|
Safety
evaluation of BacoMind trade mark in healthy volunteers: A phase I
study.
Phytomedicine.
2007 May;14(5):301-8. Epub 2007 Apr 17
*
Pravina K, * Ravindra KR, * Goudar KS, * Vinod DR, * Joshua AJ, *
Wasim P, * Venkateshwarlu K, * Saxena VS, * Amit A.
Department
of Pharmacology and Toxicology, R&D Centre, Natural Remedies Pvt.
Ltd., Bangalore 560 100, India.
BacoMindtrade
mark is an enriched phytochemical composition of Bacopa monniera (B.
monniera), a common medicinal plant used in the traditional systems
of medicine as a memory-enhancing agent. BacoMind trade mark was
standardized with reference to bioactive compounds and was evaluated
for short-term safety and tolerability in healthy adult volunteers.
The study plan employed randomized, open label, dose escalation
design. Each of 23 participants were orally given one single capsule
of BacoMind trade mark daily for 30 days, i.e., 300mg for first 15
days and 450mg for next 15 days. Detailed examination of clinical,
hematological, biochemical and electrocardiographic parameters done
in pre and post-treatment periods did not indicate any untoward
effects in any of the treated volunteers. Mild adverse events related
to gastrointestinal system were observed in the trial, which subsided
spontaneously. BacoMind trade mark was found to meet the safety
criteria at the dose administered for the given duration of trial
period in healthy adult volunteers.
PMID:
17442556 [PubMed - in process] Glycosides
of 20-Deoxy Derivatives of Jujubogenin and Pseudojujubogenin from
Bacopa monniera.
Planta
Med. 2007 Apr;73(4):380-3. Epub 2007 Mar 29
*
Pawar RS,* Khan SI, * Khan IA.
National
Center for Natural Products Research, Research Institute of
Pharmaceutical Sciences, University of Mississippi, University, MS,
USA.
A
detailed phytochemical investigation of an extract of BACOPA MONNIERA
resulted in the isolation of two new dammarane glycosides along with
eight known compounds. They have been identified as glycosides of the
20-deoxy derivatives of jujubogenin and pseudojujubogenin. The
structures were established by different spectroscopic methods that
included 1D and 2D NMR experiments. The compounds were tested for
their cytotoxicity, antileishmanial, antimalarial, antioxidant, and
anti-inflammatory activities. Only few compounds exhibited mild to
moderate cytotoxicity towards non-cancerous kidney cell lines.
PMID:
17394105 [PubMed - in process] Effect
of Bacopa monniera on stress induced changes in plasma corticosterone
and brain monoamines in rats.
J
Ethnopharmacol. 2007 May 22;111(3):671-6. Epub 2007 Jan 30.
*
Sheikh N,* Ahmad A, * Siripurapu KB, * Kuchibhotla VK, * Singh S, *
Palit G.
Division
of Pharmacology, Central Drug Research Institute, P.B. No. 173,
Lucknow 226001, Uttar Pradesh, India.
Bacopa
monniera (BM) is well known for its neuropharmacological effects. Our
previous studies indicated the adaptogenic effect of standardized
extract of BM in various stress models. In the present study, effect
of BM was evaluated on acute stress (AS) and chronic unpredictable
stress (CUS) induced changes in plasma corticosterone and
monoamines-noradrenaline (NA), dopamine (DA) and serotonin (5-HT) in
cortex and hippocampus regions of brain in rats. Panax root powder
(Panax quinquefolium) was taken as standard. Subjecting animals to AS
(immobilization for 150min once only) and CUS (different stressors
for 7 days) resulted in significant elevation in plasma
corticosterone levels, which was significantly countered by treatment
with BM at a dose of 40 and 80mg/kg p.o. similar to the effects of
Panax quinquefolium (PQ) at 100mg/kg p.o. AS exposure significantly
increased the levels of 5-HT and decreased NA content in both the
brain regions while DA content was significantly increased in cortex
and decreased in hippocampus regions. In CUS regimen, levels of NA,
DA and 5-HT were significantly depleted in cortex and hippocampus
regions of brain. Treatment with BM (40 and 80mg/kg) attenuated the
stress induced changes in levels of 5-HT and DA in cortex and
hippocampus regions but was ineffective in normalizing the NA levels
in AS model, whereas PQ treatment significantly reverted back the
effects of stress. In CUS model, pretreatment with BM and PQ
significantly elevated the levels of NA, DA and 5-HT levels in cortex
and levels of NA and 5-HT in hippocampus regions. Hence, our study
indicates that the adaptogenic activity of BM might be due to the
normalization of stress induced alteration in plasma corticosterone
and levels of monoamines like NA, 5-HT and DA in cortex and
hippocampus regions of the brain, which are more vulnerable to
stressful conditions analogous to the effects of PQ.
PMID:
17321089 [PubMed - in process] Protective
activity of Bacopa monniera Linn. on nicotine-induced toxicity in
mice.
Phytother
Res. 2007 Apr;21(4):378-81.
*
Vijayan V, * Helen A.
Department
of Biochemistry, University of Kerala, Kariavattom,
Thiruvananthapuram 695 581, India.
Nicotine,
a pharmacologically active component of cigarettes smoke causes
devastating effects in important biomolecules of the cell through
generation of free radicals leading to genomic instability. Bacopa
monniera is a reputed drug in Ayurveda known for its hepatoprotective
and DNA protective effects. In this study, an aqueous extract of
Bacopa monniera (BAE, 50 mg/kg i.p.) was investigated for its ability
to reduce nicotine-induced lipid peroxidation (LPO) and confer
genoprotection in Swiss mice. Genoprotective effect was assayed using
micronucleus (MN) assay. LPO status was studied by evaluating MDA
levels and antioxidant status. Nicotine altered hepatic function as
evident by increased ALP and GST levels and decreased SOD, catalase
and GPx activities. BAE treatment restored antioxidant enzymes such
as SOD, catalase and GPx in liver. BAE treatment also significantly
reduced the frequency of micronuclei induced by nicotine by
decreasing the incidence of micronucleated polychromatic erythrocytes
(MN-PCE). Hepatic GSH, ALP and GST levels were brought to normal
values indicating protection. The results of the present study
suggest that BAE exerts protective effects by modulating the extent
of lipid peroxidation and enhancing the antioxidant status.
PMID:
17236174 [PubMed - in process] Bacopa
monniera prevents from aluminium neurotoxicity in the cerebral cortex
of rat brain.
J
Ethnopharmacol. 2007 Apr 20;111(1):56-62. Epub 2006 Nov 11.
*
Jyoti A, * Sethi P, * Sharma D.
Neurobiology
Laboratory, School of Life Sciences, Jawaharlal Nehru University, New
Delhi-67, India.
Bacopa
monniera is a perennial herb, and is used as a nerve tonic in
ayurveda, a traditional medicinal system in India. Aluminium-induced
neurotoxicity is well known and different salts of aluminium have
been reported to accelerate oxidative damage to biomolecules like
lipids, proteins and nucleic acids. The objective of the present
study was to investigate whether Bacopa monniera could potentially
inhibit aluminium toxicity in the cerebral cortex. Male Wister rats
(8 months old) were administered with AlCl(3) orally at a dose of
50mg/kg/day in drinking water for 1 month. Experimental rats were
given AlCl(3) along with Bacopa monniera extract at a dose of
40mg/kg/day. One group of rats was treated with l-deprenyl at a dose
of 1mg/kg/day along with AlCl(3) treatment. We have observed that
Bacopa monniera prevented accumulation of lipid and protein damage
significantly, which resulted from aluminium intake. Decline in the
activity of endogenous antioxidant enzymes associated with aluminium
administration was also inhibited by Bacopa monniera extract. The
potential of Bacopa monniera to inhibit Al-induced oxidative stress
was observed to be similar to that of l-deprenyl, which was taken as
standard. The potential of Bacopa monniera extract to prevent
aluminium neurotoxicity was reflected at the microscopic level as
well, indicative of its neuroprotective effects. These findings
strongly implicate that Bacopa monniera has potential to protect
brain from oxidative damage resulting from aluminium toxicity.
PMID:
17189676 [PubMed - in process] Plant
metabolites as nootropics and cognitives
Ceska
Slov Farm. 2006 Sep;55(5):219-29.
*
Cervenka F, * Jahodar L.
Univerzita
Karlova v Praze, Farmaceuticka fakulta v Hradci Kralove, Katedra
farmaceuticke botaniky a ekologie. frantisek.cervenka@faf.cuni.cz
Nowadays
several millions of people suffer from Alzheimer's disease and other
types of dementia. Etiology of these diseases is not known very well.
There occur different levels of neurotransmitters, the level of
acetylcholine in the brain is decreased and pathological changes
affect the brain tissue. Organic and toxic damage of the brain, free
radicals, and other changes participate in the development of these
diseases. Drugs as nootropics, cognitives, and neuroprotectives are
commonly used to treat these diseases. Some of these drugs have often
side and undesirable effects. In recent years some natural substances
(galanthamine, huperzine A, vinpocetine), and standardized plant
extracts (Ginkgo biloba L., Centella asiatica L.) Urban, Bacopa
monniera L., Evolvulus alsinoides L.) are often used. These plant
preparations produce fewer undesirable effects and the same
effectiveness as the classic therapy, or these preparations are used
as a supplement to the classic therapy.
PMID:
17128592 [PubMed - indexed for MEDLINE] Bacopa
monniera extract reduces amyloid levels in PSAPP mice.
J
Alzheimers Dis. 2006 Aug;9(3):243-51.
*
Holcomb LA, * Dhanasekaran M, * Hitt AR, * Young KA, * Riggs M, *
Manyam BV.
Department
of Psychiatry and Behavioral Science, Texas A&M, University
System HSC College of Medicine, Temple, TX 76508, USA.
PSAPP
mice expressing the "Swedish" amyloid precursor protein and
M146L presenilin-1 mutations are a well-characterized model for
spontaneous amyloid plaque formation. Bacopa monniera has a long
history of use in India as an anti-aging and memory-enhancing
ethnobotanical therapy. To evaluate the effect of Bacopa monniera
extract (BME) on amyloid (Abeta) pathology in PSAPP mice, two doses
of BME (40 or 160 mg/kg/day) were administered starting at 2 months
of age for either 2 or 8 months. Our present data suggests that BME
lowers Abeta 1-40 and 1-42 levels in cortex by as much as 60%, and
reverses Y-maze performance and open field hyperlocomotion behavioral
changes present in PSAPP mice. The areas encompassed by Congo
Red-positive fibrillar amyloid deposits, however, were not altered by
BME treatment. The data suggest that BME has potential application in
Alzheimer's disease therapeutics.
PMID:
16914834 [PubMed - indexed for MEDLINE] Neuroprotective
role of Bacopa monniera extract against aluminium-induced oxidative
stress in the hippocampus of rat brain.
Neurotoxicology.
2006 Jul;27(4):451-7. Epub 2006 Feb 24.
*
Jyoti A, * Sharma D.
Neurobiology
Laboratory, School of Life Sciences, Jawaharlal Nehru University, New
Delhi 110067, India.
Bacopa
monniera is a nerve tonic used extensively in traditional Indian
medicinal system "Ayurveda". Reports regarding its various
antioxidative, adaptogenic and memory enhancing roles have already
appeared in the last few decades. In the present study, aluminium
chloride (AlCl(3)) was used to generate neurotoxicity. We have
investigated the neuroprotective effect of Bacopa extract against
aluminium-induced changes in peroxidative products, such as
thio-barbituric acid-reactive substance (TBA-RS) and protein carbonyl
contents and superoxide dismutase (SOD) activity. Effect on
lipofuscin (age pigments) accumulation and ultrastructural changes
were also studied. Bacopa effects were compared with those of
l-deprenyl. Co-administration of Bacopa extract during aluminium
treatment significantly prevented the aluminium-induced decrease in
SOD activity as well as the increased oxidative damage to lipids and
proteins. Protective effect was also observed at microscopic level.
Fluorescence and electron microscopic studies revealed considerable
inhibition of intraneuronal lipofuscin accumulation and necrotic
alteration in the CA1 region of the hippocampus. Observations showed
that Bacopa's neuroprotective effects were comparable to those of
l-deprenyl at both biochemical and microscopic levels.
PMID:
16500707 [PubMed - indexed for MEDLINE]
Phytomedicine.
2006 Feb;13(3):205-8. Epub 2005 Aug 15.
Herbal
remedies for anxiety - a systematic review of controlled clinical
trials.
*
Ernst E.
Complementary
Medicine Peninsula Medical School, Universities of Exeter Plymouth,
UK. edzard.ernst@pms.ac.uk
Anxiety
is a prominent indication for herbal medicine. This systematic review
was therefore aimed at summarising the evidence for or against the
anxiolytic efficacy of such treatments. Six databases were searched
for all randomised clinical trials testing herbal monopreparations in
the alleviation of anxiety. Seven such studies and one systematic
review were located. Eight different herbals were studied. The herbal
medicines, which, according to these data are associated with
anxiolytic activity in humans, are Piper methysticum and Bacopa
monniera. Only for kava were independent replications available. It
was concluded that there is a lack of rigorous studies in this area
and that only kava has been shown beyond reasonable doubt to have
anxiolytic effects in humans.
PMID:
16428031 [PubMed - indexed for MEDLINE] Anti-inflammatory
activity of Bacopa monniera in rodents.
J
Ethnopharmacol. 2006 Mar 8;104(1-2):286-9. Epub 2005 Dec 15.
Channa
S, * Dar A, * Anjum S, * Yaqoob M, * Atta-Ur-Rahman.
Department
of Pharmacology and Therapeutics, Frontier Medical College,
Abbottabad, Pakistan.
shabanachanna@hotmail.com
The
ethanol extract of Bacopa monniera (Scrophulariaceae) exhibited
marked anti-inflammatory activity against carrageenan-induced paw
edema in mice and rats, an acute inflammatory model. To assess the
possible mechanism of anti-inflammatory action against carrageenan,
the ethanol extract was treated with chemical mediators (histamine,
serotonin, bradykinin, prostaglandin E(2) and arachidonic
acid)-induced edema in rats. The extract selectively inhibited
prostaglandin E(2)-induced inflammation. Thus, it may be inferred
that B. monniera possesses significant anti-inflammatory activity
that may well be relevant for its effectiveness in the healing of
various inflammatory conditions in traditional medicine.
PMID:
16343831 [PubMed - indexed for MEDLINE]
Effect
of bacoside A on brain antioxidant status in cigarette smoke exposed
rats.
Life
Sci. 2006 Feb 16;78(12):1378-84. Epub 2005 Oct 13.
Anbarasi
K, * Vani G, * Balakrishna K, * Devi CS.
Department
of Biochemistry, University of Madras, Guindy Campus, Chennai-600
025, India. anbarasii@yahoo.co.in
Free
radicals mediated oxidative stress has been implicated in the
pathogenesis of smoking-related diseases and antioxidant nutrients
are reported to prevent the oxidative damage induced by smoking.
Therefore, the present study was conducted to evaluate the
antioxidant role of bacoside A (triterpenoid saponin isolated from
Bacopa monniera) against chronic cigarette smoking induced oxidative
damage in rat brain. Adult male albino rats were exposed to cigarette
smoke for a period of 12 weeks and simultaneously administered with
bacoside A (10 mg/kg b.w./day, p.o.). Antioxidant status of the brain
was assessed from the levels of reduced glutathione, vitamin C,
vitamin E, and vitamin A and the activities of superoxide dismutase,
catalase, glutathione peroxidase and glutathione reductase. The
levels of copper, iron, zinc and selenium in brain and serum
ceruloplasmin activity were also measured. Oxidative stress was
evident from the diminished levels of both enzymatic and
non-enzymatic antioxidants. Alterations in the levels of trace
elements with accumulation of copper and iron, and depletion of zinc
and selenium were also observed. Bacoside A administration improved
the antioxidant status and maintained the levels of trace elements.
These results suggest that chronic cigarette smoke exposure enhances
oxidative stress, thereby disturbing the tissue defense system and
bacoside A protects the brain from the oxidative damage through its
antioxidant potential.
PMID:
16226278 [PubMed - indexed for MEDLINE] Effect
of bacosides, alcoholic extract of Bacopa monniera Linn. (brahmi), on
experimental amnesia in mice.
Indian
J Exp Biol. 2005 Jul;43(7):640-5.
Kishore
K, * Singh M. Department
of Pharmacy, M.J.P. Rohilkhand University, Bareilly 243 006, India.
kamalbareilly@yahoo.co.in
To
investigate the effect of bacosides (alcoholic extract of brahmi) on
scopolamine (3 mg kg(-1), ip), sodium nitrite (75 mg kg(-1), ip) and
BN52021 (15 mg kg(-1), ip) induced experimental amnesia in mice,
using Morris water maze test, all the agents were administered 30 min
before the acquisition trials on each day and repeated for 4
consecutive days, and on 5th day during the retrieval trials.
Bacosides on anterograde administration (before training) in mice,
significantly decreased the escape latency time (ELT) during the
acquisition trials for 4 consecutive days and increased the time
spent (TS) in target quadrant during the retrieval trials on 5th day,
and on retrograde administration (after training) bacosides were
found not to affect TS significantly. Bacosides also significantly
decreased the ELT and increased the TS in mice treated anterogradely
with scopolamine and sodium nitrite. Bacosides did not exhibit any
significant effect on TS of mice treated retrogradely with sodium
nitrite. On the other hand, bacosides significantly increased the TS
of mice treated retrogradely with BN52021. On the basis of the
present results it can be concluded that bacosides facilitate
anterograde memory and attenuate anterograde experimental amnesia
induced by scopolamine and sodium nitrite possibly by improving
acetylcholine level and hypoxic conditions, respectively. Beside this
bacosides also reversed BN52021 induced retrograde amnesia, probably
due to increase in platelet activating factor (PAF) synthesis by
enhancing cerebral glutamate level.
PMID:
16053272 [PubMed - indexed for MEDLINE] Protective
effect of bacoside A on cigarette smoking-induced brain mitochondrial
dysfunction in rats.
J
Environ Pathol Toxicol Oncol. 2005;24(3):225-34.
*
Anbarasi K, * Vani G, * Devi CS.
Department
of Biochemistry, University of Madras, Chennai, India.
Chronic
exposure to cigarette smoke affects the structure and function of
mitochondria, which may account for the pathogenesis of
smoking-related diseases. Bacopa monniera Linn., used in traditional
Indian medicine for various neurological disorders, was shown to
possess mitrochondrial membrane-stabilizing properties in the rat
brain during exposure to morphine. We investigated the protective
effect of bacoside A, the active principle of Bacopa monniera,
against mitochondrial dysfunction in rat brain induced by cigarette
smoke. Male Wistar albino rats were exposed to cigarette smoke and
administered bacoside A for a period of 12 weeks. The mitochondrial
damage in the brain was assessed by examining the levels of lipid
peroxides, cholesterol, phospholipid, cholesterol/phospholipid (C/P)
ratio, and the activities of isocitrate dehydrogenase,
alpha-ketoglutarate dehydrogenase, succinate dehydrogenase, malate
dehydrogenase, NADH dehydrogenase, and cytochrome C oxidase. The
oxidative phosphorylation (rate of succinate oxidation, respiratory
control ratio and ADP/O ratio, and the levels of ATP) was evaluated
for the assessment of mitochondrial functional capacity. We found
significantly elevated levels of lipid peroxides, cholesterol, and
C/P ratio, and decreased levels of phospholipids and mitochondrial
enzymes in the rats exposed to cigarette smoke. Measurement of
oxidative phosphorylation revealed a marked depletion in all the
variables studied. Administration of bacoside A prevented the
structural and functional impairment of mitochondria upon exposure to
cigarette smoke. From the results, we suggest that chronic cigarette
smoke exposure induces damage to the mitochondria and that bacoside A
protects the brain from this damage by maintaining the structural and
functional integrity of the mitochondrial membrane.
PMID:
16050806 [PubMed - indexed for MEDLINE] Antioxidant
activity of DHC-1, an herbal formulation, in experimentally-induced
cardiac and renal damage.
Phytother
Res. 2005 Mar;19(3):216-21.
*
Bafna PA, * Balaraman R.
Pharmacy
Department, Faculty of Technology and Engineering, The M.S.
University of Baroda, Baroda -390
001,
Gujarat, India.
DHC-1,
an herbal formulation derived from the popular plants Bacopa
monniera, Emblica officinalis, Glycyrrhiza glabra, Mangifera indica
and Syzygium aromaticum was studied for its antioxidant activity. The
protective effect of DHC-1 in isoproterenol-induced myocardial
infarction and cisplatin-induced renal damage were studied. A
significant reduction in the serum markers of heart and kidney damage
and the extent of lipid peroxidation with a concomitant increase in
the enzymatic (SOD and CAT) and non-enzymatic antioxidants (reduced
glutathione) were observed in DHC-1 pretreated animals compared with
the isoproterenol or cisplatin alone treated animals. Thus it can be
concluded that DHC-1 possesses a protective effect against both
damaged heart and kidneys in rats. This beneficial effect may be
attributed, at least in part, to its antioxidant activity. Copyright
2005 John Wiley & Sons, Ltd.
PMID:
15934019 [PubMed - indexed for MEDLINE] Bacopa
monniera, a reputed nootropic plant: an overview.
Phytomedicine.
2005 Apr;12(4):305-17.
*
Russo A, * Borrelli F.
Department
of Biological Chemistry, Medical Chemistry and Molecular Biology,
University of Catania, Catania, Italy. alrusso@unict.it
Bacopa
monniera (BM), a traditional Ayurvedic medicine, used for centuries
as a memory enhancing, anti-inflammatory, analgesic, antipyretic,
sedative and antiepileptic agent. The plant, plant extract and
isolated bacosides (the major active principles) have been
extensively investigated in several laboratories for their
neuropharmacological effects and a number of reports are available
confirming their nootropic action. In addition, researchers have
evaluated the anti-inflammatory, cardiotonic and other
pharmacological effects of BM preparations/extracts. Therefore, in
view of the important activities performed by this plant,
investigation must be continued in the recently observed actions
described in this paper. Moreover, other clinical studies have to be
encouraged, also to evidence any side effects and possible
interactions between this herbal medicine and synthetic drugs.
PMID:
15898709 [PubMed - indexed for MEDLINE] Effect
of bacoside A on membrane-bound ATPases in the brain of rats exposed
to cigarette smoke.
J
Biochem Mol Toxicol. 2005;19(1):59-65.
*
Anbarasi K,* Vani G, * Balakrishna K, * Devi CS.
Department
of Biochemistry, University of Madras, Guindy Campus, Chennai--600
025, India. cssdevi@yahoo.com
Membrane-bound
enzymes play a vital role in neuronal function through maintenance of
membrane potential and impulse propagation. We have evaluated the
harmful effects of chronic cigarette smoking on membrane-bound
ATPases and the protective effect of Bacoside A in rat brain. Adult
male albino rats were exposed to cigarette smoke for a period of 12
weeks and simultaneously administered with Bacoside A (the active
principle isolated from Bacopa monniera) at a dosage of 10 mg/kg
b.w/day, p.o. The levels of lipid peroxides as marker for evaluating
the extent of membrane damage, the activities of Na+/K+-ATPase,
Ca2+-ATPase and Mg2+-ATPase, and associated cations sodium (Na+),
potassium (K+), calcium (Ca2+), and magnesium (Mg2+) were
investigated in the brain. Neuronal membrane damage was evident from
the elevated levels of lipid peroxides and decreased activities of
membrane-bound enzymes. Disturbances in the electrolyte balance with
accumulation of Na+ and Ca2+ and depletion of K+ and Mg2+ were also
observed. Administration of Bacoside A inhibited lipid peroxidation,
improved the activities of ATPases, and maintained the ionic
equilibrium. The results of our study indicate that Bacoside A
protects the brain from cigarette smoking induced membrane damage.
Copyright 2005 Wiley Periodicals, Inc.
PMID:
15736152 [PubMed - indexed for MEDLINE] Creatine
kinase isoenzyme patterns upon chronic exposure to cigarette smoke:
protective effect of Bacoside A.
Vascul
Pharmacol. 2005 Jan;42(2):57-61.
*
Anbarasi K, * Vani G, * Balakrishna K, * Devi CS.
Department
of Biochemistry, University of Madras, Guindy Campus, Chennai-600
025, India.
Cigarette
smoking is implicated as a major risk factor in the development of
cardiovascular and cerebrovascular diseases. Creatine kinase (CK) and
its isoforms (CK-MM, MB, BB) have been advocated as sensitive markers
in the assessment of cardiac and cerebral damage. Therefore, in the
present study, we report the isoenzyme patterns of CK in rats upon
exposure to cigarette smoke and the protective effect of Bacoside A
against chronic smoking induced toxicity. Adult male albino rats were
exposed to cigarette smoke and simultaneously administered with
Bacoside A, the active constituent from the plant Bacopa monniera,
for a period of 12 weeks. The activity of CK was assayed in serum,
heart and brain, and its isoenzymes in serum were separated
electrophoretically. Rats exposed to cigarette smoke showed
significant increase in serum CK activity with concomitant decrease
in heart and brain. Also cigarette smoke exposure resulted in a
marked increase in all the three isoforms in serum. Administration of
Bacoside A prevented these alterations induced by cigarette smoking.
Cigarette smoking is known to cause free radical mediated lipid
peroxidation leading to increased membrane permeability and cellular
damage in the heart and brain resulting in the release of CK into the
circulation. The protective effect of Bacoside A on the structural
and functional integrity of the membrane prevented the leakage of CK
from the respective tissues, which could be attributed to its free
radical scavenging and anti-lipid peroxidative effect.
PMID:
15722250 [PubMed - indexed for MEDLINE]
Free
radical scavenging capacity and protective effect of Bacopa monniera
L. on DNA damage.
Phytother
Res. 2003 Sep;17(8):870-5.
*
Russo A, * Izzo AA, * Borrelli F, * Renis M, * Vanella A.
Department
of Biochemistry, Medical Chemistry and Molecular Biology, University
of Catania, V.le A. Doria 6, 95125, Catania, Italy. alrusso@unict.it
Bacopa
monniera L. (family Scrophulariaceae) (BM) is an Ayurvedic medicine,
clinically used for memory enhancing, epilepsy, insomnia and as a
mild sedative. In this work, the free radical scavenging capacity of
a methanol extract of BM and the effect on DNA cleavage induced by
H2O2 UV-photolysis was investigated. In addition, we examined whether
this plant extract is capable of reducing the hydrogen
peroxide-induced cytotoxicity and DNA damage in human
non-immortalized fibroblasts. It showed a dose-dependent free radical
scavenging capacity and a protective effect on DNA cleavage. These
results were confirmed by a significant protective effect on
H2O2-induced cytoxicity and DNA damage in human non-immortalized
fibroblasts. The antioxidant capacity of BM may explain, at least in
part, the reported antistress, immunomodulatory,
cognition-facilitating, antiinflammatory and antiaging effects
produced by it in experimental animals and in clinical situations and
may justify further investigation of its other beneficial properties.
Moreover, this experimental evidence suggests that because of its
antioxidant activity, this Ayurvedic drug may be useful in the
treatment of human pathologies in which free radical production plays
a key role. Copyright 2003 John Wiley & Sons, Ltd.
PMID:
13680815 [PubMed - indexed for MEDLINE] A
comparative study in rodents of standardized extracts of Bacopa
monniera and Ginkgo biloba: anticholinesterase and cognitive
enhancing activities.
Pharmacol
Biochem Behav. 2002 Nov;73(4):893-900.
Das
A, * Shanker G, * Nath C, * Pal R, * Singh S, * Singh H.
Division
of Pharmacology, Central Drug Research Institute, P.O. Box 173,
Lucknow, 226 001, India. amitavadascdri@rediffmail.com
Bacopa
monniera and Ginkgo biloba are well-known cognitive enhancers in
Indian and Chinese traditional medicine systems. Standardized
extracts of B. monniera and G. biloba were used to evaluate the
antidementic and anticholinesterase activities in adult male Swiss
mice. Antidementic activity was tested against scopolamine (3 mg/kg
ip)-induced deficits in passive avoidance test. Three different
extracts of B. monniera (30 mg/kg) and extract of G. biloba (15, 30
and 60 mg/kg) were administered postoperatively, daily for 7 days and
60 min after the last dose, i.e., on Day 7, first trial was
conducted. In passive avoidance test, increased transfer latency time
(TLT) and no transfer response (NTR) were taken as criteria for
learning. TLT and NTR were significantly increased and decreased in
second trial, 24 h after the first trial in control group and
scopolamine-dementia group, respectively. The B. monniera- and G.
biloba-treated groups produced significant increase in TLT and NTR on
second trial (40-80%) after scopolamine treatment, thus, attenuating
its antidementic effect. Both the extracts showed a dose (10-1000
microg)-dependent inhibitory effect on acetylcholinesterase (AChE)
activity (in vitro), performed spectrophotometrically. IC(50) of G.
biloba was 268.33 microg, whereas none of the extracts of B. monniera
showed more than 50% inhibition. At a dose concentration of 30 and 60
mg/kg, extracts of G. biloba showed a cognitive enhancing property
and, at the same time, a significant decrease in AChE-specific
activity in both per se and scopolamine-dementia groups. These
extracts possess a significant anticholinesterase and antidementic
properties, which may be useful in the treatment of dementia.
PMID:
12213536 [PubMed - indexed for MEDLINE] Chronic
effects of Brahmi (Bacopa monnieri) on human memory.
Neuropsychopharmacology.
2002 Aug;27(2):279-81.
*
Roodenrys S, * Booth D, * Bulzomi S, * Phipps A, * Micallef C, *
Smoker J.
Department
of Psychology, University of Wollongong, Woolongong, Australia.
steven_roodenrys@uow.edu.au A
study is reported on the effects of Brahmi (Bacopa monniera) on human
memory. Seventy-six adults aged between 40 and 65 years took part in
a double-blind randomized, placebo control study in which various
memory functions were tested and levels of anxiety measured. There
were three testing sessions: one prior to the trial, one after three
months on the trial, and one six weeks after the completion of the
trial. The results show a significant effect of the Brahmi on a test
for the retention of new information. Follow-up tests showed that the
rate of learning was unaffected, suggesting that Brahmi decreases the
rate of forgetting of newly acquired information. Tasks assessing
attention, verbal and visual short-term memory and the retrieval of
pre-experimental knowledge were unaffected. Questionnaire measures of
everyday memory function and anxiety levels were also unaffected.
PMID:
12093601 [PubMed - indexed for MEDLINE] Antidepressant
activity of standardized extract of Bacopa monniera in experimental
models of depression in rats.
Phytomedicine.
2002 Apr;9(3):207-11.
*
Sairam K, * Dorababu M, * Goel RK, * Bhattacharya SK.
Department
of Pharmacology, Institute of Medical Sciences, Banaras Hindu
University, Varanasi, India.
Bacopa
monniera Wettst. (syn. Herpestis monniera L.; Scrophulariaceae) is a
commonly used Ayurvedic drug for mental disorders. The standardized
extract was reported earlier to have significant anti-oxidant effect,
anxiolytic activity and improve memory retention in Alzheimer's
disease. Presently, the standardized methanolic extract of Bacopa
monniera (bacoside A - 38.0+/-0.9) was investigated for potential
antidepressant activity in rodent models of depression. The effect
was compared with the standard antidepressant drug imipramine (15
mg/kg, ip). The extract when given in the dose of 20 and 40 mg/kg,
orally once daily for 5 days was found to have significant
antidepressant activity in forced swim and learned helplessness
models of depression and was comparable to that of imipramine.
PMID:
12046860 [PubMed - indexed for MEDLINE] The
chronic effects of an extract of Bacopa monniera (Brahmi) on
cognitive function in healthy human subjects.
Psychopharmacology
(Berl). 2001 Aug;156(4):481-4.
Stough
C, * Lloyd J, * Clarke J, * Downey LA, * Hutchison CW, * Rodgers T, *
Nathan PJ.
Neuropsychology
Laboratory, School of Biophysical Science and Electrical Engineering,
Victoria, Australia.
RATIONALE:
Extracts of Bacopa monniera have been reported to exert cognitive
enhancing effects in animals. However, the effects on human cognition
are inconclusive. OBJECTIVE: The current study examined the chronic
effects of an extract of B. monniera (Keenmind) on cognitive function
in healthy human subjects. METHODS: The study was a double-blind
placebo-controlled independent-group design in which subjects were
randomly allocated to one of two treatment conditions, B. monniera
(300 mg) or placebo. Neuropsychological testing was conducted
pre-(baseline) and at 5 and 12 weeks post drug administration.
RESULTS: B. monniera significantly improved speed of visual
information processing measured by the IT task, learning rate and
memory consolidation measured by the AVLT (P<0.05), and state
anxiety (P<0.001) compared to placebo, with maximal effects
evident after 12 weeks. CONCLUSIONS: These findings suggest that B.
monniera may improve higher order cognitive processes that are
critically dependent on the input of information from our environment
such as learning and memory.
PMID:
11498727 [PubMed - indexed for MEDLINE] Protection
from phenytoin-induced cognitive deficit by Bacopa monniera, a
reputed Indian nootropic plant.
J
Ethnopharmacol. 2000 Aug;71(3):383-90.
*
Vohora D, * Pal SN, * Pillai KK.
Department
of Pharmacology, Faculty of Pharmacy, Jamia Hamdard, 110 062, New
Delhi, India.
Many
epileptic patients suffer from cognitive impairments; both the
underlying pathology and antiepileptic drug therapy can cause such
deficits. Phenytoin, one of the widely used anticonvulsants, is known
to adversely affect cognitive function. A reputed Indian nootropic
plant Bacopa monniera (BM) was evaluated alone and in combination
with phenytoin for its effect on (a) passive-avoidance (PA) task; (b)
maximal electroshock seizures; and (c) locomotor activity in mice.
Phenytoin (PHT, 25 mg/kg po x 14 days) adversely affected cognitive
function in the PA task. BM extract (40 mg/kg x 7 days), given along
with phenytoin in the second week of the two-week regimen,
significantly reversed PHT-induced impairment. Both acquisition and
retention of memory showed improvement without affecting its
anticonvulsant activity. The observed cognitive effects of PHT and BM
were found to be independent of motor stimulation. The results
provide evidence for potential corrective effect of BM in cognitive
deficit associated with PHT therapy.
PMID:
10940574 [PubMed - indexed for MEDLINE] Antioxidant
activity of Bacopa monniera in rat frontal cortex, striatum and
hippocampus.
Phytother
Res. 2000 May;14(3):174-9.
*
Bhattacharya SK, * Bhattacharya A, * Kumar A, * Ghosal S.
Department
of Phamacology, Institute of Medical Sciences, Banaras Hindu
University, Varanasi - 221005, India.
The
effect of a standardized extract of Bacopa monniera Linn. was
assessed on rat brain frontal cortical, striatal and hippocampal
superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase
(GPX) activities, following administration for 7, 14 or 21 days. The
effects induced by this extract (bacoside A content 82% +/- 0.5%),
administered in doses of 5 and 10 mg/kg, orally, were compared with
the effects induced by (-) deprenyl (2 mg/kg, p. o.) administered for
the same time periods. Bacopa monniera (BM) induced a dose-related
increase in SOD, CAT and GPX activities, in all the brain regions
investigated, after 14 and 21 days of drug administration. On the
contrary, deprenyl induced an increase in SOD, CAT and GPX activities
in the frontal cortex and striatum, but not in the hippocampus, after
treatment for 14 or 21 days. The results suggest that BM, like
deprenyl, exhibits a significant antioxidant effect after subchronic
administration which, unlike the latter, extends to the hippocampus
as well. The results suggest that the increase in oxidative free
radical scavenging activity by BM may explain, at least in part, the
cognition- facilitating action of BM, recorded in Ayurvedic texts,
and demonstrated experimentally and clinically. Copyright 2000 John
Wiley & Sons, Ltd.
PMID:
10815010 [PubMed - indexed for MEDLINE] A
review of nutrients and botanicals in the integrative management of
cognitive dysfunction.
Altern
Med Rev. 1999 Jun;4(3):144-61.
*
Kidd PM.
Dementias
and other severe cognitive dysfunction states pose a daunting
challenge to existing medical management strategies. An integrative,
early intervention approach seems warranted. Whereas, allopathic
treatment options are highly limited, nutritional and botanical
therapies are available which have proven degrees of efficacy and
generally favorable benefit-to-risk profiles. This review covers five
such therapies: phosphatidylserine (PS), acetyl-l-carnitine (ALC),
vinpocetine, Ginkgo biloba extract (GbE), and Bacopa monniera
(Bacopa). PS is a phospholipid enriched in the brain, validated
through double-blind trials for improving memory, learning,
concentration, word recall, and mood in middle-aged and elderly
subjects with dementia or age-related cognitive decline. PS has an
excellent benefit-to-risk profile. ALC is an energizer and metabolic
cofactor which also benefits various cognitive functions in the
middle-aged and elderly, but with a slightly less favorable
benefit-to-risk profile. Vinpocetine, found in the lesser periwinkle
Vinca minor, is an excellent vasodilator and cerebral metabolic
enhancer with proven benefits for vascular-based cognitive
dysfunction. Two meta-analyses of GbE demonstrate the best
preparations offer limited benefits for vascular insufficiencies and
even more limited benefits for Alzheimer's, while "commodity"
GbE products offer little benefit, if any at all. GbE (and probably
also vinpocetine) is incompatible with blood-thinning drugs. Bacopa
is an Ayurvedic botanical with apparent anti-anxiety, anti-fatigue,
and memory-strengthening effects. These five substances offer
interesting contributions to a personalized approach for restoring
cognitive function, perhaps eventually in conjunction with the
judicious application of growth factors.
PMID:
10383479 [PubMed - indexed for MEDLINE]
|