Toxicological evaluation, brine shrimp lethality assay, in vivo and ex vivo antioxidant assessment followed by GC–MS study of the extracts obtained from Olax psittacorum (Lam.) Vahl
Autor: | Chowdhury Mobaswar Hossain, Raja Majumder, Jinamitra Sahu, Lopamudra Adhikari, Moonmun Dhara |
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Rok vydání: | 2019 |
Předmět: |
Antioxidant
biology Traditional medicine medicine.medical_treatment Brine shrimp biology.organism_classification 01 natural sciences 030205 complementary & alternative medicine 0104 chemical sciences Lipid peroxidation 010404 medicinal & biomolecular chemistry 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Complementary and alternative medicine chemistry Catalase In vivo Toxicity medicine biology.protein Cytotoxicity Ex vivo |
Zdroj: | Advances in Traditional Medicine. 20:303-325 |
ISSN: | 2662-4060 2662-4052 |
DOI: | 10.1007/s13596-019-00384-y |
Popis: | Olax psittacorum (Lam.) Vahl. has versatile ethnopharmacological healing property in addition with incomplete research are adequate pieces of information to support the choice of the plant to build up proper data in acute and sub-chronic toxicological, cytotoxicity with ex vivo and in vivo antioxidant profile as well as qualitative analytical illustration through GC–MS of the selected extracts obtained from different parts of the plant. We have extracted leaf methanolic extract (LME), stem methanolic extract (SME), stem aqueous extract (SAE) and fruits aqueous extract (FrAE) for the above mentioned respective studies. OECD guideline 420 and 407, brine shrimp lethality (BSLA), lipid peroxidation, catalase assay was conducted to gather information on toxicity, cytotoxicity, and antioxidant properties respectively. BSLA study indicates that LME may be a good choice to develop as an anticancer drug for future perspective (LC50 = 41.88 µg/ml). Both LME and SME have been selected for ex vivo and in vivo antioxidant analysis on the basis of their low toxicity and GCMS analysis. Moreover, in vivo lipidperoxidation as well as catalase assay both having significant difference (P |
Databáze: | OpenAIRE |
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