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THE JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINEVolume 7, Number 5, 2001, pp. 405–515Mary Ann Liebert, Inc.
Therapeutic Plants of Ayurveda: A Review of SelectedClinical and Other Studies for 166 Species
SARAH KHAN M.S., M.P.H., C.N.S., and MICHAEL J. BALICK, Ph.D.
ABSTRACT
This paper reports on the results of a literature survey involving 166 different species of plantsused in the Ayurvedic pharmacopoeia, based on a sampling of the literature available to us. Wefound a wide range of clinical and other in vivo studies for many of the plant-based therapiesutilized in the Ayurvedic system. Of the 166 plants investigated, 72 (43%) had at least one ormore human studies and 103 (62%) had one or more animal studies. These results appear to con-tradict the generally held notion that herbal remedies used in non-Western systems of botani-cal medicine have not been evaluated in human or in vivo trials. Some of these studies are notalways as large or methodologically rigorous as clinical studies reported in major medical jour-nals. Indeed, a critical assessment of the research according to the standards of evidence-basedmedicine would eliminate many of these studies for lack of rigor according to criteria of ran-domization, sample size, adequacy of controls, etc. However, the studies do suggest whichspecies might be appropriate for larger and better-controlled trials in the future. Accordingly, asynopsis of the plants, their therapeutic applications, and their clinical or experimental evalua-tions is presented.
405
INTRODUCTION
Non-Western healing systems that utilizebotanical medicines are often criticized be-cause of a supposed paucity of in vivo studies tosupport the safety and efficacy of individualplants or plant mixtures. For example, Barrett etal. (1999) state that therapies outside the med-ical mainstream suffer from a dearth of researchand critical evaluation. From a biomedical par-adigm, rigorous studies include those that pro-vide randomized controlled data on efficacy aswell as information on toxicity, dosage, method
of use, and adverse reactions. Few herbals orother references available to practitioners ofbotanical medicine contain information about,or citations of, clinical trials or related studies.At the same time, billions of people around theworld have studied and utilized ancient med-ical systems such as Ayurveda (translated as the“science of life”) for centuries.
To evaluate the availability of studies onplants used in Ayurveda, we conducted asearch in two databases as well as other sourcesof information, using a list of 166 species thatare important to this system of medicine.
Institute of Economic Botany, The New York Botanical Garden, Bronx, NY.
ORIGINAL PAPERS
KHAN AND BALICK406
MATERIALS AND METHODS
The research was conducted between Janu-ary 1996 and January 2000. The databasessearched were MEDLINE® and NAPRALERT.In addition, we collected literature on tradi-tional medicine and searched two Indian jour-nals not included in MEDLINE: Aryavaidyanand the Indian Journal of Medical Research. Thesepublications were selected, based on theiravailability to us, as examples of Indian jour-nals that report on studies of plants and theirtreatment of disease. There are many other In-dian journals that contain a great deal of valu-able information; however, they were not ac-cessible to us—we expect that, if access to thistype of traditional knowledge can be facilitatedin some way, much more information of inter-est could be located. In this paper, we only con-sider those studies that include individualplants or mixtures of plants consistent with thephilosophy of Ayurveda. We did not includesix species that have been reported on in manyjournals, in both human and animal studies: Al-lium sativum L., Cannabis indica Lam., Digitalispurpurea L., Papaver somniferum L., Rauwolfiaserpentina L., and Zingiber officinalis Roscoe.However, we did include these species in thecalculation of percentage of animal and humantrials of the 166 Ayurvedic medicinal plants.
RESULTS AND DISCUSSION
Summary of human studies
A summary of the human studies and thespecies included in the plant mixtures are pre-sented in Table 1: Ayurvedic Plants and Hu-man Studies. The disease categories listed inTable 1 are graphically depicted in Figure 1 asbreakdown into eleven disease categories forthe 166 plants (minus the six species alreadydocumented) with human studies. The diseasecategories include: antimicrobial; antimuta-gens; cardiovascular; dermatology; Diabetesmellitus; gastrointestinal; liver dysfunction; nervous system; pain/inflammation; renal/blood/immune system; and other. There are atotal of 145 effects based on the 66 human stud-ies. In a few instances, when one plant demon-
strated more than one effect, i.e., reduction ofboth blood glucose and triglyceride levels, theeffect was counted in both the cardiovascularand Diabetes mellitus categories. For the sake ofcomparison, Figure 2 represents a breakdownof drugs used in the U.S. pharmacopoeia ac-cording to treatment category based on thework of Paul Cox (1994).
Table 2 is a detailed list of all the plants, or-ganized by genus and species, with the familynames. Information on common Sanskrit andEnglish names is also presented, as well asmention of the plant part used, preparation anddosage used in the study, design, model andsample size when known, results (negative andpositive), and the original reference that wasexamined. Forty-three percent (43%) (a total of72) of the species in Table 2 contain referenceto one or more studies with humans and 62%(a total of 103) of the species listed in this tablecontain reference to at least one animal trial.Careful examination of the studies revealed avariation in sample size, quality of research,and presentation of results. However, there isa great deal of interesting information con-tained in these studies, representing a signifi-cant accumulation of evidence supporting theefficacy of plant therapies used in Ayurveda.Although the table is quite long and detailed,there are a number of plants exhibiting im-pressive therapeutic effects in humans. At thesame time, this corpus of information serves topoint the way to species that deserve furtherstudy, both in animal models and at the clinic.Toward this end, we suggest the adoption of“Good Botanical Practices” (Balick, 1999) withproperly collected, vouchered materials usedto produce the phytotherapies under study.This is the only way that reproducibility of re-sults can be assured, should further testing bewarranted.
CONCLUSIONS
Plants have long been the principal tools oftraditional medical systems. Although ancientin origins, many traditional medical paradigmsand their pharmacopoeias have evolved intoquite sophisticated healing systems, usingthousands of plants and other natural materi-
THERAPEUTIC PLANTS OF AYURVEDA 407
als such as minerals and animal products. Inmany parts of the world, traditional medicineis still used to provide the major part of pri-mary health care. The World Health Organiza-tion has estimated that the majority of theworld’s population depends on botanical med-icines for basic health care needs (Akerele,1985). Reasons for this include the fact thatthese local systems are culturally acceptable,cheaper for many conditions as compared tobiomedicine, and efficacious in many of the cir-cumstances in which they are used.
In a recent editorial in the New England Jour-nal of Medicine, the editors cautioned against the
use of herbal medicines as “a reversion to irra-tional approaches to medical practice” (Angelland Kassirer, 1998). In this paper, we have at-tempted to dispel the all-too-commonly heldnotion that no clinical or other evidence existsto support the use of plants used in traditionalmedical systems. We acknowledge that someof the studies are not as rigorous as desired be-cause of resource or other limitations. How-ever, the work described in this review canserve to help guide future studies by pointingout promising therapies, and thus research av-enues, for specific conditions. In the case ofAyurvedic medicine, Indian journals, often re-
FIG. 1. Ayurvedic medicinal plant uses, classified according to the treatment categories. (Based on human studies,n 5 66).
FIG. 2. U.S. Pharmacopoeia drug uses, classified according to the treatment categories. From Cox, 1994.
gional or those published by individual re-search centers, are rich in experimental studiesas well. This exercise has also pointed out theneed for access to such publications, via greaterinternational cooperation involving informa-tion exchange.*
This study has been limited by our own ac-cess to information and there are numerous ad-ditional journals that contain information onplants and complex mixtures of plants pre-pared according to traditional formulationsused in the Ayurvedic medical system. Wehave undertaken this task in the hope that someof the initial studies presented may help to di-rect research on plants deserving of more in-tensive evaluation as clinical therapies.
ACKNOWLEDGMENTS
We are grateful to Scott Gerson, M.D., Ph.D.,medical director of the National Institute ofAyurvedic Medicine, Brewster, NY, for pro-viding us with a listing of the species ofAyurvedic medicinal plants discussed in thispaper. We would like to thank the following:the NAPRALERT staff for providing informa-tion on clinical trials, The New York BotanicalGarden Library (for interlibrary loans); JenniferCooper of Nature’s Herbs for providing refer-ences on some of the plants; The Asian Eco-nomic Botany Fund of The New York BotanicalGarden (for funding travel and SK salary); andThe New York Botanical Garden Institute of
Economic Botany, Bronx, NY, staff and interns:Jan Stevenson, Kate Armstrong (1998 EverettPublic Service Intern), Kelvin Chan (volunteer),with special thanks to Rebekka Stone (ResearchAssistant), and Roberta Lee M.D. We wouldalso like to express our gratitude to GerryBodeker, Ed.D., for his thoughtful commentson the piece, and to Jackie Wootton, M.Ed., andKim Jobst, M.A., D.M., M.R.C.P., M.F.Hom.
We are also grateful to The Philecology Trustand The Metropolitan Life Foundation for theirgenerous support of Michael Balick’s researchprogram in ethnomedicine.
REFERENCES
Angell M, Kassirer, JP. Alternative medicine: The risks ofuntested and unregulated remedies [editorial]. N Eng-land J Med 1998;339:839–841.
Akerele O. The WHO Traditional Medicine Programme:Policy and Implementation. International TraditionalHealth Newsletter. Geneva, Switzerland: World HealthOrganizations, 1985;1:1.
Balick MJ. Good Botanical Practices. In Eskinazi D (ed)Botanical Medicine: Efficacy, Quality, Assurance, andRegulation. Larchmont, NY: Mary Ann Liebert, Inc.,1999:121–125.
Barrett B, Kiefer D, Rabago D. Assessing the risks andbenefits of herbal medicine: An overview of scientificevidence. Altern Ther Health Med 1999;5(4):40–49.
Cox, P. The ethnobotanical approach to drug discovery:Strengths and limitations. In: Chadwick D, Marsh J(eds). Ethnobotany and the Search for New Drugs. JohnWiley & Sons, 1994:25–36.
Address reprint requests to:Michael J. Balick, Ph.D.
The New York Botanical GardenBronx, NY 10458
E-mail: [email protected]
KHAN AND BALICK408
*The Foundation for the Revitilization of Local HealthTraditions (www.frlht-india.org) founded by DarshanShankar in 1991 is one such pioneering organization ded-icated to the conservation of Indian biodiversity and lo-cal health traditions and cultures.
http://www.frlht-india.orghttp://giorgio.catchword.com/nw=1/rpsv/cgi-bin/linker?ext=a&reqidx=/0028-4793^281998^29339L.839[aid=950136]http://giorgio.catchword.com/nw=1/rpsv/cgi-bin/linker?ext=a&reqidx=/1078-6791^281999^295:4L.40[aid=1955117]http://giorgio.catchword.com/nw=1/rpsv/cgi-bin/linker?ext=a&reqidx=/0028-4793^281998^29339L.839[aid=950136]
409
APPENDIX toTherapeutic Plants of AyurvedaTables 1 and 2 and Illustrations
410
TABLE 1. AYURVEDIC PLANTS WITH HUMAN STUDIES
Aegle marmelos Irritable bowel syndromeShigellosis
Allium cepa ColicHyperlipidemiaScar treatmentStomach carcinoma
Aloe barbendensis AntidiabeticBurn woundsPsoriasis
Andrographis paniculata Common cold (23)Fever, sore throatHepatocellular jaundicePyuria, hematuriaStenosis, restenosisViral hepatitis
Areca catechu Diphyllobothrium latum infectionInflammatory bowel disease
Artemisia vulgaris Postoperative blood loss, bacteriuriaAsparagus racemosus Calculi on kidney, urinary bladder
Gastric emptyingAzadirachta indica Congestive heart failure
Mosquito repellant (23)ScabiesVaginal contraceptiveVitiligo
Bacopa monnieri Irritable bowel syndromeBoerhavia diffusa Congestive heart failureBoswellia serrata Ulcerative colitis
OsteoarthritisRheumatoid arthritis
Butea monosperma GiardiasisWorm infestations, Ascaris lumbricoides
Capsicum annuum Cluster headaches (23)Diabetic neuropathy (23)Herpes zosterHerpetic neuralgia (33)Local stump pain due to amputationPost herpetic neuralgia (23) Postmastectomy pain syndromeSmall fiber function
Carum carvi ObstipationCedrus deodara Congestive heart failureCocos nucifera Coronary heart disease
ImmunotherapyOral rehydration therapy
Cuminum cyminum Diabetes mellitusCurcuma longa Cancerous lesions (external)
Gastric ulcersOsteoarthritisScabiesSerum lipid peroxides (decrease)Urinary mutagens (decrease)
Cyperus rotundus Intestinal metaplasia, atypical hyperplasia of gastricmucosa
Daucus carota Inhibition of endogenous nitrosationMalignant mesotheliomaMetabolic parameters (no adverse changes)Oxidation in copper-oxidized LDL (decrease)Risk of vulvar cancer (decrease)
Dolichos biflorus Binding to healthy oral mucosaEmbelia ribes Acne vulgaris
Worm infestation, Ascaris lumbricoidesEmblica officinalis Gastrointestinal disease
Serum cholesterol levelsViral hepatitis
Eugenia jambolana Decreases in mean blood sugar valuesFoeniculum vulgare Chronic nonspecific colitis
411
Glycyrrhiza glabra Acne vulgarisChronic duodenal ulcers (23)Chronic hepatitisHyperkalemia in Diabetes mellitus
Gossypium herbaceum Male antifertility (33)Gymnema sylvestre Mean blood sugar values (decrease) (23)
Serum lipids (decrease)Sweetness perception (decrease)
Holarrhena antidysenterica Facial acneHydrocotyle asiatica ShigellosisLinum usitatissimum N-3 fatty acids (increase)
Postprandrial glucose (decrease)Mallotus philippensis Worm infestations, Ascaris lumbricoidesMoringa oleifera Perceived pain relief, accelerated expulsion of wormsMucuna pruriens Parkinson’s diseaseMyristica fagrans Calculi in kidneys and urinary bladderNardostachys jatamansi Facial acneNelumbo nucifera HyperlipidemiaOcimum sanctum Non-insulin dependent Diabetes mellitusOryza sativa Oral rehydration therapyPaederia foetida ShigellosisPeucedanum graveolens Vitamin A/b-carotene contentPicrorhiza kurrooa Bronchial asthma
Congestive heart failureViral hepatitisVitiligo
Piper longum Bioavailability of certain drugs (increase)Disappearance of Giardia lamblia
Piper nigrum No damage to human gastric mucosaPueraria tuberosa Migraine headachesRaphanus sativus No adverse effects to metabolic parametersRheum emodi Prevent chronic renal failureRicinus communis Binding of healthy oral mucosaRubia cordifolia Cardiac functionSalvadora persica Peridontal diseaseSantalum album Facial acne
Urinary tract infectionSaussurea lappa Reduced frequency of anginaSesamum indicum WartsStrychnos nux-vomica Nonketotic hyperglycemiaSwertia chirata Decrease in mean blood sugar valuesTamarindus indica Bioavailability of drugs (increase) (23)
Decrease pain, accelerated expulsion of wormsTaraxacum officinale Chronic colitisTephrosia purpurea Decrease in mean blood sugar valuesTerminalia arjuna Severe refractory heart failure
Stable angina pectorisTerminalia bellirica Acne vulgarisTerminalia chebula Acne vulgaris
Congestive cardiac failureTinospora cordifolia Calculi on kidney or urinary bladder
Congestive heart failureManagement of obstructive jaundice
Tribulus terrestris Calculi on kidney and urinary bladderRemission of angina pectoris
Trigonella foenum-graecum Hypolipidemic effect (23)Postprandial glucose levels (decrease)Total cholesterol, LDL, VLDL, triglycerides (decrease)
Valeriana jatamansi Infantile rotavirus enteritisMild hypnotic actionMild insomnia, decrease sleep latencySleep quality
Withania somnifera Calculi on kidney and urinary bladderOsteoarthritisPsychomotor performanceRheumatoid arthritis
LDL, low-density lipoprotein cholesterol; VLDL, very low-density lipoprotein cho-lesterol.
412
TABLE2.
PLANTSU
SED
INAYURVEDICPHARMACOPOEIA
Genus, species
family
Common name
(Sanskrit)
Common name
Plant part used,
Design
(English)
preparation, and dosage
and model
Results
References
Acorus calamus
L.
Alcoh
olic extract of dried
Rats
Decrease in sev
erity of m
axim
um
Martis G, et al. Neu
roph
armacolog
ical
ACORACEAE
rhizom
es: 1 kg
coa
rse
electric sho
ck ind
uced seizu
res in rats
activity of Acorus calamus
L.
Vacha
pow
der
was dem
onstrated.
Fitoterapia LXII, 1
991;4:33
1–33
7.Sw
eet Flat
Acorus calamus
Ethan
olic extract of Acorus
Rats, m
ice
Extract has sho
wn sedative, ana
lgesic,
Voh
ora SB
, et al. Cen
tral nervo
uscalamus rhizo
mes. H
ot
mod
erately hy
potensive an
dsy
stem
studies on an
ethan
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extract distilla
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33
resp
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poo
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Aegle marmelos
Dried
unr
ipe fruit pow
der
Ran
domized
,Treatmen
t of shige
llosis with these
Haider R
, et al. Eva
luation of ind
ige-
(L.) Corrêa
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dou
ble-blind,
plan
ts did not sho
w any
clin
ical
nous plan
ts in the trea
tmen
t of
RUTACEAE
dried
pow
der plant of
clinical trial:
impr
ovem
ent or bacteriolog
ical cure
acute shige
llosis. Trop G
eogr M
edBilu
aHydrocotyle asiatica;
82 m
en w
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.Bael tree
dried
pow
der of Poederia
shigellosis
foetida
Aegle marmelos
Metha
nolic
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Mice
Extract inh
ibited
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spo
ntan
eous
Kak
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nstitu-
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10
0 mg/
mL
myo
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ial cells
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spon
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ous be
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50%.
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. Plan
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Clin
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In 57 pa
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yurved
ic prepa
ration
Yad
av SK, e
t al. Irritable bo
wel syn
-Aegle marmelos
and
rand
omized
was effective
in 64.9%, w
hile stand
ard
drome: the
rapeu
tic ev
alua
tion
of
Bacopa monnieri
controlle
d:
therap
y (w
ith clidinium bromide,
indigen
ous dru
gs. Ind
ian J Med
Res
169 pa
tien
tsch
lord
iaze
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aghu
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6–50
3.with irritable
60 patients was useful 78
.3%. L
ong-
bowel
term
follow-up sh
owed
both form
s of
synd
rome
therap
y were no
better than
placebo
in lim
iting the relaps
e.
Aegle marmelos
Plants lack
ing pyrroliz
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Feed
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tha
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Hemidesmus indicus,
central ve
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chebulaan
d Withania somnifera
trad
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413
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Aegle marmelos
Aqu
eous decoc
tion
s of
Lab
oratory
All plan
ts dem
onstrated significant
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ke EH, e
t al. Oral hy
po-
Aegle marmelos,
anim
als
hypo
glyc
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ir ability to
glyc
emic activity of som
e med
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Momordica charantia,
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d gluco
seplants of Sri Lan
ka. J Ethno
pha
rm
Salacia reticulata
leve
l an
d impr
ove gluc
ose toleranc
e.19
84;11(2):223
–231
.Momordica charantia
had the
highe
steffect w
hile Salacia reticulataha
d the
lowest.
Alangium
Extracted
with n-
Mice ex
tract
Sage
is a po
tent inh
ibitor of TPA-ind
uced
Oku
yama T, et al. Studies on
can
cer
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(L.f.)
hexa
ne, ethy
l acetate
exam
ined
mou
se ear edem
a. A
ntitum
or
bioc
hemop
reve
ntion of natural
Wan
gerin
and m
etha
nol.
on TPA-
promoting activity guided
the
resources:X
. 1
inhibitory effect of
ALA
NGIA
CEAE
Alls
pice, b
asil, bay
induc
ed ear
separation of the
relatively active
spices onTPA
-enh
anced 3H-cho
line
Ank
ola
leav
es, card
amom
seed,
edem
asp
ices and
led
to the isolation of
inco
rporation in pho
spho
lipids of
Sage
leave
scinn
amon
, cu
min, d
illursolic acid from sag
e. A
ll plan
tsC3h
10T1/
2 cells
and
on TPA
-seed
, dry ginge
r,were high
ly poten
t inhibitors of TPA
-induc
ed m
ouse ear edem
a.
ging
er, h
orseradish,
induc
ed m
ouse ear edem
a.Chin Pha
rm J 199
5;47
(5):4
21–4
30.
marjoram, oreg
ano,
parsley, pink pep
per,
red pe
ppe
r, ros
emary,
sage
, tarrag
on, thym
e,turm
eric, w
hite pep
per
Allium
cepaL.
Allium
cepaintake
Mailed
To assess relations
hips am
ong
Lus
t KD, e
t al. Materna
l intake
of
ALL
IACEAE
question
naire:
compon
ents of the materna
l diet an
dcruc
iferou
s ve
getables and
other
Palan
du
272 mothe
rs:
presenc
e of colic sym
ptom
s am
ong
food
s an
d colic sym
ptom
s in
Onion
infants
527
3ex
clusive
ly breast-fed infan
ts. S
tudy
exclusive
ly breast-fed infan
ts. J A
m
reve
aled
initial eviden
ce tha
t materna
lDietetic Assoc
199
6;96(1):4
6–48
.intake
of on
ions
during
exclusive
breast-feeding is assoc
iated w
ith co
licsymptoms in you
ng infan
ts.
Allium
cepa
Allium
cepaan
d Allium
Nethe
rlan
ds
Strong
inv
erse assoc
iation
between on
ion
Doran
t E, et al. Con
sumption of onion
sativum
cons
umption
Coh
ort Study
cons
umption an
d stomach carcinom
a.an
d red
uced risk of stomach
on diet an
d
carcinom
a. G
asterolenterolog
y canc
er: n
519
96;110
(1):1
2–20
.12
0,85
2 men
an
d w
omen
55
–69 ye
ars
Allium
cepa
Aqu
eous
extracts of
Rats
Garlic
and
onion
can
be inge
sted
Bordia T
, et al. An ev
aluation of
Allium
cepaor Allium
freq
uen
tly in low
dos
es w
itho
ut an
yga
rlic and
onion
as an
tithrombo
tic
sativum
administered
side
effects, a
nd can
still pr
oduc
e a
agen
ts. P
rostag
land
ins Le
uko
Essen
torally or intrap
eri-
sign
ifican
t an
tithrombo
tic effect.
Fatty Acids 19
96;54(3):183
–186
.tone
ally, d
aily for
4 weeks
414
Allium
cepa
Con
tractube
x ge
lClin
ical trial: 3
8In C
ontractube
x grou
p, e
valuation of
Marag
akis M
, et al. Possibilities of
(Mertz 1
Co., D-
child
ren with
therap
eutic resu
lt w
as “go
od” an
dscar treatmen
t after thoracic
Fran
kfurt/Main),
scar formation
“very go
od” in 84%
of cases as
surgery. D
rugs
Und
er Exp
. Clin
containing
10%
onion
after thoracic
compared
to 59
% of untreated
cases.
Res 199
5;21
(5):1
99–2
06.
extract, 50
U sod
ium
surgery.
In treated
group
, scar size w
ashe
parin/
g of gel and
1%
Con
tract-
marke
dly low
er, q
uicke
r paling, and
allantoin
ubex
-treated
conv
ersion
to hy
pertroph
ic or ke
loidal
and 27
scars was less freq
uen
t. Sc
ar specific
untrea
ted
effects of C
ontractube
x persisted
after
compared
.the en
d of trea
tmen
t.Allium
cepa
S-methy
l cy
steine
Allo
xan-
Administration of SM-C
S sign
ifican
tly
Kumari K, et al. Antidiabe
tic an
d
sulpho
xide (SM-C
S)diabe
tic rats
controlle
d blood
gluco
se, lip
id serum
hy
polip
idem
ic effects of S-methy
l isolated
from onion
.an
d altered
the
activities of liver
cysteine
sulfox
ide isolated
from
Oral ad
ministration
hexo
kina
se, g
luco
se 6-pho
spha
tase
Allium
cepaLinn. Ind
J Bioch
emdaily at a dose of 200
and H
MG C
oA red
uctase toward
Biophy
sics 199
5;32
(1):4
9–54
.mg/
kg bod
y weigh
t for
norm
al. Effects of SM-C
S were
45 day
sco
mparab
le to those of glib
enclam
ide
and ins
ulin
.Allium
cepa
Allium
cepa, Allium
27 hea
lthy
Tolbu
tamide, Cucurbita ficifolia, Phaseolus
Rom
an R
R, et al. Antihyp
erglyc
emic
sativa, Brassica oleracea,
rabb
its
vulgaris, Opuntia streptacantha, Spinacea
effect of some ed
ible plants.
Cucurbita ficifolia,
oleracea, Cucum
is sativus,a
nd Cum
inum
J Ethno
pha
rm 199
5;48
(1):2
5–32
.Cum
inum
cyminum
, cyminum
sign
ifican
tly decreased
the
Cucum
is sativus, Lactuca
area und
er the
gluco
se toleran
ce cur
vesativa, Opuntia
and the
hyp
erglyc
emic pea
k. Brassica
streptacantha, Phaseolus
oleracea, Allium
cepa an
d Allium
vulgaris, Psidum guajava,
sativum
only decreased
the
Spinacea oleracea
hype
rglycemic peak. The
glycemic
decreases cau
sed by Psidum guajava,
Brassica oleracea
and Lactuca sativa
were no
t sign
ifican
t.Allium
cepa
Oral ad
ministration of
Allo
xan-
Diabe
tic co
ndition ch
aracterized by
Sheela C
G, et al. Anti-diabe
tic
onion su
lfox
ide am
ino
diabe
tic rats
glucose intoleran
ce, w
eigh
t loss,
effects on
onion
and
garlic
acids
dep
letion
of liv
er glyco
gen im
prove
dsu
lfox
ide am
ino acids in rats.
compared
to rats treated
with
Planta Med
ica 19
95;61(4):356
–357
.gliben
clam
ide an
d ins
ulin.
TABLE2.
PLANTSU
SED
INAYURVEDICPHARMACOPOEIA
(CONT’D)
Genus, species
family
Common name
(Sanskrit)
Common name
Plant part used,
Design
(English)
preparation, and dosage
and model
Results
References
415
(continued)
Allium
cepa
Allium
cepaaq
ueou
sMice
A significant inc
rease in the
weigh
t of
Al-Bek
airi A
M, e
t al. Tox
icity studies
extract give
n to m
ice for
testes and
epididym
us of the
treated
on Allium
cepa, its effect on
3 mon
ths at a dose of
anim
als was observe
d. Sp
erm cou
ntestrad
iol trea
ted m
ice an
d on
100 mg/
kg in the
was significantly inc
reased
, supp
orting
ep
ididym
al spe
rmatoz
oa.
drink
ing water
an aphr
odisiac poten
tial. Allium
cepa
Fitoterapia LXII, 1
991;4:30
1–30
6.did not sho
w an estrog
enic or
antiestrog
enic activity an
d w
as dev
oid
of spermatotox
ic poten
tial.
Allium
cepa
Ether extract of Allium
Albino rats
Extract sign
ifican
tly pr
even
ted an increa
se
Lata S, e
t al. Ben
eficial effects of
cepa
in serum
cho
lesterol and
triglyc
eride
Allium
sativum
, Allium
cepaan
d
leve
ls, c
aused by an
atherog
enic diet.
Com
mipho
ra m
ukul on
The
extract provided
significant
experim
ental hy
perlip
idem
ia and
protection ag
ains
t athe
roge
nic diet-
athe
rosclerosis—
A com
parative
induc
ed atherosclerosis.
evalua
tion
. JPostgrad Med
199
1;(3):1
32–1
35.
Allium
cepa
10–1
0,00
0 mg Allium
cepa
Mice
The
tum
or yield and
inc
iden
ce of
Belm
an S. O
nion
and
garlic
oil inhibit
oil an
d Allium
sativum
pho
rbol-m
yristate-acetate promotion
tumor production. C
arcino
gene
sis
oil, ap
plied 3
3per w
eek
were inhibited in a dose-dep
enden
t19
83;4(8):1
063–
1065
.man
ner ov
er the
ran
ge of 10
–100
,000
mg
of onion
oil. G
arlic
oil was also
inhibitory but was less effective.
Allium
cepa
Extracted
onion
or ga
rlic
Human
trial:
Onion
and
garlic
had
a significant
Bord
ia A
, et al. E
ffect of the
essen
tial
juice or equ
ivalen
t of
10 hea
lthy
protective action
aga
inst fat-ind
uced
oils of ga
rlic and
onion
on alim
en-
ethe
r-ex
tracted essen
tial
subjects
increa
ses in serum cho
lesterol and
tary hyp
erlip
idem
ia. A
therosclerosis
oils: a
dministered 4
plasm
a fibrinog
en and
a decrease in
1975
;21(1):15–
19.
rand
omly different day
sco
agulation time an
d fibrino
lytic
during 1 week
activity.
Aloe barbadensis
Aloe barbadensisa poly-
Rats an
d m
ice
Benz
o[a]pyren
e-DNA adduc
t form
ation
Kim
HS, Lee BM. Inh
ibition of
Mill.
saccha
ride fraction
extract.
was significantly inh
ibited
in
benz
o[a]pyren
e-DNA adduc
t ASP
HODELA
CEAE
Mice ad
ministered oral
variou
s orga
ns (p
,0.00
1) w
hen mice
form
ation by
Aloe barbadensis
Kumari
dose of 10 mg follo
wed
were pretrea
ted w
ith aloe
. The
se results
Miller. C
arcino
gene
sis 19
97;18(4):
Aloe ve
rawith 16
day
s of treatmen
t su
ggest a ch
emop
rotective effect.
771–
776.
at 50 mg per m
ouse
Aloe barbadensis
Aloe vera
juice prep
ared
Placebo
-Bloo
d suga
r leve
ls and
triglyc
eride
Yon
gcha
iyud
ha SV, e
t al.
from
aloe ge
l. 1 tablespoo
n co
ntrolle
dleve
ls w
ere decreased
significantly.
Antidiabe
tic activity of Aloe vera
23pe
r day
for at least
and single-
Whe
n give
n Aloe vera
juice.
L. juice. I. Clin
ical trial in ne
w2 weeks
blind trial:
cases of diabe
tes mellitus
.50
men
, 22
Phy
tomed
199
6;3(3):241
–243
.wom
en w
ith
diabe
tes
416
Aloe barbadensis
Aloe vera
gel ve
rsus
no
Phase III
Dermatitis sco
res were virtua
lly iden
tical
Williams MS, et al. Pha
se III
trea
tmen
tdou
ble-blind
on both trea
tmen
t arms dur
ing bo
th
dou
ble-blind eva
luation of an
rand
omized
the trials. T
his dose sche
dule of an Aloe
aloe
vera ge
l as a proph
ylactic
trial. Trial 1:
vera
gel doe
s no
t pr
otect ag
ains
t ag
ent for radiation
-ind
uced
skin
194 wom
en;
radiation
.toxicity. Int J R
adiat Onc
ol, B
iol,
Trial 2: 10
8Phy
sics 199
6;36
(2):3
45–3
49.
wom
enAloe barbadensis
Aloe vera
extract cream 0.5%,
Dou
ble-blind,
Patien
ts w
ith slight to mod
erate ch
ronic
Syed
TA, e
t al. M
anag
emen
t of
100 g of placebo
or active
placebo
-plaqu
e-type
psoriasis w
ere treated.
psoriasis w
ith Aloe ve
ra extract in
ingred
ient 3
3 daily for
controlle
d,
By the en
d of the study, 25/
30a hy
drophilic
cream
: A placebo
5 co
nsecutive
day
s pe
r study: 60
(83.3%
) were cu
red com
pared to 2/
30co
ntrolle
d, dou
ble-blind study.
week (m
axim
um 4 w
eeks)
patients with
(6.6%) in the
placebo
group, Pso
riasis
Trop Med
Int H
ealth 19
96;1(4):
psoriasis
and A
rea an
d Sev
erity Index
sco
re50
5–50
9.decreased
to a mea
n of 2.2.
Aloe barbadensis
CARN 750
is a po
lydispersed
Mye
losu
p-Su
bcutan
eous ad
ministration sign
ifican
tly
Egg
er SF, et al. Hem
atop
oietic
b(1,4)-lin
ked acetylated
pressed
(7 Gy)
increased splenic an
d periphe
ral bloo
d
augm
entation
by a be
ta-(1,4)-
man
nan isolated
from
C57BL/6 mice
cellu
larity, a
s well as hem
atop
oietic
linke
d m
anna
n. C
ancer Im
mun
ol
Aloe barbadensis
proge
nitors in sp
leen
and
bon
e marrow
Immuno
ther. 1
996;43(4):1
95–2
05.
(hem
atop
oietic aug
men
tation
).Aloe barbadensis
Aloe vera
gel
Clin
ical and
Patien
ts w
ere treated w
ith Aloe vera
Visuthiko
sol V, et al. Effect of
histolog
icge
l co
mpared
with va
selin
e ga
uze.
Aloe ve
ra gel to he
aling of burn
study:
The
aloe trea
ted-group
hea
led
wou
nd and
clin
ical and
histologic
27 patients
sign
ifican
tly faster in 11
.98 day
sstudy. JMed
Assoc
Tha
iland
199
5;with partial
whe
reas petroleum
jelly
-treated
group
78(8):4
03–4
09.
thickn
ess bu
rns
healed
in 18
.19 day
s (p
,0.00
2)Aloe barbadensis
Top
ical applic
ation of
Mice
Top
ical app
lication of gel impr
oved
Strick
land
FM, e
t al. Pr
even
tion
of
0.16
7–1.67
% aloe ge
lUV-ind
uced
immune
suppr
ession
by
ultraviolet rad
iation
-ind
uced
after each
irrad
iation
a mecha
nism
tha
t doe
s no
t invo
lve
supp
ression of con
tact and
delay
edDNA dam
age or rep
air.
hypersens
itivity by
Aloe barbadensis
gel ex
tract. JInv
est Dermatol 199
4;10
2(2):197
–204
.Aloe barbadensis
Ethan
ol or water extracts
Rats orally
Aqu
eous or 90%
ethan
ol extracts of
Nath D, e
t al. Com
mon
ly used
of pow
dered
plant
dosed
for 10
the plants were studied
in rats for 10
Indian ab
ortifacien
t plants with
material: Adhatoda vasica,
day
sday
s after insemination with sp
ecial
special referenc
e to the
ir teratolog
ic
Abrus precatorius, Acacia
referenc
e to effects of fetal
effects in rats. J Ethno
pharm 199
2;arabica, Aloe barbadensis,
dev
elop
men
t. Leaf ex
tracts of
36:147
–154
.Anethum
sowa, Apium
Moringa oleifera
and Adhatoda
petroselinium, Banbusa
vasica
were 10
0% abo
rtive at doses
TABLE2.
PLANTSU
SED
INAYURVEDICPHARMACOPOEIA
(CONT’D)
Genus, species
family
Common name
(Sanskrit)
Common name
Plant part used,
Design
(English)
preparation, and dosage
and model
Results
References
417
(continued)
arundensis, Blepharis
equivalen
t to 175
mg/
kg starting dry
edulis, Butea monosperma,
material. Only the flow
ers of Acacia
Hibiscus rosa-sinensis,
arabicaan
d Hibiscus rosa-sinensis
Lepidum sativum
, Mesua
appea
red to lack
teratolog
ic poten
tial
ferrea, Moringa oleifera,
at the
doses tested.
Mucuna pruriens,
Raphanus sativus, Sida
cordifolia, Trachyspermum
ammai
Aloe barbadensis
Aceman
nan, the
USA
NMice, rats,
No sign
ifican
t sign
s of intox
ication an
d
Foglem
an R
W, e
t al. Tox
icolog
ic
accepted
nam
e for the
and dog
sno
dea
ths oc
curred
in an
imals trea
ted
evaluation of injectable acem
anna
n long
-cha
in polyd
ispe
rsed
with
the
single injection of A
ceman
nan
in the
mou
se, rat an
d dog
. Vet
b-(1,4)-acetylated
at dosag
es of 80
mg/
kg IV or 20
0 mg/
Hum Tox
icol 199
2;34
(3):2
01–2
05.
polyman
nose w
ith
kg IP in m
ice, 15 mg/
kg or 50 m
g/kg
interspersed o-acetylated
IP in rats, an
d 10 mg/
kg IV or 50
mg/
grou
ps, extracted
from
kgIP in dog
s.Aloe barbadensis. 1 m
g/mL
solution
eithe
r as a 1
dose or rep
eated at
4-day
interva
ls for 8
doses by IV
or IP rou
tes
Aloe barbadensis
Aloe barbadensis,
Mice: m
urine
Sarcom
as grew in 10
0% of the co
ntrol
Peng
SY, e
t al. Decreased
mortality
Aceman
nan, lon
g ch
ain
sarcom
a cells
an
imals an
d resulted in mortality in
of N
orman
mur
ine sarcom
a in
polydispersed b
(1,4)-
subc
utan
eously
20–4
6 day
s dep
ending on
the
num
ber
mice trea
ted w
ith im
muno
-lin
ked m
anna
n polym
ers
implan
ted.
of cells implan
ted; 4
0% of an
imals
mod
ulator, Aceman
nan. M
ol
with rand
om O
-acetyl
trea
ted w
ith Aceman
nan su
rvived
.Biother 199
1;3(3):79–
87.
grou
ps give
n IP
Aloe barbadensis
Gastric administration of
Rab
bits
Results sho
wed
tha
t tolbutamide an
dRom
an-R
amos
R, e
t al. Exp
erim
ental
water, tolbu
tamide or a
studied plants, excep
t Aloe barbadensis,
study of the
hyp
oglycemic effect
plan
t preparation
decreased
significantly the
area un
der
of som
e an
tidiabe
tic plan
ts. A
rch
the gluco
se toleran
ce curve, in
Inve
st M
ed (Mex
) 19
91;22:87–9
3.relation
to the water con
trol group
.Aloe barbadensis
Exu
date of Aloe barbadensis
Allo
xan-diabe
tic
Hyp
oglycemic effects of aloe
on seru
m
Ajabn
oor MA. Effect of aloes on
leav
es and
bitter
mice
gluc
ose leve
ls w
ere insign
ifican
t bloo
d gluco
se lev
els in normal
principle. A
dministered
whe
reas the
bitter pr
inciple w
as
and allo
xan diabe
tic mice.
orally, 50
0 mg/
kg.
high
ly significant and
exten
ded ove
r a
JEthno
pha
rm 199
0;28
(2):2
15–2
20.
The
bitter pr
inciple w
asperiod of 24
hou
rs. The
max
imum
ad
ministered IP, 5 m
g/kg
decrease in plasm
a gluc
ose leve
l was
observed
at day
5 in bo
th cases.
Alpinia galanga
Ethan
olic extract of
Mice
Alpinia galanga
trea
tmen
t sign
ifican
tly
Quresh
i S, et al. Effect of Alpinia
(L.) Sw
.Alpinia galanga
decreased
the
effect of ind
uced
galangatrea
tmen
t on
cytolog
ical
ZIN
GIBERACEAE
rhizom
es. Minim
um
micronu
clea
ted polyc
hrom
atic
and bioch
emical cha
nges ind
uced
Malay
avacha
effective dose was 125
erythr
ocytes (MPE
) witho
ut altering
by cyc
lopho
spha
mide in m
ice.
Java
galan
gal
mg/
kg bod
y weigh
tcy
totoxicity. B
ioch
emical cha
nges
Int J Ph
armacog
199
4;32
(2):1
71–1
77.
caus
ed by MPE in the liv
er w
ere
also significantly inh
ibited
.
418
Alpinia galanga
Ethan
olic extract of
Rats
Sign
ifican
t decrease in the
inten
sity of
Al-Yah
ya M
A, et al. Gastric
Alpinia galanga
at a
muco
sal dam
age was gastric observe
d.
antisecretory, antiulcer and
dose of 500 m
g/kg
Alpinia galanga
prod
uced a significant
cytoprotective properties of
decrease in gastric secretion
in py
loru
s etha
nolic
extract of A. galanga
ligated
rats an
d a highly sign
ifican
t W
illd in rats. P
hytother R
es 199
0;cy
toprotective effect aga
inst ind
uced
4(3):112
–114
.cy
todestruction.
Alpinia galanga
Ethan
olic extract of
Mice
Tox
icities studies were don
e. N
oQuresh
i S, et al. Tox
icity studies on
rhizom
es of Alpinia
sign
ifican
t mortality co
mpared
to
Alpinia galanga
and Curcuma longa.
galangaan
d Curcuma
controls w
as noted
. The
gain in
Planta Med
199
2;58
(2):1
24–1
27.
longa. A
cute dos
ages
weigh
ts of sexu
al organ
s an
d0.5, 1.0, an
d 3 g/kg
bod
yincrea
sed spe
rm m
otility and
spe
rmweigh
t. Chr
onic dos
age
counts were ob
served
in bo
th groups
100 mg/
kg per day
The
se cha
nges w
ere high
ly significant
in the
Alpinia galanga-treated
group.
Both ex
tracts failed to sh
ow any
spermatotox
ic effects.
Ananas comosus
Bromelain, a proteolytic
Piglets
Administration of bromelain can
Myn
ott TL, e
t al. Oral ad
ministration
(L.) Merr.
extract ob
tained
from
inhibit Enterotox
igen
ic Escherichia
of protease inhibits enterotox
igen
ic
BROMELIA
CEAE
pine
apple stems
coli(ETEC) receptor activity in vivo an
dEscherichia colireceptor activity in
Ana
nas
may
be us
eful for preve
ntion of K
881
piglet small intestine. G
ut 1996;38(1):
Pineapple
ETEC-ind
uced
diarrhe
a.28
–32.
Ananas
Enz
yme fraction
s derived
12
rats with
Results ind
icate de
bridem
ent (the
Row
an A
D, et al. Deb
ridem
ent of
Comosus
from
the
stem of
full thickn
ess
remov
al of un
healthy tissue) of the
experim
ental full-thickn
ess sk
in
pine
apple
skin burns
injury cou
ld be effected
rap
idly
burns of rats with en
zyme fraction
s (w
ithin 4 ho
urs). Pineapple ha
sderived
from pinea
pple stems.
poten
tial as a no
nsurgical deb
riding
Burns 19
90;16(4):243
–246
.ag
ent.
Andrographis
Kan
Jan
g, herba
l extract
Ran
dom
ized
No sign
ifican
t differenc
e in the
occurren
ceCaceres D
D, et al. Preve
ntion of
paniculata
principle ing
redient is
dou
ble-blind
of colds be
tween the study grou
p an
dco
mmon
colds with Andrographis
(Burm.f.) Nees
Andrographis paniculata,
study; 107
the placebo
con
trol. In the third m
onth,
paniculata
dried
extract. A
pilo
tACANTHACEAE
approximately 2 tablet
healthy vo
l-there was a significant decrease in the
dou
ble blind trial. P
hytomed
icine
Kirta
per day
of 10
0 mg ea
chun
teers all
occu
rren
ce of co
ld in the stud
y grou
p19
97;4(2):1
01–1
04.
King of Bitters
approximately
compared
to the placebo
.18
yea
rs old
TABLE2.
PLANTSU
SED
INAYURVEDICPHARMACOPOEIA
(CONT’D)
Genus, species
family
Common name
(Sanskrit)
Common name
Plant part used,
Design
(English)
preparation, and dosage
and model
Results
References
419
(continued)
Andrographis
Kan
jang
tab
lets, s
tand
ardized
Con
trolled,
A decrease of the
subjective
sym
ptom
s Melch
ior J, et al. Con
trolled clin
ical
paniculata
Andrographis paniculata
dou
ble-blind
and dur
ation of sym
ptoms of the
study of stand
ardized
Andrographis
extract
pilot study:
common
cold w
ere sign
ifican
tly
paniculata
extract in com
mon
cold—
50 patients
reduc
ed (p
,0.02
5)a pilo
t trial. Phy
tomed
icine 19
96/
1997
;3(4):3
15–3
18.
Andrographis
Aqu
eous ex
tract of
Spon
tane
ously
Dose-dep
enden
t hy
poten
sive
effect on
Zha
ng C
Y, T
an BK. H
ypoten
sive
paniculata
Andrographis paniculata.
hypertens
ive
systolic blood
pressur
e was studied.
activity of aq
ueou
s ex
tract of
Chr
onic IP infusion
s rats and
Plasm
a an
gioten
sin-co
nverting
Andrographis paniculata
in rats.
by osm
otic pum
ps
Wistar-
enzy
me activities as well as kidne
yClin
Exp
Pha
rm Phy
s 19
96;23(8):
Kyo
to rats
thioba
rbitur
ic acid lev
el w
ere
675–
678.
sign
ifican
tly decreased
in ex
tract-
trea
ted versu
s co
ntrols.
Andrographis
Adrographis paniculata
Dog
mod
elFind
ings
ind
icate that Andrographis
Guo ZL, et al. An ex
perimen
tal
paniculata
paniculata
may
decrease the ne
gative
study of the
mecha
nism
of
effects of ische
mic rep
erfusion
(by
Andrographis paniculata
Nees(APN)
decreasing the ha
rmful effects of free-
in alle
viating the Ca(21
)-ov
er-
radical dam
age).
load
ing in the
process of myo
- card
ial isch
emic rep
erfusion
. J.
Ton
gji Med
Univ 1995
;15(4):205
–208
.Andrographis
Andrographis paniculata
Clin
ical trial:
Results sho
w tha
t post Extraco
rporea
lMuan
gman
V, e
t al. The
usage
of
paniculata
tablets (250
mg),
100 patients
Shoc
k W
ave Litho
tripsy (ESW
L)
Andrographis paniculata
follo
wing
4 tablets tid 25 patients
with rena
lpyu
ria an
d hem
aturia in patients
Extraco
rporea
l Sh
ock W
ave
give
n co
trim
oxazole
ston
es and
receiving Andrographis paniculata
Litho
tripsy
(ESW
L). J Med
2 tablets bid, 2
5 patients
norm
al ren
alwere reduced to 0.69
and
0.55
Assoc
Tha
iland
199
5;78
(6):3
10–3
13.
received
norflox
acin
func
tion
compared
to pre-ESW
L value.
200 mg bid
Authors co
nclude Andrographis
paniculata
is ben
eficial for post-
ESW
L urina
ry tract infection
.Andrographis
Extract of Andrographis
Clin
ical trial:
Extract can
significantly alle
viate
Wan
g DW
, Hua
YZ. Prev
ention
of
paniculata
paniculata
patien
tsathe
rosclerotic sten
osis and
resteno
sis
athe
rosclerotic arterial steno
sis
with sten
osis
after ex
perimen
tal an
giop
lasty. A
4-
and resteno
sis after an
giop
lasty
week follo
w-up show
ed dila
ted ilia
cwith Andrographis paniculata
arteries in co
ntrol grou
p all ha
d sev
ere
nees and
fish oil. Chine
se M
ed J
resten
osis, b
ut Andrographis
(Eng
lish Ed) 19
94;107
(6):4
64–4
70.
paniculata-treated
group
had
no or
only m
ild resteno
sis oc
cur.
Andrographis
Andrographis paniculata
Ran
dom
ized
,Efficacy of paracetam
ol or high
dose
Tha
mlik
itku
l V, e
t al. Efficacy
of
paniculata
3 g/
d or 6 g/
d for
dou
ble-blind
of Andrographis paniculata
was
Andrographis paniculata, N
ees for
7 da
ys or Pa
racetamol
study
: 15
2sign
ifican
tly more effective than
low
pha
ryng
oton
sillitis in adults. J Med
ad
ults with
dose of Andrographis paniculata
atAssoc
Tha
iland
199
1;74
(10):437
–442
.ph
aryn
go-
day
3 in term
s of the
relief of fev
ertons
illitis
and sore throat.
420
Andrographis
And
rograp
holid
e, a
Rats
Andrographis paniculata
exhibited stron
g Tripathi G
S, T
ripathi Y
B. C
holeretic
paniculata
diterpe
ne, iso
lated from
choleratic action whe
n ad
ministered
action
of And
rograp
holid
e ob
tained
Andrographis
IP. The
sub
stan
ce ind
uced an increa
se
from
Andrographis paniculata
in
paniculata
in bile
flow and
a cha
nge in phy
sical
rats. P
hytother R
es 199
1;5:17
6–17
8.properties of bile secretion
.Andrographis
A m
ixture of Andrographis
Hum
an trial:
Herba
l mixture w
as administered to
Ram
ji, et al. E
ffect of K
almeg
ha and
paniculata
paniculata
and Emblica
35 patients
patients with Hep
atitis B
1, B
2, a
ndAmlaki com
pou
nd on viral
officinalis
hepa
titis B
1,
post he
patitis syn
drome. The
mixture
hepatitis (Kos
htha
-Sha
khashr
ita
hepa
titis B
2,
dem
onstrated efficacy in red
ucing
Kam
ala) A
ryav
aidya
n 19
92;5(3):
and post-
clinical sym
ptom
s, improving
liver
164–
169.
hepa
titis
func
tion
, an
d album
in.
synd
rome
Andrographis
Decoc
tion
of Andrographis
Hum
anHep
atoc
ellular jaund
ice was m
onitored
. Tom
ar G
S, Singh
RN. Treatmen
t of
paniculata
paniculata
of 60 ml/
trial: 60
Yellow color of the co
njunc
tiva
he
patoc
ellular jaund
ice with
day
(eq
uiva
lent to 40
gpa
tien
tsim
prove
d 100%, ten
der hep
atic
Kalmeg
h (Andrographis paniculata).
of cru
de drug) in 3
with he
pato-
enlargem
ent decreased
in 96
% w
ithin
Aryav
aidya
n 19
90;11(3–
3):156
–162
.divided
dos
es. A
verage
cellu
lar
20 day
s of treatmen
t. Loss of
trea
tmen
t 23
1/2
4 day
sjaund
ice
appetite in 100
% w
as improve
d after
4–5 da
ys. S
everal tests w
ere high
lysign
ifican
t after trea
tmen
t: seru
mbilirubin, alkaline pho
spha
tase, s
erum
tran
sferase.
Andrographis
Alcoh
ol extract of
Guinea
pigs
Extract ex
hibited sign
ifican
t an
tidiarrhe
alGupta S, et al. A
ntidiarrho
eal activity
paniculata
Andrographis
and rab
bits
activity aga
inst Escherichia coli en
terotoxins
of diterpen
es of Andrographis
paniculata
in animal m
odels.
paniculata
(Kal-M
egh) aga
inst
Escherichia colien
terotoxin in in
vivo
mod
els. Int JCru
de Drig Res
1990
;(4):2
73–2
83.
Andrographis
Andrographis
Rats
Rep
eated administration of leaf
Cho
udhu
ry BR, et al. In vivoan
d
paniculata
paniculata
leaf extract
extract positively effected
microsomal
in vitro
effects of K
almeg
h an
d and
rograp
holid
edru
g metab
olizing en
zyme system
s of
(Andrographis paniculata) ex
tract an
dthe rat liv
er (he
patic m
icroso
mal
andrograp
holid
e on
hep
atic
aniline
hydroxy
lase, N
-dem
ethy
lase,
microsomal dru
g metab
olizing
and O
-dem
ethy
lase enz
ymes).
enzy
mes. P
lanta Med
198
7;53
:13
5–14
0.
TABLE2.
PLANTSU
SED
INAYURVEDICPHARMACOPOEIA
(CONT’D)
Genus, species
family
Common name
(Sanskrit)
Common name
Plant part used,
Design
(English)
preparation, and dosage
and model
Results
References
421
(continued)
Apium
graveolens L.
Aqu
eous celery extract
Rats
Seru
m cho
lesterol con
centration
was
Tsi D
, Tan
BK. E
ffects of celery
UMBELLIFE
RAE
administered
sign
ifican
tly decreased
(p
,0.05)
extract an
d 3-N
-butylphtha
lide
Ajm
oda
intrap
eriton
eally
compared
to co
ntrols. Celery ex
tract
on lipid lev
els in gen
etically
Celery
was effective
in prev
enting
the
rise of
hype
rcho
lesterolae
mic (RIC
O) rats.
cholesterol leve
l in rats.
Clin
Exp
Pha
rmacol Phy
siol
1996
;23(3):214
–217
.Apium
graveolens
Metha
nolic
extract of
Rats with
A significant hep
atop
rotective activity
Sing
h A, H
anda SS
. Hep
atop
rotective
the seed
s of Apium
paracetamol-
of the
metha
nolic
extract of the seed
sactivity of Apium
graveolensan
dgraveolens
and
induced
of both plants was rep
orted.
Hygrophila auriculataag
ains
tHygrophila auriculata
liver
paracetam
ol and
thioa
cetamide
dam
age
intoxication
in rats. JE
thno
pharm
1995
;15;49
(3):1
19–1
26.
Apium
graveolens
Aqu
eous celery extract:
Wistar rats
At the en
d of 8 weeks, a
significant
Tsi D
, et al. Effects of a aq
ueou
s 2 grou
ps fed high fat
decrease was fou
nd in total seru
m
celery (Apium
graveolens) extract
diets, 1
group also fed
cholesterol, LD
L ch
olesterol, an
d
on lipid param
eters of rats fed a
aqueo
us celery extract
triglyceride co
ncen
trations
.high
fat diet. Plan
ta M
ed 199
5;61(1):
18–2
1.Apium
graveolens
From
celery seed
oil, 3-
Mice with
After treatmen
t with co
mpou
nds,
Zhe
ng G
Q, et al. Che
mop
reve
ntion
n-bu
tylphtha
lide,
benz
o[a]
tumor inc
iden
ce w
as decreased
from
of ben
z-[a]pyren
e-induc
ed fore-
sedan
olide, and
pyrene
-68
% to 30% and
11%
. A red
uction in
stom
ach canc
er in mice by
natur
al
p-men
tha-2,8-dien-1-ol
induced
tumor m
ultiplic
ity of 67%
and
83%
phtha
lides from celery root seed
were tested
tumorigen
esis
was observe
d w
ith 3-n-bu
tylphtha
lide
oil. Nutr C
ancer 19
93;19(1):77–
86.
and sed
anolide. D
ata indicate bo
thwere active
in tumor inh
ibition.
Apium
graveolens
80% ethan
olic extract of
Rats with
Results sh
owed
tha
t the plan
tsAl-Hindaw
i MK, e
t al. Anti-
Achillea santolina,
carrag
eena
n-possessed
varying
deg
rees of an
ti-
inflam
matory activity of some
Apium
graveolens,
induced
inflam
matory activity in the follo
wing
Iraq
i plants using
intact rats.
Matricaria chamomilla,
paw edem
adescend
ing order: W
ithania somnifera,
JEthno
pha
rm 198
9;26
(2):1
63–1
68.
Myrtus communis,
Apium
graveolens, Achillea santolina,
Withania somnifera
and
Matricaria chamomilla, Myrtus communis.
Acetylsalicylic acid used
as stand
ard drug.
Areca catechu
L.
Betel nut ch
ewing
Mailed question
-11
6 resp
onses to question
naire
Lee CN, et al. Betel nut an
d sm
oking.
PALMAE
naire, 223
co
mpared
to he
althy mem
bers of the
Are the
y bo
th protective in
Poo
gapa
tien
ts w
ith
community. It ap
pears that smok
ing
ulcerative co
litis? A pilo
t study.
Areca nut
inflam
matory
and betel nut ch
ewing reduce the
risk
Arquivos de Gastroe
nterol
bowel disea
seof dev
elop
ing ulcerative
colitis
1996
;33(1):3–5
.Areca catechu
Betel nut ch
ewing
Con
trolled
A significant inc
rease in m
itom
ycin C
Trive
di AH, e
t al. Eleva
ted m
utag
en
clinical
(MMC)-induc
ed sister ch
romatid
suscep
tibility in cultured
trial: 40
exch
ange
(SC
E)/cell va
lues w
ere
lymph
ocytes of oral can
cer
oral can
cer;
observed
amon
g oral can
cer patients
patie
nts. A
ntican
cer Res 1995;15
(6B):
40 tob
acco
(betel nut ch
ewers) as co
mpared
to
2589
–259
2.ch
ewers; 40
healthy no
nche
wer con
trols.
healthy
individuals
422
Areca catechu
Betel quid che
wing
Hum
anRea
ctive ox
ygen
spe
cies, O
H rad
ical,
Nair UJ, et al. Ortho
- an
dcons
isting
of be
tel leaf,
trial: 5
are form
ed in the hu
man
oral cavity
metatyros
ine form
ation from
areca qu
id, catech
u an
dvo
lunteers
during
betel quid che
wing an
d m
ay be
phe
nylalanine
in hu
man
saliva as
slak
ed lim
e (w
itho
ut
implic
ated
in the ge
netic dam
age that
a marke
r of hyd
roxy
l radical
toba
cco)
has be
en obs
erve
d in oral epithe
lial
gene
ration
during be
tel qu
idcells
of ch
ewers.
chew
ing. C
arcino
gene
sis
(Oxford) 19
95;16(5):119
5–11
98.
Areca catechu
Che
wing an
d smok
ing
Case-controlle
dIncreased risk of oral su
bmuco
us
Mah
er R
. Role of areca nut in the
habits and
oral
clinical
fibros
is w
as obs
erve
d for areca nu
tcaus
ation of oral su
bmuco
us
subm
uco
us fibrosis
trial: 15
7ch
ewing. W
hen the ha
bit was
fibros
is: a case-con
trol study in
(OSF
)cases an
dpracticed
alone
, app
eared to ha
vePak
istan. JOral Patho
l Med
199
4;15
7 co
ntrols
high
est risk followed
by “p
aan”
with
23(2):6
5–69
.or w
itho
ut toba
cco. D
aily con
sumption
rates ap
pea
red to be
more im
portant
with resp
ect to risk than
lifetim
e duration
of ha
bit.
Areca catechu
Areca nut pow
der added
Mice
Areca nut decreased
mace-indu
ced
Sing
h A, Rao
AR. Mod
ulatory effect
to feed
increa
ses in hep
atic glutathione
-S-
of areca nut on
the
action of m
ace
tran
sferase an
d sulphh
ydryl leve
ls and
(Myristica fragrans, H
outt) on
the
elev
ated
fur
ther inc
reases in the leve
lshe
patic detox
ification sy
stem
in
of cytochr
ome b5
and
P-450
.mice. Foo
d C
hem Tox
ic 199
3;31
(7):
517–
521.
Areca catechu
Oral ha
bits
Retrosp
ective
Ana
lyses confirmed
an association
van W
yk C
W, et al. The
areca nut
study:
betw
een nu
t ch
ewing an
d che
ekch
ewing ha
bit an
d oral sq
uamou
s 14
3 men
canc
er. T
he data sh
owed
tha
t areca
cell carcinom
a in Sou
th A
frican
an
d w
omen
nut ha
bit with or w
itho
ut toba
cco use
Indians
. A retrosp
ective
study.
with oral
is important in the dev
elop
men
t of
South A
frican
Med
J 199
3;83
(6):
squa
mou
soral squ
amou
s carcinom
a.42
5–42
9.carcinom
aAreca catechu
Areca nut decoction
Case stud
yA case stud
y dem
onstrated the
Fu H
H, e
t al. Areca nut in the
effectiven
ess of areca nut decoc
tion
in
trea
tmen
t of diphy
llobo
thrium
the trea
tmen
t of Diphyllobothrium
latum infection
:Rep
ort of a
latum
infection
case study. C
hin Med
J 195
1;69
:40
7–40
9.
TABLE2.
PLANTSU
SED
INAYURVEDICPHARMACOPOEIA
(CONT’D)
Genus, species
family
Common name
(Sanskrit)
Common name
Plant part used,
Design
(English)
preparation, and dosage
and model
Results
References
423
(continued)
Artemisia vulgaris L.
Infusion
: Urtica dioica,
Human
An he
rbal infusion
used to irriga
te the
Dav
idov
MI, et al. Po
stad
enom
ectomy
COMPO
SITAE
Hypericum
trial: 22
blad
der after prostate ad
enom
ectomy
phy
toperfusion
of the blad
der.
Nag
adam
niperformatum
,pa
tien
ts post-
reduc
ed post op
erative bloo
d loss,
Urologiya
INefrologiya
199
5;0(5):
Mug
wort
Matricaria recutita,
pros
tate
bacteriuria, preve
nted
hem
orrh
agic
19–2
0.Plantaginis majoris,
aden
omectomy
and puru
lent inflammation.
Herba millefolii,
Betula, Artemisia
vulgaris, Fragaria vesca
Asparagus
Asparagus racemosus,
Mice
All plan
ts significantly inh
ibited
the
Dhu
ley JN
. Effect of som
e Indian
racemosus
Willd.
Picrorhiza kurrooa,
carcinog
en och
ratoxin-induced
herbs on
macroph
age func
tion
s ASP
ARAGACEA
ETinospora cordifolia,
supp
ression of che
motactic activity
in och
ratoxin A treated
mice. J
Shatau
ari
Withania somnifera
and the
produc
tion
of interleu
kin-1
Ethno
pha
rm 199
7;58
(5):1
5–20
.Asp
arag
us
and tumor necrosis factor-a
bymacroph
ages.
Asparagus
1 capsu
le 3
3pe
r day
30
patients
The
herba
l co
mbina
tion
was fou
nd to
Karnick
CR. Clin
ical eva
luation of
racemosus
with luke
warm w
ater
with calculi
alleviate no
t on
ly pain bu
t also in its
composite Ayu
rved
ic dru
gs, o
ncontaining
: Asparagus
on kidne
ys,
ability to slow
ly disintegrate bo
thcalculi, in the kidne
y an
d the
racemosus,5
0 mg;
ureters, or
calcium-oxa
late and
calcium
urina
ry bladder. A
ryav
aidya
n Bergenia ligulata,
100
blad
ders
carbon
ate crys
tals in a sp
an of 72
1992
;6(2):1
04–1
08.
mg; Eclipta alba,
100
hours and
com
plete disch
arging
of
mg; Myristica fragrans,
crystals w
ithin 15
–30 day
s. C
omplete
10 m
g; Tinospora
disch
arge
occur
red in grea
ter than
cordifolia,1
00 m
g;80
% of the patients.
Tribulus terrestris, 50
mg; Withania somnifera,
50 m
gAsparagus
2 g pow
dered
roo
t of
Clin
ical crossov
erBasal gastric emptying t1/2
was 159
.9Dalvi SS, et al. Effect of Asparagus
racemosus
Asparagus racemosus
study
: 8
that w
as red
uced by Asparagus
racemosus
(Sha
tava
ri) on
gastric
compa
red to stan
dard
norm
alracemosus
to 101
(p
,0.00
1) and
by
emptying time in normal hea
lthy
treatm
ent of 10 mg
healthy male
metoc
lopr
amide to 85.3 (p
,0.00
1).
volunteers. J Postgrad M
ed 199
0;tablet m
etoclopramide
volunteers
Asparagus racemosus
and
36(2):9
1–94
.metoc
lopr
amide did not differ
sign
ifican
tly in the
ir effect.
Asparagus
Asparagus racemosus,
Mice
Whe
n co
mpared
with co
ntrol grou
ps,
Tha
tte UM, Dah
anuka
r SA
.racemosus
Tinospora cordifolia,
all four
dru
gs preve
nted
, to va
rying
Com
parative stud
y of
glucan an
d lithium
for
deg
rees, leuc
open
ia. Both indigen
ous
immuno
mod
ulating activity of
15 day
splants were poten
t im
muno
stim
ulants
Indian
med
icinal plants, lithium
with effects comparab
le to lithium
carbon
ate an
d glucan. M
etho
ds
and glucan.
Find
Exp
Clin
Pha
rmacol
1988
;10(10
):639
–644
.Azadirachta indica
Pur
ified ne
em extracts,
Rats, bab
oons
, Pr
egna
ncy was terminated
(with oral
Talwar G
P, et al. Ind
uced
termination
A. Juss.
orally delivered
and m
onke
ysne
em) su
ccessfully in roden
tsof pregn
ancy
by pur
ified extracts
MELIA
CEAE
and primates w
ith no
significant side
of Azadirachta indica(N
eem):
Arish
taeffects
Mecha
nism
s invo
lved
. Am J
Neem
Rep
rod Immun
ol 1997;37(6):4
85–4
91.
424
Azadirachta indica
Lea
f po
wder of
Male albino
rats
Results sugg
est a po
ssible rev
ersible
Joshi AR, e
t al. Effect of Azadirachta
Azadirachta indica
antian
droge
nic pr
operty of the leav
es.
indica
leav
es on testis and
its
reco
very in albino
rats. Ind
ian
JExp
Biol 19
96;34(11
):109
1–10
94.
Azadirachta indica
Neem oil in m
ixed
in
Con
trolled
Results rev
ealed 81%
–91%
mosqu
ito
Mishr
a AK, e
t al. Use of ne
em oil as
coconu
t oil (1%–4%)
field study:
repellant action during
12-ho
ur pe
riod
a mosqu
ito repe
llent in tribal
exposed
of observa
tion
from bites of
villa
ges of M
andla district, Mad
hya
body pa
rts
anop
helin
e mosqu
itoe
s.Pradesh. Ind
ian J Malariol 19
95;
of hum
an32
(3):9
9–10
3.vo
lunteers
Azadirachta indica
Neem cream
Con
trolled
App
lication of neem cream
to ex
posed
Dua
VK. Rep
ellent action of neem
field study:
body parts sho
wed
78%
, 89
%, a
nd
cream aga
inst m
osqu
itoe
s. Ind
ian J
exposed
94.4% protection ag
ains
t Aed
es,
Malariology
199
5;32
(2):4
7–53
.bo
dy pa
rts
Culex
, and
Ano
phe
les mos
quitoe
s,of hum
anresp
ective
ly. Sign
ifican
t differenc
evo
lunteers
was observe
d between ne
em cream
-trea
ted and
untreated
group for Aed
emos
quitoe
s.Azadirachta indica
Azadirachta indica,
Mice with
Infected
mice were prophy
lactically
Sohn
i YR, e
t al. Pr
ophy
lactic the
rapy
Boerhavia diffusa,
septicem
iaad
ministered postinfective
, preinfective,
of Salmonella typhi
septicemia in
Picrorhiza kurrooa,
from
sing
le and
multiple dos
es of ex
tract
mice with a trad
itiona
lly prescribe
d
Terminalia chebula,
Salmonella
and had
a significant the
rapeu
tic
crud
e dru
g form
ulation
. J
Tinospora cordifolia,
typhi
effect in reduc
ing septicemia.
Ethno
pha
rm 199
5;45
:141
–147
.Trichosanthes dioica,
Zingiber officinale.
Extracted
in 80%
aque
ous alco
hol etha
nol.
1% stock solution us
edto prepa
re dilu
tion
s.Oral or subc
utane
ous
administration
Azadirachta indica
Extracts of neem lea
ves
Rats
Neem dose dep
ende
ntly decreased
gastric
Garg GP, et al. The
gastric antiulcer
ulcer sev
erity in rats ub
jected
to stress
effects of the
lea
ves of the
Neem
and also decreased
ethan
ol provo
ked
tree. Plan
ta M
ed 199
3;59
:215
–217
.ga
stric muc
osal dam
age.
TABLE2.
PLANTSU
SED
INAYURVEDICPHARMACOPOEIA
(CONT’D)
Genus, species
family
Common name
(Sanskrit)
Common name
Plant part used,
Design
(English)
preparation, and dosage
and model
Results
References
425
(continued)
Azadirachta indica
Azadirachta indicaan
dPilo
t stud
y:In 97%
of the cases, a cur
e of scabies w
as
Cha
rles V
, Cha
rles SX. T
he use and
Curcuma longapa
ste
814 patients
obtained
within 3–
15 day
s of treatmen
t.efficacy
of Azadirachta indicaADR
with scab
ies
(“Neem”) and
Curcuma longa
(“Turm
eric”) in scab
ies:A pilo
tstudy. Trop G
eogr M
ed 199
2;44
:17
8–18
1.Azadirachta indica
A decoc
tion
of the follo
wing
14 cases of
All pa
tien
ts w
ere give
n the decoc
tion
and
Sati R
B, Sh
arma RK. Man
agem
ent of
herbs: Azadirachta indica,
cong
estive
Urgenic indica. Patients with isch
emic
cong
estive
cardiac failu
re w
ith
Boerhaavia diffusa, Cedrus
heart failu
rehe
art disease, card
iomyo
pathy
and
certain Ayu
rved
ic dru
gs.
deodara, Picrorhiza kurrooa,
cor pulmon
ale were give
n pow
der of
Aryav
aidy
an 199
0;4(2):123
–126
.Terminalia chebula, Tinospora
Inula racemosa, w
hile patients with
cordifolia, Trichosantes lobata;
rheu
matic heart disea
se w
ere give
nInula raceomosa2 g, 8
Commiphora mukul. A
fter 2 w
eeks
hourly; Commiphora mukul,
of treatmen
t all 10
patients were cu
red
1/2 g 8 ho
urly; Urgenic
completely, 2
had
bradyc
ardia and
indica 100 m
g 8 ho
urly
2 were refractory.
Azadirachta indica
Group I: Azadirachta indica
Ran
dom
Enc
ouraging
improve
men
t in treating
Nair RP, et al. Clin
ical eva
luation of
powder 4 g/33
day
, trial: 60
vitilig
o (app
earanc
e of w
hite patch
esAyu
rved
ic prepa
ration
s in vitiligo
. Pa
ste of Abrus precatorius,
patien
tson
the
skin) w
as noted
in bo
th group
s.JR
es A
yur Siddh 19
87;VIII(1–
2):
and Plumbago zeylanica
with vitilig
o30
–38.
applie
d externa
llyGroup
II:Pow
der of
Phyllanthus emblica,
Acacia catechuan
dseed
s of Psoralea
corylifolia
4 g/
33day
Azadirachta indica
Neem oil ap
plie
d w
ith
Human
and
Used intrava
gina
lly, ne
em w
as 100
%Sinh
a KC, e
t al. N
eem oil as a
an applicator
anim
aleffective in preve
nting pregn
ancy
in
vagina
l co
ntraceptive. Ind
ian
trial: rats,
subjects.
JMed
Res 198
4;79
:131
–136
.rhesus
mon
keys
,hu
man
sBacopa monnieri
Ayu
rved
ic prepa
ration
of
Dou
ble-blind,
Ayu
rved
ic preparation was effective
in
Yad
av SK, et al. Irritable bo
wel
(L.) Pe
nnell
Aegle marmelos
and Bacopa
rand
omized
64.9% w
hereas stand
ard the
rapy
was
synd
rome: the
rape
utic ev
alua
tion
SC
ROPH
ULA
RIACEA
Emonnierifor 6 weeks
trial: 16
9useful in 78.3%
. Placebo
patients
of ind
igen
ous dru
gs. Indian JM
edBrahm
ive
rsus
stand
ard the
rapy
pa
tien
ts w
ith
improve
d 32.7%
. The
rapy was
Res Sect A-Infect Dis 198
9;90
:Brahm
iof clid
inium bromide,
irritable
particu
larly be
neficial in the diarrhe
a-49
6–50
3.ch
lord
iaze
poxide, and
bowel
predom
inan
t form
of IBS.
isap
hagu
llasynd
rome
(IBS)
Bacopa monnieri
Con
stituen
ts of Bacopa
Rats
Bacosides app
eared to ha
ve a significant
Sing
h HK, et al. Effect of Bacos
ides A
monnieriaq
ueo
us
effect on men
tal retention capa
city of
and B on av
oidan
ce respon
ses in
susp
ension
of ba
cosides
rats by im
prov
ing resp
onses.
rats. P
hyto R
es 198
8;2(2):70–
75.
A and
B
426
Bacopa monnieri
Aqu
eous
susp
ension
of
Rats
In Sho
ck-M
otivated
Brigh
tness-
Sing
h HK, Dha
wan
BN.
an alcoh
olic extract of
Discrim
ination Reaction, the
treated
Effect of Bacopa monniera
Bacopa monnieri(40 mg/
kg
grou
p sho
wed
significant better
Linn. (brah
mi) extract on
orally) for 3 or m
ore day
sacqu
isition, improv
ed reten
tion
, an
dav
oida
nce resp
onses in rat. J
delay
ed extinction. In Active
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2;5(2):205
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.Con
ditione
d Flig
ht R
eacti