Eckly A E, Stoclet J C, Lugnier C
Université Louis Pasteur de Strasbourg, Laboratoire de Pharmacologie et Physiopathologie cellulaires, CNRS URA 0600, Illkirch, France.
Eur J Pharmacol. 1994 Dec 12;271(1):237-40. doi: 10.1016/0014-2999(94)90287-9.
The role of endothelium in isoprenaline-induced relaxation was investigated in aortic rings brought to different levels of pre-contraction. Relaxation elicited by isoprenaline decreased with increasing pre-contraction. However, relaxation was identical in rings with and without endothelium brought to the same initial tension by adjusting the noradrenaline concentration. Furthermore, isoprenaline increased cAMP and cGMP contents to the same levels whether endothelium was present or not. These results do not support an obligatory role for the endothelium in isoprenaline-induced relaxation in rat aorta. They indicate that relaxation induced by isoprenaline can be enhanced by the endothelium as a consequence of its effect on the precontraction level of the aorta.
在不同预收缩水平的主动脉环中研究了内皮在异丙肾上腺素诱导的舒张中的作用。异丙肾上腺素引起的舒张随着预收缩程度的增加而降低。然而,通过调节去甲肾上腺素浓度使有内皮和无内皮的环达到相同的初始张力时,舒张情况是相同的。此外,无论有无内皮,异丙肾上腺素均可将环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)含量提高到相同水平。这些结果不支持内皮在大鼠主动脉异丙肾上腺素诱导的舒张中起必不可少的作用。它们表明,由于内皮对主动脉预收缩水平的影响,异丙肾上腺素诱导的舒张可被增强。