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人类高血压中自主神经控制的异常。

Abnormalities of autonomic nervous control in human hypertension.

作者信息

Julius S

机构信息

Division of Hypertension, University of Michigan Medical School, Ann Arbor 48109-0356.

出版信息

Cardiovasc Drugs Ther. 1994 Mar;8 Suppl 1:11-20. doi: 10.1007/BF00877080.

Abstract

The pathophysiology of various stages of hypertension is different. In early hyperkinetic borderline hypertension, the sympathetic drive to the heart and blood vessels is increased while the parasympathetic cardiac inhibition is decreased. The elevated cardiac output, vascular resistance, and blood pressure at that stage can be fully normalized by autonomic blockade. As hypertension advances, a hyperkinetic circulation is less evident, since beta-adrenergic responsiveness and cardiac compliance tend to decrease. Simultaneously hypertrophy of the resistance vessels increases the baseline vascular resistance and the vessels' responsiveness to constrictive stimuli. Eventually a picture of a normal cardiac output/high vascular resistance typical for established essential hypertension emerges. As the blood vessels become hyperreactive, the same degree of vasoconstriction/blood pressure elevation can be achieved with less sympathetic tone. In that phase the sympathetic overactivity is less evident, as the brain resets itself to maintain the same blood pressure elevation with a small amount of sympathetic discharge. While sympathetic overactivity may be less evident in established hypertension, it remains an important pathophysiologic factor, not only for the maintenance of blood pressure, but also for a number of other abnormalities in hypertension. Hypertension is intimately associated with higher levels of pressure-unrelated risk for development of atherosclerosis: dyslipidemia, overweight, and hyperinsulinemia. Furthermore, a number of factors in hypertension favor a poorer outcome from coronary heart disease. These pressure-independent factors increase the risk of coronary thrombosis, arrhythmic deaths, and coronary spasms. Sympathetic overreactivity appears to be crucially implicated in the evolution of this added coronary risk in hypertension. Understanding the pathophysiology of coronary risk and its relationship to sympathetic overreactivity in hypertension is helpful in seeking further improvements in clinical practice. At present antihypertensive treatment is less efficacious in reducing coronary events in hypertension than would be expected. Judicious use of appropriate drugs promises to further improve the efficacy of antihypertensive treatment in those patients who, in addition to high blood pressure, also have other associated risk factors.

摘要

高血压各阶段的病理生理学有所不同。在早期的高动力性临界高血压阶段,心脏和血管的交感神经驱动力增加,而副交感神经对心脏的抑制作用减弱。该阶段升高的心输出量、血管阻力和血压可通过自主神经阻滞完全恢复正常。随着高血压病情进展,高动力性循环不那么明显,因为β-肾上腺素能反应性和心脏顺应性趋于降低。同时,阻力血管的肥厚增加了基线血管阻力以及血管对收缩性刺激的反应性。最终会出现典型的原发性高血压所具有的正常心输出量/高血管阻力的情况。随着血管反应性增强,在交感神经张力较低的情况下就能实现相同程度的血管收缩/血压升高。在该阶段,交感神经过度活跃不太明显,因为大脑会自我调整,通过少量的交感神经放电来维持相同程度的血压升高。虽然在已确诊的高血压中交感神经过度活跃可能不太明显,但它仍然是一个重要的病理生理因素,不仅与血压维持有关,还与高血压的许多其他异常情况有关。高血压与动脉粥样硬化发生发展中与压力无关的较高风险密切相关:血脂异常、超重和高胰岛素血症。此外,高血压中的一些因素会使冠心病的预后更差。这些与压力无关的因素增加了冠状动脉血栓形成、心律失常性死亡和冠状动脉痉挛的风险。交感神经过度反应似乎在高血压中这种额外的冠状动脉风险的演变中起关键作用。了解冠状动脉风险的病理生理学及其与高血压中交感神经过度反应的关系有助于在临床实践中寻求进一步的改善。目前,抗高血压治疗在降低高血压患者冠状动脉事件方面的效果不如预期。明智地使用合适的药物有望进一步提高对那些除高血压外还伴有其他相关危险因素的患者的抗高血压治疗效果。

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