- Part 11

Gotu Kola

General Information


Common Name:

Gotu Kola

Latin Name:

Centella Asiatica

Family:

Umbelliferae [Apiaceae]

Other Names:

  • Centella-a specific variety of Gotu Kola. This contains the highest amounts of the active ingredients;
  • Indian penny wort;
  • Hydrocotyle;
  • Marsh penny;
  • Sheep rot;
  • Water penny wort;
  • Talepetrako.

Indications & Historical Uses

  • Increases sex drive;
  • Decreases fatigue and depression;
  • Central nervous system stimulant; enhances memory and learning;
  • Treatment of skin conditions such as psoriasis, eczema, lupus , varicose ulcers and leprosy;
  • Healing of post surgical wounds, burns, open wounds, sores, cuts, ulcers,- applied topically or taken internally;
  • For promoting longevity.

Contraindications & Precautions

Contraindications:
None known. See Caution.

Precautions:
None known. See Caution.

Adverse Side Effects:
None known. See Caution.

Drug Interactions:
None known. See Caution.

Dosage Information

How Supplied:

50 & 100 mg tablets.
1% preparation for local use.

Dosage:

50 mg to 100 mg per day orally.
Topical: 1% preparation twice a day.

Pharmacology

Asiaticosides stimulate the reticulo-endothelial system, and help in the healing process by connective tissue development. Centella also enhances the process of keratinisation, the process of building more skin in areas of skin damage such as sores and ulcers. Asiaticosides also stimulate the synthesis of lipids and proteins which are essential for healthy skin. Centella strengthens veins by repairing tissues surrounding the veins, and by decreasing capillary fragility. Gotu Kola applied locally has both skin healing and anti-inflammatory properties. Extracts of Asiaticosides have proved valuable in stimulating a scar- free wound healing in surgical wounds, skin ulcers, fistulas, episiotomies [perineal lesions occurring during deliveries and obstetrical manipulations], radiation ulcers, skin grafts ,skin tuberculosis and lupus lesion. In a small 1973 study, painful psoriasis lesions responded positively to gotukola cream[ containing oil and water extracts of the leaves]. In 5 out of 7 subjects ,the welts resolved completely within 3 to 7 weeks. Gotu Kola asiaticosides also enhance sexual function in both males and females by stimulating the central nervous system and historically has been used for this purpose on the Indian subcontinent. It has also been used as an antidepressant and in the treatment of fatigue.

Active Ingredients:

  • Asiaticosides;
  • Triterpenes.

Origin

It is a creeping perennial found in wet ,swampy areas in India ,Sri-Lanka, South Africa , Madagascar and other Tropical environments .Some of its common names e.g Indian penny wort ,refers to the size of its fan-shaped leaves which are the size of an old British penny. The leaves are used medicinally. The plant also bears fruits and clusters of small red flowers.

Processing

All aerial parts are used in the extraction process. Extraction is carried out with acetone-based solutions. The extract is then dried & standardized.

Scientific References

Mowrey, D. (1990) Guaranteed Potency Herbs.

Balch & Balch: Prescription for Nutritional Healing. 2nd Ed. (1997). Avery Publishing N.Y.

T.D.Babu et al ,Journal of Ethnopharmacolgy ,48 [1995]:53.

S. Natarajan and P.P.Paily, ,Indian Journal of Dermatology, 18[4] [1973] :82.

F. Damis et al, Semaine des Hospitaux de Paris ,55 [1979] 1749-50.

H.C.Eun and A,Y.Lee, Contact Dermatitis, 13 [5] [1985] :310.

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Ginseng

General Information


Common Name:

Ginseng

Latin Name:

Panax quinquefolium (American Ginseng)
Panax ginseng (China, Korea, Japan and Russia)
Panax pseudo-ginseng

Family:

Araliaceae

Other Names:

  • Korean Ginseng;
  • Panax Ginseng.

Indications & Historical Uses

  • CNS depressant, tranquilizer;
  • Sedative, relaxant;
  • Treatment for Insomnia, anxiety, poor appetite;
  • Agitation;
  • Increase vitality in conditions of weakness, prolonged stress, poor immunity, or chronic disease;
  • Hypotensive;
  • Improves gastro-intestinal motility;
  • Immune system stimulant;
  • Increase synthesis of cholesterol in liver;
  • Helps to regulate blood sugar and lipid levels;
  • Regulates adrenal gland function.

Widely cultivated, Korean ginseng is used as a natural restorative, and valued for its adaptogenic properties. An adaptogen is supposed to help the body adapt to internal and external stressors and prevent stress induced damage and illnesses .Herbal practitioners define adaptogens as normalizers but adaptogen has no medical definition.. People use ginseng to increase their endurance and stamina, to fight off stress, to recuperate from a debilitating illness, to fight fatigue and to enhance their performance-physical, mental and even sexual. Ginseng is therefore sometimes used as an aphrodisiac. Ginseng extracts have been shown to have antioxidant activity, and to protect against radiation damage . European studies have shown that ginseng increases reaction times, alertness, concentration, and enhances coordination .

Contraindications & Precautions

Should not be used by persons with hypoglycaemia, insulin dependent diabetes, high blood pressure or heart disorders, unless approved by their physician.
See Caution.

Adverse Side Effects:
May cause nervousness, increased blood pressure, irritability in high doses. See Caution. Ginseng and /or adulterants have estrogenic activity and may cause vaginal bleeding and mastalgia [breast soreness] and patients with estrogen dependent malignancies may need to avoid ginseng.

weiDrug Interactions:
Patients on anticoagulants e.g coumadin should avoid ginseng because ginseng is known to increase or decrease blood coagulation. Ginseng has potential to cause hypoglycaemia , because some components of ginseng can elevate plasma insulin levels. Therefore, diabetics who take ginseng must have their blood sugars monitored closely .

Dosage Information

How Supplied:

250 mg soft gel capsules.

Dosage:

500 mg per day of extract.

Pharmacology

The main active ingredients of ginseng are the more than 20 saponin triterpenoid glycosides called ginsenosides or panaxosides. These range from Rb 1 group of ginsenoside (sedative and metabolic effects) to Rg 1 group (more arousing and stimulating). Rb1 Ginsenosides also have CNS depressant activity, weak anti-inflammatory activity, and increase bowel motility, as well as have some anti-pyretic, anti-convulsant and analgesic properties. The Rg1 ginsenosides have weak CNS stimulating properties, and protect against fatigue, as well as increase motor activity. There are no apparent major differences between American Ginseng & Oriental Ginseng. Siberian Ginseng is a different plant (Eleutherococcus Senticoccus), which has differing properties, and should not be confused with Panax Ginseng.

Origin

Panax quinquefolium is a deciduous perennial shrub whose fleshy roots take 4 years to cultivate. Cultivated in Canada, Eastern U.S., Wisconsin, China, Korea. American ginseng is more sedative and relaxing and increases yin energy while Korean ginseng is more stimulating and increases the yang energy.

Processing

4 year old roots are harvested and dried.

Scientific References

Weiner, M. (1990) Weiner’s Herbal. Mill Valley: Quantum: Books.

Foster, S.: American ginseng: Panx Quinquarfolians, Botanical series no. 308, American Botanical Council, Austin, Tex. (1991) 8 pp.

Baldwin, CS et al. (1986) What pharmacists should know about Ginseng. Pharm. J. Nov 8th: 582.

Brekhman, I.I. and Dardymov, I.V. (1969) New substances of plant origin which increase nonspecific resistance. Ann Rev Pharm. 9:419..

Hia, et al. (1979) Stimulation of pituitary adrenocortical system by ginseng saponins. Endocrinol. Japonica. 26(6): 661.

Mowrey, D. (1990) Guaranteed Potency Herbs. A Compilation of writings on the subject.

Oshima, Y et al. (1987) J. Nat. Prod. 50.

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Glucosamine

General Information


Common Name:

Glucosamine

Scientific Name:

2_Amino-2 deoxyglucose

Other Names:

  • Chitosamine;
  • Glucosamine sulphate.

What is it?

An Aminoglycoside or Aminosugar. Glucosamine is not an herbal extract. Glucosamine is prepared synthetically or extracted from shellfish. It is found in cell membranes, mucopolysaccharides, and chitin, the horny substance in the exoskeleton of crabs, beetles, and various marine invertebrates and microorganisms. It is included in this section because of its efficacy as an alternative treatment of osteoarthritis.

Arthritis Plan

(Ref: The Arthritis cure plan by Dr. Theodosakis).

Number

Action

Comment

  • Consultations with a physician. The author encourages a proper diagnosis be made;
  • Glucosamine and chondroitin sulphate. Doses outlined – adjusted versus symptoms and divide 2-4 time/day;
  • Vitamin C 500 – 4000mg and Manganese 50mg. Antioxidants;
  • Improve biomechanics. Physiotherapists/Sports medicine/Neuromuscular therapists;
  • Exercise PhyPhysiotherapists/Sports medicine/ Neuromuscular therapists;
  • Healthy diet. Encouraged strongly;
  • Fight Depression. Very important;
  • Use traditional medications. Surgery is a final option only;
  • Maintain a positive attitude. Don’t obsess about the condition.

Indications & Historical Uses

Relief of osteoarthritis. Other recommended uses are for tendonitis and, bursitis. Glucosamine is sold as a dietary supplement to decrease pain and improve mobility in people suffering from osteoarthritis ,a progressive disease of cartilage degeneration. It is also billed as a chemical to support healthy joint and connective tissue. It has been suggested ,by some sources , that it may even prevent or postpone the development of osteoarthritis in certain groups ,such as the elderly and the athletes.

Contraindications & Precautions

Contraindications:
None known. See Caution.

Precautions:
Patients allergic to sulphates should take glucosamine Hydrochloride (not sulphate). Also these patients must not take Chondroitin Sulfate. Since Glucosamine is extracated from shellfish, persons who are allergic to shellfish should exercise caution, though there have been no reported cases of these allergies to glucosamine. See Caution.

Adverse Side Effects:
Rare cases of nausea, vomiting, diarrhea have been reported.

Drug Interactions:
No known drug interactions. It is safe to take glucosamine with blood pressure medications, non-steroidal anti inflammatory drugs, and for diabetics on hypoglycaemic agents. ( but close monitoring of blood sugar levels is recommended).

Dosage Information

How Supplied:

500mg capsules.

Dosage:

Daily Doses of Glucosamine and Chondroitin sulphate:

Weight Glucosamine Sulphate Chondroitin sulphate

  • 1000mg 800mg;
  • 120-200 pounds 1500mg 1200mg;
  • >200 pounds 2000mg 1600mg.

If no effect within 12 weeks of treatment, discontinue treatment.

Pharmacology

Glucosamine, an amino sugar, is the building block for certain glyosaminoglycans. In vitro, it has been shown to stimulate proteoglycan synthesis by human chondrocytes. It also has some innate anti-inflammatory properties ,independent of prostaglandin synthesis. There are some studies ,mainly in the European literature, suggesting that 1500mg daily of glucosamine sulphate is equivalent to1200mg of ibuprofen in the control of osteoarthritis symptoms. Glucosamine is also involved in the formation of nails, tendons, skin, eyes, bones, ligaments and other connective tissues in the body . Osteoarthritis involves a progressive degeneration of cartilage glycoaminoglycans [GAGs], components of cartilage that enable joints to move smoothly. The theory behind taking glucosamine supplements ,which are critical to the synthesis of GAGs, is that by flooding the system with them the production of these GAGs will be stimulated. Theoretically, the end result would be cartilage regeneration and joint repair. Many studies have shown that glucosamine is absorbed rapidly from the intestines, and transported to the connective tissues. It helps in the restoration of damaged joint tissue in osteoarthritis, especially in conjunction with Chondroitin Sulfate or devil’s claw. Chondroitin sulphate is a glycosaminoglycan and is a main constituent of proteoglycans. Like glucosamine, it has been shown to stimulate proteoglycan synthesis by human chondrocytes. Chondroitin sulphate also has some innate anti-inflammatory properties, independent of prostaglandin synthesis. Both compounds are natural and may be beneficial in the treatment of osteoarthritis.

Active Ingredients:

Glucosamine is a combination of glucose and glutamine

Origin & Processing

Glucosamine is extracted from shellfish, and purified & standardized to form Glucosamine Sulfate. Glucosamine is also prepared synthetically.

Scientific References

Bassleer C, Malaise M, University of L B (1997): Chondroitin Sulfate: its in-vitro Effects on Human Articular Chondrocytes Cultivated in Clusters. 3rd, International Congress of the Osteoarthritis Research Society Osteoarthritis in Focus: 5, Suppl A,:69.

Bassleer C, Henrotin Y, Franchiment P. (1992): in-vitro Evaluation of Drugs Proposed as Chondroprotective Agents. Int J Tissue React, 14:231-241.

Bourgeois P I. Chales G, Dehais J, Delcambre B, Dreyfus P, Kuntz J, Rosenberg S (1997): Efficacy and Tolerability of Chondrotin Sulfate 1200mg/dfe Vs. Chondrotin Sulfate 3 x 400 mg/d Vs. Placebo. 3rd, International Congress of the Osteoarthritis Research Society Osteoarthritis in Focus: 5, Suppl A,:69.

Bucci L, Podr G et al (1997): Efficacy and Tolerability of 2 x 400 Mg Oral Chondroitin Sulfate as a Single dose in the Treatment of Knee Osteoarthritis. 3rd, International Congress of the Osteoarthritis Research Society Osteoarthritis in focus: 5, Suppl A:69.

Camus J P (1972): verification de action de l’acid Chondroitin suifurique cnez des malades arthrosiques. Laboratories Gremy-Longuet. Paris.

Crivelli E, Voy E D (1987): Etude de pnase IV sur action des soses orales del sulfate articulations. Der informaierte Artz Gazette Medicinale, 3.

Crolle G, D’Este E (1980): Glucosamine sulphate for the management of arthrosis. Current Medical Research and Opinion Vol.7, No.2.

D’Angnolo B (1986): Valutazione degli effetti coilaterali e della efficacia nel sintmo del dolore (in pazienti artosici) del galattosamino glucuronogllcano solfato. Clin. Eur. Fasc., XXV (March-April). 275-280.

Droranti A, Bignamini A A, Rorati A I, Italy (1980): Therapeutic Activity of Oral Glucosamine in Osteoarthrosis: a placebo-controlled double-blind investigation Clinical therapeutics, vol. 3, no. 4.

D’Ambrosio, Casa B, Bompani R, Scali G (1981): Glucosamine Sulphate: a Controlled Clinical Investigation in arthrosis. Pharmatheutica, 2 (8):504.

Fioravanti A., Franci A., Anselmi F., Fattorini L., Marcolongo R. (1991) Clinical Efficacy and tolerance of Galactosoaminoglucuronoglycan Sulfate in the Treatment of Osteoarthritis. Drugs Exptl. Clin. Res. XVII (1) 41-44.

Garzya G. (1986): Orale Chondroitin sulfatmedikation zur Benandung von Arthrosen: Therapiewoche, 33, 4238.

Hardingham T (1997): Chondroitin Sulphate and Joint Disease. 3rd, International Congress of the Osteoarthritis Research Society Osteoarthritis in Focus: 5, Wuppl A,:69.

Helli MP, Vignon E, annefeld M, Richard M (1996): The Effects of Glucosamine on the Human Osteoarthritic Chondrocytes. The 9th Eular Symposium, Madrid, 7-10.

Jenoure P. et al (1986): Lesions degeneratives du gerou. Der informierte Artz/Gazette Medicinale, 7.

Jimenez SA, Dodge G R, Thomas J (1996): the Effects of Glucosamine On Human Chondrocyte Gene Expression. The 9th Eular symposium, Madrid, 7-10 October, pp 8-10.

Karzel K. domenjoz R (1971): Effect of Hexosamine Derivatives and Uronic Acid Derivatives on Glycosaminoglycan Metabolism of fibroblast Cultures. Pharmacol, 5:337-345.

Kim JJ, Conrad H E (1974): Effect of D-glucosamine Concentration on the Kinetics of Mucopolysaccharides Biosynthesis in Cultured Chick Embryo Vertebral Cartilage. J Biol Chem, 249: 3091-3097.

Maier R, Wilhelmi G (1982): Neue experimentelle Ergebnisse uber korperdestruktion und Protektion. Der Kassernartz, 22. 16.

McCarty MF (1994): the Neglect of Glucosamine as a Treatment for Osteoarthritis – a Personal Perspective. Medical Hypotheses, 42:323-327.

Muller-fabender Hans, Gerhard L, Bach, Wolfgang Haase, Rovati L C (1994): Glucosamine sulfate Compared to Ibuprofen in Osteoarthritis of the Knee. Osteoarthritis and Cartilage 2, 61-69.

Nerucci F, Fioravanti A, Bisogno S, Spinelli G, Marcolongo R, (1997): evaluation of the Chondroitin Sulfate Effects on Chondrocytes’ cultures Placed in a Pressurization System. 3rd, International Congress of the Osteoarthritis Research society Osteoarthritis in Focus: 5, Suppl A, :69, May.

Noack W, Fischer M, Forster K K, Rovati, L C , Setnikar I (1994): Glucosamine Sulfate in Osteoarthritis of the Knee. Osteoarthritis Cartilage (United Kingdom), 2/1 (51-59).

Oliviero U, sorrentino GP, De Paola P, Tranfaglia E, D’alessandro A, Carifi S, Porfido FA, Cerio R, Grasso A M, Policicchio D, Di Grezia F, Sorrentino P, Lingetti M (1991): Effects of the Treatment with Matrix on Elderly People with Chronic Articular Degeneration Drugs Exptl-Clin. Res. XVII (1) 45-51.

Paroli E, Antonilli L and Biffoni M (1991): a Pharmacological Approach to Glycosaminoglycans. Drugs under Experimental and Clinical Research, XVII (1):9-20.

Rietro M, Manopulo R, Galati M, Boccanera L, Saponati G and Bocchi L (1996): Comparison of the Antiinflammatory Efficacy of Chondroitin Sulfate and Diclofenac Sodium in Patients with Knee Osteoarthxifis. J Rheumaro I, 23: 1385-91.

Pujalte J M, Llavore E P, and Ylescupidez F R, (1980): double-blind Clinical Evaluation of Oral Glucosamine Sulphate in the Basic Treatment of Osteoarthrosis Current Medical Research and Opinion Vol.7, No.2.

Raiss R (1985): Effect of D-glucosamine on Experimentally Injured Articular Cartilage. Comparative Morphometry of the Ultra Structure of Chondrocytes. Fortschritte Der Medizin. 103 (24) 658.

Reichelt A, Fbrsterc KK, Fischer M B, Rovatie L C, and Setnikar I (1994): Efficacy and Safety of Intramuscular Glucosamine Sulfate in Oseoarthritis of the Knee. Arzneim. Forsch./Drug Res. 44 (1), Nr. 1.

Roden, L (1956): Effect of Hexosamines on the Synthesis of Chondroitin sulphuric Acid in-vitro. Ark. Kemi., 10, 345.

Ronca G (1997): Anti-inflammatory Activity of chondroitin sulfate. 3rd, International Congress of the International Congress of the Osteoarthritis Research Society Osteoarthritis in Focus: 5, Suppl A, :69.

Rovetta G (1991): Galactosaminoglycuronoglycan Sulfate (Matrix) in Therapy of Tibiofibular Osteoarthritis of The Knee. Drugs Exptl. Clin. Res. XVII (1) 53-57.

Serni U (1993): Profile of Glucosamine as a Example of Slow Acting Drug in Osteoarthritis. In: Proceedings of the Xviii th Congress of Rheumatology. Rev Esp Reumatol, 20(suppl):222.

Setnikar I, Cerada R, Pacinic M A, et al. (1991 b): Antireactive Properties of Glucosamine sulfate. Arzneimittel-forshung, 41 (1), Nr. 2, 157-161.

Tapadinhas M J (1982): Oral glucosamine sulphate in the management of arthrosis: report on a multi-centre open investigation in Portugal. Pharmatherapeutica, 3, 157.

Uebelhart D, Zhang J, Thonar E, Williams J (1997): Acute Degradation of Articular Cartilage in the Rabbit: Protective Effect of Chondroitin 4 & 6 sulfate. 3rd, International Congress of the Osteoarthritis Research Society Osteoarthritis Focus: 5, Suppl A, :69.

Vidal Y., Plana R R, Bizzarri D, Rovatie A I, (1978): Articular Cartilage Pharmacology, I. In-vitro Studies on Glucosamine and Nonsteroidal Anti-inflammatory Drugs. Pharmacol. Res. Comm., 10, 557.

Vajaradul Y (1981): Double-Blind Clincal Evaluation of Intra-Articular Glucosamine in Outpatients with Gonarthrosis. Clinical Therapeutics/vol. 3, No. 5.

Vaz A L (1982): Double-Blind Clinical Evaluation of the Relative Efficacy of Ibuprofen and Glucosamine Sulphate in the Management of Osteoarthrosis of the Knee in Out-patients. Current Medical Research and Opinion: Vol. 8, 145.

Weyers W, Iseli D (1987): Pharmakologische Untersuchungen zur antiphalogistisch Wirksamkeit Von Chondroitinsulfat. II Mittelung. Therapiewoche Schweiz, 3, 864.

EVIDENCE OF BIOAVAILABILITY.

Setnikar I, Giachetti C, Zanolo G. (1986): Pharmacokinetics of Glucosamine in the Dog and in Man. Drug Research, 36 (1):729-735.

Setnikar I, Giachetti C and Zanolo G. (1984): Absorption, Distribution and Excretion of Radioactivity after a Single Intravenous or Oral Parmatherapeutica, 3, (8)538.

Setnikar I, R. Palumbo, S. Canali, and G. Zanolo, (1993): Pharmacokinetics of Glucosamine in Man. Arzneim-Forsch / Drug Res. 43(II), Nr 10.

Conte A (1995), Volpi N, Palmiera L, et Al. Biochemical and Pharmacokinetic Aspects of Oral Treatment with Chondroitin Sulfate. Arzneimittel-forshung, 45: 918-925.

Palmieri L. Conte A. Giovannini L. Lualdi P. Ronca G. (1990): Metabolic Fate of Exogenous Chondroitin Sulfate in the Experimental Animal. Arzneimittel-forschung. 40(3):319-23.

CURRENT CLINICAL TRIAL ON GLUCOSAMINE AND CHONDROITIN.

HUMAN CLINICAL TRIAL #1.

Principal investigator: Amal K. Das, Jr., M.D.(an orthopedic surgeon).

Institiution: Henderson Orthopedic Research Associates, North Carolina. Study design: Almost 100 patients with chronic pain and osteoarthritis (confirmed by X-Ray) in a double-blinded, placebo-controlled, six-month clinical trial using Cosamin DS (combination of 1,500 milligrams glucosamine and 1,200 milligrams of chondroitin daily).

Results: Knee osteoarthritis symptoms were measured by summary disease scores and patient assessment of treatment effect, recorded at clinic visits and in a dairy. The summary disease score incorporated pain, stiffness and function using validated questionnaires. Adverse events: Recorded, if any, in a daily dairy specifying severity and no adverse reactions were note. More details to follow up0on the publication of this study.

HUMAN CLINICAL TRIAL #2.

Prinicpal investigators: Dr. Alan Philippi, LCDR, MC, USNR and Dr. Christopher Leffler, MD.

Institution: Medical Department Naval Special Warfare (SEAL). Group Two, Naval Amphibious Base, Little Creek. Study design: 16-week, randomized, double-blinded,placebo-controlled crossover design in 34 Navy SEALs, and divers by the Portsmouth Naval Medical Center in Virginia.

Results: Significant relief of knee pain but no improvement in function after eight weeks on the supplements. More details to follow upon the publication of this study.

HUMAN CLINICAL TRIAL #3.

Principal investigators: Dr. Joseph B. Houpt (Toronto, Canada).

Study design: Double-blinded, placebo-controlled using glucosamine in patients with oseoarthritis.

Results: Still pending.

HUMAN CLINICAL TRIAL #4.

Principal investigators: Jason Theodosakis, M.D.,James Weaver, D.D.S.

Study design: Double-blinded, placebo-controlled using glucosamine and chondroitin for prevention and treatment of osteoarthritis in the TMJ.

Results: Study is still in design and approval phase.

Several new university-based, large animal studies, along with basic science research continues to point to the disease-modifying benefits of the two supplements on joint cartilage. For example, Dr. Louis Lippiello, Ph.D., the Director of Basic Science at the Harrington Arthritis Research Center in Phoenix, has found that glucosamine and chondroitin work synergistically in promoting cartilage cell activity

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Garlic

General Information


Common Name:

Garlic

Latin Name:

Allium Sativum 

Family:

Liliaceae

Other Names:

  • Allium;
  • Camphor of the poor;
  • Nectar of the gods;
  • Camphor of the poor.

Indications & Historical Uses

  • Protect the circulation, lower cholesterol;
  • Protect against and fight infections, colds, and flu;
  • Enhances immune function;
  • Aids in the treatment of arthritis, arteriosclerosis, digestive problems, insomnia, and liver disease;

Contraindications & Precautions

Nil known. Please See Caution.

Precautions: See Caution. 

Adverse Side Effects: Garlic does not have many adverse effects. The most commonly reported adverse effects are the taste or offensive odor of garlic. However some commercial products do not have this odor. There are rare reports of garlic extracts causing burning of the mouth and stomach, nausea, sweating and light-headedness. Raw garlic and garlic oil may irritate the digestive system and therefore should be taken with meals.

Drug Interactions: Not known

Dosage Information

How Supplied:

100mg, 200mg, 400mg tablets enteric coated. It is important to note that both Allin and Allicin are unstable in gastric fluid and therefore it has been suggested the best formulations of garlic are enteric-coated tablets or capsules of dried garlic or garlic powder.

Dosage:

400 mg per day of standardized extract. (Equivalent to 1200mg of fresh garlic per day)

Pharmacology

The intact cells of garlic contain an odorless sulfur-containing amino-acid – Allin ((+) S-ALLYL-L-CYSTEINE SULFOXIDE) When these cells are crushed, the allin combines with allinase in the neighboring cells to produce allicin (diallyl thiosulfinate), which is a very potent antibiotic: The allicin is unstable, and decomposes to other strong smelling sulfur compounds, including various diallyl-sulfides and ajoenes (ah-jo-weens). The ajoenes are responsible for the anti-thrombotic properties of garlic, while allicin itself has been shown to possess anti-platelet, antibiotic and anti-lipaemic properties.

The effectiveness of garlic in reducing cholesterol and serum lipids is still controversial. However in a number of experimental double blind studies garlic has been shown to reduce total cholesterol on the average by about 6-9%. LDL Cholesterol by about 11% and triglycerides by as much as 17%. In many cases a rise in HDLCholesterol was also noted. The mechanism by which garlic causes reduction in cholesterol is not completely clear. It is speculated that the disulphide compounds in garlic oil affect thiol groups found in many enzymes. The blood pressure lowering and anti platelet effects of garlic are probably due to the compounds that influence calcium dependent processes. Some of these have an effect on platelet aggregation, lysosomal enzyme release and maintenance of vascular muscle tone. Reduction in platelet aggregation is due to the interference with thromboxane synthesis. The antimicrobial and anticancer properties of garlic are probably attributable to the organic sulphur compounds in garlic. These compounds may fight infections by interfering with microbial structure or function; they may fight cancer by reducing the formation and the activity of carcinogens.   It is important to note that although garlic may help reduce blood pressure and cholesterol, it will be most effective in conjunction with appropriate life style modifications, such as appropriate diet, exercise and smoking cessation.

Active Ingredients:

  • Allin;
  • Allinase;
  • Allicin;
  • Vitamins A, B, &C.

Enhancing Agents:

Origin

Xianjiang Province, China

Now widely grown Garlic is the bulb of the tall flowering plant Allium savium that bears pink to purple flowers. Humans have been cultivating garlic for more than five thousand years. The bulb has been handed down through the centuries as a preventive medicine and cure-all that many medieval folk healers claimed could ward off vampires, witches and other unwanted imaginary creatures. Widely used as an antiseptic for generations, garlic became known as” Russian penicillin” in the days of penicillin shortages during World war II, when people resorted to applying garlic juice to open wounds.

Processing

Chinese garlic is meticulously dried at ultra-low temperatures to protect its TAP and enzyme activity.

The powder is compressed into tablets, coated with an enteric coating and a clear protein coating to lock in freshness and to eliminate odor.

Scientific References

Foster S: Garlic: Allium Sativum, Botanical series 311, American Botanical Council, Austin Texas, 1991. 7pp.

Kleijpen J., Krispschild P, & Tao Peit, G: British Journal of Clinical Pharmacology 28:535-544(1989).

Bordia, A. (1981) Effect of garlic on blood lipids in patients with coronary heart disease. Amer. J. Clin. Nurtr.34 (10): 2100.

Weiner, M. (1990) Weiner’s Herbal. Mill Valley: Quantum Books.

Nishimo, H. et al. (1989) Antitumor-Promoting activity of garlic extracts. Oncology 46(4): 277.

Mowrey, D. (1986) The Scientific Validation of Herbal Medicine. Cormorant Books.

McCaleb, R. (1992) Garlic fantastic health aid. Better Nutrition for Today’s Living. Feb 92:36.

Bordia, A. and Bansal, H.C. (1973) Essential oil of garlic in prevention of atherosclerosis. Lancet ii: 1491.

Tyler V.E., Herbs of Choice, pp.104-108, 1994.

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Flaxseed Oil

General Information


Common Name:

Flaxseed Oil

Latin Name:

Linum usitatissimum

Family:

Linaceae

Other Names:

  • Flaxseed Oil;
  • Linseed Oil.

Indications & Historical Uses

Flaxseed oil is used orally as food oil, as a supplemental source of alpha- linolenic acid and for certain medical conditions outlined below:

  • Arthritis;
  • For hyperlipidemia;
  • To prevent heart attacks;
  • Cancer;
  • Anxiety;
  • Benign prostatic hypertrophy;
  • Constipation;
  • Vaginitis.

Contraindications & Precautions

Not to be used in pregnancy and if nursing. See Caution.
No adverse reactions have been reported.

Drug Interactions:
Non known.

Dosage Information

How Supplied:

750 mg. Capsules.
Also available for topical use

Dosage:

1 to 2 capsules two times daily or as advised by physician/ health professional.

Pharmacology

Flaxseed oil is the best natural source of alpha-linolenic acid. Linolenic and alpha-linolenic acid are required for the structural integrity of cell membranes. They are transformed into longer chain, more polyunsaturated fatty acids that are precursors to a group of hormone-like compounds called prostaglandins and leukotrienes. Some studies show that flaxseed oil offers protection against cardiovascular disease probably by decreasing platelet aggregation and also by improving lipid profiles in people with hyperlipoprotinemia.

Active Ingredients:

  • Alpha-linolenic acid;
  • linolenic;
  • oleic acids.

Origin and Processing

Oil is extracted from flaxseed. Commercial preparations are available for oral and topical use.

Scientific References

The Review ofNatiural Products by Facts and Comparisions: St. Louis,MO: Wolters Kluwer Co., 1999

Mann , Trusswell AS. Eds. Essentials of Human Nutrition .Oxford. Oxford University Press 1998

Rozanova IA, et al. ” Effect of antiartherosclerotic diet, containing polyunsaturated fatty acids of the omega-3 family from flax oil, on fatty acid composition of cell membranes of patients with ischemic heart disease, hypertensive disease and hyperlipoprotinemia. Vopr Pitan 1997: (5): 15-7

Allman MA, Penna MM, Pang D,” Supplementation with flaxseed oil versus sunflower seed oil in healthy young men consuming a low fat diet: effects on platelet composition and function.” Eur J Clin Nutr , 1995; 49 (3): 169-178.

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Feverfew

General Information


Common Name:

Feverfew

Latin Name:

Tanacetum parthenium

Family:

Asteraceae

Other Names:

  • Altamisa;
  • Featherfoil;
  • Febrifuge plant;
  • Midsummer daisy;
  • Nosebleed;
  • Wild chamomilee;
  • Santa Maria.

Indications & Historical Uses

Feverfew was known to the ancient Egyptians and Greeks as a valuable herbal remedy and was used as an anti-inflammatory agent. It was used to treat headaches and for promoting menstrual flow. Recent clinical trials have substantiated its effectiveness as a remedy for migraine headaches. It is used effectively for the prevention and treatment of migraine headaches. It has also been suggested for inflammations, nausea and vomiting, vertigo, arthritis, and as a digestive aid .

Contraindications & Precautions

Contraindications:
None known at present (See Caution).

Precautions:
See Drug Interactions.

Adverse Side Effects:
Feverfew is usually well-tolerated and no serious side-effects have been reported. Rarely, individuals allergic to the Compositae family of flowers [e.g ragweed and chamomile ] may show hypersensitivity. 10% of people taking fever few may develop mouth ulcers.

Drug Interactions:
It has been shown that the concomitant use of NSAIDS or steroids may reduce the effectiveness of Feverfew. Feverfew also has the potential to decrease platelet aggregation and therefore patients on anticoagulants should be closely monitored. See Caution.

Dosage Information

How Supplied:

As capsules containing 500mg of parthenolide.

Dosage:

One capsule of extract containing 500 mg parthenolide per day. Feverfew has to be taken for an entire month before beneficial effects are noticeable in case of migraine prophylaxis. Also much higher doses are required to abort an acute attack of migraine. [1-2 gm ].

Pharmacology

The most pharmacologically active ingredient is Parthenolide. Feverfew contains a number of other not so active, bitter tasting sesquiterpene lactones. Research studies have determined that parthenolide, michefuscalide, and chrysanthenyl acetate inhibit the production of prostaglandins. Though it does not directly inhibit cyclo-oxygenase like ASA or NSAIDS, it does appear to inhibit the release of arachidonic acid which reduces substrate for both prostaglandins and leukotriene synthesis. Feverfew also inhibits degranulation in platelets and leukocytes, and this in turn results in the decreased secretion of serotonin and histamine. Inhibition of prostaglandins production results in reduction of inflammation, decreased secretion of histamine, decreased activation of inflammatory cells and a reduction of fever, hence the name. While the anti- inflammatory effect is of some benefit, the major beneficial effect is due to its effects on histamine and serotonin. It is postulated that it is the inhibtion of serotonin and histamine release that reduces the spasm of the cerebral blood vessels, thus preventing and controlling migraine headaches. In addition to its anti-inflammatory activities, feverfew is also known for relaxing the smooth muscles in the uterus and promoting menstrual flow and for inhibiting platelet aggregation and excessive blood clotting. As a bitter herb, feverfew has been used in stimulating digestion and improving the function of the liver.

Active Ingredients:

Principal active ingredient is parthenolide – a sequestrene lactone. Other sequesterpene lactones are chrysanthemonin, Chrysartemin A and B and Santamarin. Other active substances are tannins, betafarnesene and camphor. Standardized amount of active ingredient is 0.1 – 0.5 % parthenolide.

Origin

Feverfew is a member of the daisy family, similar to the tansy and chrysanthemum. It is native to Germany, Holland, U.K. and Israel. Feverfew is a short , bushy perennial with daisylike yellow and white flowers and closely resembles chamomile. The yellow-green leaves are used medicinally.

Processing

Active ingredient is extracted from the harvested leaves. The extract is then concentrated to the guaranteed potency.

Scientific References

S. Foster: Feverfew, Tanacetum parthenium, Botanical series No 310. American Botanical Council, Austin,Texas (1991) p.p. 8.

Weiner, M. (1990) Weiner’s Herbal. Mill Valley, CA: Quantum Books.

Grieve, M. (1978) A Modern Herbal. Middlesex, UK: Penguin Books.

Heptinstall, S. (1988) Feverfew– An ancient remedy for modern times? J. Royal Soc. Med. 81:373-374.

Bohlmann, F. and Zdero, C. (1982) Sesquiterpene lactones and other constituents from Tanacetum parthenum. Phytochemistry 21:2543

Makheja, A. and Bailey, J. (1981) The active principle of Feverfew. Lancet 2:1054.

Jhnson, E.S. et al. (1985) Efficacy of Feverfew as prophylactic treatment of migraine. Brit. Med. J. 291:569.

Murphy, J.J. et al. (1988) Randomised double-blind trial of Feverfew in migraine prevention. The Lancet 2:189.

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Dong Quai

General Information


Common Name:
Dong Quai

Latin Name:

Angelica Sinesis

Indications & Historical Uses

Has historically been used for menstrual symptoms, fatigue, debility, and as a liver tonic, anti-inflammatory and anti-spasmodic.

Contraindications & Precautions

Contraindications:
This herbal has major contra-indications, and is not recommended. See Warning, and Pharmacology. Precautions: See below.

Adverse Side Effects:
Major adverse effects. See Pharmacology

Drug Interactions:
See below.

Dosage Information

Dosage:

Not recommended.

How Supplied:

See below.

Pharmacology

Seven different coumarin derivatives have been identified in Dong Quai, including psoralen, oxypevledanin, osthole, imperotorin, and bergapten. Some of these have a central nervous system stimulant effect, and some act as vasodilators and anti spasmodics. However, psoralen and berapten cause severe photosensitive dermatitis, and investigators have concluded that these ingredients cause sufficient risks to humans and should be avoided. Substantial clinical evidence is lacking to support the effectiveness of Dong Quai for the various clinical conditions it is purported to alleviate, and consequently the use of this herb is not recommended.

Active Ingredients:

See Above.

Origin

Asia, primarily China, Korea and Japan.

Processing

In the Far East, the roots of the plant are harvested, dried, and extracted by using water and alcohol.

Scientific References

G.W. Ivie, D.L. Holt & M.C. Ivey: Science 213: 909-910, 1981.

M. Tierra : The Way of Herbs, Unity press, Santa Cruz, Ca, 1980. Pg. 124-145.

K. Hata, M. Kozawa, Y. Ikesmiro: Yagasaku Zassmi. 87: 464-465, 1967.

Teeguarden, R (1984) Chinese Tonic Herbs. Japan Publications Inc. N.Y.

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Echinacea

General Information

Common Name:

Echinacea

Latin Name:

  • Echinacea Purpurea
  • Echinacea Angustifolia
  • Echinacea Pallido

Family:

Asteraceae

Other Names:

  • American coneflower
  • Black Sampson
  • Missouri snake root
  • Rudbeckia
  • Scurvy root

Indications & Historical Uses

  • Immunity booster, especially against colds and flu.
  • As an anti-inflammatory, analgesic, sedative and anti-spasmodic.
  • As an adjunct to treatment of throat infections.
  • Anti-viral.
  • Wound healing.

For skin conditions like eczema ,psoriasis and herpes

Echinacea is the forgotten herb , recently, rediscovered and appreciated for its ability to enhance our innate infection-fighting ability. For centuries, many native North American tribes such as the Cheyennes and Comanches have used Echinacea,or purple cone flower, in topical and ingestible medicinal herb preparations .This herb was used by native Americans to aid in healing insect bites, skin wounds, toothaches and to treat mumps, colds, arthritis and a wide variety of other medical conditions. Although its use was largely abandoned once antibiotics became popular, the medical community is recognizing its usefulness once again, especially in this age of antibiotic resistance .Recent clinical trials support the use of Echinacea to treat colds and flu and to strengthen the immune system to optimize our infection fighting ability against a variety of other illnesses, such as herpes, bronchitis, tonsillitis, influenza, meningitis ,tuberculosis, abscesses, whooping cough, arthritis, ear infections and many other conditions.

Contraindications & Precautions

Contraindictions:
Should not be used by persons suffering from severe systemic illnesses such as collagen diseases, multiple sclerosis, asthma, diabetes, leukemia, tuberculosis, immunocompromised individuals (HIV/ AIDS) and individuals receiving immunosuppressive therapy (such as corticosteroids and cyclosporine). Also See Caution.

Precautions:
See above and Caution. Do not use if you are allergic to sunflowers .Prolonged use of echinacea may depress the immune system probably because of overstimulation and therefore echinacea should be taken for only 2-3 months at a time or on and off alternating schedule every few weeks.

Drug Interaction:
May interfere with immunosuppressive therapy.

Dosage Information

How Supplied:

500 mg capsules.

Dosage:

500mg. extract two times a day during flu season.

Pharmacology

Roots and leaves contain the most potent immunostimulating components. Echinacea contains Polysaccharides and Phytosterols, which have stimulatory effects on the immune system, particularly the complement pathway. It increases phagocytosis, and promotes the activity of lymphocytes, increasing release of tumor necrosis factor[TNF]. It also stimulates adrenal cortical activity, induces production of interferon and properidin and inhibits production of hyaluronidase and as a result promotes wound healing and has anti-inflammatory effects. Echinacosides appear to have antibacterial activity. All these actions tend to increase the body’s resistance to viral and bacterial activity. .

Active Ingredients:

  • Polysacharrides
  • Echinacosides
  • Caffeic Acid Glycoside
  • Essential oils [ humulene,caryophylene]
  • Polyacetylenes
  • Sesquiterpene Esters
  • Flavonoids

Enhancing Agents:

  • Golden seal
  • Ginseng
  • Astragalus
  • Licorice

Origin

Echinacea Angustifolia ,a member of the daisy family, is native to the American Midwest. It has thick narrow leaves and bears a single flower distinguished by purple rays emanating from a coned shaped centre. The black root stock is used medicinally.

Processing

Cold water/ethanol extraction (repercolation) Evaporation at low temperature, low pressure.

Scientific References

Foster, S. (1991) Echinacea, The Purple Cornflower. American Botanical Council, No. 301.

Hobbs, C.(1989) The Echinacea handbook. Portland, OR: Eclectic Medical Publication.

Mowrey, D. (1990) Guaranteed Potency Herbs. A Compilation of writings on the subject.

Mowrey, D. (1986) The Scientific Validation of Herbal Medicine. Cormorant Books.

Samochowiez, E. et al. (1979) Evaluation of the effect of Calendula officinalis and Echinacea angustifolia on Trichomonas vaginalis in vitro. Wiadmosci Parazytologiczne. 25(1):77.

Tragni,E. et al. (1985) Evidence from two classic irritation tests for an anti-inflammatory action of a natural extract, Echinacin B. Food and Chem. Toxic. 23(1):317.

Wacker, A. and Hilbig, A. (1981) An immunostimulating active principle from Echinacea purpurea. Agnew. Phytother. 2(5):166.

Weiner,M. (1990) Weiner’s Herbal. Mill Valley: Quantum Books.

Brophy, J.J.: “Chapter 19” in current Medical Diagnosis & Treatment 1990, S.A. Schroeder, M.A. Krupp, L.M. Tierney, Jr., and S.J. McPhee, eds., Appleton & Lange, Norwalk, Connecticut, 1990, pp.710-714.

Foster, S.: Asian Ginseng: Panax ginseng, Botanical Series No. 303, American Botanical Council, Austin, Texas, 1991, 7 pp.

Foster, S.: American Ginseng: Panax quinquefolius, Botanical Series No. 308, American Botanical Council, Austin, Texas, 1991, 8 pp.

Chandler, R.F.: Canadian Pharmaceutical Journal 121:36-38 (1988).

Lawrence Review of Natural Products: March, 1990.

Wren, R.C.: Potter’s New Cyclopaedia of Botanical Drugs and Preparations, rev. ed., D.W. Daniel, Saffron Walden, England, 1988, pp. 129-130.

Barna, P.: Lancet II:548 (1985).

Staba, E.J.: Lancet II:1309-1310 (1985).

Lewis, W.H.: “Chapter 15” in Plants in Indigenous Medicine & Diet: Biobehavioral Approaches, N.L. Etkin, ed., Redgrave Publishing, Bedford Hills, New York, 1986, pp. 290-305.

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Devil’s Claw

General Information

Common Name:

Devil’s Claw

Latin Name:

Harpagophytum procumbens

Family:

Pedaliaceae

Other Names:

  • grapple plant
  • wood spider

Indications & Historical Uses

This medicinal tuber derives its unique name from the menacingly barbed, claw-shaped fruit which has been known to trap and harm livestock grazing nearby. It was originally used by natives of the Kalahari Desert and Namibian steppes as a treatment for indigestion and a myriad of other gastrointestinal disorders. Main indication is in arthritis, gout, rheumatism and lower back pain due to spondylosis. Devils Claw has strong anti inflammatory properties and is therefore very helpful for people with arthritis and inflammatory diseases. The British Herbal Pharmacopoeia does recognize Devils Claw as having anti- inflammatory, anti-rheumatic, analgesic, sedative and diuretic properties. Devils Claw has also proven to be effective in treating complaints such as dyspepsia and conditions relating to the proper functioning of bile salts, the gall bladder and the entero-hepatic circulation .

Contraindications & Precautions

Contraindications:
Devils Claw should not be taken during pregnancy, as it has been known to stimulate uterine muscle.

Also contraindicated in anyone with gastric or duodenal ulcers.

Precautions:
See Caution.

Adverse Effects:
None known at present. Devils Claw has extemely low toxicity.

Drug Interactions:
None known at present.

Dosage Information

Dosage:

100mg per day of 5% standardized extract.

Pharmacology

The tuber, or root , of the Devil’s Claw plant contains a trio of bitter-tasting iridoid glyocsides and beta-sitosterol which endow the plant with its biological activity on the immune system, the gastrointestinal tract , ,the micturition reflex, and the sensations of pain and anxiety. These compounds increase the mobility of and increase the secretions into the gastrointestinal tract and they modify the immune system such that production of prostaglandins is reduced. Two components of the plant, harpogoside and beta-sitosterol ,have anti inflammatory properties. However whole devil’s claw was found to be superior to just isolated harpogoside. Various studies have shown it to be more effective than aspirin, indomethacin, and other synthetic and semi-synthetic anti-inflammatories, and it is now known to be 6000 times more effective than western bitters (e.g. gentian bitters) in the treatment of gastrointestinal disorders. However , the active components of devil’s claw are very labile and mass-produced tablets often contain harpagoside in the absence of other irido glycosides or beta-sitosterol , thus rendering them biologically inactive and ineffective.

Active Ingredients:

Iridoid glycosides (Harpagoside, harpagide and procumbine), sugars, gum resin and beta-sitosterol. They are extracted from the tuber [underground stems] and roots of the plant.

Enhancing Agents:

Gluc osamine.

Chondroitin Sulphate.

Circuma Longa.

Origin

Devils claw is found in Africa, particularly South Africa. Devil’s Claw is a South African plant and derives its unique name from the plant’s peculiar fruits which seem to be covered with miniature claw-like hooks, which have been known to trap and harm livestock grazing nearby. It was originally used by natives of the Kalahari Desert and Namibian steppes as a treatment for indigestion and a myriad of other gastrointestinal disorders.

Processing

Processing is by aqueous extract from the tuber and roots of the plant. Standard amount of the active ingredient should be 5% harpagosides, whole plant material.

Scientific References

Mowrey, D. (1990) Guaranteed Potency Herbs. A Compilation of writings on the subject

Mowrey, D. (1986) The Scientific Validation of Herbal Medicine. Cormorant Books

R. Jaspersan-Schib: Deutsche Apotheker Zieting 130:71-73, 1990.

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Trailing Swamp Cranberry

General Information

Common Name:

Trailing Swamp Cranberry

Latin Name:

Vaccinium macrocarpon Ait

Family:

Ericaceae

Indications & Historical Uses

For more than a century, American Indians consumed crushed cranberries to prevent and treat urinary tract infections (UTI). Today, even after the introduction of antibiotics capable of eradicating the bacteria responsible for the urinary tract infection, many women still swear by this remedy. Many women drink cranberry juice to treat cystitis (inflammation of the urinary bladder). The juice is also reported to deodorize the urine.

Contraindications & Precautions

No known contraindications.

It is important to note that no one should self medicate a urinary tract infection as antibiotics are almost always warranted. Therefore, if a urinary tract infection is suspected one should always consult a physician.

Large amounts of juice may cause diarrhea and stomach upset.

Drug Interaction:
None known.

Dosage Information

How Supplied:

Trailing swamp cranberry can be consumed in capsules containing the dried cranberry powder. Six capsules are equivalent to 90mL of cranberry cocktail.

Alternatively, one can consume fresh or frozen cranberries. Forty-five grams would be equivalent to 90mL of cranberry cocktail, however, it would be difficult to consume this quantity, as these berries are sour tasting and acidic.

Recommended dose of cranberry juice cocktail.

As a UTI preventive is 90mL (or 3 fl.oz.) – about 1/3 of this is pure juice.

As UTI treatment is 360-960mL (12-32 fl.oz.).

Active ingredients:

Two constituents:

  1. Fructose
  2. Various carbohydrates and fiber as well as plant acids including benzoic and citric acid.

Pharmacology

It is a popular belief that cranberry juice effectively prevents urinary tract infections. An important study in 1994 reported in the Journal of the American Medical Association found that cranberry juice was more effective in treating than preventing urinary tract infection. It was the first placebo controlled large-scale trial to show that cranberry juice truly does reduce levels of bacteria in the urine. It also showed that cranberry juice increases the influx of white blood cells (immune cells) into the urine to fight the infection. Currently the US Pharmacopoeia lists cranberry juice as an effective remedy for preventing UTIs. It is not known how cranberry works, but several theories have been proposed. In the early 1920s, scientists believed that cranberry juice works by making the urine more acidic; the increased acidity possibly inhibits bacterial development as bacteria flourish in an alkaline (basic) environment. Recent research indicates that the benefits are more likely due to cranberry’’s ability to make the urinary tract unfavorable to these bacteria in another way. Namely, by preventing the microorganisms from adhering to the epithelial cells that line the urinary tract. The most common bacteria causing UTI is Eschericia coli. It produces two constituents (known as adherins) that cause the organisms to cling to the epithelial cells where they multiply rapidly. Two different constituents of cranberry juice inhibit adherin activity. Recent findings suggest that cranberry juice works to reduce the odor of incontinent individuals by acidifying the urine and reducing the bacterial activity (especially of E.coli).

Origin

Cranberry is a well-known red acidic fruit or berry of a small evergreen shrub. A number of species are cultivated throughout the United States. The medicinal part is the juice of the cranberry.

Processing

Berries are processed into juice and marketed as cranberry cocktail or prepared as a powder and marketed as a capsule.

Scientific References

W.J.Hopkins et al, Journal of American Medical Association (Letter) 272(8)(1994):588-9.

Lawrence Review Natural Products (St. Louis:Facts and comparisions,July 1994).

I.Oek et al, New England Journal of Medicine,(324)(1991): 1599 .M.S.Soloway and R.A. Smith,)Journal of American Association,260(1998) :1465A.E.Sabota ,Journal of Urology,131 (1984):1013-16.

R.Goodfriend , Journal of American Association ,72(8) (1992):588.

Lawerence Review of Natural Products (St. Louis :Facts and Comparisons, July 1994).

J.Avor et al ,Journal of American Medical Association ,271(1994):751.

N.R.Blatherwich and M.L. Long ,Journal of Biological Chemistry,57(19923):815-18.

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