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外源性三磷酸腺苷(ATP)、腺苷、三磷酸鸟苷(GTP)和鸟苷对大鼠肠系膜动脉血管张力和环核苷酸积累的内皮依赖性和非内皮依赖性作用。

Endothelium-dependent and -independent effects of exogenous ATP, adenosine, GTP and guanosine on vascular tone and cyclic nucleotide accumulation of rat mesenteric artery.

作者信息

Vuorinen P, Pörsti I, Metsä-Ketelä T, Manninen V, Vapaatalo H, Laustiola K E

机构信息

Department of Biomedical Sciences, University of Tampere, Finland.

出版信息

Br J Pharmacol. 1992 Feb;105(2):279-84. doi: 10.1111/j.1476-5381.1992.tb14246.x.

DOI:10.1111/j.1476-5381.1992.tb14246.x
PMID:1313722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908667/
Abstract
  1. The effects of exogenous guanosine 5'-triphosphate (GTP) and guanosine on vascular tone and cyclic nucleotide accumulation of noradrenaline-precontracted endothelium-intact and endothelium-denuded rat mesenteric artery rings were compared with the effects of the known purinoceptor agonists adenosine 5'-triphosphate (ATP) and adenosine. 2. GTP (10 microM-1 mM) dose-dependently relaxed endothelium-intact mesenteric artery rings by producing a rapid initial response followed by sustained relaxation resembling the relaxant response to acetylcholine. GTP also slightly relaxed endothelium-denuded artery rings. The acetylcholine- and GTP-induced relaxations of endothelium-intact rings were attenuated by NG-nitro L-arginine methyl ester (L-NAME, 330 microM) which attenuation was reversed with L-arginine (1 mM). 3. Guanosine (10 microM-1 mM) relaxed both endothelium-intact and -denuded artery rings in a dose-dependent manner. The relaxations were more pronounced in endothelium-intact preparations and were only slightly attenuated by L-NAME (330 microM). 4. ATP (1 microM-1 mM) and adenosine (10 microM-1 mM) dose-dependently relaxed endothelium-intact and -denuded artery rings. The responses were more pronounced in endothelium-intact vascular preparations. 5. GTP (100 microM) and guanosine (100 microM) increased guanosine 3':5'-cyclic monophosphate (cyclic GMP) accumulation in both endothelium-intact and -denuded artery rings corresponding to the relaxations observed. The concentrations of adenosine 3':5'-cyclic monophosphate (cyclic AMP) were not affected. 6. ATP (100 microM) increased cyclic GMP concentration of endothelium-intact artery rings. The concentrations of cyclic AMP were not affected by ATP (100 microM) and adenosine (100 microM) in endothelium-intact and -denuded vascular preparations.7. These results provide evidence that exogenous GTP and guanosine relax precontracted endothelium-intact and -denuded rat mesenteric artery rings by increasing cyclic GMP accumulation. The response to GTP of endothelium-intact rings can mainly be explained by the release of endothelium-derived relaxing factor (EDRF), but that of guanosine is only partly due to EDRF, and is a combination of endothelium-dependent and -independent effects. The endothelium-independent response of GTP and guanosine is a direct, unknown effect on smooth muscle and guanylate cyclase.
摘要
  1. 将外源性鸟苷 5'-三磷酸(GTP)和鸟苷对去甲肾上腺素预收缩的完整内皮和去内皮大鼠肠系膜动脉环的血管张力及环核苷酸积累的影响,与已知嘌呤受体激动剂腺苷 5'-三磷酸(ATP)和腺苷的作用进行比较。2. GTP(10 μM - 1 mM)以剂量依赖方式使完整内皮的肠系膜动脉环舒张,产生快速的初始反应,随后是持续舒张,类似于对乙酰胆碱的舒张反应。GTP 也使去内皮动脉环略有舒张。NG-硝基-L-精氨酸甲酯(L-NAME,330 μM)减弱了完整内皮环由乙酰胆碱和 GTP 诱导的舒张,而 L-精氨酸(1 mM)可逆转这种减弱。3. 鸟苷(10 μM - 1 mM)以剂量依赖方式使完整内皮和去内皮的动脉环舒张。在完整内皮的标本中舒张更明显,且仅被 L-NAME(330 μM)轻微减弱。4. ATP(1 μM - 1 mM)和腺苷(10 μM - 1 mM)以剂量依赖方式使完整内皮和去内皮的动脉环舒张。在完整内皮的血管标本中反应更明显。5. GTP(100 μM)和鸟苷(100 μM)使完整内皮和去内皮的动脉环中鸟苷 3':5'-环一磷酸(环鸟苷酸)积累增加,这与观察到的舒张相对应。腺苷 3':5'-环一磷酸(环腺苷酸)的浓度未受影响。6. ATP(100 μM)增加了完整内皮动脉环的环鸟苷酸浓度。在完整内皮和去内皮的血管标本中,ATP(100 μM)和腺苷(100 μM)均未影响环腺苷酸的浓度。7. 这些结果表明,外源性 GTP 和鸟苷通过增加环鸟苷酸积累使预收缩的完整内皮和去内皮大鼠肠系膜动脉环舒张。完整内皮环对 GTP 的反应主要可由内皮源性舒张因子(EDRF)的释放来解释,但鸟苷的反应仅部分归因于 EDRF,是内皮依赖性和非依赖性作用的组合。GTP 和鸟苷的非内皮依赖性反应是对平滑肌和鸟苷酸环化酶的直接且未知的作用。

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