
Arthritis:
Numerous forms of arthritis exist, but the most common two are osteoarthritis, and rheumatoid arthritis. These conditions can effect the body's movable joints in the knees, wrists, elbows, fingers, toes, hips, and shoulders as well as the bones of the spine on the neck and back. The Indian herb Ashwagandha
has been shown to be effective in reducing the pain of arthritis. A joint is where two bones come together.
Their surfaces are covered with a layer of smooth, rubbery, blue-white
tissue called cartilage. A fluid-filled capsule made up of a tough, fibrous
tissue called ligaments surrounds these bones and cartilage. Thanks to this
liquid and the cartilage that covers then end of these bones, the bones
within the joint normally glide smoothly past one another. If anything goes
wrong with any of these parts of a joint, arthritis can result. The swelling
and deformity that takes place in arthritic joints can result from the
thickening of the membrane, the fluid, enlargement of the bones, or some
combination of these factors. Other forms of arthritis are spondyloarthropathies, including psoriatic arthritis, ankylosing spondylitis, Reiter's syndrome (a group of disorders that tend to affect the spine), systemic lupus, juvenile rheurmatoid arthritis, infectious arthritis, and kawasaki syndrome. Arthritis can also be caused by bacterial, viral or fungal infection of a joint. Usually the infecting organism travels to the joint through the blood stream from an infection elsewhere in the body, but injury or even surgery can result in joint infection as well. Symptoms not only include the pain and tenderness effecting the joint, but also include symptoms of systemic infections such as fever, chills and body aches. Standard Treatment: If your joints are swollen and painful,
you're probably not going to be in the mood for exercise, but physical
activity can help prevent the swelling, stiffness and pain in the joints.
Remember to stretch especially before exercise. Regular walking, stretching,
and weight lifting can reduce knee joint pain and improve the range of
motion. There are nutritional supplements that the
body needs if one has arthritis. Below is a list of the vitamins that
should be taken to handle your body's nutritional needs. Omega 3 oils are of great value in reducing the symptoms of rheumatoid arthritis. Omega 3 oil is also known as linolenic acid, it can reduce the swelling, stiffness and inflammation typical of arthritis. This can be gotten from such supplements as Emu Oil from Australia (the emu is a close relative of the ostrich), hemp oil, borage oil and flaxseed oil. Omega 3 oils are essential to good health and should be taken by everyone (see article Essential Fatty Acids) Herbs and other Remedies: For more info on nutritional handling of Arthritis
|
| : Altern Med Rev 2000 Aug;5(4):334-46 | Related Articles, Links |
DESIGN: This review is in a narrative format and consists
of all publications relevant to ashwagandha that were identified by the authors
through a systematic search of major computerized medical databases; no
statistical pooling of results or evaluation of the quality of the studies was
performed due to the widely different methods employed by each study.
RESULTS: Studies indicate ashwagandha possesses anti-inflammatory, antitumor, antistress, antioxidant, immunomodulatory, hemopoietic, and rejuvenating properties. It also appears to exert a positive influence on the endocrine, cardiopulmonary, and central nervous systems.
The mechanisms of action for these properties are not fully understood.
Toxicity studies reveal that ashwagandha appears to be a safe compound.
CONCLUSION: Preliminary studies have found various
constituents of ashwagandha exhibit a variety of therapeutic effects with little
or no associated toxicity. These results are very encouraging and indicate this
herb should be studied more extensively to confirm these results and reveal
other potential therapeutic effects. Clinical trials using ashwagandha for a
variety of conditions should also be conducted.
Publication Types:
PMID: 10956379 [PubMed - indexed for MEDLINE]
| J Ethnopharmacol 1991 May-Jun;33(1-2):91-5 | Related Articles, Links |
Treatment of osteoarthritis with a herbomineral formulation:
a double-blind, placebo-controlled, cross-over study.After a one-month single blind run-in period, 42 patients with osteoarthritis were randomly allocated to receive either a drug treatment or a matching placebo for a period of three months.
After a 15-day wash-out period the patients were transferred to the other treatment for a further period of three months.
Clinical efficacy was evaluated every fortnight on the basis of severity of pain, morning stiffness, Ritchie articular index, joint score, disability score and grip strength.
Other parameters like erythrocyte sedimentation rate and radiological examination were carried out on a monthly basis.
Treatment with the herbomineral formulation produced a
significant drop in severity of pain (P less than 0.001) and disability score (P
less than 0.05). Radiological assessment, however, did not show any significant
changes in both the groups. Side effects observed with this formulation did not
necessitate withdrawal of treatment.
Publication Types:
PMID: 1943180 [PubMed - indexed for MEDLINE]
Ayurvedic Medicinal Plants: Ashwagandha
SANSKRIT
NAME: Ashvagandha, "smelling like
a horse"
Botanical Name:
Withania somnifera, Solanaceae
Common Name: Asgandh (H), Amukkira (T), Winter Cherry (E)
Part Used: root, leaves, fruit
Dravyguna: root.
·Rasa: tikta, kashaya
·Vipaka: katu
·Virya: ushna
·Karma: Vatapittahara, Kaphakopa, balyam, vajikarana, tonic,
adaptogen, relaxing nervine, post-partum tonic, immunomodulant, astringent,
galactagogue, diuretic, thermogenic (Dash 1991, 59; Dash and Junius 1983, 155;
Frawley and Lad 1986, 160; Varier 1996, 409)
Indications:
·Root: asthma, bronchitis, edema, leucoderma, anorexia, consumption,
asthenia, anemia, exhaustion, aging, insomnia, ADD/ADHD, neurasthenia,
infertility, impotence, repeated miscarriage, paralysis, memory loss, multiple
sclerosis, immune-dysfunction, carcinoma, rheumatism, arthritis,
lumbago (Dash 1991 59; Dash and Junius 1987, 155; Kirtikar and Basu 1993,
1775-76; Frawley and Lad 1986, 160; Nadkarni 1976, 1293-94; Varier 1996, 409)
·Leaves: used internally for fever and hemorrhoids; externally for
wounds, hemorrhoids, tumors, tuberculous glands, anthrax pustules, syphylitic
sores, erysipelas, and in ophthalmitis (Kirtikar and Basu 1993 1775-76; Varier
1996, 409)
·Fruit: used externally in ringworm (Kirtikar and Basu 1993 1775-76)
Contraindications: Caution should be used with clients on anticonvulsants, barbituates and benzodiazepines. Ashvagandha is traditionally avoided in lymphatic congestion, during colds and flu, or symptoms of ama (Frawley and Lad 1986, 160).
Toxicity: None reported (Aphale et al 1998).
Dosage: root
·Churna: 3 5 g b.i.d. - t.i.d.
·Kashaya: 100 mL t.i.d.
·Tincture: fresh root, 95%, 1:2; dried root, 50%, 1:4; 1 10 mL t.i.d.
Pharmacology:
·Adaptogen: The traditional use of
Ashvagandha as a rasayana [definition] has
been validated by scientific investigation. Wistar rats treated with an extract
of Withania somnifera showed better stress tolerance in cold water
swimming tests (Archana and Namasivayam 1999).
·Antiinflammatory: A methanolic extract of the
aerial parts of Withania somnifera had antiinflammatory activities
comparable to that of hydrocortisone sodium succinate (al-Hindawi et al 1992).
An 80% ethanolic extract of Withania somnifera displayed significant
antiinflammatory activity on carrageenan-induced paw edema (al-Hindawi 1989).
·Antioxidant: An aqueous suspension of root extract of Ashvagandha prevented the rise of experimentally induced lipid peroxidation in rabbits and mice (Dhuley 1998a). An extract of Withania somnifera, consisting of equimolar concentrations of sitoindosides VII-X and withaferin A, induced an increase in the levels of superoxide dismutase, catalase and glutathione peroxidase in rat brain, consistent with other research that reports an antioxidant, immunomodulant and antiinflammatory activity (Bhattacharya et al 1997).
·Cancer: The administration of Ashvagandha rasayana (an Ayurvedic polyherbal formulation containing Ashvagandha) significantly reduced the lung tumor nodule formation by 55.6% in experimental animals (Menon et al. 1997). An alcoholic extract of the dried roots as well as withaferin A isolated from the extract showed significant antitumor and radiosensitizing effects in experimental tumors in Chinese hamster cells, without any noticeable systemic toxicity (Devi 1996). The steroidal lactone withaferin A displayed significant antitumor and radiosensitizing effects, inhibiting tumor growth and increasing survival in Swiss mice inoculated with Ehrlich ascites carcinoma (Devi et al 1995; Sharad et al 1996). The administration of an extract of Withania somnifera was found to significantly reduce leucopenia induced by cyclophosphamide treated experimental animals, indicating its usefulness in cancer therapy (Davis and Kuttan 1998). The administration of methanolic extract of Ashvagandha was found to significantly increase the WBC count in normal Balb/c mice and reduce leucopenia induced by a sublethal dose of gamma radiation. Withania increased bone marrow cellularity and normalised the ratio of normochromatic erythrocytes and polychromatic erythrocytes. This observed activity was thought to be due to stem cell proliferation (Kuttan 1996).
·Central Nervous system: Isolated constituents of Withania somnifera (sitoindosides VII-X and withaferin-A) increased cortical muscarinic acetylcholine receptor capacity, partly explaining the cognition-enhancing and memory-improving effects traditionally attributed to Ashvagandha (Schliebs et al 1997). A methanolic extract of Withania somnifera inhibited the specific binding of [3H]GABA and [35S]TBPS, and enhanced the binding of [3H]flunitrazepam to their putative receptor sites, suggesting a GABA-mimetic activity (Mehta et al 1991). A commercial root extract of Withania somnifera used repeatedly over 9 days attenuated the development of tolerance to the analgesic effect of morphine and suppressed morphine-withdrawal jumps (Kulkarni and Ninan 1997).
·Immunity: Myelosuppressed mice treated with an extract of Ashvagandha displayed a significant increase in hemoglobin concentration, red blood cell count, white blood cell count, platelet count and body weight as compared to controls, as well as increased hemolytic antibody responses towards human erythrocytes (Ziauddin et al 1996). Researchers at the Amala Cancer Research Centre in Kerala, India, found that the administration of an extract from the powdered root of Withania somnifera enhanced the levels of interferon gamma, interleukin-2 and granulocyte macrophage colony stimulating factor in normal and cyclophosphamide-treated mice, suggesting an immunopotentiating and myeloprotective effect (Davis and Kuttan 1999). Mice infected intravenously with Aspergillus fumigatus and treated for 7 consecutive days with an oral preparation of an extract of Withania somnifera at a dose of 100mg/kg displayed increased phagocytic activity and prolonged survival time (Dhuley 1998). The antifungal activity of Withania has been confirmed elsewhere, attributed to the withanolides (Choudhary et al 1995).
·Musculo-skeletal: A herbomineral formulation containing roots of Withania somnifera, the stem of Boswellia serrata, rhizomes of Curcuma longa and a zinc complex (Articulin-F), was evaluated in a randomized, double-blind, placebo controlled, cross-over study in clients with osteoarthritis. The results produced a significant drop in severity of pain and disability, although radiological assessment did not show any significant changes. Sideeffects were minimal and did not necessitate the withdrawal of treatment. (Kulkarni et al 1991)
Comments:
Ashvagandha is the Indian equivalent to Ginseng (Panax ginseng),
but unlike Ginseng, Ashvagandha has a sedative rather than stimulant
action on the central nervous system, making it a superior medicine for
exhaustion with nervous irritability. A rejuvenating preparation can be made by
mixing Ashvagandha with 10-15% Pippali, taken with one half part
ghrita and 1 part honey on an empty stomach, morning and evening.
Ashvagandha is a useful nervine, taken before bed to relax and nourish the
body in deficiency diseases, but is only seen to be efficacious when taken on a
sustained basis- it is not a sufficient sedative to treat acute insomnia. For
poor memory, lack of concentration and in the treatment of ADD/ADHD
Ashvagandha may be used in equal proportions with
Mandukaparni and
Ling zhi (Ganoderma lucidum). Ashvagandha is widely used in any
debility, emaciation or consumptive condition, in both adults and children (Kirtikar
and Basu 1993, 1775; Nadkarni 1976, 1294).
Ashvagandha may be used by men as sexual tonic in the treatment of spermatopathia, impotence and "seminal depletion" (Nadkarni 1976, 1293). When mixed with equal parts Shatavari, it is an appropriate treatment for female infertility and frigidity and is useful in threatened miscarriage.
For poor eyesight Ashvagandha powder is mixed with equal proportions of Licorice (Glycyrrhiza glabra root) powder and the fresh juice of Amalaki (Emblica officinalis fruit) (Nadkarni, 1294). An infusion of the leaves may be used in in the treatment of ophthalmia (Kirtikar and Basu 1993, 1776).
In the form of Narayana taila, Ashvagandha may be taken internally, 3 10 gtt. b.i.d. for consumption and emaciation in children, and as an enema for anal fistula (Nadkarni 1976, 1294). Narayana taila may also be taken as nasya (2-3 gtt.) in cases of hearing loss and in abhyanga in cases of paralysis, tetanus, rheumatism and lumbago (Nadkarni 1976, 1294).
Nadkarni mentions that Ashvagandha is used in the treatment of antiinflammatory joint disease (1976, 1293), but as Lad and Frawley suggest, Ashvagandha can facilitate the production of ama (1986, 160), and thus an eliminative regimen is best utilized prior to using this botanical. Likewise, Ashvagandha is an appropriate remedy in the treatment of asthma and bronchitis (Kirtikar and Basu 1993, 1775-6), but should be used concurrently with dravyas that have a dipana-pachana property to avoid the production of ama.
Varrier mentions that a paste made of the roots and bruised leaves may be applied to carbuncles, ulcers and painful swellings (1996, 409).
References:
al-Hindawi, M.K., I.H. Al-Deen, M.H.
Nabi, and M.H. Ismail. 1989. Anti-inflammatory activity of some Iraqi plants
using intact rats. J Ethnopharmacol. Sep; 26(2):163-8
Aphale A.A., A.D. Chhibba, N.R. Kumbhakarna, M. Mateenuddin and S.H. Dahat.
1998. Subacute toxicity study of the combination of ginseng (Panax ginseng) and
ashwagandha (Withania somnifera) in rats: a safety assessment. Indian
J Physiol Pharmacol Apr; 42(2):299-302
Archana, R. and A. Namasivayam. 1999. Antistressor effect of Withania
somnifera. J Ethnopharmacol. Jan; 64(1):91-3
Bhattacharya, S.K., K.S. Satyan and S. Ghosal. 1997. Antioxidant activity of
glycowithanolides from Withania somnifera. Indian J Exp Biol. Mar;
35(3):236-9
Choudhary, M.I., Dur-e-Shahwar, Z. Parveen, A. Jabbar , I. Ali, Atta-ur-Rahman.
1995. Antifungal steroidal lactones from Withania coagulance.
Phytochemistry Nov; 40(4):1243-6
Dash, Bhagwan. 1991. Materia Medica of Ayurveda. New Delhi: B. Jain
Publishers.
----------- and Manfred Junius. 1983. A Handbook of Ayurveda. New Delhi:
Concept Publishing.
Davis, L. and G. Kuttan. 1999. Effect of Withania somnifera on cytokine
production in normal and cyclophosphamide treated mice. Immunopharmacol
Immunotoxicol Nov; 21(4):695-703
Davis L. and G. Kuttan. 1998. Suppressive effect of cyclophosphamide-induced
toxicity by Withania somnifera extract in mice. J Ethnopharmacol.
Oct; 62(3):209-14
Devi, P.U. 1996. Withania somnifera Dunal (Ashwagandha): potential plant
source of a promising drug for cancer chemotherapy and radiosensitization.
Indian J Exp Biol. Oct; 34(10):927-32
Devi, P.U., A.C. Sharada, and F.E. Solomon. 1995. In vivo growth inhibitory and
radiosensitizing effects of withaferin A on mouse Ehrlich ascites carcinoma.
Cancer Lett. Aug 16; 95(1-2):189-93
Dhuley, J.N. 1998a. Effect of Ashwagandha on lipid peroxidation in
stress-induced animals. J Ethnopharmacol. Mar; 60(2):173-8
Dhuley, J.N. 1998b. Therapeutic efficacy of Ashwagandha against experimental
aspergillosis in mice. Immunopharmacol Immunotoxicol. Feb; 20(1):191-8
Frawley, David and Vasant Lad. 1986. The Yoga Of Herbs: An Ayurvedic Guide to
Herbal Medicine. Santa Fe: Lotus Press.
Kirtikar KR and BD Basu. 1993. Indian Medicinal Plants. 2nd ed. Vol. 1-4.
1935. Reprint. Delhi: Periodical Experts.
Kulkarni, S.K. and I. Ninan. 1997. Inhibition of morphine tolerance and
dependence by Withania somnifera in mice. J Ethnopharmacol. Aug;
57(3):213-7
Kulkarni, R.R., P.S. Patki, V.P. Jog, S.G. Gandage and B. Patwardhan. 1991.
Treatment of osteoarthritis with a herbomineral formulation: a double-blind,
placebo-controlled, cross-over study. J Ethnopharmacol. May-Jun;
33(1-2):91-5
Kuttan, G. 1996. Use of Withania somnifera Dunal as an adjuvant during
radiation therapy. Indian J Exp Biol. Sep; 34(9):854-6
Mehta, A.K., P. Binkley, S.S. Gandhi, and M.K. Ticku. 1991. Pharmacological
effects of Withania somnifera root extract on GABAA receptor complex.
Indian J Med Res. Aug; 94:312-5
Menon L.G., R. Kuttan, and G. Kuttan. 1997. Effect of rasayanas in the
inhibition of lung metastasis induced by B16F-10 melanoma cells. J Exp Clin
Cancer Res. Dec; 16(4):365-8
Nadkarni, Dr. K.M. 1976. The Indian Materia Medica, with Ayurvedic, Unani and
Home Remedies. Revised and enlarged by A.K. Nadkarni. 1954. Reprint. Bombay:
Bombay Popular Prakashan PVP.
Schliebs, R., A. Liebmann , S.K. Bhattacharya, A. Kumar, S. Ghosal, and V. Bigl.
1997. Systemic administration of defined extracts from Withania somnifera
(Indian Ginseng) and Shilajit differentially affects cholinergic but not
glutamatergic and GABAergic markers in rat brain. Neurochem Int. Feb;
30(2):181-90
Sharad, A.C., F.E. Solomon, P.U. Devi, N. Udupa, and K.K. Srinivasan. 1996.
Antitumor and radiosensitizing effects of withaferin A on mouse Ehrlich ascites
carcinoma in vivo. Acta Oncol. 35(1):95-100
Varrier, P.S. 1996. Indian Medicinal Plants: A Compendium of 500 species.
Edited by PK Warrier, VPK Nambiar and C Ramankutty. vol 5. Hyderabad: Orient
Longman.
Ziauddin, M., N. Phansalkar, P. Patki , S. Diwanay, B. Patwardhan. 1996. Studies
on the immunomodulatory effects of Ashwagandha. J Ethnopharmacol. Feb;
50(2):69-76
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Withaferin
Ashowed marked tumour-inhibitory
activity when tested in vitroagainst cells derived from human carcinoma of
nasopharynx (KB). It also acted as a mitotic poison arresting the division of
cultured humanlarynx carcinoma cells at metaphase and in HeLa cultures similar
to star -metaphase. It also produced significant retardation of the growth of
Ehrlich ascites carcinoma, Sarcoma 180, Sarcoma Black (SBL), and E 0771 mammary
adenocarcinoma in mice in doses of 10, 12, 15 mg./kg. body-wt. Growth of Ehrlich
ascites carcinoma was completely inhibited in more than half the mice which
survived for 100 days without the evidence of growth of the tumour. Withaferin A
caused mitotic arrest in embryonal chicken fibroblast cells. Methylthiodeacetyl
colchicine potentiated the effect of withaferin A. The presence of an
unsaturated lactone in the side-chain to which an allylic primary alcohol group
is attached at C25 and the highly oxygenated rings at the other end of the
molecule may well suggest specific chemical systems possessing carcinostatic
properties (Kupchan et al., J. Amer. chem. Soc.,1965, 87,
5805; Shohat et al.,loc. cit.; Chem. Abstr.,1973, 79, 139; 1970, 72, 130740;
Lavie et al., J. chem. Soc.,1965, 75171).
Withaferin
A
exhibits fairly potent anti-arthritic and anti-inflammatory activities. It was
found to suppress arthritic syndrome without any toxic effect. Unlike
hydrocortisone-treated animals which lost weight, the animals treated with
withaferin A showed gain in weight in arthritic syndrome. It is interesting that
withaferin A seems to be more potent than hydrocortisone in adjuvant-induced
arthritis in rats, a close experimental approximation to human rheumatoid
arthritis. In its oedema-inhibiting activity, the compound gave a good
dose-response in the dose-range of 12-25 mg./kg. body-wt. of albino rats
intraperitoneally and a single dose had a good duration of action, as it could
effectively suppress the inflammation after four hours of its administration.
The effect of the withanoloide in suppressing granulation-tissue formation
appeared to be similar to that of hydrocortisone. The locally induced graft
(lymphocytes)-versus-host reaction in chicks was strongly inhibited by
withaferin A (Sethi et al., Indian J Pharmacol.,1970, 2, 165; Chem. Abstr.,1973,
79, 142880)
Extract of ashwagandha induced a significant decrease in the arterial and
diastolic blood pressure in normotensive pentobarbital anaesthetized dogs. It
also prevented the hypotensive effect of acetylcholine and increased the
hypertensive effect of adrenaline. Alcoholic extract of the drug produced good
response against mouse tumor, Sarcoma 180. In combination with gamma-radiation
and hyperthermia treatment, ashwagandha significantly increased the tumor cure,
growth delay of partially responding tumors and animal survival. Ashwangandha,
in addition to having inhibitory effect, also acts as radio sensitizer and heat
enhancer Ahumad(a et al, Phytother Res, 1991, 5, 111; Uma
Devi et al, Indian J Exp Biol, 1992, 30, 169;
1993, 31, 607).
Ashwagandha
is classified as tranquilizer, adaptogenic and antiinflammatory. The herbal drug
is found to decrease the degree of anxiety and depression and can be used as
antidepresent. The effect of extract of the drug on mouse central nervous system
has demonstrated a significant increase of the narcosis time. The recovery of
righting reflex was sex and dose dependent. Alongwith Panax ginseng and Tribulus
terrestris, ashwagandha was found to give improvement over all psychomotor
functions including adaptability of patients, to various stresses and in the
building of tissues. The methanolic extract of the drug inhibited the specific
binding of GABA showing GABA recepter mediated anticonvulsent activity in mice
[Dandiya, East Pharm, 1990, 33 (396), 39; Singh et al, J
Res Ayur Siddha, 1990, 11, 1; Ahmuda et al, Phytother Res, 1991, 5, 29; Karnick,
Indian Med, 1992, 4 (1), 1; Jayaram et al, Indian Drugs, 1993, 30, 498; Mehta et
al, Indian J Med Res [B], 1991, 94, 312; Kulkarni et al, Indian Drugs, 1993, 30,
305].
Ashwagandha
is used in several Ayurvedic preparations alongwith other herbal drugs such as -
`Laksha Guggulu', `Raktawardak', `Abana', BR-16A etc in the treatment of
hypercholesteroemia, mental disturbances, convulsions, etc
[Panda, J Res Ayur Siddha ,1990, 11(1-4), 7; Poehlmann, Deerghayu Int, 1993, 9
(4), 8; Shukla et al, Probe, 1994, 33, 133; Shah & Patkar, ibid, 1993, 33, 20;
Kulkarni & Verma, Indian Drugs, 1993, 30, 97].
Ashwagandha alters the concentration of Neurotransmitters - Chemical substances
that are known to play an important role in Brain Processes such as Memory. An
abnormally high level of Gamma Amino Butyric Acid (GABA) or a reduction in the
level of Acetylcholine, both Neurotransmitters can affect Memory. The roots
contain Fe (0.218), K (1.87), Mg (0.19) and Ni (0.126 mg/gm of dry plant
material), along with other elements, which are reported to play a significant
role in the diuretic and aphrodisiac activity of the drug
(Lohar et al, Indian Drugs, 1992, 29, 271).
Ashwagandha
(Withania Somnifera) is commercially available in the following forms:-
|
EXTRACT TYPE |
Thick Paste |
|
DESCRIPTION |
Dark brown thick paste. |
|
HERB EXTRACT RATIO |
5 : 1 |
|
SOLVENT |
Hydroalcohol (50 % EtOH) |
|
EXTRACTIVES IN EtOH |
Not less than 70 % |
|
TOTAL ALKALOIDS |
Not less than 0.50 % |
|
TOTAL WITHANALOIDS |
Not less than 1.0 % |
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|
EXTRACT TYPE |
Dry Powder |
|
DESCRIPTION |
Light brown Powder with Bitter Taste. |
|
HERB EXTRACT RATIO |
5 : 1 |
|
SOLVENT |
Hydroalcohol (50 % EtOH) |
|
IDENTIFICATION |
TLC test for Alkaloids to pass |
|
EXTRACTIVES IN EtOH |
Not less than 75 % |
|
TOTAL ALKALOIDS |
Not less than 1.0 % |
|
TOTAL WITHANALOIDES |
Not less than 1.50 % |
NOTE: PRODUCT OF HIGHER ALKALOID & WITHANALOID CONTENT CAN BE PROVIDED.
USES:
OTHER REFERENCES::
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The Banner Here Indicates They Will "Manufacture" each product/purchase FRESH within on day
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Ashwaghanda is an Ayurvedic herb similar to Indian ginseng that has been traditionally used for libido, fatigue, mental problems, concentration, memory, general debility, nervous and sexual debility, headaches, drug burnout, rejuvenation and recovery from prolonged illness. Official Latin Name:
Withania somnifera |
|
Historical Uses:
Ashwaghanda is also known by the names Ashwagandha, Winter Cherry, Indian Ginseng, and Withania. Ashwaghanda, which belongs to the pepper family, is found in India, Pakistan, Sri Lanka, and Africa. The medicinal part of this herb is the root. The shoots and seeds are also used as food, and to thicken milk. Ashwaghanda is an important herb used in Ayurveda. The name comes from the peculiar odor of this herb, a smell akin to that of a sweaty horse.
Ashwaghanda
in India is akin to
Ginseng in
other parts of the Orient. Both herbs are touted for their longevity enhancing
and sexually stimulating properties, however Ashwaghanda is considered to be
milder and less stimulating than Ginseng. Ashwaghanda has been used for 4000
years in traditional Indian medicine - it was used for tumors, inflammation (including
arthritis), and a wide range of infectious diseases.
Traditional uses of Ashwaghanda among tribal peoples in Africa included fevers and inflammatory conditions. Modern herbalists classify Ashwaghanda as an adaptogen, a substance said to increase the body's ability to withstand stress of all types. Like other adaptogens, Ashwaghanda is supposed to improve physical energy, exercise capacity, and overall health. It also strengthens immunity (against colds, flu, and other infections), increases sexual capacity, improves fertility, and normalizes cholesterol levels. As its name "somnifera" suggests, it is also sometimes said to produce mild sedation (an effect potentially useful for those troubled by insomnia or anxiety). However, as yet the evidence for these and other potential benefits is limited to highly preliminary studies at best.
The primary chemical constituents of this herb include alkaloids, steroidal lactones, and iron.
Studies with rats and human volunteers have shown that Ashwaghanda is helpful in putting cancer tumors into regression (used as an alcoholic root extract) and in reducing inflammation in rheumatoid arthritis.
The plant's high steroid content was found to be more potent than hydrocortisone in animal and human arthritis.
Compounds known as withanolides are believed to account for the multiple medicinal applications of this herb. Ashwaghanda has also been shown to relieve pain by lowering serotonin levels, which contribute to the sensitivity of pain receptors in the body. It is considered a good tonic for the mind and useful for those who have overindulged in work, drugs, or alcohol.
Available Product Form:
Capsules - 570 mg. each (Standard Gelatin, Pure Vegetable, –and- Certified Kosher capsules are available)
Available Purchase Sizes:
Sealed Bottles of 30, 60 or 350 capsules.
Herbal Ingredients:
100% Ashwaghanda 4:1
(This product does NOT contain fillers, grains, soy, yeast, sugars, binders, excipients, starches, or synthetic materials.)
Recommended Dosage:
Take two (2) capsules, two (2) times each day with water at mealtimes.
Product Warnings:
This product has no known warnings or contraindications.
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Ashwaghanda
3 bottle sizes |
SPECIAL PRICING DISCOUNT: Order three or more bottles of any of the items listed below, and you'll receive an automatic 10% price discount for that item. | |
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30 Capsule Bottle -
Item #S111-30 @ $8.68 each |
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60 Capsule Bottle -
Item #S111-60 @ $15.16 each |
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350 Capsule Bottle -
Item #S111-350 @ $73.00 each |
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Withania somnifera Dunal
PLANT PART
USED :
Roots, leaves and seeds. DESCRIPTION : A branched erect shrub, 0.3-1.5 m. Leaves 5-10 x 2.5-5 cm and ovate. Flowers greenish or lurid yellow, about 5 together in an umbellate cyme. PHYTOACTIVE : The roots contain choline, tropanol, pseudotropanol,cuscohygrene,3-tigloyloxytropane, isopelletierine, anaferine and anahygrine'. Withasomnine also has been isolated from the roots2. The roots also have been reported to contain withaferin A and several other steroidal lactones including pharmacologically active with- anolides. These were also isolated as minor constituents of the leaves. DIRECTIONS FOR USE : Acetone soluble alkaloid fraction of the roots showed C.N.S. depressant effect in dogs, albino rats and mice. Convulsions produced by metrazol were exacerbated in rats but the animals were protected against supraorbital electroshock seizures. It produced hypnosis in mice. Potentiation of barbiturate, ethanol and urethane- induced hypnosis were observed in mice". Increase in 5 HT and depletion of calcium was also observed. Alcoholic extract potentiated thiopental-induced sleep in albino mice. It was not effective in antagonising rnetrazol and strychnine induced convulsions and mortality7. The functional activity of normal human T lymphocytes as assessed by local xenogenic graft via host reaction was also affected by withanolide and withaferine'. Withaferine affects both T and B lymphoeytes'. Adaptogenic antistress action of pi 'ant extract from defatted seeds was shown by the increa'se in duration of sleeping time, and prevention of the reduction of ascorbic acid and cortisol contents of adrenals in mice significantly in comparison with controls. Significant protection against aspirin and stress-induced ulcers was also observed in rats. A dose of 60 mglkg for three days showed 50% inhibition of milk-induced leucocytosis in albino rats". The effect of Ashwagandharishta-medicated wine prepared from the roots of Withania somnifera was studied in 30 patients with anxiety neurosis. Moderate improvement in palpitation, tremors, headache, anorexia, lack of concentration, dyspepsia, fatigue and irritability was observed, while maximum improvement was seen in nervousness with 49 ml of Ashwagandharishta administered in two divided doses for one month",". Root powder was studied in 46 patients of rheumatoid arthritis with a dose of 4, 6 or 9 gm/day for a period of 3 to 4 weeks. Pain and swelling disappeared completely in 14 patients; considerable improvement was observed in 10 patients and 11 patients showed mild improvement. There was no relief in 4 patients and 7 patients discontinued the treatments. CONTRAINDICATION : Root powder in a dose of 9 gm/day in divided doses used for 3 to 4 weeks in patients with arthritis was well tolerated. No side effects were observed with Ashwagandharishta in a dose of 40 ml/day in two divided doses given for a month to thirty patients with anxiety neurosis. In acute toxicity studies LD,0 of the alcoholic extract of seeds was 1750 141 mg (P. O.) in albino mice.
FORMULATION AND DOSAGE : Root powder : 2 - 3 gm t.i.d. Ashagandharishta : 20 - 30 ml b.i.d.
REFERENCES : 1. Khanna, K. L. cl al. - Lloydia 26: 258 (1963). 2. Schroter, H. B. et al.: Tetrahedron (London) 22: 2895 (1966). 3. Abraham, A et al.: Phytochemistry 14..189 (1975). 4. Lavic, D. et al.: J. Chem. Soc. 7517: 31 (1965). 5. Schwarting, A. E. et al.: Llyodia 26: 273 (1963). 6. Prasad, L. and C. L. Malhotra: Ind. J. Physiol. & Pharmacol. 12: 175 (1986), 7. Dey, P. K. and B. K. Chatterjec: J. Res. Ind. Med. 3: 1 (1968). 8. Bahr, V. and Hansel, R.: Planta Med. 44: 32 (1982). 9. Shobal, B. et al... Biomedicine 28: 18 (1978). 10. Singh, N. et al.: Int. J. Crude Drug Res. 20..'29 (1982). 11. Singh, R. S. and P. C. Malaviya, J. Res. Ind. Med. Yoga & Homeo, 13: 15 (1978). 12. Daye, D.. Personal Communication. 13. Bector, N. P. et al.: Ind. J. Med. Res. 56: 1581 (1968). 14. Sharma, A. K. and R. H. Singh: Bull. Med. Ethnobot. Res. 1: 262 (1980).
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