4.7 Article

Dose-dependent antihypertensive determination and toxicological studies of tilianin isolated from Agastache mexicana

期刊

JOURNAL OF ETHNOPHARMACOLOGY
卷 146, 期 1, 页码 187-191

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ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2012.12.029

关键词

Agastache mexicana; Antihypertensive; Median effective dose; Median lethal dose; Safety pharmacology; Tilianin

资金

  1. Apoyo a la Mejora del Perfil Individual del profesorado de tiempo completo (Fondo para la Consolidacion de las Universidades Publicas Estatales y con Apoyo Solidario Ejercicio)
  2. Facultad de Farmacia, UAEM Budgets

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Ethnopharmacological relevance: Agastache mexicana is used in Mexican traditional medicine for the treatment of hypertension, anxiety and related diseases. Aim of the study: Current work was developed to establish pharmacological/toxicological parameters of tilianin, a fiavone extracted from Agastache mexicana in order to propose it for clinical trials. Materials and methods: Acute and sub-acute toxicology studies in Imprinting Control Region (ICR) mice and median effective dose (ED50) determination in conscious spontaneously hypertensive rats (SHR) were done. Results: A median lethal dose (LD50) of 6624 mg/kg (6201, 7076) in mice and significant antihypertensive effect (ED50=53.51 mg/kg) in SHR were determined. Moreover, sub-acute oral administration of tilianin did not alter body weight, clinical chemistry parameters (alanine amino-transferase, aspartate amino-transferase, total cholesterol, high density lipoprotein, low density lipoprotein, triglycerides, glucose and insulin), and also did not induce any toxic or adverse effects on kidney, heart, liver, and lung functions. Conclusions: We have shown that tilianin, isolated from Agastache mexicana, was not toxic for rodents. Also, its antihypertensive effect was dose-dependent and ED50 (53.51 mg/kg) calculated was lesser than LD50 determined (6624 mg/kg), which suggest a wide range of pharmacology-toxicology patterns. Results support the hypothesis that tilianin must be investigated and developed for clinical trials as antihypertensive drug. (C) 2012 Elsevier Ireland Ltd. All rights reserved.

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