The Renal System Juxtaglomerulous Apparatus &Bladder (1)

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    The Renal System Juxtaglomerulousapparatus &bladder

    By Associate Professor Dr /Sohair AlyHassan

    College of medicine,[RCMP] Perak

    &National Research Center/Cairo, Egypt

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    Chapter 14: The Kidneys and Regulation of

    Water and Inorganic Ions

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    L objectives

    At the end of this lecture, the students shouldbe able to:

    discuss the functional unit of the kideny

    Nephron discuss the blood flow to the kidney

    c) explain the basic mechanisms of Glomerular

    filtration, tubular reabsorption and secretiondiscuss the different cell types in thejuxtaglomerular apparatus

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    Section A:

    Basic Principles of Renal Physiology:

    1- Glomerular filtration

    2- Tubular reabsorption

    3- Tubular secretion

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    The paired kidneys form a filtrate of the blood that is modified by

    reabsorption and secretion; urine designated for excretion moves along

    the ureters to the bladder.

    Figure 14-1

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    Fluid filtered from the blood in the glomerular

    capillaries is altered by reabsorption and secretion

    along the length of the 1,000,000 nephrons/kidney.

    Figure 14-2

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    Nephrone

    Create osmotic gradient assisting in

    water reasorption

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    Due to the hydrostatic

    pressure of the cardiac

    pump, fluid is filtered from

    the blood through fenestra inthe glomerular capillaries

    into slit pores in the capsule.

    Figure 14-3

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    The outer layer

    of the kidney is

    the renal cortex;

    it is the site of

    glomerular filtration

    and the convoluted

    tubules.

    The inner part of

    the kidney is the

    renal medulla; this is

    the location of the

    longer loops of Henle,and the drainage of the

    collecting ducts into

    the renal pelvis and ureter.

    Figure 14-4

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    The intersection of the macula densa in the distal tubule

    with the afferent and efferent arterioles forms the

    juxtaglomerular apparatus, which secretes the endocrine

    signal known as renin into blood in the afferent arteriole.

    Figure 14-5

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    juxtaglomerular cells(JG cells, or granular cells) are

    cells in the kidney that synthesize, store, and secrete the enzyme renin. They are

    specialized smooth muscle cells in the wall of the afferent arteriole that delivers blood to

    the glomerulus. In synthesizing renin, they play a critical role in the renin-angiotensin

    system and thus in renal autoregulation, the self-governance of the kidney

    http://en.wikipedia.org/wiki/Cell_(biology)http://en.wikipedia.org/wiki/Kidneyhttp://en.wikipedia.org/wiki/Reninhttp://en.wikipedia.org/wiki/Smooth_muscle_cellhttp://en.wikipedia.org/wiki/Nephronhttp://en.wikipedia.org/wiki/Glomerulus_(kidney)http://en.wikipedia.org/wiki/Renin-angiotensin_systemhttp://en.wikipedia.org/wiki/Renin-angiotensin_systemhttp://en.wikipedia.org/wiki/Renal_autoregulationhttp://en.wikipedia.org/wiki/Renal_autoregulationhttp://en.wikipedia.org/wiki/Renal_autoregulationhttp://en.wikipedia.org/wiki/Renin-angiotensin_systemhttp://en.wikipedia.org/wiki/Renin-angiotensin_systemhttp://en.wikipedia.org/wiki/Renin-angiotensin_systemhttp://en.wikipedia.org/wiki/Renin-angiotensin_systemhttp://en.wikipedia.org/wiki/Renin-angiotensin_systemhttp://en.wikipedia.org/wiki/Glomerulus_(kidney)http://en.wikipedia.org/wiki/Nephronhttp://en.wikipedia.org/wiki/Smooth_muscle_cellhttp://en.wikipedia.org/wiki/Reninhttp://en.wikipedia.org/wiki/Kidneyhttp://en.wikipedia.org/wiki/Cell_(biology)
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    1. Glomerular filtration

    refers to the

    movement of fluid

    and solutes from the

    glomerular capillaries

    into Bowmans space.

    Figure 14-6

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    2. Tubular secretionrefers to the

    secretion of solutes

    from the peritubular

    capillaries into the

    tubules.

    1. Glomerular filtration

    refers to the

    movement of fluid

    and solutes from the

    glomerular capillaries

    into Bowmans space.

    Figure 14-6

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    3. Tubular reabsorption refers to the movement of materials from the

    filtrate in the tubules into the peritubular capillaries.

    2. Tubular secretionrefers to the

    secretion of solutes

    from the peritubular

    capillaries into the

    tubules.

    1. Glomerular filtration

    refers to the

    movement of fluid

    and solutes from the

    glomerular capillaries

    into Bowmans space.

    Figure 14-6

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    Substance X is filtered and secreted but not reabsorbed.

    Substance Y is filtered and some of it is reabsorbed.

    Substance Z is filtered and completely reabsorbed. Glucose

    Figure 14-7

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    Formation of the glomerular filtrate in Bowmans capsule

    is the outcome of opposing pressures:

    hydrostatic pressure from the heart favors filtration, osmotic and

    hydrostatic pressure of the filtrate oppose it.

    Figure 14-8

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    GLOMERULAR FILTRATION

    Depends upon the interaction of a number of forces:

    1. Glomerular blood hydrostatic pressure (GBHP) - This is the chief force. It is the

    pressure of blood in the glomerular capillaries, i.e., 75mm.

    2. Capsular hydrostatic pressure (CHP) - CHP is a back pressure due to the presence of

    fluid already in the renal tubule and the resistance of the tubule walls.

    3. Blood Colloid osmotic pressure (BCOP) - The presence of non-filtrating proteins inthe blood of the glomerular capillaries creates an osmotic pull on water in the

    relatively protein-free filtrate.

    Pressure #1 is opposed by Pressures #2 and #3, This produces an effective filtration

    pressure (Peff) of 25mm Hg

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    As vasodilation and vasoconstriction of the afferent and

    efferent arterioles alter the blood flow through the

    glomerular capillaries, there are corresponding alterations

    in the glomerular filtration rate (GFR).

    Figure 14-9

    http://www.wisc-

    online.com/objects/Vie

    wObject.aspx?ID=ap22

    04

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    Glomerular Filtration

    [GFR ]is the volume of fluid filtered from the

    glomeruli into Bowmans space per unite time

    Determined by

    permeability of the corpuscular membranes

    Surface area available for filtration

    GFR for normal person is 125ml/min or 180L /day /

    the renal plasma flow is about 625 ml/min in a

    'normal' kidney

    clearance values/ml/min

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    The luminal

    section of the

    plasma

    membrane of

    the tubule cells

    faces the

    filtrate,

    whereas the

    basolateral

    section is in

    close proximity

    to the peritubularcapillary.

    Figure 14-10

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    Reabsorpition

    Tubular reapsorpition

    Diffusion

    Mediated have a limited amounts of material they cantransport/unit time [transport maximum Tm] this is

    because the binding site on the membrane transport

    proteins become saturated when the concentration ofthe transported substance increases to a certain level.

    Eg glucose[normal is 150 mg/100ml Fig 14-11 Glucouria when start to appear in urine[in hyperglycemia] or

    Drop in the nephron efficiency to reabsorb the excess of filtered load of glucose[nephropathy] active

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    Tubular Secretion move substances from

    peritubular capillaries into the tubular lumen

    Occure by diffusion

    Mediated transport

    Substances secreted are H,K, choline ,

    creatinine

    penicillin

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    Kidney Concept of Clearance

    Is the vol of plasma from which the substance

    is completely removed [cleared] by kidney

    per unit time.

    Cs= Mass of S excreted/unit time/plasma

    concentration of S

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    Inulin, a biologically inert polysaccharide, can be used

    to estimate the glomerular filtration rate since it is

    filtered, but not reaborbed or secreted.

    Figure 14-11 CONCEPT OF RENAL CLEARANCE

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    Release of urine from the bladder, called

    micturition, is coordinated by a combination of

    smooth and skeletal muscle relaxation and

    contraction.

    Figure 14-12

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    MICTURITION

    Micturition is the process by which urine is

    expelled from the bladder.

    The neural mechanism causing micturition is

    called Micturition reflex.

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    Micturition cycle occurs two phases .

    it consist of a filling phase and emptying phase.

    Each phase requires a coordination interactionbetween the bladder and the nervous system.

    Urine formed by the nephrone is ultimately carried

    to the urinary bladder.

    Where it is stored till a voluntary signal is given by

    the central nervous system [CNS].

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    The signal is initiated by the stretching of the

    urinary bladder as it gets filled with urine.

    In response ,the stretch receptors on the walls of

    the bladder send signals to the CNS.

    The CNS passes on motor messages to initiate the

    contraction of smooth muscles of the bladder .

    The simultaneous relaxation of the urethralsphincter causing the release of urine.

    This type urine releasing process are called

    MICTURITION

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    Bladder control problems

    For the urinary system to do its job, muscles and

    nerves must work together to hold urine in the

    bladder and then release it at the right time. Nerves carry messages from the bladder to the

    brain to let it know when the bladder is full.

    They also carry messages from the brain to thebladder, telling muscles either to tighten or release

    . A nerve problem might affect your bladder control

    if the nerves that are supposed to carry messages

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    in case nerve damage?

    Nerves that work poorly can lead to three different

    kinds ofbladder control problems.

    1-Overactive bladder. Damaged nerves may sendsignals to the bladder at the wrong time, causing its

    muscles to squeeze without warning. The

    symptoms of overactive bladder includeurinary frequency-defined as urination eight or more times a day or two or more

    times at night

    urinary urgency-the sudden, strong need to urinate immediately

    urge incontinence-leakage of urine that follows a sudden, strong urge to urinate

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    2-Poor control of sphincter muscles.

    Sphincter muscles surround the urethra and keep it closed to hold urine in the bladder. If the

    nerves to the sphincter muscles are damaged, the muscles may become loose and allow leakage

    or stay tight when you are trying to release urine.

    Urine retention.

    For some people, nerve damage means their bladder muscles do not get the message that it istime to release urine or are too weak to completely empty the bladder. If the bladder becomes

    too full, urine may back up and the increasing pressure may damage the kidneys. Or urine that

    stays too long may lead to an infection in the kidneys or bladder. Urine retention may also lead

    to overflow incontinence.

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    What causes nerve damage?

    Many events or conditions can damage nerves and nerve pathways. Some of the

    most common causes are

    vaginal childbirth

    infections of the brain or spinal cord

    diabetesstroke

    accidents that injure the brain or spinal cord

    multiple sclerosis

    heavy metal poisoning

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