Pool J L, Lenz M L, Taylor A A
Department of Medicine, Baylor College of Medicine, Houston, Texas.
J Hum Hypertens. 1990 Oct;4 Suppl 3:23-33.
For the past 40 years, adrenoreceptors have been studied as the biomolecular mediators of tissue response to catecholamines. An expanded role of alpha-adrenoreceptors in the regulation of risk factors for coronary heart disease (CHD) has recently emerged. Hypercholesterolaemia, hypertension, and cigarette smoking are the major risk factors and their interactions are associated with increased mortality. Control of hypertension alone has failed to reduce the risk of CHD. Conversely, reduction of elevated total cholesterol and low density lipoprotein (LDL)-cholesterol has been shown to lower the risk of CHD. As a result, multiple risk factor approaches to the management of patients have evolved in attempts to reduce deaths from CHD. Selective alpha 1-adrenoreceptor antagonists appear to have a dual function in CHD risk management since they control elevated blood pressure by peripheral vasodilatation and reduce atherogenic lipids by several mechanisms. With selective alpha 1-blockade, the number of LDL-cholesterol receptors is up-regulated and 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG Co-A reductase) activity is suppressed causing reductions in total cholesterol, LDL-cholesterol, and apoprotein B levels. Effects on intermediary metabolism reduce synthesis of very low density lipoprotein (VLDL) which contributes to a reduction of total triglyceride levels and, to a lesser extent, to a reduction of total cholesterol levels. Increased lipoprotein lipase activity leads to reduced total triglyceride and VLDL levels and to increased high density lipoprotein (HDL)-cholesterol levels. As demonstrated by the initial prospective data from Phase I of the Treatment of Mild Hypertension Study (TOMHS), both reduction of raised blood pressure and beneficial lipid modifications are sustained (1 year) with selective alpha 1-blockade. The prospective benefits on morbidity and mortality from CHD of such favourable changes in these two major risk factors remain to be quantified.
在过去40年里,肾上腺素能受体一直被作为组织对儿茶酚胺反应的生物分子介质进行研究。最近,α-肾上腺素能受体在冠心病(CHD)危险因素调节中的作用得到了扩展。高胆固醇血症、高血压和吸烟是主要的危险因素,它们之间的相互作用与死亡率增加有关。仅控制高血压并不能降低冠心病风险。相反,降低升高的总胆固醇和低密度脂蛋白(LDL)胆固醇已被证明可降低冠心病风险。因此,针对患者管理的多危险因素方法不断发展,试图减少冠心病死亡人数。选择性α1-肾上腺素能受体拮抗剂在冠心病风险管理中似乎具有双重作用,因为它们通过外周血管舒张控制血压升高,并通过多种机制降低致动脉粥样硬化脂质。通过选择性α1-阻断,LDL胆固醇受体数量上调,3-羟基-3-甲基戊二酰辅酶A还原酶(HMG Co-A还原酶)活性受到抑制,导致总胆固醇、LDL胆固醇和载脂蛋白B水平降低。对中间代谢的影响减少了极低密度脂蛋白(VLDL)的合成,这有助于降低总甘油三酯水平,并在较小程度上降低总胆固醇水平。脂蛋白脂肪酶活性增加导致总甘油三酯和VLDL水平降低,高密度脂蛋白(HDL)胆固醇水平升高。治疗轻度高血压研究(TOMHS)第一阶段的初步前瞻性数据表明,选择性α1-阻断可使升高的血压降低和有益的血脂改变持续(1年)。这两个主要危险因素的这些有利变化对冠心病发病率和死亡率的前瞻性益处仍有待量化。