Acute and repeated-doses (28 days) toxicity study of Hypericum polyanthemum Klotzsch ex Reichardt (Guttiferare) in mice

• Published in: Food and chemical toxicology Vol. 50; no. 7; pp. 2349 - 2355
• Main Authors: Betti, Andresa Heemann, Stein, Ana Cristina, Dallegrave, Eliane, Wouters, Angelica Terezinha Barth, Watanabe, Tatiane Terumi Negrão, Driemeier, Davi, Buffon, Andréia, Rates, Stela Maris Kuze
• Format: Journal Article
• Language: English
• Published: Oxford Elsevier Ltd 01.07.2012; Elsevier
• Subjects: Acute oral toxicity; acute toxicity; Animals; behavior change; Biological and medical sciences; Chromatography, High Pressure Liquid; Dose-Response Relationship, Drug; Feeding Behavior - drug effects; General pharmacology; guidelines; Hypericum; Hypericum - chemistry; Hypericum polyanthemum; liver; Male; Medical sciences; Mice; mortality; Organ Size - drug effects; Pharmacognosy. Homeopathy. Health food; Pharmacology. Drug treatments; Plant Extracts - toxicity; Repeated dose toxicity; toxicity testing; Toxicity Tests, Acute; Toxicology; weight gain; Weight Gain - drug effects; Repeated dose toxicity; Hypericum polyanthemum; Acute oral toxicity; Hypericum perforatum; Toxicity; Guttiferae; Acute; Rodentia; Medicinal plant; Multiple dose; Vertebrata; Mammalia; Mouse; Dicotyledones; Animal; Angiospermae; Plant origin; Spermatophyta
• ISSN: 0278-6915; 1873-6351
• DOI: 10.1016/j.fct.2012.04.012

► Antinociceptive and antidepressant-like effects of Hypericum polyanthemum were previously shown in mice (90mg/kg, p.o.). ► Based on OECD acute toxicity parameters H. polyanthemum can be classified as safe, named category 5. ► The liver could be the target organ on potential repeated toxicity of H. polyanthemum (450 and 900mg/kg). ► H. polyanthemum induced signs of toxicity in mice at doses 5- and/or 10-fold above the effective dose only. Hypericum polyanthemum, a South Brazilian species showed antidepressant-like and antinociceptive effects in rodents. Since limited information is available on the toxicity and safety profile of the Hypericum genus, we therefore investigated whether H. polyanthemum cyclo-hexane extract (POL) treatment could be associated with toxicity in preclinical setting using mice as an experimental model. These toxicity studies were based on the guidelines of the Organization for Economic Cooperation and Development (OECD-guidelines 423 and 407). Animals received POL single dose (2000mg/kg, p.o.) or daily for 28-days (90, 450 and 900mg/kg, p.o.). Acute toxicity study did not detect any clinical signs, changes in behavior or mortality. In repeated dose toxicity study, POL affected the body weight gain and induced biochemical, hematological and liver histological changes at 450 and 900mg/kg. Mice treated with POL 90mg/kg did not show any toxicity signs. In conclusion H. polyanthemum can be classified as safe (category 5) according to OECD acute toxicity parameters. However, the alterations observed after repeated treatment with high doses suggest that the liver could be the target organ on potential H. polyanthemum toxicity and point to the need of further toxicity studies.