Frew R, Lundy P M
Eur J Pharmacol. 1982 Jul 9;81(2):333-6. doi: 10.1016/0014-2999(82)90453-8.
THe adenosine-sensitive P1 purinoceptor antagonists 8-phenyl theophylline and 8-(p-bromophenyl)theophylline (4 microM) antagonized ATP-induced relaxation of spontaneous tone in guinea pig stomach, but caused no significant modification of relaxation to electrical field stimulation (0.2 - 10 Hz, 1 msec for 30 sec, atropine 1.5 microM, and guanethidine 4 microM treated). These results suggest that in fundic muscle ATP acts via hydrolysis to adenosine, with subsequent activation of P1 purinoceptors, and that ATP is not the nonadrenergic, noncholinergic inhibitory transmitter in stomach fundus.
腺苷敏感的P1嘌呤受体拮抗剂8-苯基茶碱和8-(对溴苯基)茶碱(4微摩尔)拮抗ATP诱导的豚鼠胃自发张力松弛,但对电场刺激(0.2 - 10赫兹,1毫秒,持续30秒,经1.5微摩尔阿托品和4微摩尔胍乙啶处理)引起的松弛无显著影响。这些结果表明,在胃底肌中,ATP通过水解为腺苷起作用,随后激活P1嘌呤受体,并且ATP不是胃底的非肾上腺素能、非胆碱能抑制性递质。