Pharmacological effects and toxicity of Costus pulverulentus C. Presl (Costaceae)
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Ethnopharmacological relevance Costus pulverulentus C. Presl (Costaceae), a species endemic to Mexico, is used for the empirical treatment of cancer, pain, and inflammation. Aim of the study The objective of this study was to evaluate the toxicity, as well as the cytotoxic, antinociceptive, anti-inflammatory and sedative effects of an ethanol extract from Costus pulverulentus stem (CPE). Materials and methods The chemical characterization of CPE was performed by Gas chromatography-mass spectrometry (GC-MS). The toxicity of CPE was evaluated using the comet assay (10-1000 μg/ml during 5 h) and the acute toxicity test (500-5000 mg/kg p.o. and i.p. during 14 days). The cytotoxic effect of CPE (1-250 μg/ml) on human cancer cells was evaluated using the MTT assay. The antinociceptive effects of CPE (50-200 mg/kg p.o.) were evaluated using thermal-induced nociception tests (hot plate and tail flick) and the chemical-induced nociceptive tests (acetic acid and formalin). The sedative activity of CPE (50-200 mg/kg p.o.) was evaluated using the ketamine-induced sleeping time test. Results CPE showed the presence of compounds such as campesterol, stigmasterol β-sitosterol, vanillic acid, among others. In the comet assay, CPE at 200 μg/ml or higher concentrations induced DNA damage. In the acute toxicity test, the LD50 estimated for CPE was>5000 mg/kg p.o. or i.p. CEP showed moderate cytotoxic effects on prostate carcinoma cells PC-3 cells (IC50=179±23.2 μg/ml). In the chemical-induced nociception models, CPE (100 and 200 mg/kg p.o.) showed antinociceptive effects with similar activity to 100 mg/kg naproxen. In the thermal-induced nociception tests, CPE tested at 200 mg/kg showed moderate antinociceptive effects by 28%25 (hot plate test) and by 25%25 (tail flick test). In the ketamine-induced sleeping time test, CPE showed no sedative effects. Conclusions C. pulverulents exerts moderate cytotoxic effects in human cancer cells, moderate anti-inflammatory and antinociceptive effects. C. pulverulentus induces antinociceptive effects without inducing sedation. © 2016 Elsevier Ireland Ltd. All rights reserved.
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Antiinflammatory; Antinociceptive; Cancer; Costus pulverulentus; Gas chromatography-mass spectrometry; Toxicity acetic acid; antiinflammatory agent; antinociceptive agent; campesterol; chemical compound; Costus pulverulentus extract; formaldehyde; ketamine; naproxen; sedative agent; sitosterol; stigmasterol; unclassified drug; vanillic acid; analgesic agent; anesthetic agent; antiinflammatory agent; ketamine; plant extract; acute toxicity; animal cell; animal experiment; antiinflammatory activity; Article; cancer cell; comet assay; controlled study; Costus; cytotoxicity; DNA damage; drug cytotoxicity; drug effect; gas chromatography; hot plate test; human; human cell; LD50; male; mass spectrometry; mouse; nociception; nonhuman; prostate carcinoma; sedation; sleep time; tail flick test; thermal analysis; animal; Bagg albino mouse; cell survival; chemically induced; drug effects; edema; heat; metabolism; mononuclear cell; pain; plant stem; tumor cell line; Acetic Acid; Analgesics; Anesthetics, Dissociative; Animals; Anti-Inflammatory Agents; Cell Line, Tumor; Cell Survival; Comet Assay; Costus; Edema; Formaldehyde; Hot Temperature; Humans; Ketamine; Lethal Dose 50; Leukocytes, Mononuclear; Male; Mice, Inbred BALB C; Pain; Plant Extracts; Plant Stems
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