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佐匹克隆对高脂血症大鼠血糖水平和血脂的急性影响。与PK 11195和氟马西尼的相互作用。

Acute effects of zopiclone on blood glucose level and serum lipids in hyperlipidemic rats. Interactions with PK 11195 and flumazenil.

作者信息

Horák J, Cuparencu B, Horák A

机构信息

Department of Pharmacology, Faculty of Medicine and Pharmacy, University of Oradea, Cluj-Napoca, Romania.

出版信息

Acta Physiol Hung. 2000;87(2):185-92.

Abstract

UNLABELLED

Intraperitoneal administration of 5 mg/kg zopiclone a cyclopyrolone acting on the central benzodiazepine receptors was found to produce significant reduction of total lipids, total cholesterol and triglyceride in rats randered hyperlipidemic by intraperitoneal injection of Triton W-1339. Blood glucose level was also reduced. Flumazenil (10 mg/kg) potentiated the hypoglicemic effect of zopiclone but had no additional effect on serum lipids. PK 11195 (25 mg/kg) antagonized the hypolipidemic effects of zopiclone.

IN CONCLUSION

  1. The central benzodiazepine receptors are not involved in the hypolipidemic activity of zopiclone. 2. The peripheral type benzodiazepine receptors are partly responsible, for the hypolipidemic activity of this cyclopirrolone. 3. The changes of blood glucose level induced by these drugs does not seem to be related to benzodiazepine receptors.
摘要

未标记

腹腔注射5毫克/千克佐匹克隆(一种作用于中枢苯二氮䓬受体的环吡咯酮),可使腹腔注射Triton W - 1339致高脂血症的大鼠的总脂质、总胆固醇和甘油三酯显著降低。血糖水平也降低。氟马西尼(10毫克/千克)增强了佐匹克隆的降血糖作用,但对血清脂质无额外影响。PK 11195(25毫克/千克)拮抗了佐匹克隆的降血脂作用。

结论

  1. 中枢苯二氮䓬受体不参与佐匹克隆的降血脂活性。2. 外周型苯二氮䓬受体部分负责这种环吡咯酮的降血脂活性。3. 这些药物引起的血糖水平变化似乎与苯二氮䓬受体无关。

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