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A Hand Note on
Physiology
A Hand Note on Physiology
Composed & distributed by bdvets.wordpress.com authority Page 2
A Hand Note on
Physiology
Veterinary & Animal Science
bdvets.wordpress.com
Composed & Designed by
Md. Arifur Rahman
A big thanks to
Nur Ahmed
Resources www.wikipedia.org
physiology.org
physiology.ucla.edu
physiology.case.edu
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Physiology
Physiology is a biological science which deals with the normal function and phenomena of living organism.
Cellular physiology
Cellular physiology is the branch of physiology which deals with the natural function and phenomena of live cell.
The basic theme of physiology is the interaction between a living organism and it’s environment.
Major Branches of Physiology
Some major branches of physiology are as follow:
Cell Physiology/Cytophysiology
This branch deals with the functioning of a cell. It includes the study of growth, maintenance, regulation and division of a cell and interaction between the nucleus and the cytoplasm. It may be further divided according to the particular organelle we are studying. For example, in membrane physiology we study the functioning of cell membranes.
General Physiology
In general physiology, those functions and vital processes are focused which are common to all living organisms.
Special (or Organ) Physiology
In this branch, functioning of a particular organ is studied.
System Physiology
In this branch, functional aspects of a particular system of the body are studied. System physiology can be divided in to various sub-branches depending upon the system under study. For example, renal physiology deals with the functioning of the kidneys, endocrinology deals with the functioning of the endocrine system (consisting of hormones and endocrine glands), immune physiology deals with the functioning of the immune system, etc.
Pathophysiology/Morbid Physiology
In this branch, disordered functions or functions in diseased tissues are studied.
Developmental Physiology
In this branch, physiological processes are studied in relation to their embryonic development.
Comparative Physiology
In this branch, physiological processes of different species are compared with one another.
Environmental Physiology
In this branch, physiological processes occurring in living organisms are studied in relation to their environment. It includes the study of adaptations that occur in organisms under different evironmental stresses.
Exercise Physiology
In this branch of physiology, we study different processes and changes that occur in body during exercise. It also includes the study of long lasting effects of exercise on the body and the beneficial or adverse effects of exercise in various pathological conditions.
Space Physiology
Physiology
Basic theme of Physiology
Branches of Physiology
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In this branch, physiological processes and changes are studied in relation to the space, that is, in astronauts.
Aviation Physiology
In this branch, physiological processes and changes are studied in relation to the aircraft pilots.
High Altitude Physiology
This branch deals with the study of physiological processes and adaptations taking place in the people living at high altitudes.
Deep Sea Physiology
In this branch, physiological processes and changes are studied in the people who have to go deep in the sea. These people include professional divers and navy submarine crew.
Cell
Cell defined as structural & functional unit of the living organism.
Cell organelles chronologically
1. Cell membrane
2. Cytoplasm
Mitochondria
Endoplasmic reticulum
Ribosome
Golgi bodies
Lysosome
Chromosome
3. Nucleus
Nuclear membrane
Nucleoplasm
Nuclelous
Chromatin
Biological cell
Biological cell is called especial for life because it is the structural and functional unit of the living organism.
Basic characteristics of Biological cell
1. It needs energy to function.
2. Every cell generates it’s own energy. 3. Most of the cell have the capability to reproduce it’s own species.
Cell membrane
Cell membrane is a thin elastic structure composed of lipid bi-layer interposed with sandwitch of protein that
envelops the cell. The lipid bi-layers are phospholipid and cholesterol.
The phospholipid have a phosphate radical that is hydrophilic (water soluble) and a fatty acid radical that is
hydrophobic (fat soluble). The cholesterol has hydroxyl (OH-) radical and sterol radical. The membrane protein is
mainly glycoprotein.
Function
1. Maintains the shape of the cell.
Physiology of Cell
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2. Regulates cell-cell interaction.
3. Separates and protects the nucleus and cytoplasm.
4. Acts as a selective barrier that control the passage of certain materials into and out of the cell.
5. It can recognize certain signals due the presence of cell surface receptor.
Mitochondria
1. It produces DNA, RNA, Sperm & Ovum.
2. It controls Creb’s Cycle.
3. It produces ATP & heat by means of oxidative phosphorylation. For this reason it is called power house
of cell.
4. Mitochondria contains DNA & hence these are involved in the synthesis of RNA and protein.
Ribosome
1. Ribosome plays an important role in protein synthesis.
2. It helps in metabolism of fat materials.
3. Free ribosomes are involved in the synthesis of protein for intra-cellular.
ER (Endoplasmic Reticulum)
There are two types of ER. They are-
1. Rough ER &
2. Smooth ER.
Function of RER (rough endoplasmic reticulum)
1. The synthesis of phospholipid.
2. Helps in synthesis of protein.
3. The assembly of multi chain proteins.
Function of SER (smooth endoplasmic reticulum)
1. Participates in lipid synthesis
2. Participates in contraction process of muscles.
3. Participates in metabolism of lipid, certain fat(?) in Liver Cell.
Golgi body
1. Helps in secretion of hormones.
2. Helps in the making of acrosome of sperm.
3. Modification of protein, synthesized RER, packaging and placing of these proteins to the specific sites
within the cell.
Lysosome
1. Helps in Mitosis Cell Division.
2. Plays an important role the cell economy by acting as Intracellular Schavangers.
3. They digest foreign particles and unwanted cell organelles.
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Membrane Transport
a) Non carrier mediated transport.
eg:
-Simple diffusion
-Osmosis
b) Carrier mediated transport.
eg:
-Facillated diffusion
-Active transport
-Co-transport
-Counter transport
-Endocytosis, Pinocytosis,
Phagocytosis.
Mechanism of membrane transport
Difference between Active transport and Facilitated Diffusion
SL Points Active Transport Facilitated Diffusion
01 Movement of molecule or ions
Movement of the molecule and/or ions from lower concentration to higher concentration.
Movement of the molecule or ions from higher concentration to lower concentration.
02 Energy Energy is utilized. No need of energy.
Carrier mediated transport
Four type of transportation are available-
1. Facilitated diffusion
Movement of the molecule and/or ion from higher concentration to lower concentration by binding with carrier protein in the cell membrane is called facilitated diffusion.
eg: - Absorption of fructose from the gut.
- Glucose or amino acid is transported from cell to extra cellular fluid.
Criteria of facilitated diffusion:
1. Carrier is needed. 2. No need of energy. 3. Molecule or ions move from higher concentration to lower concentration.
2. Active transport
Movement of the molecule and/or ions against concentration and electrochemical gradient by binding with carrier protein and utilization of energy (ATP).
Membrane transport system
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eg:
- Na+-k+ pump in almost all cells in the body.
- H+-K+ pump or proton pump in gastric cell.
- Na+-H+ exchanges in renal tube.
Criteria of active transport
1. Carrier is needed.
2. Energy is utilized. 3. Transport of substance against concentration gradient and electrochemical gradient (Lower to higher).
3.Co-transportation
Movement of two substances in the same direction across the membrane by carrier protein is called sys-port or co-transport.
eg: Glucose entry with Na+-k- pump.
4.Counter-transportation
Movement of two substances in opposite direction across the membrane by a currier protein is called counter-transport or antiport.
eg. Na+-K+ pump.
We also found two types of carrier mediated transport systems. These are-
1.Endocytosis
It is an energy dependant process by which the cell membrane engulf particulate matter or extracellular fluid along with content. It is biologically important for the uptake into cell of substance of large molecular weight such as protein which can’t otherwise cross the plasma membrane.
It has two forms-
Pinocytosis (cell drinking): Endocytic uptake of soluble materials into cells.
Phagocytosis: It refers to the engulfing the particles by the cell. eg. Bacteria and virus neutrophil.
2.Exocytosis
Release of intracellular substances into the extracellular fluid by fusion or intracellular vesicles with the plasma membrane is called exocytosis. eg. Release of peptide hormone and secretion of exocrine gland in the gut.
Basic difference between ECF and ICF
SL Points Extra Cellular Fluid Intracellular Fluid
01 Definition The fluid which is present outside of the cell is called Extra cellular fluid.
The fluid which is present inside the cell is called intracellular fluid.
02 Contains less protein. Contains high protein.
03 In the extra cellular fluid the amount of Na+, Cl- ,HCO3
- is very high. In the intracellular fluid the amount of Amino acid K+, Mg++ is very high.
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Na+-K+ pump
It is one of the most important active transport mechanism in the body. It also one of the major energy using process in the body.
Movement of 3Na+ ions from inside to outside the cell with simultaneous movement of 2K+ ions from outside to inside by splitting ATP is called Na+-K+ pulp.
Function
1. Responsible for membrane potential. 2. Control of cell volume. 3. Basis of nerve function. 4. There is a link between Na+ and K+ transport and
metabolism.
The greater rate of pumping the more ADP is formed. The supply of ADP determines the rate at which ATP is formed by oxidative phosphorylation.
Related Question:
Q. Mention the most important active transport process in the body with their function.
Physiological importance of Na+-K+ pump in preventing cell bursting.
One of the most important functions of the Na+-K+ pump is to control the volume of the cells, without function of
this pump, most cell of the body will swell until they burst. If a cell begins to swell for any reason, this device pumps three Na+ ions from inside to the outside the cell with simultaneous movement of 2K+ ions from outside to inside by splitting ATP. Also the membrane is far permeable to sodium ions than potassium ions. So, once the sodium ions are on the outside, They have a strong tendency to stay there. Thus this represents a continual net loss of ions out of the cell as well. So, in this way Na+-K+ prevents the cell volume from bursting.
Figure: Na+-K+ Pump
Na+-K+ pump
The process of moving sodium and potassium ions across the cell membrance is an active transport process involving the hydrolysis of ATP to provide the necessary energy. It involves an enzyme referred to as Na+/K+-ATPase. This process is responsible for maintaining the large excess of Na+ outside the cell and the large excess of K+ ions on the inside. It accomplishes the transport of three Na+ to the outside of the cell and the transport of two K+ ions to the inside. This unbalanced charge transfer contributes to the separation of charge across the membrane. The sodium-potassium pump is an
important contributer to action potential produced by nerve cells. This pump is called a P-type ion pump because the ATP interactions phosphorylates the transport protein and causes a change in its conformation.
Na+-K+ cv¤c
Na+-K+ cv¤c nj †mvwWqvg Ges cUvwmqvg Avq‡bi GKwUf Uªv݇cvU© cÖ‡m‡mi gva¨‡g †mj †gg‡eªb AwZµg Kivi cÖwµqv hv kw³ Drcv`‡bi Rb¨ ATP Gi nvB‡WªvjvBwmm Gi mv‡_ RwoZ | G‡Z Na+/K+-ATPase GbRvBg KvR K‡i | GwU †mj †_‡K AwZwi³ gvÎvq Na+ †ei n‡q hvIqv I †m‡ji g‡a¨ AwZwi³ gvÎvq K+ Gi cÖ‡ek wbqš¿‡Yi Rb¨v `vqx | G‡Z 3wU †mvwWqvg Avqb †ei n‡q hvq Ges 2wU cUvwmqvg Avqb cÖ‡ek K‡i | Pv‡R©i GB AmgZv †gg‡eª‡bi gva¨‡g c„_K _v‡K | bvf© †m‡ji Action Potential ˆZwi‡Z †mvwWqvg-cUvwmqvg cv¤c ¸i“Z¡c~Y© Ae`vb iv‡L | ATP Gi gva¨‡g Uªv݇cvU© †cÖvwU‡bi dm‡dvivB‡jkb NUvi d‡j cv¤cwUi MvVwbK cwieZ©b nq e‡j GB cv¤c †K "
N O
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Na+-K+ pump
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Blood
Definition
Blood is a specialized type of liquid connective tissue composed of fluid portion “Plasma” and cellular elements circulating through the cardiovascular system and carrying substances essential for living.
Composition Blood composed of mainly two compounds-
1. A cellular fluid portion or plasma – 55% 2. Cellular elements or formed elements – 45%
Special feature of blood
Color: i) Red due to hemoglobin (Hb), ii) Arterial blood is bright red due to oxyhemoglobin, iii) venous blood is dark red due to carboxyhemoglobin.
Specific quality: 1.050-1.060.
pH: 7.4 average.
Reaction: Alkaline.
Volume: 5-6 L.
Osmotic pressure: 25-30 mmHg.
Temperature: 37º average.
Function of blood
Blood performs mainly two major functions-
1. Transport
2. Defense of the body against infection 1. Transport
i. Transport of respiratory gases (O2 and CO2) RBC carries O2 by binding with hemoglobin fromlung to tissue and carries CO2 from the tissue to lung.
ii. Transport of nutrients from GIT to tissue. iii. Transport metabolic waste products to the site elimination.
2. Defense of the body against infection 3. Blood act as a vehicle for hormones and other agents. That regulates cell function. 4. Blood carries antibody for immunity of the body. 5. Blood contains buffer system. These contributing the regulation of acid-base balance in the body. 6. It also maintains water balance. 7. Blood regulates body temperature.
Hematopoiesis
It is a process by which blood cells are produced under normal physiological condition from blood forming organ i.e: bone marrow with the action of growth factor.
Growth factors of Hemopoiesis
1. Erythropoietin 2. Interleukins 3. Thrombopoietn 4. Colony stimulating factor
1. Erythropoietin
Proliferation and differentiation of erythrocytes.
2. Interleukins
Proliferation and differentiation of lymphoid progenitors.
Physiology of Blood
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Plasma
Solid 10%
Inorganic
Na+, K+, Ca++, Mg++, HCO3
-, CL-, Mn, Iron, Copper etc.
Organic
Plasma protein
-Albumen: Colloidal
-Globulin: Defense
-Fibrinogen: Blood clot
Various enzymes
Blood clotting factors
Antibody
Hormones
NPN as Urea, Uric acid, Creatinine
Neutral fat, phospholipid, cholesterol, glucose, amino acid
Antitoxin
Water 90%
3. Thrombopoietin
Stimulates the production of megakaryocytes.
4. Colony stimulating factor
Proliferation and differentiation of myeloid progenitors (eosinophil, neutrophil, basophil).
These all types of growth factors are produced from T-lymphocyte, monocyte, endothelial cells, fibroblast cells and kidney.
Plasma Plasma is the fluid portion of the blood which is a vasculareable(?) solution containing water and immense number of ions, organic and inorganic substances is called plasma.
Physical and biological features of plasma
Amount: 55% of blood. Color: Yellowish.
Chemical nature: Colloidal solution.
pH: 7.33-7.51 over 7.4
Sp. gravity: 1.026
Composition
Plasma
Figure : Megakaryocyte
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Serum Serum is what remains after the formation of fibrin clot. (The fluid portion of blood after removal of clot of coagulated blood).
Basic difference between plasma and serum
SL Points Plasma Serum
01 Definition Fluid portion of blood, containing Acellular and blood clotting factor. (Acellular fluid portion of blood)
Serum is what remains after the formation of fibrinogen clot. (The fluid portion of blood after removal of clot of coagulated blood.
02 Fibrinogen Contain fibrinogen. No fibrinogen in serum, No prothrombin, factor v and viii.
03 Serotonin Serotonin content is low. Serotonin content is high.
04 Clotting factor Plasma does not contain any degradative product of clotting factor.
Contain some degradation product of clotting factor.
05 Color is not characteristic. Straw is color.
Difference between blood and plasma.
SL Points Blood Plasma
01 Definition Blood is a specialized type of liquid connective tissue.
Plasma is the a cellular fluid portion of the blood.
02 Color Color is red due to presence of hemoglobin (HB).
Color is yellowish due to the absence of hemoglobin (HB).
Serum
i³im (Plasma)
i³im nj i‡³i GKwU ¸i“Z¡c~Y© Dcv`vb| GwU nvjKv njy`vf Zij hv mvaviYZ †`‡ni wewfbœ cÖKvi i³‡Kvl aviY K‡i| gvbe †`‡ni kZKiv cÖvq 55 fvMB nj i³im| i³im g~jZ †Kvlc`©vi evB‡ii i³MnŸ‡ii ga¨Kvi Zij c`v_©| Gi 95 kZvsk nj cvwb Ges 6-8% kZvsk wewfbœcÖKvi Avwgl (A¨vjeywgb, †Mveywjb, dvBweª‡bv‡Rb), M“‡KvR, †K¬vwUs Dcv`vb, B‡j‡±ªv‡cU (Na+, Ca2+, Mg2+, HCO-
3,
Cl-, BZ¨vw`), ni‡gvb Ges Kve©b WvBA·vBW (i³im wecvKxq msenbZ‡š¿i g~j gva¨g)| i³im gvbe‡`‡ni Avwgl msi¶‡Yi KvRI K‡i _v‡K| GwU i³MnŸ‡ii AwfmªeY cÖwµqv AUzU iv‡L hv‡Z i‡³ wewfbœ B‡j‡±ªvjvBU h_vbycv‡Z we`¨gvb _v‡K Ges gvbe‡`n RxevYy msµgY I wewea i³‰eKj¨ †_‡K gy³ _v‡K| i³im‡K ˆZwi Kiv nq †mw›UªwdD‡R A¨vw›U‡Kv¸‡j‡›Uavix weï× i‡³i bj‡K w¯cwbs K‡i; hZ¶Y bv i³‡Kvl b‡ji wb‡P c‡o hvq| Gici i³im Ab¨ GKwU cv‡Î †X‡j c„_K Kiv nq| i³i‡mi NbZ¡ cÖvq 1025 †KwR/wgUvi3, ev 1.025 MÖvg/wgwjwjUvi3 i³ wmivg nj †K¬vwUs Dcv`vb e¨ZxZ GKai‡Yi i³im|) cvRgv‡d‡iwmm nj GKai‡Yi †gwW‡Kj †_ivwc hvi g‡a¨ Av‡Q i³im G·‡UªKkb, wPwKrmv Ges wiBbwU‡MÖkb|
N
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Erythrocyte/RBC
Erythrocyte is a circular biconcave disc with a mean corpuscular diameter of 7.2 m. erythrocyte contains no nucleus and no cytoplasmic organelles. Most part if the mature RBC contains Hemoglobin.
Life span of blood cells
SL Blood Cells Life Span
01 RBC 120 days
02
WBC
Granulocytes
Neutrophil 2-4 days
Eosinophil 8-12 days
Basophil Basophil 12-15 days
Agranulocytes
Monocytes
10-20 hours in the blood. As tissue macrophages , can live for month unless destroyed which performing phagocytic function
Lymphocytes ___week or months that life span depends on the body’s need for this cells.
03 Platelets About 8-10 days/10 days
Ref. Guyton 423 page
Cellular part of Blood
How to get cell free blood
If we centrifuge the blood with the 2500-3000 rpm then it is divided into three layers, the cellular
portion of the blood let down in the lower portion of the tube. After aparting (mwi‡q †djv) the upper
two portion we get the cell free blood. N O
T E
Serum
Serum is the liquid portion of the blood obtained after a serum sample tube has been allowed to clot and is centrifuged. The serum tube may or may not contain a separator gel. The tubes that contain separator gel are commonly called Serum Separator
Tubes (SST®). For those tests requiring serum, please use the following procedure:
Use a tube with no anticoagulant (i.e. red-top tube, marbled-top tube or SST®).
Invert the tube 5 or 6 times after drawing to hasten the clotting process. Do not shake the tube. Shaking may cause hemolysis and result in specimen rejection.
Allow the specimen to clot in an upright position for 30 minutes, then centrifuge for 10-15 minutes at 2500-3000 RPM.
Serum must be removed from the clot within 45-60 minutes after collection. Transfer the required amount of serum to a plastic transfer tube and cap securely. When removing the serum, be sure not to aspirate any blood cells. If the blood was collected in a SST®, transferring the serum into a plastic transfer tube after centrifugation is not necessary.
Please label the plastic transfer tube with the patient's full name (first and last), collection date, and the requested test(s). wmivg wmivg m¨v¤cj wUD‡e i³ RgvU evuav‡bvi c‡i †mw›UªwdDRW (‡mw›UªwdDR †gwkb Øviv cÖ‡mwms) Kivi ci cvIqv Zij Ask | wmivg wUD‡e †mcv‡iUi †Rj (c„_KxKiY †Rj) e¨envi Kiv n‡ZI cv‡i bvI n‡Z cv‡i | wmivg wUD‡e †mcv‡iUi †Rj e¨envi Ki‡j Zv‡K "wmivg †mcv‡iUi wUDe" e‡j | wmivg ˆZwii c×wZt Gw›U‡Kv¸‡j›U wenxb GKwU †U÷wUDe wb‡Z nq | i³ RgvU evuav Z¡ivwš^Z Ki‡Z †U÷wUDewU‡K 5-6 evi Dëv-cvëv Ki‡Z nq | wUDewU‡K SvuKv‡Z
nqbv †h‡bv wn‡gvjvBwmm bv N‡U Ges bgybv bó bv n‡q hvq | bgybvwU Dc‡ii As‡k RgvU nIqvi Rb¨ 30wgwbU A‡c¶v Ki‡Z nq Ges c‡i 2500-3000 RPM (ivDÛ cvi
wgwbU) G 10-15wgwbU mgq a‡i †mw›UªwdDR Kiv nq | 45-60wgwb‡Ui g‡a¨ Aek¨B wmivg‡K RgvU Ask †_‡K c„_K Ki‡Z n‡e | cwiwgZ cwigvY wmivg GKwU
cvw÷K UªvÝdvi wUD‡e ¯’vbvš—i Kiv nq Ges fvjfv‡e wUD‡ei gyL eÜ Ki‡Z nq | wmivg c„_KxKi‡Yi mgq mZK© _vK‡Z nq †hb G‡Z †Kv‡bv i³KwYKv hy³ bv _v‡K | hw` i³ wmivg †mcv‡iUi wUD‡e (SST) msMÖn Kiv nq Zvn‡j Zv †mw›UªwdDR Kivi ci cvw÷K UªvÝdvi wUD‡e ¯’vbvš—i Ki‡Z nq bv |
cvw÷K UªvÝdvi wUDe †ivMxi c~Y© bvg, i³ msMÖ‡ni ZvwiL Ges cÖ‡qvRbxq †U‡÷i bvgmn fv‡jvfv‡e †j‡ewjs Ki‡Z nq |
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Erythropoiesis Formation of mature red cell under normal physiologic condition is called erythropoiesis.
Factors that are essential for RBC maturation.
1. Vitamin B12 : Nuclear division and metabolism of DNA synthesis. 2. Folic acid, Vitamin C, Vitamin E: Act as a catalyst of DNA synthesis. 3. Riboflavin: Normal erythropoiesis.
4. Amino acid: Globin synthesis. 5. Iron + pyridoxin: Heme synthesis.
Regulating factors of Erythropoiesis
1. Hypoxia
Hypoxia means decrease of tissue O2 which occurs in high altitudes, anaema, cardiac, pulmonary disease. Hypoxia stimulates erythropoiesis by erythropoietin ( a local hormone secreted by kidney and liver is response to tissue hypoxia).
2. Erythropoietin
In response to tissue hypoxia kidney release a horemone erythropoietin that on bone marrow and stimulates. Erythropoietin is a local hormone mainly secreted by kidney (90%) and liver (10%) is response to tissue Hypoxia.
3. Endocrine gland
Gonad, pituitary, thyroid, adrenal gland exerts a secondary modifying influence on erythropoiesis.
4. Miscellaneous
Vitamin, bile salt, diet-amino acid etc.
Development of RBC
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Erythropoietin stimulates
Increase proliferation
of RBC
Maturaion of RBC
Increase production
Increase Hb concentration
Increase tissue O2
No hypoxia
(-)ve feedback to
kidney
Feedback mechanism of Erythropoiesis.
Relation between Hypoxia, Erythropoietin in Erythropoiesis
Figure: Feedback mechanism of Erythropoiesis
Decrease arterial O2 content
Hypoxia developed
Erythropoietin realease from kidney
Hypoxia
Hypoxia
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Stem cell
Mature RBC. Life span 120 days
Passing through RE system
(Spleen, Liver)
Destruction of RBC
Others Hb
Heme
Re-utilized further
Biliverdin
Liver
GIT reduced by bacteria
Urobilinogen
Pass through kidney
Urobilinogen
Gives the color of urine
Through feces
Stercobilinogen
Gives color of feces
Globuline
Re-utilize
Fate of RBC Donation of blood after 120 days is scientifically correct. Because, after 120 days RBC are destroyed ultimately.
Figure: Fate of RBC
Fate of RBC
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Related Questions:
Q. Do you think donation of blood after 120 days is scientifically correct? Please explain in relation to fate of RBC.
FAQ1. Which solution between Colloid and Crystalloid therapy is more practical in severe blood loss condition? Explain with justification.
Colloid solution is more practical than crystalloid’s in severe blood loss condition. This type of solution contains protein is colloid. If the severe blood loss occur colloid solution must be added.
eg. Blood is a colloid solution.
If the severe blood loss occur colloid solution should be used because, colloids are better than crystalloids at expanding the circulatory volume, because there larger molecules are retained more easily in the intravascular space and increase osmotic pressure.
FAQ2. Which solution between colloid and crystalloid therapy is more practical in severe dehydration? Explain with justification.
Crystalloid solution is more practical than colloid in severe dehydration. Because this solution passes freely through cell membranes and vascular system walls. They flow out of the vascular system rather quickly. So, the use of crystalloid solution is more scientific than the use of colloidal solution.
Or, this type of solution contains small molecules that passes freely through the semi permeable membrane and vascular system walls and it spreads all the whole body very rapidly.
FAQ3. Why hypoxia beneficial for RBC. Explain this.
If hypoxia occur, it stimulates erythropoiesis by erythropoietin. In response to tissue hypoxia kidney release hormone erythropoietin that act on bone marrow and increases the proliferation of RBC.
So, Hypoxia is beneficial for RBC production or Erythropoiesis.
Hypoxia
This hormone act on bone
marrow (Red)
RBC production occur
Erythropoietin Hormone
Hypoxia Kidney release
FAQ- Frequently Asked Questions
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FAQ4. Mention the development of RBC.
RBC is developed in certain exclusive part of the body. Those are as follows-
1. Mesoblastic
RBC developed in mesoderm of yolk sac (Up to 8 week of life).
2. Hepatic
RBC developed in liver up to 1 month before birth.
3. Myeloid
RBC developed in bone marrow.
Blood coagulation Blood coagulation means the conversion of fluid blood to a solid gel or clot by conversion of soluble fibrinogen to insoluble fibrin.
Remaining as fluid of blood in the blood vessel
Due to-
1. Blood remain separated from the activator factor by the intact endothelium. 2. Presence of natural anticoagulant (Heparin) in the circulation. (Protein S, Protein C). 3. By the balancing action of prostocycline (PGR and thromboxane)
In case of:
Why blood clot do not occur within the normal vascular system? The answer of question mentions above.
Figure : Remaining fluid of blood in the blood vessel
Prostocycline is synthesized by the endothelial cell
Thus prevent platelets
aggregation on the normal
vessel wall
Thus blood remain fluid within
the vessel
It produce vasodilution
Opposes the action of
thromboxane
Blood Coagulation
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NB:
Some essential knowledge about different types of coagulants
SL Name of anticoagulant Origin and function
01 Heparin -Produced by the Mast cell and Basophil cell granules -It inhibits the thrombin formation
02 Protein C -It is synthesized by liver -It is a Vit-K dependent protein.
03 Protein S Synthesized by liver
Fibrinolysis
1. Streptokinase 2. Heparin 3. Hirudin
Anticoagulant
Anticoagulant are the chemical agent which prevent or hamper the coagulation process.
eg: Natural anticoagulant prevent clot formation inside the vessel.
Types of anticoagulant
There are two types of anticoagulant
1. Natural anticoagulant. 2. Artificial anticoagulant.
SL Natural anticoagulant Artificial anticoagulant
01 eg. -Antithrombin iii -Heparin -Protein C and Protein S -Other macro
eg. -EDTA -H-Na cytrate -Sodium oxalate
Difference between Natural anticoagulant and Artificial anticoagulant
SL Point Natural anticoagulant Artificial anticoagulant
01 Location They are naturally found in the vascular system.
This type of coagulant are made artificially by chemical agent.
02 Composition
Natural anticoagulant are produced by many different cells of the body, but especially large quantities are formed by the basophilic mast
cells located in the pericapillary connective tissue throughout the body.
It is artificially prepared by chemical substances.
Related Questions:
Q1. Define Blood Coagulation. Why blood remain fluid within the blood vessel?
Q2. Define Anticoagulant with their example.
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Mechanism of coagulation process of blood
Source: Wikipedia; modified
Related Questions:
Q. Mention the mechanism of how blood is coagulated during an external cut.
FAQ1. Compare the extrinsic and intrinsic pathway of blood coagulation.
SL Traits Extrinsic Pathway Intrinsic Pathway
01 Initiasion
Begins with the trauma of blood vessel or exposure of blood to extravascular tissue.
Begins with trauma to blood itself or exposure of blood to subendothelial matrix.
02 Clotting factors involve in prothrombin
activation
Factor III,IV,V,VII,X Factor IV,V,VIII,IX,X,XI,XII
03 Duration Rapid process. Slower process.
FAQ- Frequently Asked Questions
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Disorder of Hemostatis
1. Bleeding time
It is the time between bleeds, starts and stoppage of bleeding.
Bleeding time: 3-10 min.
2. Clotting time
It is the time between withdrawal of blood and clot formation.
Clotting time: 5-11 min.
3. Prothrombin time
Prothrombin time is measured by adding tissue thromboplastin, Ca to patient’s plasma.
Prothrombin time: 16-18 sec.
FAQ2. How does Vit-K helps in coagulation?
Maximum coagulation factor synthesis in the liver by the help of vit-K. Here, vit-K acts as a catalyst. Vit-K can’t help directly in blood coagulation, but it helps indirectly in blood coagulation.
Vit-K
FAQ3. How the coagulation process is hampered due to the damage of liver? Is Vit-K deficiency causes hamper of coagulation process? If it is true, explain.
The coagulation process is due to the damage of liver because the liver is the main organ for the synthesis of various coagulation factors. So, if any damage occur in liver or hepatocyte, the liver or hepatocyte incapable to synthesis the coagulation factor. Ultimately the coagulation factor is hampered.
Otherwise the deficiency of Vit-K or lack of Vit-K also hampers the coagulation process. Because, Vit-k acts as a catalyst when the coagulation factors are synthesized from the liver. So, Vit-K deficiency or lacking causes
hamper of coagulation factors synthesis.
Liver
Coagulation occur
Coagulation fact or synthesis
Figure: Function of Vit-K in blood coagulation
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Hypoxia
Hypoxia means decrease of tissue O2 which occurs in high altitudes, anaema, cardiac, pulmonary disease. Hypoxia stimulates erythropoiesis by erythropoietin ( a local hormone secreted by kidney and liver is response to tissue hypoxia).
Effect if Iron during Hypoxia
Figure: Effect of Iron in the Hypoxia
Related Questions: Q. Why Iron containing food should be supplied during Hypoxia?
During Hypoxia
Hemoglobin composed of
Heme and Globuline
Hemoglobin can’t carry O2 to
the tissue
Iron containing food increase
the amount of Heme (Fe++) in
the blood
The hemoglobin increases
Carry the O2 to the tissue
Ultimately Hypoxia (recover)
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Acidosis A decrease in the pH of Arterial plasma below 7.4 due to excessive acid accumulation, the loss of base is called acidosis. Or, Acidosis is a condition in which the acidity of body fluid and tissue abnormally great. i.e: when body pH fall below the normal value of 7.4. A pH of below 7.0 is considered life threatening.
There are two types of acidosis 1. Respiratory acidosis
It occurs as a consequence of hypoventilation when CO2 accumulates in the body as Carbonic acid.
2. Metabolic acidosis
It is caused by various changes in the body’s metabolism.
Acidosis is characterized by
1. HCO3- / S.P(?) CO2 ratio becomes less than 20:1.
2. pH falls i.e(?) H+ increased. 3. Negative base excess. 4. Hyperkalacmia (cellular K+ enter. ECF and H+ enter into cell).
Alcalosis A condition in which the alkalinity of body fluids and tissues is abnormally high. Alcalosis may be associated with loss of through vomiting or with excessive NaHCO3 administration.
Or, an increase in the pH of arterial plasma abnormal (?) 7.4 due to acumulation of base or the loss of acid is called alcalosis or alcalomia.
Alcalosis is characterized by
1. HCO3- /SP(?) CO2 ratio becomes more than 20:1
2. pH rise ie: H+ concentration decrease.
3. Positive base excess. 4. Hypokalacmia
Buffer A solution containing weak acid and it’s salt of strong base having capacity to resist change of ppH when moderate amount of acids or bases are added to it is called a buffer system.
Some important Buffer system Physiological buffer system in the body
1. Bicarbonate buffer system 2. Phosphate buffer system 3. Protein buffer system. 4. Hemoglobin buffer system.
1) Bi carbonate buffer system will contain HCO3- when a base is added it will liberate the H+ and produce water
combining with OH- ion of the base there for reducing the effect of the base and when an acid is added it will accept the H+ ion and for H2CO3 therefore the effect of the acid will be nullified.
2)Phosphates are H2O4- or HPO4
2- and it will also have the functions as mentioned in the above.
3)Proteins have an NH2 group and well as a COOH group both attached to the same molecule. Therefore when acid is added the NH2 group will neutralize it and when a base is added COOH group will neutralize it reducing the alkalinity.
Therefore all these chemicals found in the blood and other body tissue will maintain the blood pH level at a constant level acting as natural buffers.
Polycythaemia Polycythaemia is defined as an increase of hemoglobin (Hb), PCV and red cell count above the normal reference range. PCV is more reliable indicator for polycythaemia than Hb.
Types of polycythaemia
1. Primary polycythemia (polycythaemia vera): when there is pathological proliferation of red cells without Erythropoietin stimulation, then it is called polycythaemia vera. Due to
Bone marrow tumor
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X-ray radiation.
2. Secondary polycythaemia (physiological variety): When there is a physiological response pathological stimulus as in hypoxia in which the production of erythropoietin is increased. So, red cell is increased from secondary(?) to hypoxia. Due to-
Hypoxia
Pulmonary disease
Renal disease
Stress
Dehydration
Burn
Abnormal hemoglobin which has high O2
Affinity.
Related Questions:
Q. Define with example Acidosis, Alkalosis, Buffer and Polycythemia.
FAQ1. Why after severe vomiting Alkalosis occurs?
After severe vomiting the body losses excessive amount of acid or due to the accumulation of base after the vomiting.
During severe vomiting
Blood pH is increased
Body losses excessive amount
of acidic fluid
Alkalosis occurs
FAQ
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FAQ2. Why after severe diarrhoea Acidosis occurs?
After the severe diarrhoea, the body loss excessive amount of basic fluid. For this reason the rate of blood pH decreases then acidosis occurs.
Hemoglobin Hemoglobin is a complex globular protein molecule in the RBC consists of a red pigment heme and globulin or globin.
Types of Hemoglobin
1. Oxyhemoglobin
Oxyhemoglobin of hemoglobin is called oxyhemoglobin. It is dissoluble hemoglobin-oxygen complex. One molecule of Hb can carry 4 molecule of O2 due to presence of 4 heme unite in 1 molecule Hb.
Iron remaining requires Fe++ state in oxyhemeglobin. Hb bind loosly and reversly with O2.
2. Methehemoglobin
Oxidation of Hb is called methemoglobin or Ferrihemoglobin. Here Iron remains in Fe+++ (Feric) state.
3. Carboxyhemoglobin
Combination of CO with Hb forms carboxyhenoglobin. The affinity of CO for Hb is much more higher than O2.
The color of HbCO is cherry red.
4. Carbonylhemoglobin
The Hb-CO2 complex is designated as carbonylhemoglobin.
Function of Hb.
Transport of respiratory gas
Hb plays an important role in carrying O2 from lung to tissue in the forms of oxyhemoglobin and returning CO2
from tissue to lung.
Acts as a buffer
Human Hb molecule contains 36 histidine residue with pK value near pH=7 makes the Hb an excellent buffer in the physiological pH range. Then it contributes in acid-base balance.
During severe diarrhoea
Blood pH is decreased
Body losses excessive amount
of basic fluid
Acidosis occurs
Hemoglobin
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Synthesis of Hemoglobin
Hb starts to synthesis in the intermediated normoblast stage of RBC development. Heme synthesis ocurs in the mitochondria of developing RBC. The major rate limiting step is the conversion of Glycine and Succinyle CoA
to α-amino laevuilic acid (ALA) witth the help of ALA synthetase. Then a series of synthetic steps are occurred
and forms Pyrrole molecules. Then 4 pyrrole molecules combine to form/to produce protoporphyrins. Finally iron
is inserted into the mitochondria to form heme. Heme is then inserted into the globin chain to form hemoglobin.
Step 1
Succenyl CoA + Glycine Pyrrole molecule
Step 2
4 Pyrrole molecule Protoporphyrin
Step 3
Protoporphyrin + Iron (Fe) Heme
Step 4
4 Heme + Glubin Hemoglobin
Factors for Hemoglobin synthesis
Globin
Iron
Cobalt (RBC maturation)
Related Questions:
Q. Write down the synthesis of Hemoglobin with mentioning the four exclusive steps and associated factors.
Anaemia Qualitative and quantitative deficiency of the hemoglobin or RBC in the circulation in respect of age and sex of the individual is called anaemia.
Anaemia is not a disease but it is a sign of disease.
Types of anaemia
1. Deficiency anaemia: Due to deficiency of Iron, Vit-B12 and folic acid.
Heme synthesis
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2. Aplastic anaemia: Due to depression of bone marrow function. 3. Hemolytic anaemia: Due to excessive red cell destruction. 4. Sickle cell anaemia: Due to abnormality in the Hb structure.
Thalassemia It is an inherited impairment of Hb production in which there is a partial or complete failure to synthesis a specific type of globin chain.
FAQ1. Write down the advantages or importance of Encasing (residing) the Hemoglobin within the RBC.
Incase of RBC, the Hb will float free and invite some hazards-
1. The freely floating Hb will greatly increase the osmotic tension of plasma. High osmotic tension of plasma is dangerous. So, to remain alive, in this setup, the volume of plasma shall have to be great.
This means our blood volume shall have to be tremendous and our body size unmanageable.
2. A small fraction of free hemoglobin would be filtered through the kidney. This camn block the kidney tubules under suitable condition.
FAQ2. Write down the advantages or importance of Biconcavity of RBC.
Importance of Biconcavity of RBC
1. Because of the biconcavity, the thickness of the RBC at it’s center is only flattened. The oxygen from plasma has to travel to a very small distance to reach the Hb.
2. The presence biconcavity increases the surface area of the RBC, so that the oxygen gets a bigger area for diffusion and the diffusion is facilitated.
3. Because of the biconcavity, the RBC can squeeze itself in a narrow capillary more easily.
Advantages of absence of nucleus in RBC
1. Provides some extra spaces for the storage of large amount of hemoglobin within the RBC. 2. No –nucleated state of RBC also facilitates its movement in the way that it provides special ability to
change it’s shape avoiding creation of any extra tension on the membrane while passing through narrow capillaries.
FAQ3. How we can separate Crystalloid solution from Colloid solution through a semipermeable membrane?
Crystalloid solution passes easily through the membrane but the colloid solution cannot pass through the membrane. Because the crystalloid solution contains small molecules. So, it can easily pass through the semipermeable membrane, on the other hand, the colloid solution contains very complex and larger molecules. So, it can not pass through the membrane.
FAQ4. Why stomach is called hemopoietic organ?
Stomach produces intrinsic factor that carries Vit-B12. This Vit-B12 is essential for RBC maturation. For this reason stomach is called hemopoietic organ.
FAQ5. Why peptic ulcerate man shows Anaemia?
Peptic means – Stomach;
Ulcer – Sore, wound.
We know that stomach is a hemopoietic organ. So, when ulceration occurred in the stomach, the stomach can not produce intrinsic factor, no carrying of Vit-B12. Ultimately RBc maturation do not occur. So, the peptic ulcerate
man shows anaemia.
FAQ
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FAQ6. How kidney disease causes anaemia?
FAQ7. Why kidney is called Endocrine gland?
Kidney is called endocrine gland because it secrets erythropoietin hormone. This hormone directly goes into the circulation and acts on the bone marrow and produces red blood cell. So the kidney is called endocrine gland.
Kidney disease occurs
The low amount of erythropoietin
stimulate low amount of bone
marrow
Kidney produces low amount of
Erythropoietin hormone
Low amount of RBC produced
Anaemia occurs
Kidney
Produces erythropoietin hormone
Enters/goes into the circulation directly
Acts on bone marrow (Red)
Produces RBC
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Pituitary gland
Erythropoietis or RBC production
Exerts(?) a secondary modified
influence on
FAQ8. Why Edema is formed during pregnancy?
During pregnancy protein passes from mother to fetus through placental blood for fetus development. As a result, protein decreases in mother’s blood, that means hypoproteinemia develops. For hypoprotinemia osmotic pressure decreases in blood. As aresult water comes to the tissue from bloods and accumulates within the interstitial space. So, edema developed.
FAQ9. Write down the basic step of Coagulation process.
Step-1
Generation of prothrombin by extrinsic and intrinsic pathway
Step-2
Conversion of prothrombin to thrombin by prothrombin activator.
Step-3
Formation of fibrin clot.
FAQ10. Is there any co-relation between RBC, Hb and PCV?
Yes, there is a positive co-relation between RBC, Hb and PCV. i.e. If RBC number increases, there is increase amount of hemoglobin and PCV or vice versa.
FAQ11. What are the causes of PCV variation?
Increased PCV: Polycythemia, Dehydration, High PCV.
Low PCV: Anaemia, Pregnancy.
FAQ12. Why Gonad- (Ovary/Testes), Pituitary, Thyroid and Adrenal gland are called erythropoietic organ?
/ RBC
/ Hb
/PCV
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FAQ13. Why energy is needed for active transport and why energy isn’t needed for facilitated by diffusion?
In active transport system the movement of molecules against concentration and electro chemical gradient by binding with carrier protein. Due to the movement of molecules against concentration in above transport system if need energy.
And on the other hand, due the movement of molecules from higher concentration to lower concentration.
FAQ14. Why Oxyhemoglobin is better Methemoglobin?
Because, oxyhemoglobin easily bind with O2. on the other hand the Methemoglobin losses it’s capacity to bind with. For this reason it can’t transport O2.
FAQ15. Why one molecule of Hemoglobin can carry 4 molecule of O2?
1 molecule of hemoglobin contain 4 heme unit. For this reason 1 molecule of hemoglobin can carry 4 molecule of
O2. Another reason is, the hemoglobin contain pyrrole ring. This pyrrole ring is responsible for carrying of 4 molecule of O2.
FAQ16. How you can collect anticoagulant free blood?
Or, How you can collect acellular blood?
Or, How you can collect coagulation factor containing blood?
At first the collected blood is mixed with anticoagulant. Then the blood is centrifused by Centrifuse machine. The separated portion of the blood in the test tube is called acellular blood or cell less blood. This is also known as plasma.
FAQ17. How will collect the serum for immediate use?
Or, how you will collect blood clotting factor free blood?
In a test tube the blood without anticoagulant is coagulated for about 1 to 2 hours at 37ºC. Then it is transferred to a refrigerator at 4ºC overnight. The following fluid out after clot retraction which is known as serum.
FAQ18. Write down the causes of anaemia.
Causes of anaemia
1. Excessive destruction of RBC. 2. Blood loss from whatever cause. 3. Decreased formation of RBC. 4. Faulty construction of RBC. 5.
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Content of WBC
Content Amount (%)
Neutrophil 40-75%
Eosinophil 1-6%
Basophil 0-1%
Lymphocyte 20-45%
Monocyte 2-10%
General properties of WBC
Diapedesis
Neutrophil and monocyte can squeeze the pores of the blood vessels. They first adhere to the endothelium and then institute through gap between two adjacent endothelial cell. This is called “Diapedesis”.
Amoeboid Motion
Neutrophils and macrophages move through the tissue by amoeboid motion.
Chemotaxis
A purposeful & unidirectional movement of neutrophil and macrophage towards the site of injury or inflammation is called “Chemotaxis”. Chemotaxix occurs due to release of chemo-attachments at the site of infection or inflammation.
Phagocytosis
Phagocytosis means cell eating, ingestion of invading microorganisms by WBC is called phagocytosis. Neutrophil is the most specialized microbial phagocyte. These cells are extensively released during acute inflammation or tissue damage.
Phagocytosis involves three steps-
1. Requirement (recognition and attachment of foreign particles). 2. Engulfment (endocytosis of foreign particles). 3. Killing or destroying of phagocytic materials.
Recruitment
Powerful chemoattractant are released at sites of infection or inflammation. This chemoattractant cause migration of neutrophil to the site of infection by two processes-
1. Increased migration and adhesion of neutrophil to the vascular endothelium. 2. Stimulating neutrophil chemotaxis, cell passes through endothelium into tissue by diapedesis.
Engulfment
Phagocytosis occurs by the formation of pseudopodia around the organism or particle to be ingested. Due to fluidity of the cell membrane the tips eventually fused to form a membrane bound vesicle phagosome. The phagosome fused with the neutrophil cytoplasmic granules to form a phagolysosome. Within this localized environment killing occurs. Ingestion of organism is much effective if the particle is first coated or opsonized with specific antibody.
Killing
Within the phagolysosome enzymatic destruction of organism occurred by two major mechanisms-
1. O2 dependent response
In which there is production of reactive O2 metabolites such as H2O2, OH- via reduction of O2 by an NADPH-oxidase enzyme.
2. O2 independent response
Due to toxic actionof preformed antionic protein enzyme continued within the neutrophilic cytoplasm.
WBC
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Pluripotential Stem cell
CFU
CFU-GEMM
CFU-baso
Basophil
(2-5 lobes)
CFU-GMEO
CFU-GM
Neutrophil
(2-5 lobes)
Monocyte
(mono nucleur)
CFU-EO
Eosinophil
(bi-lobed)
Lymphoid stem cell
T cell
T-helper cell
T-supressor cell
N K cell
B cell
Plasma cell
The super oxidase ions are discharged to the inside of the cell or into phagolysosome. Where it encounters ingested bacteria. Killing of bacteria depends on combind action of elevated pH, super oxide ion or oxygen derivatives, H2O2, OH- present in neutrophil.
Granulopoiesis ( Development of WBC) The production of granulocyte under normal physiological condition is called Granulolpoiesis. All peripheral blood cell are produced or derived from pluripotential Stem cells by a differentiation step. The earliest detectable colony forming unit CFU gives rise to CFU-GEMM that produces-
Granulocyte
Erythrocyte
Monocyte
Megakaryocyte
Stem cells also produce lymphocyte cell through lymphoid stem cells.
From CFU-GEMM the following cell groups are developed-
CFU-GMEO
CFU-baso
From CFU-GMEO Monocyte, Neutrophil and Eosinophil are produced and Basophil is produced from CFU-baso.
Figure: Granulopoiesis
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Speciality WBC cell
Diapedesis
Amoeboid motion
Kemotoxic
Phagocytosis
i. Requirement ii. Engulfment
iii. Killing
Related Questions:
Q. What is Granulopoiesis? Explain briefly. Mention the speciality of WBC cell.
Fate of Neutrophil. After phagocytosis and killing-
Necrosis and disintegration
Apoptosis formation
Macrophage ingestion.
Opsonization Optionization means “Made ready to eat”. Some pathogens have protective coats. So, phagocytes can never destroy them. Ingestion or killing of these organisms are much more effective if the particles are first coated or opsonized with specific antibody. Serum containing natural antibody opsonin which coats the particles and make
the particles acceptable to the phagocytes. This is called optonization.
Monocyte or tissue macrophage Macrophages are derived from the bone marrow precursor (Monocyte).when monocyte is in the tissue it differentiates into macrophage. Mature macrophage forms Reticulo-endothelial system (RE) in the tissue.
Macrophage like other polymerphs are capable of phagocytic and killing of microorganiss. They also secret some important products-
Cytokinage and growth factor- Interferon, IL, TNF.
Enzymes. eg. Elastase, collagenase, phospholypase.
Enzyme inhibitors. eg. α-antitrypsin, α2-macroglobin.
Lipids. eg. Leukotriens, PGE etc.
Coagulation factors. eg.Tissue factor, thromboplastin factor: α,IX,V. Function
1. Secretory function: Monocyte and macrophage secret around 100 substances.
2. Ingestion and killing of microorganisms and waste particles. 3. Regulation of hemopoiesis via the effect of 12TNF, CSF, erithropoietin. 4. Lymphocyte activation via antigen(?) presentation. 5. Killing of tumor cell via the TNF (Tumor Nacrosis? Factoer) 6. Tissue repairing and remodeling.
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Lymphocyte Lymphocytes are two types-
1. T-lymphocyte 2. B-lymphocyte
T-lymphocyte Lymphocytes derived from the thymus are called T-lymphocyte. T-lymphocyte comprises about 75% of the lymphoid population. Immature T-cell (developed from bone marrow) enter into thymus where maturation of T-lymphocytes occur by the influence of thymic epethelial hormone “Thymosin”. Finally, T-lymphocyte is divided
into four groups-
1. Helper T-cell: Immunoregulatory function stimulate B-cell for antibody production. 2. Suppressor T-cell: Reduces the immunoactivity by releasing soluble factor or messenger. 3. Cytotoxic T-cell: Killing of the cell. 4. T-cell: That mediates delayed type of hyper sensitivity reaction.
Function of T-lymphocyte
Responsible for cellular immunity by-
1. Antigen recognition- Stimulates B-lymphocyte for antibody production and capable of cell killing. 2. Produces lymphs which results delayed type of hyper sensitivity reaction.
3. Responsible for graft rejection reaction.
Immunoglobulin (Ig)
Immunoglobulins are γ-globulin fractions of plasma protein. They are glycoproteins that are produced by a highly
specific response to an antigenic challenge.
Types of immunoglobulins
Ig G Humoral antibody
Ig A Galiva, RT secration, GIT secratin
Ig M Intravascular pool
Ig D Surface of B-lymphocyte
Ig E Mast cell and basophil cell
Immune system in the health
Two types of immunities-
1. Innate immunity: A non-specific immediate response. The main component of innate immunity-
Phagocyte: Neutrophil, Monocyte, macrophage.
Other inflammatory cell: Basophil, eosinophil.
Complement system.
Acute phase reactant such as: C-protein.
2. Specific immunity: It is the hallmark of immuno system. T & B-lymphocyts are responcible for this immuno system.
Humoral immunity: This immunity is produced by B-lymphocyte that ultimately produces plasma cell and memory cell. It is the major defense against soluble antigens.
Cellular immunity: It is performed by T-lymphocyte. It is responsible for delayed allergic reaction
and rejection of transplant of foreign tissue.
B-lymphocyte Early stage of B-lymphocytes are found in the bone marrow and then enter into bursa of Fabricious or Lymphnode and completed their maturation within this. These cells produce antibody.
Mechanism of Antibody production
B-cells are capable of producing specific antibody to a given antigen. In this process, once B-cell has been exposed to specific antigen (which is recognized through immunoglobulin molecule located in the B-cell) and in
Lymphocyte
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the presence of cytokins (IL-1,6). It is activated and divided. This is called clonal expansion following this expansion step B-lymphocyte is differentiated to become plasma cell. Which produces larger amount of antibody. Plasma cells have unique features.
1. Morphologically plasma cells are distinguished by a cytoplasm containing large amount of ER (endoplasmic reticulum).
2. Have relatively short haft(?) life. 3. Finally, they die autonomously(?).
Clonal expansion of B-cell production and production of Antibody
Antigen ‘X’
B-lymphocyte (activated & divided)
Clonal expansion
Differentiation into plasma cell
Antibody Production (reactivated specifically with
Antigen ‘X’)
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Different cell of immune system
Osmosis Diffusion of water across a semipermeable membrane
(like a cell membrane) from an area of low solute concentration to an area of high solute concentration is known as osmosis.
Membrane potentials Potential developing across the membrane due to-
Na+-K+ pump.
Resting state membrane is 50-100 times more permeable to K+ than Na+.
Donnan effect is known as membrane potential effect.
There are two types of membrane potential-
Resting membrane potential (RMP)
It is the potential difference across the membrane in resting state with the inside of the cell negative to the exterior. In the resting state, membrane is maintained in a polarized state with the outside positive relative to the inside.
Causes
Unequal distribution of diffusible ions across the membrane is due to-
Na+-K+ pump.
Bone marrow lymphatic precursor
Thymus, liver, spleen
T-lymphocyte
Cytotoxic or killer cell
Helper T-cell
Suppressor T-cell
Memory T-cell
Lymphnode or bursa of
Fabricious
B-lymphocyte
Plasma cell
Immunoglobuline
Memory B-cell
Solution
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K+ permeability is greater than Na+ in the resting state.
Donnan effect.
Action potential
When a muscle or nerve fiber is stimulated by the threshold stimulus the excitable tissues (muscles, nerves) exhibits a sequence of depolarization and repolarization of the membrane which travel along the entire length of the fiber without any change in the size. This change in the membrane potential is called action potential.
Depolarization
Upon threshold stimulus the membrane suddenly becomes very much permeable to sodium ion (Na+) ie. Potential changes to positive direction. This is called depolarization.
Repolarization
Just after depolarization Na+ channel gradually closes and K+ channel gradually opens. This causes outflux of K+
and reestablished negativity inside the cell is called repolarization.
Donnan effect When a non diffusible Anion (A-) is present on one
side of membrane. It causes an unequal distribution diffusible ions to the opposite side of thermometer. That is called Donnan effect.
The Gibbs–Donnan effect (also known as the Donnan's effect, Donnan law, Donnan equilibrium, or Gibbs–Donnan equilibrium) is a name for the behavior of charged particles near a semi-permeable membrane that sometimes fail to distribute evenly across the two sides of the membrane. The usual cause is the presence of a different charged substance that is unable to pass
through the membrane and thus creates an uneven electrical charge. For example, the large anionic proteins in blood plasma are not permeable to capillary walls. Because small cation are attracted, but are not bound to the proteins, small anions will cross capillary walls away from the anionic proteins more readily than small cations.
Donnan Effect
Action potential
In physiology, an action potential is a short-lasting event in which the electrical membrane potential of a cell rapidly rises and falls, following a consistent trajectory. Action potentials occur in several types of animal cells, called excitable cells, which include neurons, muscle cells, and endocrine cells, as well as in some plant cells. In neurons, they play a central role in cell-to-cell communication. In other types of cells, their main function is to activate intracellular processes. In muscle cells, for example, an action potential is the first step in the chain of events leading to contraction. In beta cells of the pancreas, they provoke release of insulin. Action potentials in neurons are also known as "nerve impulses" or "spikes", and the temporal
sequence of action potentials generated by a neuron is called its "spike train". A neuron that emits an action potential is often said to "fire".
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Source: Wikipedia
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Crystalloid solution
Crystalloid solutions contain small molecules that pass freely through cell membranes and vascular system walls. These solutions are useful as fluid expenders and are stored at room temperature. The crystalloid solutions are a useful source for fluid volume. They flow out of the vascular system rather quickly. Lactated Ringer’s is an example of crystalloid solutions.
Normal saline (0.9% NaCl solution)
Hartman’s solution
Ringer’s solution.
Advantages and Disadvantages
The advantage of crystalloid fluid resuscitation is that volume has not only been lost from the intravascular space, but also extracellular water has been drawn to the intravascular space by oncotic pressure.
Solutions with lower sodiun concentrations distribute more evenly throughout the total body water. This means that crystalloid solutions with higher sodiun concentrations are more effective as plasma expenders (Platt & Wade, 2002). Crystalloid therapy may, however, adversely effect microcirculatory blood flow and oxygenation when used in cases of shock, resulting hypoxia even after resuscitation (Krau, 1998).
The main disadvantage of using a crystalloid of fluid is that excessive use will cause peripheral and pulmonary oedema (Bradley, 2001).
Colloid solution The colloid solution contains molecules that are frequently very complex and much larger than those in the crystalloid solution. A solution that contains protein is colloidal. The colloidal solutions are needed when a solution is requerd to remain in the vascular system. Colloid solutions generally require refrigeration and can be stored for a limited period. Whole human blood U.S.P. and Hetastarch are examples of colloidal solutions.
Gelatins
Hetastarch
Albumin
Plasma protein fraction
Dextran.
Advantages and disadvantages
Colloids are better than crystalloids at expanding the circulatory volume, because their larger molecules are retained more easily in the intravascular space (Kwan et al, 2003) and increased osmotic pressure (Breadley, 2001).
However, excessive use of colloids can precipitate cardiac failure, pulmonary and peripheral oedema (O’Neill, 2001). Although the pulmonary oedema caused by excessive use of colloids is delayed in comparison with the caused by crystalloids, it is more sustained (Breadley, 2001).
FAQ1. What is Isotonic, Hypotonic, Hypertonic solution? Describe with example.
Isotonic solution
The solutions having osmotic pressure similar as plasma are known as isotonic solution.
eg. 0.9% NaCl solution.
Hypotonic solution
The solutions having osmotic pressure less than plasma are known as hypotonic solution.
eg. 0.45% NaCl solution.
Hypertonic solution
The dolution having osmotic pressure more than plasma are known as hypertonic solution.
eg. 3% NaCl solution.
FAQ
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FAQ2. What happens when RBC is suspended in Isotonic, Hypotonic and Hypertonic solution.
The following changes occur
In isotonic solution
No change occurs
In Hypotonic solution
Osmosis of fluid occurs from the solution to RBC RBC Swells Ultimately bursts (hemolysis).
In Hypertonic solution
Osmosis of fluid occurs from RBC to the solution RBC shrinks.
FAQ3. Mention the basic difference between Diffusion and Ultra filtration.
SL Points Diffusion Ultra filtration
01 Transformation
Solvent/water moves from higher concentration to lower concentration.
Solution moves from higher pressure to lower pressure.
02 Necessity of pressure No need Need
FAQ4. Mention the Diffusion and Osmosis.
SL Points Diffusion Osmosis
01 Transformation Solvent moves from higher concentration to lower concentration.
Solvent moves from lower concentration to higher concentration.
02 Necessity of pressure Diffusion is not a special type os
Osmosis.
Osmosis is the special type of
Diffusion.
03 Medium Diffusion occurs in both solvent and solute.
Osmosis occurs in only solvent.
04 Necessity of permeable membrane
Selectively permeable membrane may be or may not be needed.
Selectively permeable membrane must be needed.
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