Lockette W, Otsuka Y, Carretero O
Hypertension. 1986 Jun;8(6 Pt 2):II61-6. doi: 10.1161/01.hyp.8.6_pt_2.ii61.
We investigated endothelium-dependent relaxation in rat aortae, using three models of experimental hypertension: deoxycorticosterone and salt; one-kidney, one clip renovascular hypertension; and coarctation. Isolated aortae were contracted with phenylephrine, and relaxation was subsequently induced with acetylcholine or calcium ionophore A23187. Blood vessels denuded of endothelium did not relax in response to acetylcholine or A23187. Blood vessels from animals with high blood pressure had decreased relaxation responses to acetylcholine and A23187, and also to the endothelium-independent vasodilator sodium nitroprusside. Unlike acetylcholine and A23187, however, nitroprusside completely relaxed the blood vessels from the hypertensive animals, though the sensitivity to nitroprusside was much lower in these vessels. Subsequent reversal of hypertension caused a return of endothelium-dependent relaxation. Loss of endothelium-dependent relaxation occurs readily in the aortae with the development of hypertension; this phenomenon appears to be related to elevated pressure.
我们使用三种实验性高血压模型,即脱氧皮质酮盐模型、单肾单夹肾血管性高血压模型和主动脉缩窄模型,研究了大鼠主动脉的内皮依赖性舒张功能。分离的主动脉用去氧肾上腺素收缩,随后用乙酰胆碱或钙离子载体A23187诱导舒张。去除内皮的血管对乙酰胆碱或A23187无舒张反应。高血压动物的血管对乙酰胆碱、A23187以及对不依赖内皮的血管舒张剂硝普钠的舒张反应均降低。然而,与乙酰胆碱和A23187不同,硝普钠可使高血压动物的血管完全舒张,尽管这些血管对硝普钠的敏感性要低得多。随后高血压的逆转导致内皮依赖性舒张功能恢复。随着高血压的发展,主动脉中内皮依赖性舒张功能很容易丧失;这种现象似乎与血压升高有关。