4-苯基-5,5-二乙氧基-2-吡咯烷酮对大鼠脂质代谢的影响。

Acta pharmaceutica Nordica Pub Date : 1992-01-01
I H Hall, O T Wong, D J Reynolds, J J Chang
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引用次数: 0

摘要

4-苯基-5,5-二乙氧基-2-吡罗烷酮[XIV]治疗可显著降低Sprague Dawley大鼠血清胆固醇和甘油三酯水平,降低VLDL和LDL胆固醇水平。该化合物显著降低了调节酶的活性,如ATP依赖性柠檬酸裂解酶、HMG辅酶a还原酶、酰基辅酶a胆固醇酰基转移酶、胆固醇-7- α -羟化酶、asn -甘油-3-磷酸酰基转移酶和磷脂酸磷酸化水解酶。在组织培养细胞中,该化合物抑制LDL受体活性和降解,提高HDL受体活性和降解。大鼠胆汁胆固醇和磷脂升高;然而,总胆汁酸减少。原位环研究表明,该药物干扰了胆固醇和胆酸的肝间重吸收。在化合物XIV治疗剂量下,小鼠未见有害作用。
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The effects on lipid metabolism of 4-phenyl-5,5-dicarbethoxy-2-pyrrolidenone in Sprague Dawley rats.

4-Phenyl-5,5-dicarbethoxy-2-pyrrolidenone [XIV] treatment in Sprague Dawley rats caused significant reduction of serum cholesterol and triglyceride levels with reduction of VLDL and LDL cholesterol levels. The compound significantly reduced regulatory enzyme activities, e.g. ATP dependent citrate lyase, HMG CoA reductase, acyl CoA cholesterol acyl transferase, cholesterol-7-alpha-hydroxylase, sn-glycerol-3-phosphate acyl transferase and phosphatidylate phosphohydrolase. In tissue cultured cells, the compound suppressed LDL receptor activity and degradation, and elevated HDL receptor activity and HDL degradation. Rat bile cholesterol and phospholipids were elevated; however, overall bile acids were reduced. In situ loop studies suggest that the agent interfered with interhepatic reabsorption of cholesterol and cholic acids. At the therapeutic dose of compound XIV, no deleterious effects were demonstrated in mice.

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