Handbook of Medicinal Herbs

(Nandana) #1

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WOI); Edema (1; CAN; PH2); Elephantiasis (f; CRC; FEL; WOI); Encephalosis (f; DEP); Epilepsy
(f; KAP; MBB; PH2; WHO); Epistaxis (f; PH2; WHO); Failing Memory (1; PED); Fatigue (f;
PH2); Fever (1; AKT; APA; CRC; KAB; PED; VAG; VVG; WHO); Fracture (f; WHO; WO2);
Fungus (1; PED; VAG; VVG); Furunculosis (f; WHO); Gonorrhea (f; CRC); Headache (f; CRC;
KAB; PED; WO2); Hematemesis (f; WHO); Hemorrhoid (1; CRC; WHO; WOI); Hepatosis (1;
WHO); Hiccup (f; CRC); High Blood Pressure (1; PH2; VVG; WHO); Hydrocele (f; WO2);
Hysteria (f; PH2); Immunodepression (1; PNC); Induration (f; JLH); Infection (1; PED; VAG;
VVG); Inflammation (1; AKT; CRC; FNF; PED; PH2; VVG; WHO; WO2); Insanity (f; CRC; DEP;
KAB; KAP); Insomnia (1; ABS; APA; KAP; ZUL); Itch (f; CRC; DEP; PH2; WO2); Jaundice (f;
APA; CRC; WHO); Keloids (2; PNC; WHO); Leprosy (1; APA; DEP; FEL; PH2; SUW; VVG);
Leukoderma (f; CRC; KAB); Leukorrhea (f; WHO; WO2); Liver (f; CRC); Longevity (f; APA);
Lung (f; CRC); Lupus (f; APA; WBB); Lymphatic Insufficiency (f; VVG); Malaria (f; WO2);
Measles (f; WHO); Miscarriage (f; MBB); Mycosis (1; PED; VAG; VVG); Nephrosis (f; CRC;
WOI; WO2); Nervousness (1; ABS; APA; KAP; VAG; VVG; ZUL); Neuralgia (f; WHO); Neurosis
(f; APA; KAB; SUW; WHO); Ophthalmia (f; PH2); Pain (1; ABS; PH2; WHO); Pleurosis (f; CRC);
Psoriasis (1; APA; CAN; KAB); Rheumatism (1; CAN; KAP; PH2; SUW; WHO; WO2); Rib Ache
(f; CRC); Scabies (f; PH2); Scar (1; WHO); Schizophrenia (PED); Scleroderma (2; APA; SKY);
Scrofula (f; CRC; DEP; FEL); Skin Disease (f; CRC); Smallpox (f; KAB; WHO); Snakebite (f;
KAB); Sore (2; CAN; FEL; PH2; PNC; WHO); Spasm (f; CRC); Splenomegaly (f; CRC); Sprain
(f; WHO); Stomachache (PED); Stress (f; KAP); Striae gravidarum (2; ABS); Stutter (f; KAB);
Swelling (1; CAN; PH2; WHO); Syphilis (f; DEP; KAB; PED; PH2; SUW; WHO); Thirst (f;
CRC); Toothache (f; WHO); Tuberculosis (1; CRC; WBB; WO2); Tumor (1; CRC; PH2; VVG);
Ulcer (2; CAN; PED; PHR; PH2; VAG; WHO; WO2); Ulcus cruris (2; WHO); Urethrosis (f; CRC;
WHO; WOI); Urinary Discharge (f; CRC); Uterosis (f; PH2); Varicosis (1; APA; PH2; PNC; SKY;
VAG; WHO); VD (f; KAB; PED; PH2; SUW; WHO); Virus (1; ABS); Water Retention (f; CRC;
PED; SUW; VVG); Wound (2; APA; PH2; SKY; WBB; WHO; WO2).


Dosages (Gotu Kola) — 0.5–1 tsp herb/cup water 2–3 ×/day (APA; MB); 0.6 g herb, or in tea, 3
×/day (CAN); 1–2 tsp dry herb/cup water 2–3 ×/day (SKY); 0.5–1.5 g powdered herb (KAP); 2–4
g crude leaf/day (MB); 0.25 cup fresh leaf (PED); 6 g dry leaf (PED); 6 g dry leaf:30 ml alcohol/30
ml water (PED); 600 mg powdered leaf/day (PNC); 0.5–1 dropper 2–3 ×/day (APA); 2–4 ml (0.5–1
tsp) liquid extract (1:1) (MB); 12–20 ml infusion (KAP); 10–20 ml tincture 3 ×/day (SKY); 330–680
mg 3 ×/day (WHO); 60–120 mg StX/day (to 100% triterpenoids) (MB; SKY).


Contraindications, Interactions, and Side Effects (Gotu Kola) — Class 1 (AHP). “Hazards
and/or side effects not known for proper therapeutic dosages” (PH2). LRNP (December 1988) says
that, despite claims of nonallergenicity, dermatosis has been reported in some patients taking gotu
kola. Asiaticoside may be carcinogenic to the skin, following repeated applications (MB). Reading
their account, I’d not be any more afraid of gotu kola than wild lettuce. Contraindicated in epilepsy
and pregnancy; may photosensitize (MB). CAN cautions against dermatosis and phototoxicity.
Ingestion may induce pruritus (CAN). Because it is reputed to be abortifacient and to affect the
menstrual cycle, its use in pregnancy and lactation is to be avoided. May interact with other blood
pressure, cholesterol, and depression medications. “Excessive ingestion of hydrocotyle should be
avoided” (CAN). Not allowed as nonmedicinal ingredient in oral use products in Canada. (Michols,
1995). Nausea may rarely follow extremely high doses (SKY).


Extracts (Gotu Kola) — With antiedemic and antiinflammatory activity, the triterpenoids promote
healing and keratinization, stimulating the epidermis (asiaticoside may inhibit the synthesis of
collagen and mucopolysaccharides in connective tissue). Hydroethanolic extracts showed anticon-
vulsant (40, 50, 60 mg/kg orl mouse), anxiolytic (75 mg/kg orl rats cf 2 mg diazepam ipr rat), and
sedative effects (75, 150, 300 mg/kg orl mouse), but no conclusive anorective effect. Leaves
marketed in Brazil as an antiobesity compound. LD50 >675 mg/kg orl rat. Results seem to verify

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