Dohi Y, Kojima M, Sato K, Lüscher T F
Department of Internal Medicine, Nagoyashi Kohseiin Geriatric Hospital, Nagoya, Japan.
Drugs Aging. 1995 Oct;7(4):278-91. doi: 10.2165/00002512-199507040-00003.
Aging is associated with structural and functional changes in the blood vessel wall. In vascular smooth muscle, the effects of aging on the response mediated by beta-adrenoceptors have been most intensively studied. beta-adrenoceptor-mediated relaxation decreases in most arteries, but not veins, with increasing age. In contrast, studies on contractile responses to alpha-adrenergic drugs are conflicting. The response to alpha-adrenoceptor agonists appears to be unchanged for decreased by aging. The endothelium takes part in the local regulation of vascular tone as a source of several vasoactive factors. Basal release of endothelium-derived nitric oxide decreases with age in vitro studies. Aging is also associated with reduced endothelium-dependent relaxations in response to vasoactive substances such as acetylcholine, histamine or adenosine. The impairment of the relaxation is, in most cases, achieved by a decreased release and/or decreased production of endothelium-derived relaxing factors (endothelium-derived nitric oxide, hyperpolarising factor and prostacyclin). An increased release of endothelium-derived, cyclo-oxygenase-dependent contracting factor is also responsible for reduced relaxation in some tissues. On the other hand, the release of endothelin-1 from the endothelium increases with age, while the response to the peptide decreases under the same conditions, especially in small resistance arteries. The alterations of vascular smooth muscle and endothelial cells occurring with age may have important clinical implications for the pathogenesis of cardiovascular disease.
衰老与血管壁的结构和功能变化相关。在血管平滑肌中,衰老对β-肾上腺素能受体介导的反应的影响得到了最为深入的研究。随着年龄增长,大多数动脉(而非静脉)中β-肾上腺素能受体介导的舒张功能下降。相比之下,关于α-肾上腺素能药物收缩反应的研究结果相互矛盾。对α-肾上腺素能受体激动剂的反应似乎未因衰老而改变或有所降低。内皮作为多种血管活性因子的来源,参与血管张力的局部调节。体外研究表明,内皮源性一氧化氮的基础释放量随年龄增长而减少。衰老还与对诸如乙酰胆碱、组胺或腺苷等血管活性物质的内皮依赖性舒张功能降低相关。在大多数情况下,舒张功能受损是由于内皮源性舒张因子(内皮源性一氧化氮、超极化因子和前列环素)的释放减少和/或生成减少所致。内皮源性环氧化酶依赖性收缩因子的释放增加在某些组织中也导致舒张功能降低。另一方面,内皮素-1从内皮的释放量随年龄增长而增加,而在相同条件下对该肽的反应降低,尤其是在小阻力动脉中。随着年龄增长发生的血管平滑肌和内皮细胞的改变可能对心血管疾病的发病机制具有重要的临床意义。