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Acute oral toxicity evaluation of Andrographis paniculata-standardized first true leaf ethanolic extract.
Worasuttayangkurn, Luksamee; Nakareangrit, Watanyoo; Kwangjai, Jackapun; Sritangos, Pishyaporn; Pholphana, Nanthanit; Watcharasit, Piyajit; Rangkadilok, Nuchanart; Thiantanawat, Apinya; Satayavivad, Jutamaad.
Afiliação
  • Worasuttayangkurn L; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok 10210, Thailand.
  • Nakareangrit W; Translational Research Unit, Chulabhorn Research Institute, Bangkok 10210, Thailand.
  • Kwangjai J; Food and Drug Quality Unit, Chulabhorn Research Institute, Bangkok 10210, Thailand.
  • Sritangos P; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok 10210, Thailand.
  • Pholphana N; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok 10210, Thailand.
  • Watcharasit P; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok 10210, Thailand.
  • Rangkadilok N; Center of Excellence on Environmental Health and Toxicology (EHT), Office of Higher Education Commission, Ministry of Education, Bangkok 10400, Thailand.
  • Thiantanawat A; Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok 10210, Thailand.
  • Satayavivad J; Center of Excellence on Environmental Health and Toxicology (EHT), Office of Higher Education Commission, Ministry of Education, Bangkok 10400, Thailand.
Toxicol Rep ; 6: 426-430, 2019.
Article em En | MEDLINE | ID: mdl-31193040
ABSTRACT
Andrographis paniculata is widely used in traditional herbal medicines for the treatment of common cold, fever and diarrhea, in many regions of Scandinavia and Asia, including Thailand. The pharmacological activities of A. paniculata are mainly attributed to active diterpenoids including 14-deoxyandrographolide, which is uniquely high in first true leaf ethanolic extract (FTLEE) of A. paniculata. In this study, the acute toxicity of the standardized FTLEE of A. paniculata was examined according to the OECD test guideline No. 420. Mice were divided into four groups of each sex and orally received the standardized FTLEE of A. paniculata (0, 300, 2000, or 5000 mg/kg BW). Post-treatment, body weight, signs of toxicity, and/or mortality were observed for 14 days. At Day 15, animals were euthanized, internal organs were observed grossly, and blood samples collected were subjected to hematology and clinical biochemistry analyses. The results showed that all treated animals survived and no apparent adverse effects were observed during the duration of the study. Gross necropsy observation revealed no lesion in any organ of all the standardized FTLEE-treated mice. Although significant alterations in BUN, lymphocytes, neutrophils, hematocrit and hemoglobin were observed, these alterations were not treatment-related toxic effects. Therefore, we concluded that a single oral administration of the standardized FTLEE of A. paniculata with an upper fixed dose of 5000 mg/kg BW has no significant acute toxicological effects.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 3_ND Problema de saúde: 3_diarrhea Tipo de estudo: Guideline Idioma: En Revista: Toxicol Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Tailândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 3_ND Problema de saúde: 3_diarrhea Tipo de estudo: Guideline Idioma: En Revista: Toxicol Rep Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Tailândia
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