Toxicity Studies on Chloroform Extract of Solanum trilobatum: Effect on Drug Metabolizing and Antioxidant Enzymes in Rats

H. Sini, K. Devi, K. G. Nevin
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引用次数: 2

Abstract

The aim of the study was to evaluate the effect of chloroform extract of Solanum trilobatum (CST) on drug metabolizing and antioxidant defense enzymes for assessing its chemo preventive potential and protection of tissues from oxidative damage. The CST was obtained by soxhlet extraction with chloroform. Animals (Male Sprague Dawley rats) were divided into three groups: Group I-normal control, group II-CST (200 mg kgG1 b.wt.), group III-CST (800 mg kgG1 b.wt.). The CST was given by oral gavage once daily for 15 days. At the end of the experimental period all the rats were sacrificed and the livers, lungs and kidneys were taken for estimating the phase I and II drug metabolizing and antioxidant enzyme activities. The gain in body weight and the levels of GSH and lipid peroxides in these tissues were also determined. The results showed that the administration of CST could modulate the phase I and phase II enzymes that are critical for cancer protection. Administration of CST at 200 and 800 mg kgG1 b.wt. to animals did not cause any apparent clinical signs as survivability or visible changes caused by toxicity in the liver, lungs and kidney. Administration of CST at a dose of (800 mg kgG1 b.wt.) was found to be ineffective in elevating the phase I enzymes suggesting that CST could possibly prevent the biotransformation of carcinogens. These results clearly indicate that CST with its biologically active components could be used as a chemo preventive agent in treating various cancers.
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三叶龙葵氯仿提取物毒性研究:对大鼠药物代谢及抗氧化酶的影响
本研究旨在研究三叶龙葵(Solanum trilobatum, CST)氯仿提取物对药物代谢和抗氧化防御酶的影响,以评估其化学预防作用和对组织氧化损伤的保护作用。用氯仿索氏萃取法得到CST。动物(雄性Sprague Dawley大鼠)分为3组:正常对照组i组、cst组(200 mg kgG1 b.wt.)、cst组(800 mg kgG1 b.wt.)。CST给予口服灌胃,每日1次,连用15 d。实验结束时处死大鼠,取肝、肺、肾,测定ⅰ、ⅱ期药物代谢及抗氧化酶活性。体重的增加以及这些组织中谷胱甘肽和脂质过氧化物的水平也被测定。结果表明,CST的施用可以调节对癌症保护至关重要的I期和II期酶。CST在200和800 mg kgG1 b.wt的管理。对动物未造成任何明显的临床症状,如生存能力或肝、肺、肾毒性引起的明显变化。在800 mg kgG1 b.wt的剂量下,CST对提高I期酶无效,这表明CST可能阻止致癌物质的生物转化。这些结果清楚地表明,CST及其生物活性成分可作为一种化学预防剂用于治疗各种癌症。
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