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酞嗪醇(EG 626)对大鼠动脉脂肪分解酶活性的影响。

Effects of phthalazinol (EG 626) on arterial lipolytic enzyme activities in the rat.

作者信息

Tomita T, Yonekura I, Shirasaki Y, Hayashi E, Numano F

出版信息

Paroi Arterielle. 1979 Dec;5(4):181-4.

PMID:233431
Abstract

Phthalazinol (EG 626), a thromboxane A2 antagonist and cyclic AMP phosphodiesterase inhibitor, has been shown to prevent the atherosclerosis induced in cholesterol fed rabbits. In an attempt to clarify the antiatherosclerotic mechanism, the effects of this compound on the lipolytic enzyme activities (cholesterol esterase and lipoprotein lipase) of rat aorta were examined in vivo. Administration of EG 626 (100-200 mg/kg, per os, daily, 1-2 weeks) affected neither the aortic lysosomal cholesterol esterase nor the acid phosphatase activity, whereas the lipoprotein lipase activity was signficantly decreased by the treatment. These results suggest that with an elevation in HDL-cholesterol, a decrease in lipoprotein lipase activity after ingestion of EG 626 might contribute, at least to some extent, to the prevention of arterial lipid accumulation.

摘要

酞嗪醇(EG 626)是一种血栓素A2拮抗剂和环磷酸腺苷磷酸二酯酶抑制剂,已被证明可预防喂饲胆固醇的家兔动脉粥样硬化。为了阐明其抗动脉粥样硬化机制,在体内研究了该化合物对大鼠主动脉脂解酶活性(胆固醇酯酶和脂蛋白脂肪酶)的影响。给予EG 626(100 - 200毫克/千克,口服,每日,1 - 2周)对主动脉溶酶体胆固醇酯酶和酸性磷酸酶活性均无影响,而脂蛋白脂肪酶活性则因该处理而显著降低。这些结果表明,随着高密度脂蛋白胆固醇升高,摄入EG 626后脂蛋白脂肪酶活性降低可能至少在一定程度上有助于预防动脉脂质蓄积。

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