Literature DB >> 26550447

Acute and subchronic toxicity as well as evaluation of safety pharmacology of traditional Chinese medicine "Huhezi".

Yaqin Chen1, Shufan Chen1, Chenhui Song1, Zhongqiong Yin1, Zhenzhen Chen1, Renyong Jia1, Xiaoxia Liang1, Lixia Li1, Yuanfeng Zou1, Changliang He1, Gang Ye1, Cheng Lv1.   

Abstract

The study was conducted to evaluate the toxicity and safety pharmacology of the traditional Chinese medicine, "Huhezi" granules. The results of acute toxicity test showed that the granules' LD50 was more than 5000 mg/kg, which indicated that the "Huhezi" belonged to actually non-toxic drug. Subchronic toxicity study showed that non-toxic reaction were detected in high (1000 mg/kg), medium (500 mg/kg) and low dose (250 mg/kg) of "Huhezi" groups by measuring rat body weight, organ coefficient, blood physiological indexes and blood biochemical indexes. Pathological examination showed that no tissue lesions were observed in test organs except liver (mild granular degenerationand reversible vesicular degeneration), spleen (Langerhans cells infiltrating) and kidney (homogeneous red staining of renal tubule). Safety pharmacology study found that "Huhezi" had no effects on the central nervous system, respiratory system and cardiovascular system. These results suggested that the dose of "Huhezi" at or below 1000 mg/kg through oral administration is considered safe.

Entities:  

Keywords:  acute toxicity; rats; safety pharmacology; subchronic toxicity; “Huhezi” granules

Year:  2015        PMID: 26550447      PMCID: PMC4613132     

Source DB:  PubMed          Journal:  Int J Clin Exp Med        ISSN: 1940-5901


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