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新型钙拮抗剂SIM 6080可减轻喂饲胆固醇的家兔的主动脉粥样硬化。

SIM 6080, a new calcium antagonist, reduces aortic atherosclerosis in cholesterol-fed rabbits.

作者信息

Maggi F M, Bernini F, Barberi L, Fantoni M, Catapano A L

机构信息

Institute of Pharmacological Sciences, University of Milano, Italy.

出版信息

Pharmacol Res. 1993 Oct-Nov;28(3):219-27. doi: 10.1006/phrs.1993.1125.

Abstract

SIM 6080 is a new calcium antagonist, structurally related to diphenylalkylamines, which combines transmembrane and intracellular calcium antagonist activities. In the present study we investigated the effect of SIM 6080 on atherogenesis in cholesterol-fed rabbits. Subcutaneous administration of the compound at 0.33, 1, and 3 mg kg-1/bid for 60 days neither affected plasma lipids nor blood pressure. However at 1 and 3 mg kg-1/bid SIM 6080 reduced in a dose-dependent manner both the area of the aorta covered by plaques and aortic cholesterol content. Determination of SIM 6080 plasma and aortic content indicated that the compound could concentrate up to 10 times in the arterial tissue. In vitro studies demonstrated that at concentrations similar to those observed in the aorta this compound may stimulate rabbit beta VLDL catabolism by smooth muscle cells in an homologous system suggesting that the up-regulation of LDL-receptors in the aorta may contribute to the antiatherosclerotic properties of SIM 6080.

摘要

SIM 6080是一种新型钙拮抗剂,在结构上与二苯基烷基胺相关,兼具跨膜和细胞内钙拮抗剂活性。在本研究中,我们调查了SIM 6080对喂饲胆固醇的家兔动脉粥样硬化形成的影响。以0.33、1和3 mg kg-1/每日两次的剂量皮下给予该化合物60天,既不影响血脂也不影响血压。然而,以1和3 mg kg-1/每日两次的剂量,SIM 6080以剂量依赖方式减少了斑块覆盖的主动脉面积和主动脉胆固醇含量。SIM 6080血浆和主动脉含量的测定表明,该化合物在动脉组织中的浓度可高达10倍。体外研究表明,在与主动脉中观察到的浓度相似的情况下,该化合物可能在同源系统中刺激平滑肌细胞对兔β-VLDL的分解代谢,这表明主动脉中LDL受体的上调可能有助于SIM 6080的抗动脉粥样硬化特性。

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