Christofi F L, Cook M A
Can J Physiol Pharmacol. 1985 Sep;63(9):1195-7. doi: 10.1139/y85-196.
The inhibitory effect of the putative adenosine A2 receptor agonist 5'-N-ethylcarboxamidoadenosine (NECA) on acetylcholine release from the stimulated guinea pig ileum preparation and the nature of its antagonism by theophylline were investigated. NECA was shown to inhibit the response of the ileum preparation in a dose-dependent fashion, and an EC50 value of 1.62 X 10(-8) M was determined. This value was comparable with that determined for the A1 receptor agonist N6-R-phenylisopropyladenosine (R-PIA) (2.57 X 10(-8) M) using the same preparation. Competitive antagonism of the inhibitory effect of NECA by theophylline was quantitated and a pA2 value of 5.04 for the methylxanthine was obtained. This value was similar to those obtained previously for R-PIA and adenosine itself and suggests that these nucleosides may be interacting with the same receptor site on myenteric nerve endings. These findings do not permit the designation of the receptor as an A1 or A2 subtype according to current criteria.
研究了假定的腺苷A2受体激动剂5'-N-乙基羧基酰胺腺苷(NECA)对刺激的豚鼠回肠标本中乙酰胆碱释放的抑制作用,以及茶碱对其拮抗作用的性质。结果表明,NECA以剂量依赖性方式抑制回肠标本的反应,测定的EC50值为1.62×10^(-8)M。该值与使用相同标本测定的A1受体激动剂N6-R-苯基异丙基腺苷(R-PIA)(2.57×10^(-8)M)的值相当。对茶碱对NECA抑制作用的竞争性拮抗作用进行了定量分析,得到该甲基黄嘌呤的pA2值为5.04。该值与先前获得的R-PIA和腺苷本身的值相似,表明这些核苷可能与肠肌间神经末梢上的同一受体位点相互作用。根据目前的标准,这些发现无法将该受体指定为A1或A2亚型。