- Part 10

Suma

General Information


Common Name:

Suma

Latin Name:

Pffafia Paniculata

Family:

Amaranthaceae

Other Names:

Brazilian Ginseng.

Para Todo.

Indications & Historical Uses

Suma is one of the most highly regarded herbs from South America. It has been used as an adaptogen, and historically has been used as:

  • Anabolic;
  • Analgesic;
  • Anti-inflammatory;
  • Tonic and nutrient for regeneration;
  • Aid to increase resistance to stress.

Contraindications & Precautions

Contraindications:
None known

Precautions:
Do not use in pregnancy.

Adverse Side Effects:
None Known.

Drug Interactions:
None known.

Dosage Information

How Supplied:

Capsules of 200 mg.

Dosage:

200 mg capsules twice daily.

Pharmacology

The most notable ingredient of Suma is Ecdysterone. Other ingredients are the Saponins (Pffafosides and Pffafic acid), beta sitosterol, allantoin and vitamins and minerals. Suma is considered to be the richest source of B-ecdysterone. A great deal of research is being done all over the world to study the anabolic effects of ecdysterone and plant sterols. Some research from Japan indicates that it may inhibit certain types of cancer. However, more studies need to be done.

Active Ingredients:

  • Saponins;
  • Pffafosides A,B,C,D,E,F;
  • Pffafic Acid.

Origin

Brazil- Suma is one of the most highly regarded herbs from South America, and is native to the mid Atlantic forest regions of Sao Paulo and Rio Janiero State.

Processing

The roots of the Suma plant are used to prepare the extract.. The product is prepared by distilling and spraying an extract of suma using 96% pure Sugar Cane ethanol. The active ingredients are then extracted.

Scientific References

Hikino, H. and Takemoto, T., Naturwissenschaften, 59:91-98 1972.

Otaka, T. and others, Chem. Pahrm. Bull., 17:1352-1355.

Syrov, V.V. med. Sh. Uzb., 3:67-9 1986.

Kurmukov, A.G., Med. Zh.l Uzb. ISS 10 68-70 1988.

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St. John’s Wort

General Information

Common Name:
St. John’s Wort

Latin Name:

Hypericum perforatium 

Family:

Hypericaceae

Other Names:

  • St. John’s Wort;
  • Goatweed;
  • Hypericum;
  • Klamath Weed;
  • Amber touch-and- heal.

Indications & Historical Uses

St. John’s Wort is one of the most popular herbal remedies for depression. A tea prepared from the leaves and flowering tops of hypericum perforatum L. is widely used in Europe today for its anti depressive effects. It is also used to relieve anxiety and in the treatment of sleep disturbances. It is the most popular non- prescription drug for treating mild to moderate depression. Other possible benefits of St. John’s Wort are relief from menstrual cramps, promotion of wound healing and the fighting off of certain viral infections. Historically, it has been used for the following conditions:

  • Depression and other emotional illnesses;
  • Anxiety;
  • Kidney disorder;
  • Wound and burn healing (Externally);
  • Anti bacterial;
  • Anti viral – AIDS;
  • Bed wetting and childhood night terrors;
  • Gastritis, gastric ulcers and inflammatory bowel disease;
  • Menstrual cramps;
  • Diuretic;
  • Myalgia and neuralgia (Externally);
  • For PMS(premenstrual syndrome).

Contraindications & Precautions

Although, to date, there have been no reports of any serious problems in humans, this herb can be poisonous to cattle. However, prolonged and high dose (1800 mg. per day) consumption of hypericum may render the skin photosensitive especially in individuals who are already sensitive to sunlight. Therefore persons taking St. John’s Wort should avoid excessive exposure to sunlight, tanning lights or UV sources. Also anyone on any prescribed psycho-active medication should consult with their physician before combining it with St. John’s Wort. (See Caution). Topically, St. John’s wort oil is a skin irritant.

Adverse Side Effects:
Photosensitivity causing dermatitis and inflammation of mucus membranes.

Drug Interactions:
Because of its MAO inhibition type of activity, it may potentiate the effects of other MAO inhibitors. However, the MAO 1 activity in St. John’s Wort, in usual doses, is not enough to cause interaction with tyramine containing foods like red wine and cheese.

Secondly St. John’s Wort may cause serotonin syndrome when combined with other drugs which affect serotonin levels. These drugs include:

  • Selective serotonin reuptake inhibitors (SSRI’s);
  • Tricyclic antidepressants;
  • Amphetamine;
  • Mono amine oxidase inhibitors (MAOIs)s;
  • Dopamine agonist such as bromocriptine.

Therefore patients who combine these and other similar products should be advised to contact their physician if they develop any of the symptoms of “Serotonin Syndrome”. Serotonin Syndrome is characterized by sudden onset and rapid progression of some or all of these symptoms:

  • Confusion;
  • Agitation;
  • Shivering;
  • Fever;
  • Diaphoresis (profuse sweating);
  • Diarrhea;
  • Nausea;
  • Myoclonus (muscle spasms or twitching);
  • Hyperreflexia;
  • Tremor.

These reactions can be fatal.

How Supplied:

For internal use:
Capsules, fluid extract, tincture 

For external use:
oil, ointment.

Dosage:

300 mg standardized / three times daily

Pharmacology

St. John’s Wort comprises of a number of active ingredients, namely dianthrone derivatives (hypericin and pseudohypericin) flavonoids and tannins (hyperoside, quercitin, rutin, catechin), xanthrones, monoterpenes and sesquisterpenes and phytosterols (beta-sitosterol) Hypericin and xanthones and flavonoids have been shown to have mono-amine oxidase (MAO) inhibiting property. In depression, MAO inhibitors are used to reduce the breakdown of neurotransmitters such as norepinephrine and serotonin and thereby increasing their concentration in the central nervous system. Recent clinical trials using standardized hypericin extract showed improvement in symptoms of depression including anxiety, insomnia, depression and feelings of worthlessness. Most recent research at two of the world’s leading medical institutions, New York University and the Weizman Institute of Science in Israel ,found that 2 of the main constituents of St. John’s Wort namely hypercin and pseudohypericin were found to inhibit the growth of retroviruses (including HIV, the AIDS virus) in animals. Although the results of these studies are promising, more work needs to be done. The mechanism is thought to involve the production of oxygen free radicals which can damage the viral envelope. Therefore, non- enveloped viruses , e.g. Adeno virus or poliovirus are not affected by hypericin. At present, human studies involving high doses of synthetic form of hypericin (10mg) are being tested on HIV infected patients. In addition to its anti depressant and anti-viral properties, St. John’s Wort has significant wound healing properties. St. John’s Wort increases the rate of healing in second and third degree burns. The product used is sometimes known as “red oil”. It is named after the red color formed when the fresh flowers are extracted in olive oil. Increased epithelialization of wounds also occurs when St. John’s Wort is taken orally as an 1:10 tincture. It is likely that some of the wound healing activity of St. John’s Wort may come from anti bacterial activity. Additionally, the flavonoids are tannins and they exert their wound healing effects through their astringent and protein precipitating actions

Active Ingredients:

  • Glycosides (hypericin, pseudohypericin);
  • Flavonoids and tannins.

Standardized extract should contain 0.3 – 0.5% Hypericin

Enhancing Agents:

  • Beta Carotene;
  • Vitamin C.

Origin

Hypericum perforatium is an aromatic perennial herb and belongs to the family hypericaceae. It is native to Europe, but is found worldwide. It has golden yellow flowers – flowering between June and September. The flowers have the brightest appearance on June 24th , birthday of John the Baptist.

St.John’s wort is a natural source of food flavoring in Europe. It is also used in pastilles and lozenges and in alcoholic beverages. Active ingredients are extracted from the leaves and the flowering tops.

Processing

Processing involves harvesting of the aerial parts of St. John’s Wort, drying away from sunlight and extraction by water and ethanol.

Scientific References

Hobbs, C. (1989) St. John’s Wort. A review Herbal Gram 18/19:24.

Muldner, Von H. and Zoller, M. (1984) Antidepressive activity of an hypericin standardized extract of Hypericum. Arzeneim. Forschh. /Drug. Res. 34:918.

Gerhardt, J.J. and Fowkes, S. W. (1991) Antiviral activity of the photoactive plant pigment hypericin. Photchem. And Photobio. 54(1): 95.

Schinazi, R.F. et al (1988) Therapeutic agents with dramatic anti-retroviral activity and little toxicity at effective doses: aromatic polycyclic diones hypericin and pseudohypericin. Proc. Natl. Acad. Sci. (USA) 85:5230.

Weiner,M. (199)) Weiner’s Herbal. Mill Valley: Quantum Books.

Suzuki, O. et al. (1984) Inhibition of monoamine oxidase by hypericin. Planta medica 50:272.

Pahlow, M.: Duetsche Apotheker Zeitung 42:2059-2060(1984).

Wichtl,M., ed.: Teedrogen, Wissenschaftliche Verlagsgesellschaft, Stuttgart, 1984, pp. 178-180.

Holzl, J., Demisch Apotheker Zeitung 130:367 (1990).

Okpanyi, S.M.and Weischer,M.L.: Arzneimittel-Forshng 37(1):10-13 (1987)

Poginsky, B., Westendorf,J., Prosence, N. Kuppe,M., and Marquardt,H.:Deutsche Aporheker Zeitung 128:1365-1366(1988).

Kommisiion E des Bujndesgesundheitsamtes: Deutsche apotheker Zeitung 128:1499 (1988)

Roth, L.:Hypercium-Hypericin: Botanik, Inhaltssoffe, Wirkung, ecomed, Landsberg/Lech, Germany,1990,pp135-138.

James, J.S.: AIDS Treatment News No. 117:3(1990).

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Saw Palmetto

General Information


Common Name:

Saw Palmetto

Latin Name:

Serenoa Repens
Serenoa Serrulate

Family:

Palmaceae [Arecaceae]

Other Names:

  • American dwarf palm tree;
  • Sabal;
  • Cabbage palm;
  • Serenoa.

Indications & Historical Uses

  • Benign prostatic hypertrophy;
  • Prostate inflammation;
  • Impotence, low libido;
  • Urinary tract disorders, nocturia, enuresis;
  • Treatment of Male Pattern Baldness;
  • Female infertility;
  • May increase breast size in women;
  • Male and female aphrodisiac;
  • Anti-inflammatory agent;
  • Appetite stimulant;
  • General nutritional tonic to increase muscle strength.

Contraindications & Precautions

Contraindications:
None known at therapeutic doses. See Caution.
DO NOT USE IN PREGNANCY. Not advisable for anybody suffering from a hormone dependent illness such as breast cancer. Precautions:
None known. See Caution.

Adverse Side Effects:
None known. In rare instances upset stomach and headache may occur. See Caution.

Drug Interactions:
None known. See Caution. However, since mechanism of action of Saw Palmetto is similar to Finasteride (Proscar) it may be important not to use those two medications concurrently due to the possibility of an additive effect. Conversely, San Palmetto’s anti-androgenic activity could diminish the effect of therapeutic androgens. Also, may interact negatively with hormone replacement therapy.

Dosage Information

How Supplied:

500mg tablets or capsules.

Dosage:

500 mg three times per day.

Pharmacology

Saw Palmetto was once widely used for urogenital ailments prior to World War ll. Since then, European Scientists have conducted studies on Saw Palmetto and recognized its’ therapeutic value in Benign Prostatic Hyperplasia. [BPH ]. Studies have shown that Saw Palmetto extract reduced the uptake, in tissue specimens ,of both testosterone and dihydrotestosterone (DHT) by more than 40%. Other studies have shown that Saw Palmetto inhibits the conversion of the less active testosterone to the more active DHT by inhibiting the enzyme 5 alpha reductase. Hence Saw Palmetto, by blocking the binding of DHT to nuclear receptor sites and inhibiting the conversion of testosterone to DHT, decreases the proliferative effects of DHT on prostate cells (a mechanism similar to Finasteride – Proscar ,but without its side-effect. Proscar may cause hypotension and lethargy). Saw Palmetto also inhibits the cyclo-oxygenase and 5-lipoxygenase pathways, which results in prevention of biosynthesis of inflammation producing substances such as prostaglandin and leukotrienes. It also inhibits the arachidonic acid cascade, and all these account for the anti-inflammatory and anti-edematous properties of saw palmetto. Together, the anti-androgenic and anti-inflammatory effects of Saw Palmetto account for its effectiveness in treating BPH. Placebo-controlled double blind clinical studies in over 2,000 patients in Germany confirms the effectiveness of Saw Palmetto in BPH. Saw Palmetto has become a very popular herb because of its efficacy, low potential for toxicity and an increasing population of middle-aged men seeking relief from symptoms of BPH – namely urinary frequency, dysuria and nocturia. As a result of its efficacy and low potential for toxicity, it is now prescribed as a first line treatment for mild BPH. by many physicians. It is important to note that Saw Palmetto does not reduce the size of the prostate, although it relieves the urinary symptoms. Also, men should be aware that lower urinary tract symptoms ,that may be relieved by Saw Palmetto ,could be symptoms of Prostate Cancer. Such symptoms include urinary frequency, inability to urinate, trouble starting or holding back urination and a weak or interrupted flow of urine. Men experiencing these symptoms should be evaluated by their physician. In the U.S., a prescription drug called FINASTERIDE (proscar) with exactly the same mode of action has been approved for prostatic cancer and also for male pattern baldness .

Active Ingredients:

  • Steroidal saponins;
  • Fatty acids;
  • Phytosterols;
  • Volatile oil;
  • Resin;
  • Tannins.

Enhancing Agents:

  • Pygeum

Origin

Saw Palmetto is a small palm tree with large leaves and large deep red blackberries found along the North American Atlantic Coast (Florida). The berries were used by American Indians in the treatment of genito urinary tract problems including enuresis, nocturia and urinary tract disorders. Recent clinical trials have been shown that Saw Palmetto berries are very effective the treatment of Benign Prostatic Hyperplasia.

Processing

The large deep red blackberries of the Saw Palmetto are picked when ripe, then partially dried, and prepared into a purified fat soluble extract and processed into tablets or capsule form.

Scientific References

Campault, G. et al. (1984) A double blind trial of an extract of the plant Seronoa repens in benign prostatic hyperplasia. Br. J. Clin Pharm. 18:461.

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

Harischfeger, G. and Stolze, H.: Zeitschrift fur Phytotherapie 10:71-76 (1989).

El Sheikh, M.M., Dakkak, M.R. and Saddique, A.: Acta Obsterica et Gynecologica Scandinavica 67:398-399 (1988).

Casarosa, C., Di Coscio, M.C.O., and Fratta, M.: Clinical Therapeutics 10:686-588 (1988).

Sultan, C. et al. (6 other authors): Journal of Steroid Biochemistry 20:515-519 (1984).

Breu, W., Stadler, F., Hagenlocher, M. and Wagner, H.: Zeitschrift fur Phytotherapie 13:107-115 (1992).

Hansel, R. and Haas, H.: Therapie mit Phytopharmaka, Springer-Verlag, Berlin, 1984, p. 202.

Heirmann, A.: Archiv der Pharmazie 322:111-114.

Varro, E.T.: Herbs of Choice The Therapeutic Use of Phytomedicinal. Pharmaceutical Producres Press, Moriarty Press, 1994.

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Pygeum

General Information


Common Name:

Pygeum

Latin Name:

Pygeum Africanum

Other Names:

African Pygeum

Indications & Historical Uses

  • Benign Prostatic Hypertrophy;
  • Prostatitis;
  • Urinary incontinence;
  • Burning or painful urination.

Contraindications & Precautions

Contraindications:
None reported at therapeutic doses See Caution).

Precautions:
See Caution.

Adverse Side Effects:
See Caution.

Drug Interactions:
See Caution.

Dosage Information

How Supplied:

50 – 100 mg tablets.

Dosage:

100mg – 200 mg extract / day in divided doses (morning & evening for 1 -2 months).

Pharmacology

Pygeum contains three groups of active components: Phytosterols such as beta-sitosterol; pentacyclic triterpenoids, such as ursolic and oleanic acids; and ferulic esters of fatty acids, particularly the ferulic esters of docosanol and tetracosanol. The phytosterols, particucularly beta-sitosterol are found in numerous plants and are anti-inflammatory, inhibiting the synthesis of prostaglandins. Beta-sitosterol has been shown to be useful in cases of BPH [ Benign prostatic hyperplasia ] .It does this by reducing the normally elevated levels of prostaglandins in these patients, and thus reducing the size of the prostate. This helps to relieve the symptoms of BPH. The pentacyclic triterpenoids also help inhibit inflammation by blocking enzymatic activity, and reduce swelling of the prostate. The ferulic esters of long-chain fatty acids help by inhibiting both – the absorption and metabolism of cholesterol . Generally, enlarged prostates are characterized by high levels of cholesterol. Numerous double blind clinical trials have demonstrated that pygeum is effective in treating a wide range of prostatic hyperplasias. It has been shown that consumption of pygeum extract resulted in significant amelioration of symptoms of prostatic hyperplasia , namely dysuria [ painful urination ], nocturia and frequency as well as reduction in residual urine volume [post -micturition residue ]. In addition to this ,pygeum also promotes reduction in the size of the prostate and clearance of bladder neck obstruction .

Active Ingredients:

  • Phytosterols [Sitosterol];
  • Pentacyclic Triterpenoids;
  • Ferulic Esters of long chain fatty acids.

Enhancing Agents:

  • Saw Palmetto.

Origin

Pygeum is a large evergreen tree found in the higher plateaus of South Africa Active ingredients are extracted from the bark of this tree.

Processing

Air dried bark from the trunk of Pygeum africanum is passed through a screen, and extracted with chloroform to isolate the fat-soluble portions. These extracts are filtered and concentrated, and vacuum dried to eliminate chlorinated solvent.

Scientific References

Bassi, P. et al (1987) Standardized extract of pygeum africanum in the treatment of benign prostate hypertrophy. Minerva Urologica 39:45.

Marcoli, M. et al. (1985) New trends in Andro. Sci. 1:39.

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

Thierblot, L. et al. (1971) Action preventive d’un extrait d’ecorce de plante africaine “Pygeum africanum” sur l’adenome prostatique experimental chez le rat. (Preventative action of an African plant extract, “Pygeum africanum” on experimental prostate adenoma in the rat) Therapie 26:575.

Zurita, E.L. et al. (1984) Treatment of prostatic hypertrophy with extract African prunus. Rev. Bras. Med. 41:48.

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Nettles

General Information


Common Name:

Nettles

Latin Name:

Urtica Dioica

Family:

Urticaceae

Other Names:

  • Stinging Nettles;
  • Greater nettle;
  • Common nettle.

Indications & Historical Uses

Nettles have been widely used as food, medicine, cosmetics and clothing. The most recent indication in phytomedicine is in the treatment of urinary retention arising from early stages of benign prostatic hyperplasia (BHP). Usual dose is 4 – 6 grams (of the root extract) daily. Dried leaves of the nettle plant are commonly employed as a mild diuretic and their consumption does increase urine flow. Nettle leaves are ordinarily taken in the form of a tea. Tea is prepared with 3-4 teaspoonsful (about 4gms) of the botanical and 150ml of boiling water. One cup may be drunk 3 – 4 times daily together with additional water. This is not effective in the treatment of hypertension or edema of cardiac origin. Nettles have also been traditionally used as an important hair and skin tonic. The high quantity of silicon has made nettles highly useful in stimulating hair growth, improving condition of the hair and skin and treating dandruff. Nettles have been used externally and internally to treat eczema. Nettle juice has been used as an astringent or styptic to stop bleeding and to treat wounds. The best known use of nettles is in the treatment of gout and other rheumatic conditions. A decoction of the leaves or the expressed juice has been known to mobilize uric acid from the joints and eliminate it through the kidneys. Recently a randomized, double blind clinical trial has shown beneficial effects of nettles in the treatment of allergic rhinitis or hay fever. Historically, nettles has been used for the following:

  • Arthritis, tendonitis, sciatica;
  • Eczema;
  • Hair loss;
  • Allergic rhinitis, hay fever, sinus congestion;
  • Anemia;
  • Astringent; wound healing; styptic;
  • Mild diuretic;
  • Benign Prostatic hyperplasia;
  • Stimulate lactation;
  • Hypoglycemia (low blood sugar).

Contraindications & Precautions

None known at present – (See Caution.) Avoid its use in cardiac and renal impairment and in diabetes. Some experts believe that nettle causes poor glycemic (blood sugar) control in patients with diabetes and therefore diabetics should not use nettles.

Known Drug Interactions:
None known at present.

Dosage Information

Dosage:

750mg extract/day.

Pharmacology

Nettles are a rich source of trace elements, absorbing and accumulating them. As mentioned in the active ingredients, nettles contain formic acid and neurotransmitters acetylcholine, 5 hydroxy-tryptamine and histamine which are responsible for the sting. It is these substances which are thought to endow nettles with their anti-arthritic, antispasmodic, diuretic, astringent, tonic and expectorant properties. Nettle also contains steroidal and phenolic substances which inhibit the prostatic enzymes, and this leads to the beneficial structural changes in the prostate in patients with BPH [Benign prostatic hypertrophy]. Nettle suppresses cell growth of the prostate. Other compounds that have been isolated include flavonoids, vitamins and antioxidants – all of these may contribute to its therapeutic benefits. German E Commission has approved nettle for irrigation in inflammation of the urinary tract and in the prevention and treatment of kidney stones .

Active Ingredients:

  • Formic acid;
  • Histamine;
  • Acetylcholine;
  • 5-hydroxytryptamine;
  • Glucoquinones;
  • Chlorophyll;
  • Minerals (iron, magnesium, silica, potassium, sulphur);
  • Vitamins A; C; B2 and B5 and chlorophyll;
  • N.B. Standardized extract should contain 1 – 2 % plant silica.

Origin

Stinging Nettles are found all over the world. Originally found in Europe and Israel. They derive their name from the presence of stinging hairs on their leaves and stems which, when touched, inject formic acid and histamine into the skin and cause urticaria.

Processing

For processing, the young top leaves are harvested from plants grown in clean, uncontaminated areas. Extraction is by traditional alcohol and water extraction. The extract is concentrated to a paste, prepared as a liposoluble liquid for cosmetic use or spray dried to produce a stable pure powder.

Scientific References

A.Y.Leung. Encyclopedia of natural ingredients used in food, drugs and cosmetics.

Krstic-Pavlovic, N. and Dzamic, R. (1985) Astringent and mineral components in the leaves of nettle (Urtica dioica, L.) from many natural locations. Agrochemija. 1985:191-198.

Smith, T.A. (1977) Tryptamine and related compounds in plants. Phytochemistry. 16:171.

Caceres, A. et al. (1987) Diuretic activity of plants used for the treatment of urinary ailments in Guatemala. J. Ethnopharmaco. 19:233-245.

Baraibar, C. et al. (1983) Acute and chronic toxicity studies on Nettle (Urtica dioica, L.). An. Bromatol. 35:99-103.

Mittman, P.(1990) Randomized, Double-blind study of freeze-dried Urtica Dioica in the treatment of allergic rhinitis. Planta medica 56:44-47.

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Milk Thistle

General Information


Common Name:

Milk Thistle

Latin Name:

Silybum Marianum

Family:

Asteraceae [compositae]

Other Names:

  • Marian;
  • Mary thistle;
  • St Mary’s silybum.

Indications & Historical Uses

  • Protects liver from toxins, heavy metals, alcohol, poisons;
  • Liver disease, acute and chronic hepatitis;
  • Treatment of fatty degeneration of liver,. Liver cirrhosis;
  • Psoriasis;
  • Gallbladder disorders;
  • Indigestion.

Contraindications & Precautions

Contraindications:
None known. See Caution.

Precautions:
None known. See Caution.

Adverse Side Effects:
None known except mild laxative effect is occasionally reported.

Drug Interactions:
None known.

Dosage Information

How Supplied:

Capsules of 200mg of concentrated extract representing 140mg of Silymarin.

Dosage:

200 – 400 mg of extract per day.

Pharmacology

German scientists made a breakthrough in the late 1960s when they isolated the liver-protectant principles in the fruit .They called these Silymarin. Milk Thistle contains three potent liver protective flavonoids- Silybin, Silydianin & Silychristin known collectively as Sylimarin. Numerous clinical trials have shown that Silymarin protects the liver. Silymarin protects the liver against various toxins and boasts another remarkable property: namely, by encouraging the regeneration of liver cells, it can actually reverse the damage and help cure the liver. It does this by stimulating protein synthesis [RNA polymerase A ], thus activating the liver,’s ability to regenerate itself through increased formation of new liver cells called hepatocytes. Silymarin counteracts the toxic effects of a wide variety of liver poisons, including alcohol, carbon tetrachloride (used widely in the dry-cleaning industry) acetaminophen and the death cap mushroom, which can cause death within a day. The mechanisms of action of Silymarin are as follows:

  • Altering the membranes of hepatic cells to inhibit passage of toxins;
  • Increasing cellular regeneration by stimulating protein synthesis;
  • Increasing glutathione levels in liver cells;
  • Scavenging for substances called free radicals that can damage the liver -because of it’s powerful anti-oxidant properties in the liver cells, stomach and intestine.

As a result, Silymarin (at a dose of 140 mg. three times daily), can significantly reduce patient mortality in alcohol-induced liver cirrhosis. Acute viral hepatitis can be treated with Silymarin (at a dose of 70 mg. three times daily) to lower levels of bilirubin and the transaminases (liver enzymes). Silymarin has also been used in death angel or death cap mushroom poisoning, and fatal outcome can be prevented if treatment is begun at an early stage. However liver diseases are serious ailments; consult your doctor before taking this or any other medication for them.

Active Ingredients:

Flavonoids – (SILYBIN, SILYDIANIN, & SILYCHRISTIN together known as SILYMARIN)

Origin

Milk thistle is native to the Mediterranean region but now grows in many parts of Europe and North America ,including California and the Eastern seaboard of the United States. It is a tall, weed -like plant with large prickly leaves and the stems contain a milky sap that oozes out when cracked open. Small fruits ‘seeds’ nestle in the reddish purple flowers and are used to make the medicinal extract known as silymarin.

Processing

Parts of Plant used:
Seeds of the milk thistle plant. The seeds are harvested, and extracted by methyl alcohol. The solution is filtered and vacuum evaporated. The final defatted suspension is dried in ventilation ovens.

Scientific References

Campos, R. et al. (1989) Silybin Dihemisuccinate protects against glutathione depletion and lipid peroxidation induced by acetaminophen on rat liver. Planta Medica. 55:417.

Canini, F. et al. (1985) The use of silymarin in the treatment of alcoholic hepatic cirrhosis Clin. Ther. 114:307.

Ferenci, P. et al. (1989) Randomized controlled trial of silymarin treatment in patients with cirrhosis of the liver. J. Hepat. 9:105.

Hruby, C. (1984) Silibinin in the treatment of Deathcap Fungus poisoning.; Forum 6:23.

Koch, HP et al. (1985) Silymarin: Potent inhibitor of cyclic AMP phosphodiesterase. Meth. Find. Espt. Clin Pharm. 7:409.

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

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

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

R.F. Weiss: Herbal Medicine. Beaconsfield Publishers Ltd, Beacons England, 1988, pp. 82-85.

A. Osol and G.E. Farrar, Jr., Eds.: The Dispensatory of the United States of America, 24th Ed. J.B. Lippincott Company, Philadelphia, 1947, p. 1629.

H. Wagner and O. Seligmann: In Advances in Chinese Medicinal Maters Scientific Publishing Co., Singapore, 1985, pp. 247-256.

S. Foster: Milk Thistle, Silybum marianum, Botanical Series No. 305 American Botanical Council, Austin, Texas, 1991, 7pp.

Bundesanzeiger, March 13, 1986.

I. Merfort and G. Willuhn: Deutsche Apotheker Zeitung 125: 695 (1985).

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Hawthorne

General Information


Common Name:

Hawthorne

Latin Name:

Categus
Oxyacantha

Family:

Rosaceae

Other Names:

  • Haw;
  • May;
  • Mayflower;
  • Mayblossom;
  • Maybush;
  • Whitehom.

Indications & Historical Uses

Indications:
Hawthorne is one of the most valuable herbal cardiovascular tonics available. It is described in most modern herbal literature as a valuable drug for the treatment of various heart ailments and circulatory disorders. Hawthorne has been used in the treatment of irregular heartbeats, high blood pressure, spasms of arteries (e.g. Raynaud’s) and certain nervous disorders. It has also been used to control atherosclerosis. Hawthorne has potential to be a very valuable drug. However, further scientific studies are needed to substantiate the beneficial effects of the drug. Until additional research has been carried out., prospective users of hawthorne , for heart and circulatory disorders should consider all the consequences and seek medical advice before self-treatment.

Historically
It has been used in the following conditions:

  • Cardiotonic;
  • Spasm of arteries (Raynaud’s);
  • High and low blood pressure;
  • Old age vascular problems;
  • Nervous disorders;
  • Insomnia;
  • Coronary artery and perfusion disordersn [mild stable angina];
  • Irregular heartbeats;
  • Dyspepsia and diarrhea.

Toxicity is low and becomes evident only in large doses,. Therefore, it is relatively harmless if taken in recommended doses. It seems to be a relatively harmless mild heart tonic which apparently has been beneficial in many conditions where this kind of treatment is required.

Contraindications & Precautions

Hawthorne may potentiate the action of digitalis and other drugs that have cardiovascular effects. (See Caution).

Drug Interaction:
May potentiate action of digitalis and other cardiac drugs. Therefore, patients on these drugs should refrain from using Hawthorne unless supervised by a physician. (See Caution) .

Dosage Information

Dosage:

250mg/day.

Pharmacology

Modern research has revealed some interesting properties of hawthorne. It’s berries are rich in flavonoids and they act on the body in 2 ways: First, they dilate the blood vessels, especially the coronary vessels, and secondly, they reduce peripheral resistance and thus lower blood pressure. Therefore, it reduces the tendency to angina attacks.  Additionally, flavonoids have a direct favorable effect on the heart itself , which is especially apparent in cases of heart damage. Hawthorn’s action is not immediate, but develops very slowly and is relatively harmless if taken in the recommended doses. It takes up to two weeks to acquire high enough tissue concentrations of hawthorn to produce observable effects. (See Precautions). Because of its slow onset of action ,it is not useful for acute attacks of angina, but is helpful in reducing the tendency to angina. Hawthorne is also known to have a positive ionotropic effect on the heart and accelerates the heart, increases nerve conductivity and heart muscle functioning. Hawthorne is also known for its sedative effect .

Active Ingredients:

Mixture of:

  • Flavonoids;
  • Saponins;
  • Procyanidins;
  • Trimethylamine;
  • Tannins.

Enhancing Agents:

  • Valerian root;
  • Motherwort.

Origin

Hawthorne is a small thorny tree with white and red flowers and berries. It is found in England, Europe and North America. Hawthorne is widely used in Europe, especially Germany. Three dozen different preparations containing extracts of these plant parts, either singly or in combination with other drugs, are currently marketed in Germany. Active ingredients are extracted mainly from the berries, although the flowers and the leaves also contain some of the active ingredients Because the berries, leaves and flowers all contain compounds which affect the heart and the circulatory system, products containing them should not be used indiscriminately.

Processing

Processing involves only alcoholic extraction.
Standardized extract should contain 2% Vitexin and 2% Vitexen Rhamnoside.

Scientific References

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

Ullsperger, R. (1951) Preliminary communication concerning a coronary vessel dilating principle from hawthorne. Pharmazie 6(4):141-144.

Rewerski, W and Lewak, S. (1970) Hypotonic and sedative polyphenol and procyanidin extracts from hawthorne. Ger. Offen. 2:145-211.

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

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Guarana

General Information


Common Name:

Guarana

Latin Name:

Paullinia Crysan
Paullinia sorbilis

Family:

Sapindaceae

Other Names:

  • Brazilian cocoa;
  • Brazilian cola;
  • Uabeno;
  • Guarana gum.

Indications & Historical Uses

  • Central Nervous System stimulant;
  • Used for treatment of fatigue, nerve tonic;
  • For Diarrhea, gastrointestinal complaints;
  • For symptoms of PMS: listlessness, lack of concentration and headaches;
  • Appetite suppressant;
  • Historically used as an aphrodisiac;
  • A popular beverage in South America.

Contraindications & Precautions

Guarana contains two to three times more caffeine than coffee or tea. Do not overuse. Exercise caution in pregnancy, and heart conditions.
See Caution.

Adverse Side Effects:
Dysuria is a common side effect of guarana.

Drug Interactions:
None known.

Dosage Information

How Supplied:

50 mg tablets, capsules.

Dosage:

50-100mg per day.

Pharmacology

Guarana contains Xanthines, which are potent CNS stimulants. Guarana contains two to three times more caffeine than coffee or tea. Xanthines are used as stimulants, diuretics and anti diarrheal, as well as appetite suppressant. Researchers have identified high levels of tannins [5-6% ] in guarana. These astringent substances explain its reputation for alleviating diarrhea; tannins are believed to control or stop diarrhea by reducing inflammation in the intestine. In addition to the high caffeine content ,the presence of associated alkaloids [theophylline and theobromine ] also explains guarana’s traditonal use in treating migraine headache and as an appetite stimulant.

Active Ingredients:

Xanthines:

  • Guarnine (caffeine);
  • Theobromine;
  • Theophylline.

In Brazil ,Guarana is made into a popular carbonated cola drink and it is considered the national beverage of Brazil .People drink it for energy and for stimulation. The caffeine driven energy boost provided by Guarana capsules and tablets has earned them the nickname ” Zoom”. It is also available as a dried herb ,extract , powder ,syrup, and tea

Origin

It is a climbing evergreen shrub , native to the Brazilian Rain Forests, South.

Processing

America. Extracts are prepared from the seeds ,which are found in the orange yellow fruits of these perennials. Guarana seeds are dry roasted, crushed and powdered and zanthines are extracted by hydroalcoholic process. The extract is then dried & standardized.

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.

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Green Tea

General Information


Common Name:

Green Tea Extract

Latin Name:

Camellia Sinensis

Family:

Theceae

Other Names:

Tea

Indications & Historical Uses

Green tea extract is a bioflavonoid-rich potent extract which is a powerful free-radical antagonist and anti-oxidant. It is used primarily for its antioxidant & free-radical fighting properties. Thus it is used for prevention of atherosclerotic disease, and reducing blood pressure by its suppression of angiotensin I converting enzyme. It also reduces platelet aggregation, and these properties are applied in preventing atherosclerosis, and thereby preventing heart disease and stroke. It also combats mental fatigue, and may lower the risk of esophageal, stomach, colon and skin cancer.

Contraindications & Precautions

Should not be used in large quantities during pregnancy and while nursing. Persons with anxiety disorders, irregular heartbeat should limit their intake of Green Tea.

Adverse Side Effects/Drug Interactions:
None known at present. See Caution.

Dosage Information

Dosage:

250 mg to 500 mg of EGCG content daily.

Pharmacology

The polyphenols in green tea are catechins, with multiple linked ring-like structures. The dominant polyphenol is EGCG( Epigallocatechin Gallate), a potent antioxidant, and anti infective. EGCG is over 200 times more effective than Vitamin E in neutralizing pro-oxidants and free radicals that attack brain lipids, in vivo. EGCG is suppressive for Angiotension I converting enzyme, which is a key factor in essential hypertension. EGCG also reduces platelet aggregation, inhibits pathogenic bacteria and finally may be effective in prevention of dental caries by blocking the attachment of caries-causing bacteria to the teeth and gum tissue.

Active Ingredients:

Catechins, especially (-) Epigallocatechin Gallate (EGCG) a potent antioxidant

Origin

Semi-tropical shrub native to China, Japan, South East Asia. About 20%of the World,s tea market consists of Green Tea.

Processing

Extraction with hydromethanolic or hydroacetonic solution.

Scientific References

Chem. Pharm. Bull., vol. 38,pg. 1049, 1990.

Tohoku J. Exp. Med., vol. 166, pg. 475, 1992.

Carcinogenesis, vol. 13, pp. 947 & 1491, 1992.

Cancer Res., vol. 52, pp. 1162, 1943, 3875, 4050, 6657 & 6890, 1992.

Cancer Lett., vol. 65, pg. 51, 1992.

Muramatsu, K., Fukuyo, M., & Hara, Y., Effect of green Tea Catechin on Plasma Cholesterol Level in Cholesterol-Fed Rats, J. Nutr.Sci. Vitaminol., vol. 32, pp. 613-622, 1986.

Sagasaka-Mitane, Y., Miwa, M., & Okada, S., Platelet Aggregation Inhibitors in Hot Water Extract of Green Tea, Chem. Pharm. Bull., vol.38(3), pp. 789-793, 1990.

Horiba, N., et al., A Pilot Study of Japanese Green Tea as a Medicament: Antibacterial and Bactericidal Effects, Journal of Endodontic, vol, 17 (3), pp. 122-124, 1991.

Hattori, M., et al., Chem. Pharm. Bull., vol. 38, pg. 717, 1990.

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Goldenseal

General Information


Common Name:

Goldenseal

Latin Name:

Hydrostis Canadensis

Family:

Ranunculaceae

Other Names:

  • Yellow root;
  • Indian turmenric;
  • Jaundice root;
  • Eye balm;
  • Ground raspberry;
  • Indian dye.

Indications & Historical Uses

  • Inflammatory conditions of digestive system and of joints;
  • Peptic ulcer disease, gastritis, flatulence, diarrhea, dyspepsia;
  • Liver and gallbladder problems;
  • Skin infections, impetigo, eczema and ringworm;
  • Sedative;
  • Anti-viral, antibacterial;
  • Eye inflammations;
  • Disturbances of endocrine functions;
  • Vaginitis, urethritis and rectal inflammations.

Goldenseal has been used to treat mucous membrane infections caused by bacteria, fungus or protozoa. These types of infections are commonly found in the mouth, respiratory, gastrointestinal and genitourinary tracts. Goldenseal is also used to treat inflammations of the gall-bladder, and to correct some of the metabolic effects of liver cirrhosis. Goldenseal root has been used by native Americans for a wide range of ailments, especially for localized skin and eye irritations. It is still used today as an ingredient in a number of commercial sterile eye washes.

Contraindications & Precautions

At high doses (over 2-3 grams per day) may cause bradycardia (slow heart beat), and also may stimulate the nervous system. Do not use during pregnancy as berberine stimulates the uterus and may cause abortion.

Adverse effects:
See Caution.

Drug Interactions:
See Caution.

Dosage Information

How Supplied:

250 mg tablets of extract.

Dosage:

250 mg once or twice a day.

Pharmacology

The active ingredients of goldenseal include a group of alkaloids, hydrastine, berberine & tetrahydroberberine The Alkaloids, primarily hydrastine and berberine have antiseptic and astringent properties, and therefore help reduce inflammation of mucous membranes. The Alkaloids also have an effect on inflammation, help to lower blood pressure, and stimulate peristalsis. Berberine also has some antibiotic properties. A few clinical trials testing berberine’s antibiotic properties show that goldenseal can successfully treat diarrhea caused by E.Coli (traveller’s diarrhea), Shigella, salmonella , Klebsiella and cholera. It has been shown that in Vitro, berberine can inhibit many common bacteria, including Staphylococcus, Streptococcus, Chlamydia, E. Coli, Psuedomonas and others. In Vitro, Berberine has been shown to inhibit protozoa such as Giardia and Trichomonas. In one study in pediatric patients, berberine was shown to be as effective as metronidazole in control of Giardiasis. Clinical studies have also been carried out to study the effectiveness of goldenseal in the treatment of trachoma, an eye infection caused by Chlamydia trachomatis In comparison to conventional therapy, Berberine was found to be less effective in reducing acute symptoms such as conjunctivitis and edema, but as effective in eradicating the pathogen and preventing recurrences .

Enhancing Agents:

May be combined with Echinacea and/or Garlic for enhanced effect.

Origin

Goldenseal is a perennial and it grows deep in moist rich woods along the East Coast of North America, and has been used by Native American healers for a wide range of conditions. In spring, the small erect stems produce large hand-shaped flowers ,and dark orange-red berries.The parts of the plant used medicinally are the dried rhizomes [underground stems] and roots. Golden seal is now scarce in the wild , probably because of over harvesting.

Processing

It is processed with ethanol/water extraction at low temperature, with pH adjusted for maximum yield and extraction.

Scientific References

Datta, D. et al. (1971) Thin layer chromatography and UV spectrophotometry of alcoholic extracts of Hydrastis canadensis. Planta Medica 19(3):258.

Foster, S. (1991) Goldenseal. American Botanical Council, Botanical Series No. 309.

Gupta, S. (1975) Use of berberine in the treatment of giardiasis. Amer. J. dis. Childhood. 129:866.

Ikram, M. (1975) A review of the chemical and pharmacological aspects of genus berberis. Planta Medica 28:353.

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

Sharda, D. (1970) Berberine in the treatment of diarrhea of infancy and childhood. J.Ind. Med. Assoc. 54(1):22.

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

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