Division of Cellular Pharmacology, Department of Pharmacology, Escola Paulista de Medicina, Universidade Federal de São Paulo (EPM/UNIFESP), São Paulo, Brazil.
Division of Cellular Pharmacology, Department of Pharmacology, Escola Paulista de Medicina, Universidade Federal de São Paulo (EPM/UNIFESP), São Paulo, Brazil
J Pharmacol Exp Ther. 2018 Jul;366(1):75-83. doi: 10.1124/jpet.118.247734. Epub 2018 Apr 23.
In the respiratory tract, intracellular cAMP has a key role in the smooth muscle relaxation induced by the -adrenoceptor/Gs protein/adenylyl cyclase axis. In other tissues, cAMP also works as an extracellular messenger, after its efflux and interstitial conversion to adenosine by ectoenzymes. The aim of this study was to identify cAMP efflux and the "extracellular cAMP-adenosine pathway" in the airway smooth muscle. First, we tested the ability of -adrenoceptor agonists formoterol or fenoterol to increase the extracellular cAMP in isolated tracheal rings from adult male Wistar rats. The effects of adenosine, cAMP, 8-Br-cAMP, fenoterol, or formoterol were also evaluated in the isometric contraction of control or carbachol (CCh) precontracted tracheas, normalized as the percentage of CCh-induced response. Fenoterol and formoterol induced 70%-80% relaxation and increased extracellular cAMP levels by up to 280%-450%. Although exogenous cAMP or adenosine evoked phasic contractions, the membrane-permeable cAMP analog 8-Br-cAMP induced relaxation of CCh-precontracted tracheas. The simultaneous inhibition of adenosine degradation/uptake with EHNA [erythro9-(2-hydroxy-3-nonyl) adenine hydrochloride] plus uridine increased by 3-fold the maximum cAMP-induced contraction, whereas it was significantly reduced by AMPCP [adenosine 5'-(,-methylene)diphosphate; an ecto-5'-nucleotidase inhibitor], and by adenosine receptor antagonists CGS-15943 (nonselective) or DPCPX (8-cyclopentyl-1,3-dipropylxanthine) (A selective). Finally, CGS-15943 shifted to the left the concentration-relaxation curve for fenoterol. In conclusion, our results show that airway smooth muscle expresses the extracellular cAMP-adenosine pathway associated with contracting effects mediated by A receptors. The cAMP efflux triggered by fenoterol/formoterol indicates that the extracellular cAMP-adenosine pathway may play a role in balancing the relaxant effects of -adrenoceptor agonists in airways, which may impact their bronchodilation effects.
在呼吸道中,细胞内的 cAMP 在β-肾上腺素能受体/Gs 蛋白/腺苷酸环化酶轴诱导的平滑肌松弛中起着关键作用。在其他组织中,cAMP 也作为细胞外信使发挥作用,在其通过细胞外酶流出并在细胞间隙转化为腺苷后。本研究的目的是鉴定气道平滑肌中的 cAMP 外排和“细胞外 cAMP-腺苷途径”。首先,我们测试了β-肾上腺素能激动剂福莫特罗或特布他林增加成年雄性 Wistar 大鼠离体气管环细胞外 cAMP 的能力。还评估了腺苷、cAMP、8-Br-cAMP、特布他林或福莫特罗在对照或卡巴可(CCh)预收缩气管的等长收缩中的作用,以 CCh 诱导反应的百分比表示。福莫特罗和特布他林诱导 70%-80%的松弛,并将细胞外 cAMP 水平提高 280%-450%。尽管外源性 cAMP 或腺苷诱发了相性收缩,但膜通透的 cAMP 类似物 8-Br-cAMP 诱导了 CCh 预收缩气管的松弛。EHNA[盐酸红霉素 9-(2-羟基-3-壬基)腺嘌呤]加尿嘧啶同时抑制腺苷降解/摄取,将最大 cAMP 诱导收缩增加 3 倍,而 AMPCP[腺苷 5'-(,-亚甲基)二磷酸;一种外切 5'-核苷酸酶抑制剂]和腺苷受体拮抗剂 CGS-15943(非选择性)或 DPCPX(8-环戊基-1,3-二丙基黄嘌呤)(A 选择性)显著降低。最后,CGS-15943 将福莫特罗的浓度-松弛曲线向左移动。总之,我们的结果表明,气道平滑肌表达与 A 受体介导的收缩作用相关的细胞外 cAMP-腺苷途径。福莫特罗/特布他林触发的 cAMP 外排表明,细胞外 cAMP-腺苷途径可能在平衡β-肾上腺素能受体激动剂在气道中的松弛作用方面发挥作用,这可能影响它们的支气管扩张作用。