苯巴比妥对大鼠肝素后血浆和组织中脂溶活性的调节。

D M Goldberg, M W Roomi, A Yu
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引用次数: 7

摘要

雄性大鼠以100mg /kg剂量注射苯巴比妥5天,空腹血浆的肝后溶脂活性增加。鱼精蛋白硫酸盐、1m NaCl和十二烷基硫酸钠的抑制作用表明,肝磷脂后血浆中脂蛋白脂肪酶和肝甘油三酯脂肪酶的活性均升高。苯巴比妥治疗的大鼠脂肪组织脂蛋白脂肪酶活性也增加。肝素洗脱的肝切片甘油三酯脂肪酶活性和肝微粒体残留活性显著升高。苯巴比妥对心肌和红骨骼肌的脂蛋白脂肪酶无明显影响。空腹服用苯巴比妥的大鼠肝素后溶脂活性的增加似乎是通过脂肪组织脂蛋白脂肪酶活性的增加和肝脏甘油三酯脂肪酶活性的增加来解释的,正如先前报道的那样,这两者都可能导致药物介导的空腹血清甘油三酯浓度的降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation by phenobarbital of lipolytic activity in postheparin plasma and tissues of the rat.

Male rats injected with phenobarbital at a dose of 100 mg/kg for 5 days manifested increased postheparin lipolytic activity of fasting plasma. Inhibition studies with protamine sulphate, 1 M NaCl, and sodium dodecyl sulphate revealed that the activities of both lipoprotein lipase and hepatic triacylglycerol lipase were increased in the postheparin plasma of the drug-treated rats. Adipose tissue lipoprotein lipase activity was also increased in the phenobarbital-treated rats. The triacylglycerol lipase activity elutable by heparin from liver slices and the residual activity of liver microsomes increased significantly in the drug-treated rats. Lipoprotein lipase of cardiac muscle and red skeletal muscle was unaltered by phenobarbital treatment. The increased postheparin lipolytic activity of fasting phenobarbital-treated rats seems to be accountable through increased lipoprotein lipase activity of adipose tissue and increased triacylglycerol lipase activity of liver, both of which may contribute to the lowered fasting concentrations of serum triacylglycerol mediated by the drug, as previously reported.

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