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来自内皮的一氧化氮可减弱低氧性肺动脉高压大鼠离体肺动脉的固有张力的证据。

Evidence that nitric oxide from the endothelium attenuates inherent tone in isolated pulmonary arteries from rats with hypoxic pulmonary hypertension.

作者信息

Wanstall J C, Hughes I E, O'Donnell S R

机构信息

Department of Physiology and Pharmacology, University of Queensland, Brisbane, Australia.

出版信息

Br J Pharmacol. 1995 Jan;114(1):109-14. doi: 10.1111/j.1476-5381.1995.tb14913.x.

Abstract
  1. The inherent contractile tone, and its modulation by the endothelium, have been studied in isolated pulmonary artery preparations taken from rats in which pulmonary hypertension was induced by exposure to a hypoxic environment (10% O2) for 14 days. Control rats were housed in room air. 2. All preparations in which the endothelium was left intact relaxed in response to acetylcholine (43 +/- 4% and 54 +/- 9%, reversal of the noradrenaline-induced contraction in control and hypoxic rats, respectively) indicating that the endothelium was functional in both groups of rats. 3. Exposure of the preparations to Ca(2+)-free physiological salt solution containing 2 mM EGTA for 30-40 min had no effect on preparations from control rats but caused relaxation in preparations from hypoxic rats. The relaxation (taken as a measure of the inherent tone in the preparations) was larger in preparations without endothelium (14.5 +/- 1.9 mN mm-2; n = 5) than in preparations with endothelium (9.1 +/- 1.2 mN mm-2; n = 5). 4. In preparations from hypoxic rats the magnitudes of the contractions to 80 mM K+ and to noradrenaline (0.1 microM) were less than in preparations from control rats. This may have been because the preparations from hypoxic rats were already partially contracted due to the inherent tone. 5.The nitric oxide (NO) synthase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME, 0.1-1 100 microM)had negligible effect on preparations from control rats or on endothelium-denuded preparations from hypoxic rats, but produced concentration-dependent contractions (maximum contraction 7.4 +/- 0.7 mN mm-2 (n = 4) with 100 micro M) in endothelium-intact preparations from hypoxic rats. This effect of L-NAME was prevented by L-arginine (1 mM) but not by D-arginine (1 mM).6. Contractions to L-NAME were also seen in endothelium-intact arteries from control rats if the preparations were first partially contracted by exposure to K+, endothelin, U46619 (thromboxane mimetic)or noradrenaline.7 It is concluded that isolated pulmonary artery rings from hypoxic rats, but not those from control rats, have substantial inherent tone. This inherent tone is normally attenuated by the generation of an endothelium-derived factor that is probably NO. A stimulus for the release of NO from the endothelium may be the contraction of the underlying smooth muscle, whether the contraction is inherent in the tissue, as in preparations from hypoxic rats, or is induced by a vasoconstrictor spasmogen.
摘要
  1. 在从暴露于低氧环境(10%氧气)14天诱导出肺动脉高压的大鼠身上获取的离体肺动脉标本中,研究了其固有收缩张力及其受内皮细胞的调节作用。对照大鼠饲养在正常空气中。2. 所有内皮完整的标本对乙酰胆碱均有舒张反应(分别使对照大鼠和低氧大鼠中去甲肾上腺素诱导的收缩反转了43±4%和54±9%),这表明两组大鼠的内皮均有功能。3. 将标本暴露于含2 mM EGTA的无钙生理盐溶液中30 - 40分钟,对对照大鼠的标本无影响,但使低氧大鼠的标本出现舒张。无内皮标本的舒张(作为标本固有张力的指标)(14.5±1.9 mN·mm⁻²;n = 5)比有内皮标本(9.1±1.2 mN·mm⁻²;n = 5)更大。4. 在低氧大鼠的标本中,对80 mM钾离子和去甲肾上腺素(0.1 μM)的收缩幅度小于对照大鼠的标本。这可能是因为低氧大鼠的标本由于固有张力已经部分收缩。5. 一氧化氮(NO)合酶抑制剂NG - 硝基 - L - 精氨酸甲酯(L - NAME,0.1 - 100 μM)对对照大鼠的标本或低氧大鼠的去内皮标本影响可忽略不计,但在低氧大鼠的内皮完整标本中产生浓度依赖性收缩(100 μM时最大收缩为7.4±0.7 mN·mm⁻²(n = 4))。L - 精氨酸(1 mM)可阻止L - NAME的这种作用,而D - 精氨酸(1 mM)则不能。6. 如果先将对照大鼠的内皮完整动脉标本通过暴露于钾离子、内皮素、U46619(血栓素类似物)或去甲肾上腺素使其部分收缩,也会出现对L - NAME的收缩反应。7. 得出的结论是,低氧大鼠的离体肺动脉环有显著的固有张力,而对照大鼠的则没有。这种固有张力通常被一种可能是NO的内皮衍生因子的产生所减弱。内皮释放NO的刺激可能是其下方平滑肌的收缩,无论这种收缩是组织固有的,如低氧大鼠标本中的情况,还是由血管收缩剂致痉剂诱导的。

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