EVALUATION OF HEPATOPROTECTIVE POTENTIAL OF LEAF AND LEAF CALLUS EXTRACTS OF ANISOCHILUS CARNOSUS (L) WALL.

N. Reshi, Sudarahana Mysore Shankarsingh, Girish Hodiyala Vasanaika
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引用次数: 2

Abstract

The study was carried out to evaluate the hepatoprotective activity of leaf and leaf callus extracts of Anisochilus carnosus (L) Wall. against alcohol induced toxicity using HepG2 cell line. Leaf explants were cultured on Murashige and Skoog solid medium supplemented with different growth regulators. Prior to the determination of hepatoprotective property leaf and leaf callus extracts were subjected to the toxic dose study. The degree of hepatoprotection of extracts was determined by measuring cell viability percentage by MTT assay. The preliminary phytochemical analysis of leaf and leaf callus was carried out by qualitative analysis. Maximum percentage of callus formation (98%) was obtained in MS medium fortified with 3 mg/l 2,4-D. HepG2 cells were pretreated with the different concentrations (below toxic dose) of leaf and leaf callus extracts for 72 hours followed by alcohol intoxication. Results revealed that ethanolic leaf extract pretreated HepG2 cells show 94% cell viability compared to the standard silymarin pretreated HepG2 cells which showed 81% cell viability. Leaf callus extracts also exhibited significant hepatoprotective activity where ethanolic callus extract pretreated HepG2 cells showed 86% viability after intoxication with alcohol. Results revealed that HepG2 cell viability percentage is dose dependent. Phytochemical studies revealed the presence of different secondary metabolites in leaf and leaf callus extracts. The bio-efficacy study confirms the presence of secondary metabolites of hepatoprotective nature in leaf and leaf callus of A. carnosus.
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山楂叶和愈伤组织提取物对肝脏保护作用的评价。
研究了山楂叶和愈伤组织提取物对肝脏的保护作用。HepG2细胞抗酒精毒性的实验研究叶片外植体在添加不同生长调节剂的Murashige和Skoog固体培养基上培养。在确定其肝保护作用之前,对其叶片和愈伤组织提取物进行了毒性剂量研究。MTT法测定细胞存活率,测定提取物的保肝作用。采用定性分析方法对叶片和愈伤组织进行了初步的植物化学分析。在添加3 mg/l 2,4- d的MS培养基中愈伤组织形成率最高(98%)。用不同浓度(低于中毒剂量)的叶片和愈伤组织提取物预处理HepG2细胞72小时,然后酒精中毒。结果表明,乙醇叶提取物预处理的HepG2细胞的细胞存活率为94%,而水飞蓟素预处理的HepG2细胞的细胞存活率为81%。叶片愈伤组织提取物也表现出显著的肝保护作用,乙醇愈伤组织提取物预处理HepG2细胞后,酒精中毒后的存活率为86%。结果显示HepG2细胞存活率呈剂量依赖性。植物化学研究表明,叶片和愈伤组织提取物中存在不同的次生代谢物。生物功效研究证实了牛油果叶片和叶片愈伤组织中存在具有保肝作用的次生代谢产物。
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