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与年龄相关的组胺诱导的血管舒张功能下降可能是由于环鸟苷酸生成减少所致。

Age-associated decrease in histamine-induced vasodilation may be due to reduction of cyclic GMP formation.

作者信息

Moritoki H, Tanioka A, Maeshiba Y, Iwamoto T, Ishida Y, Araki H

机构信息

Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokushima, Japan.

出版信息

Br J Pharmacol. 1988 Dec;95(4):1015-22. doi: 10.1111/j.1476-5381.1988.tb11734.x.

Abstract
  1. The effects of aging on histamine-induced vasodilatation and cyclic GMP production in rat thoracic aorta were investigated. 2. This histamine-induced dilatation of the aorta was mediated by H1-receptors and was dependent on the endothelium. 3. Histamine induced the greatest dilatation of arteries of 3-4 week old rats, progressively less of those of rats of 8 to 56 weeks old, and scarcely detectable dilatation of those of 100 week old rats. 4. Histamine induced cyclic GMP production in aorta from rats of 4 weeks old, with no change in the cyclic AMP level. This increase in the cyclic GMP level induced by histamine also decreased with age, being about 70% as great at 8 weeks, 50% as great at 50-60 weeks, and 10% as great at 130 weeks of age. 5. Removal of the endothelium completely abolished the histamine-induced increase in cyclic GMP. 6. The dilator effect of nitroprusside, which enhances cyclic GMP production by stimulating guanylate cyclase directly (not indirectly via the endothelium derived relaxing factor, EDRF), also showed age-related attenuation. 7. The dilator effect of 8-bromo cyclic GMP, which stimulates cyclic GMP-dependent protein kinase, also decreased during aging. 8. These results suggest that aging reduces the ability of the endothelium to produce EDRF, which stimulates guanylate cyclase, and so decreases cyclic GMP production. Thus the decreased dilator response of the arteries to histamine during aging is probably due to both loss of endothelial function and reduction of guanylate cyclase activity. Alteration of cyclic GMP-dependent protein kinase activity may also participate in the age-related changes.
摘要
  1. 研究了衰老对大鼠胸主动脉中组胺诱导的血管舒张和环磷酸鸟苷(cGMP)生成的影响。2. 这种组胺诱导的主动脉舒张由H1受体介导且依赖于内皮。3. 组胺诱导3 - 4周龄大鼠的动脉产生最大程度的舒张,8至56周龄大鼠的动脉舒张程度逐渐降低,而100周龄大鼠的动脉几乎检测不到舒张。4. 组胺诱导4周龄大鼠主动脉中cGMP生成,环磷酸腺苷(cAMP)水平无变化。组胺诱导的cGMP水平升高也随年龄降低,8周龄时约为70%,50 - 60周龄时为50%,130周龄时为10%。5. 去除内皮完全消除了组胺诱导的cGMP增加。6. 硝普钠的舒张作用,其通过直接刺激鸟苷酸环化酶(而非经由内皮衍生舒张因子,EDRF间接刺激)增强cGMP生成,也显示出与年龄相关的减弱。7. 8 - 溴环磷酸鸟苷的舒张作用,其刺激依赖cGMP的蛋白激酶,在衰老过程中也降低。8. 这些结果表明,衰老降低了内皮产生EDRF的能力,EDRF刺激鸟苷酸环化酶,从而减少cGMP生成。因此,衰老过程中动脉对组胺的舒张反应降低可能是由于内皮功能丧失和鸟苷酸环化酶活性降低。依赖cGMP的蛋白激酶活性改变也可能参与了与年龄相关的变化。

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