首页> 美国卫生研究院文献>Iranian Journal of Pharmaceutical Research : IJPR >Investigating The Role of Novel Bioactive Compound from Ficus Virens Ait on Cigarette Smoke Induced Oxidative Stress and Hyperlipidemia in Rats
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Investigating The Role of Novel Bioactive Compound from Ficus Virens Ait on Cigarette Smoke Induced Oxidative Stress and Hyperlipidemia in Rats

机译:研究来自榕榕的新型生物活性化合物对香烟烟雾诱导的大鼠氧化应激和高脂血症的作用

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摘要

The present study is premeditated to extenuate the role of Ficus virens extract and its bioactive compound on cigarette smoke, an important risk factor for CVD, induced oxidative stress and hyperlipidemia. Cigarette smoke (CS) exposure to rats results in significant loss of body weight and increases blood carbon monoxide saturation (carboxyhemoglobin), nicotine, plasma TC, TG, and LDL-C levels but reduced level of antiatherogenic HDL-C. Moreover, owing to substantial oxidative stress generated in rats due to cigarette smoke a significant increase in plasma and erythrocytes lipid peroxidation products were observed which was well correlated with increase in ex-vivo BDC (48%) and MDA (53%) level (p < 0.001). Simultaneous administration of FVBM extract at higher dose (100 mg/rat) and F18 (n-Octadecanyl-O-α-D-glucopyranosyl(6’→1’’)-O-α-D-glucopyranoside) compound to CS-exposed rats effectively blocked the increase in plasma lipid and lipoprotein levels (p < 0.001) which was due to the marked suppression in the hepatic HMG-CoA reductase activity (p < 0.001) and significantly inhibit the lipid peroxidation process thus preventing the membrane damage, LDL oxidation, and in turn subsequent atherosclerosis. Thus, the results clearly demonstrated the protective role of FVBM extract and F18 compound in risk factor induced cardiovascular disease.
机译:本研究预示着减轻榕树提取物及其生物活性化合物对香烟烟雾的作用,香烟烟雾是CVD,诱发氧化应激和高脂血症的重要危险因素。暴露于大鼠的香烟烟雾(CS)导致体重显着减少,并增加血液中的一氧化碳饱和度(羧基血红蛋白),尼古丁,血浆TC,TG和LDL-C水平,但抗动脉粥样硬化HDL-C水平降低。此外,由于香烟烟雾在大鼠中产生了巨大的氧化应激,血浆和红细胞脂质过氧化产物显着增加,这与离体BDC(48%)和MDA(53%)水平的升高密切相关(p <0.001)。将高剂量(100 mg /大鼠)的FVBM提取物和F18(正十八烷基-O-α-D-吡喃葡萄糖基(6'→1'')-O-α-D-吡喃葡萄糖苷)同时给药于CS暴露大鼠有效地阻止了血浆脂质和脂蛋白水平的增加(p <0.001),这是由于肝脏HMG-CoA还原酶活性的显着抑制(p <0.001),并显着抑制了脂质过氧化过程,从而防止了膜损伤,LDL氧化,继而导致随后的动脉粥样硬化。因此,结果清楚地证明了FVBM提取物和F18化合物在危险因素诱发的心血管疾病中的保护作用。

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