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首页> 外文期刊>Current drug targets. Cardiovascular & haematological disorders >The Possible Therapeutic Actions of Peroxisome Proliferator-Activated Receptor alpha (PPARalpha) Agonists, PPARgamma Agonists, 3-Hydroxy-3-Methylglutaryl Coenzyme A (HMG-CoA) Reductase Inhibitors, Angiotensin Converting Enzyme (ACE) Inhibitors and Ca
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The Possible Therapeutic Actions of Peroxisome Proliferator-Activated Receptor alpha (PPARalpha) Agonists, PPARgamma Agonists, 3-Hydroxy-3-Methylglutaryl Coenzyme A (HMG-CoA) Reductase Inhibitors, Angiotensin Converting Enzyme (ACE) Inhibitors and Ca

机译:过氧化物酶体增殖物激活受体α(PPARalpha)激动剂,PPARγ激动剂,3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂,血管紧张素转换酶(ACE)抑制剂和Ca的可能治疗作用

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摘要

Several intervention studies have shown that some hypolipidemic and hypotensive drugs such as fibrates, 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors, angiotensin converting enzyme (ACE) inhibitors and calcium (Ca)-antagonists prevent atherosclerosis. The main pathological findings in atherosclerosis include abnormal reactions of neutrophils, lymphocytes and monocytes/ macrophages, vascular smooth muscle cells and vascular endothelial cells, and the accumulation of cholesterol ester in the arterial wall. Therefore, investigating the effects of these drugs on the arterial wall may improve understanding of the mechanisms underlying atherosclerosis. Here, based on recent studies including our own, we describe the relationships between risk factors for atherosclerosis, especially hyperlipidemia and hypertension, and the molecular mechanisms that govern lipid metabolism in the arteries.
机译:几项干预研究表明,某些降血脂和降压药,例如贝特类,3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂,血管紧张素转化酶(ACE)抑制剂和钙(Ca)拮抗剂可预防动脉粥样硬化。动脉粥样硬化的主要病理发现包括嗜中性粒细胞,淋巴细胞和单核细胞/巨噬细胞,血管平滑肌细胞和血管内皮细胞的异常反应,以及胆固醇酯在动脉壁中的积累。因此,研究这些药物对动脉壁的作用可能会增进对动脉粥样硬化潜在机制的了解。在此,基于包括我们自己在内的最新研究,我们描述了动脉粥样硬化的危险因素,特别是高脂血症和高血压,与控制动脉脂质代谢的分子机制之间的关系。

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