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环磷酸鸟苷参与腺苷诱导的、年龄依赖性血管舒张的证据。

Evidence for the involvement of cyclic GMP in adenosine-induced, age-dependent vasodilatation.

作者信息

Moritoki H, Matsugi T, Takase H, Ueda H, Tanioka A

机构信息

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

出版信息

Br J Pharmacol. 1990 Jul;100(3):569-75. doi: 10.1111/j.1476-5381.1990.tb15848.x.

DOI:10.1111/j.1476-5381.1990.tb15848.x
PMID:2167736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917775/
Abstract
  1. Adenosine-induced dilatation of rat aorta was present in aorta taken from 4 week-old rats, attenuated with increase in age of rats to 8 weeks, and was virtually absent in the aorta from 12 week-old rats. 2. Removal of the endothelium by mechanical rubbing attenuated adenosine-induced dilatation. 3. Haemoglobin and methylene blue partly reversed the adenosine-induced endothelium-dependent dilatation. 4. The order of potency of adenosine derivatives was 5'-(N-ethylcarboxamido)adenosine (NECA) greater than 2-phenylaminoadenosine (CV-1808) greater than 2-chloroadenosine greater than N6-([R]-[-]-phenylisopropyl)adenosine (R-PIA) greater than adenosine greater than N6-cyclohexyladenosine (CHA) greater than N6-([S]-[+]-phenylisopropyl)adenosine (S-PIA), indicating that adenosine receptors mediating the dilatation are of the A2 subtype. 5. [3H]-NECA bound to preparations of membranes from rats of 4 weeks old; it was displaced more effectively by NECA and the A2 ligand CV-1808 than by the A1 ligands CHA and S-PIA. ligands CHA and S-PIA. 6. The number but not affinity of specific binding sites for NECA decreased considerably with increase in age of rats to 8 weeks, and binding sites for [3H]-NECA were hardly detected in membrane preparations from rats of 20 weeks old. 7. Adenosine caused a marked increase in cyclic GMP production, but did not induce an increase in the cyclic AMP level. 8. This increase in cyclic GMP production induced by adenosine was abolished by methylene blue or 8-phenyltheophylline, or by removal of the endothelium. 9. The age-associated decrease in adenosine-induced dilatation was found to be associated with a reduction in the formation of cyclic GMP, but not of cyclic AMP. 10. These results suggest that adenosine causes dilatation via A2 receptors by inducing production of an endothelium-derived relaxing factor (EDRF), which in turn stimulates soluble guanylate cyclase, and so increases production of cyclic GMP. It is also suggested that the main reason for the age-associated decrease in adenosine-induced dilatation is a decrease in the number of A2-receptors or the ability of the endothelium to produce EDRF, leading to decreased production of cyclic GMP.
摘要
  1. 腺苷诱导的大鼠主动脉扩张在4周龄大鼠的主动脉中存在,随着大鼠年龄增长至8周而减弱,在12周龄大鼠的主动脉中几乎不存在。2. 通过机械摩擦去除内皮会减弱腺苷诱导的扩张。3. 血红蛋白和亚甲蓝部分逆转了腺苷诱导的内皮依赖性扩张。4. 腺苷衍生物的效力顺序为5'-(N-乙基甲酰胺基)腺苷(NECA)大于2-苯氨基腺苷(CV-1808)大于2-氯腺苷大于N6-([R]-[-]-苯异丙基)腺苷(R-PIA)大于腺苷大于N6-环己基腺苷(CHA)大于N6-([S]-[+]-苯异丙基)腺苷(S-PIA),表明介导扩张的腺苷受体是A2亚型。5. [3H]-NECA与4周龄大鼠的膜制剂结合;NECA和A2配体CV-1808比A1配体CHA和S-PIA更有效地取代它。6. 随着大鼠年龄增长至8周,NECA特异性结合位点的数量而非亲和力显著下降,在20周龄大鼠的膜制剂中几乎检测不到[3H]-NECA的结合位点。7. 腺苷导致环鸟苷酸(cGMP)生成显著增加,但未诱导环磷酸腺苷(cAMP)水平升高。8. 腺苷诱导的这种cGMP生成增加被亚甲蓝或8-苯基茶碱或去除内皮所消除。9. 发现腺苷诱导的扩张与年龄相关的下降与cGMP形成减少有关,而非cAMP形成减少有关。10. 这些结果表明,腺苷通过诱导内皮衍生舒张因子(EDRF)的产生,经由A2受体引起扩张,EDRF进而刺激可溶性鸟苷酸环化酶,从而增加cGMP的生成。还表明,腺苷诱导的扩张与年龄相关下降的主要原因是A2受体数量减少或内皮产生EDRF的能力下降,导致cGMP生成减少。

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Adenosine relaxes the aorta by interacting with an A2 receptor and an intracellular site.腺苷通过与A2受体及细胞内位点相互作用,使主动脉舒张。
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Agonist-induced endothelium-dependent relaxation in rat thoracic aorta may be mediated through cGMP.激动剂诱导的大鼠胸主动脉内皮依赖性舒张可能通过环磷酸鸟苷(cGMP)介导。
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