Billig H, Thelander H, Rosberg S
Department of Physiology, University of Göteborg, Sweden.
Endocrinology. 1988 Jan;122(1):52-61. doi: 10.1210/endo-122-1-52.
The influence of nonmetabolizable adenosine analogs on cAMP production was investigated in preovulatory rat granulosa cells. 5'-(N-ethyl)Carboxamido-adenosine (NECA), a stimulatory A2-adenosine receptor agonist, stimulated cAMP accumulation, and NECA and 2-chloro-adenosine also potentiated the response to FSH. The adenosine receptor antagonist 8-phenyltheophylline antagonized the effect of NECA, shown by a shift in the dose-response curve to the right. The stimulatory effect of NECA was also seen in an ovarian membrane preparation, where NECA stimulated adenylate cyclase in both the presence and absence of FSH. The stimulatory effect of NECA was also decreased by 8-phenyltheophylline in this preparation. The A1-receptor agonists N6-(R-phenyl-isopropyl)-adenosine (R-PIA) and N6-(S-phenyl-isopropyl)-adenosine (S-PIA) both inhibited FSH-stimulated cAMP accumulation. The inhibitory effects of R-PIA and S-PIA, but not the stimulatory effects of NECA, could be counteracted by dipyridamole, a nucleoside transport inhibitor. Furthermore, R-PIA and S-PIA inhibited adenosine uptake into granulosa cells. Thus, the inhibitory effects of R-PIA and S-PIA are not likely to be mediated via membrane-bound inhibitory A1-adenosine receptors. Neither the stimulatory effects of NECA nor the inhibitory effects of R- and S-PIA could be attributed to changes in ATP levels, since the ATP levels were unaffected by these analogs. The results of this study indicate the existence of stimulatory A2-adenosine receptors in preovulatory rat granulosa cells and suggest a membrane-associated modulatory role of adenosine in preovulatory granulosa cells.
在排卵前大鼠颗粒细胞中研究了不可代谢的腺苷类似物对环磷酸腺苷(cAMP)生成的影响。5'-(N-乙基)羧酰胺腺苷(NECA),一种刺激性A2-腺苷受体激动剂,刺激了cAMP的积累,并且NECA和2-氯腺苷也增强了对促卵泡激素(FSH)的反应。腺苷受体拮抗剂8-苯基茶碱拮抗NECA的作用,表现为剂量反应曲线右移。在卵巢膜制剂中也观察到NECA的刺激作用,其中NECA在有和没有FSH的情况下均刺激腺苷酸环化酶。在该制剂中,8-苯基茶碱也降低了NECA的刺激作用。A1受体激动剂N6-(R-苯基-异丙基)腺苷(R-PIA)和N6-(S-苯基-异丙基)腺苷(S-PIA)均抑制FSH刺激的cAMP积累。核苷转运抑制剂双嘧达莫可以抵消R-PIA和S-PIA的抑制作用,但不能抵消NECA的刺激作用。此外,R-PIA和S-PIA抑制颗粒细胞对腺苷的摄取。因此,R-PIA和S-PIA的抑制作用不太可能通过膜结合的抑制性A1-腺苷受体介导。NECA的刺激作用和R-及S-PIA的抑制作用均不能归因于ATP水平的变化,因为这些类似物未影响ATP水平。本研究结果表明排卵前大鼠颗粒细胞中存在刺激性A2-腺苷受体,并提示腺苷在排卵前颗粒细胞中具有膜相关的调节作用。