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首页> 外文期刊>Biochemistry and Cell Biology >Effects of ethanol and haloperidol on plasma levels of hepatic enzymes, lipid profile, and apolipoprotein in rats.
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Effects of ethanol and haloperidol on plasma levels of hepatic enzymes, lipid profile, and apolipoprotein in rats.

机译:乙醇和氟哌啶醇对大鼠血浆肝酶,脂质谱和载脂蛋白的影响。

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摘要

This work studied the effects of ethanol in the absence and presence of haloperidol under two experimental conditions. In protocol 1, rats were treated daily with ethanol (4 g/kg, p.o.) for 7 days, and received only haloperidol (1 mg/kg, i.p.) from the 8th day to the 14th day. In protocol 2, animals received ethanol, and the treatment continued with ethanol and haloperidol from the 8th day to the 14th day. Results show increases in alanine transaminase (ALT; 48% and 55%) and aspartate transaminase (AST; 32% and 22%) levels after ethanol or haloperidol (14 days) treatments, as compared with controls. Apolipoprotein A-1 (APO A1) levels were increased by haloperidol, after 7- (148%) but not after 14-day treatments, as compared with controls. Levels of lipoprotein (high-density lipoprotein (HDL-C)) tended to be increased only by ethanol treatment for 14 days. ALT (80%) and AST (43%) levels were increased in the haloperidol plus ethanol group (protocol 2), as compared with controls. However, an increase in APO A1 levels was observed in the haloperidol group pretreated with ethanol (protocol 1), as compared with controls and ethanol 7-day treatments. Triglyceride (TG) levels were increased in the combination of ethanol and haloperidol in protocol 1 (234%) and 2 (106%), as compared with controls. Except for a small decrease in haloperidol groups, with or without ethanol, as related to ethanol alone, no other effect was observed in HDL-C levels. In conclusion, we showed that haloperidol might be effective in moderating lipid alterations caused by chronic alcohol intake.
机译:这项工作在两种实验条件下研究了在没有氟哌啶醇存在的情况下乙醇的作用。在方案1中,每天用乙醇(4 g / kg,p.o.)处理大鼠7天,从第8天到第14天仅接受氟哌啶醇(1 mg / kg,i.p.)。在方案2中,动物接受了乙醇,从第8天到第14天,继续用乙醇和氟哌啶醇进行治疗。结果显示,与对照组相比,乙醇或氟哌啶醇(14天)治疗后丙氨酸转氨酶(ALT; 48%和55%)和天冬氨酸转氨酶(AST; 32%和22%)水平增加。与对照组相比,氟哌啶醇在7-(148%)治疗后(但在14天治疗后)未增加氟哌啶醇的载脂蛋白A-1(APO A1)水平。仅通过乙醇处理14天,脂蛋白(高密度脂蛋白(HDL-C))的水平趋于增加。与对照组相比,氟哌啶醇加乙醇组(协议2)的ALT(80%)和AST(43%)水平升高。然而,与对照和乙醇7天治疗相比,在用乙醇(协议1)预处理的氟哌啶醇组中观察到APO A1水平增加。与对照组相比,方案1(234%)和2(106%)的乙醇和氟哌啶醇组合中的甘油三酸酯(TG)水平升高。除了单独或与乙醇有关的氟哌啶醇组有或没有乙醇的少量减少外,在HDL-C水平上未观察到其他影响。总之,我们表明氟哌啶醇可能有效减轻慢性饮酒引起的脂质改变。

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