Phytochemical investigation and pharmacological evaluation of ehretia microphylla dipteracanthus patulus and hydnocarpus lorifolia
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Abstract
Liver is a vital organ involved in metabolism of foreign compounds entering into the
newlinebody and regulates the internal chemical environment. Human exposure to toxic
newlinesubstances causes liver toxicity inflicted by hepatotoxic agents. According to WHO, liver
newlinedisease rates have been progressively growing over the years. Conventional drugs used
newlineto cure liver toxicity are inefficient, and there is an imperative need to find drugs that
newlinepossess not only improved liver protection but also significant antioxidant property.
newlineEhretia microphylla (EM), Dipteracanthus patulus (DP) and Hydnocarpus lorifolia (HL)
newlinehave been used to treat various liver diseases by folk medicinal practitioners in the
newlineWayanad hills of Western Ghats of India, but there is no strong scientific evidence to
newlineprove their medicinal claims. The present study was proposed to evaluate the antioxidant
newlineand hepatoprotective activities of various extracts (petroleum ether, chloroform, ethyl
newlineacetate and methanol) of selected medicinal plants. In vitro antioxidant studies confirmed
newlinethe antioxidant potential of the plant extracts and these extracts were also studied for their
newlinehepatoprotective activity against paracetamol-induced liver toxicity in rat model. The
newlineparacetamol-induced rats showed elevated levels of hepatic enzymes SGOT, SGPT, ALP
newlineand billurubin and decreased level of antioxidant parameters such as SOD, CAT, GPx
newlineand GSH. These altered parameters were significantly normalized by different extracts
newlineof EM, DP and HL. The histopathological studies also confirmed the hepatoprotective
newlinenature of the plant extracts. When compared all extracts, chloroform extract of EM
newline(CEM) showed potent antioxidant and hepatoprotective activity. Further isolation and
newlinecharacterisation studies revealed CEM posses a novel triterpenoid 11-oxo amyrin
newline(C30H48O2), along with bauerenol (C30H50O) and and#946;-sitosterol (C29H50O). The cytotoxicity