Spedding M, Weetman D F
Br J Pharmacol. 1978 Aug;63(4):659-64. doi: 10.1111/j.1476-5381.1978.tb17279.x.
1 2-2'-Pyridylisatogen tosylate (PIT) slowly relaxed taenia caeci preparationg of the guinea-pig in a concentration-dependent manner (threshold 2.5 muM). The relaxant effect did not show tachyphylaxis.2 The relaxation was not affected by tetrodotoxin (0.3 muM), guanethidine (17 muM) nor by a combination of phentolamine (36 muM) and propranolol (4 muM)3 In taenia caeci preparations suspended in K(+)-depolarizing, Ca(2+)-free Ringer, addition of Ca(2+) (0.1 to 30 mM) resulted in a slow contraction. PIT (50 muM) and papaverine (15 muM) antagonized these contractions, whereas indomethacin (28 muM) was ineffective.4 Although PIT (50 muM for 30 min) caused a relaxation of the taenia, and, when the tone of the preparations was restored with carbachol, antagonized adenosine 5'-triphosphate (ATP)-induced relaxations, relaxation of the taenia with papaverine (30 muM for 5 min) did not antagonize ATP-induced relaxations. It is concluded that the relaxant and ATP-receptor blocking actions of PIT are independent properties of the compound.
1 甲苯磺酸2-2'-吡啶异靛红(PIT)能以浓度依赖性方式缓慢舒张豚鼠盲肠带制备物(阈值为2.5 μM)。该舒张作用未表现出快速耐受性。
2 这种舒张不受河豚毒素(0.3 μM)、胍乙啶(17 μM)的影响,也不受酚妥拉明(36 μM)和普萘洛尔(4 μM)联合使用的影响。
3 在悬浮于K⁺去极化、无Ca²⁺的林格液中的盲肠带制备物中,加入Ca²⁺(0.1至30 mM)会导致缓慢收缩。PIT(50 μM)和罂粟碱(15 μM)可拮抗这些收缩,而吲哚美辛(28 μM)则无效。
4 尽管PIT(50 μM,作用30分钟)可使盲肠带舒张,并且当用卡巴胆碱恢复制备物的张力时,PIT可拮抗三磷酸腺苷(ATP)诱导的舒张,但罂粟碱(30 μM,作用5分钟)使盲肠带舒张却不能拮抗ATP诱导的舒张。结论是,PIT的舒张作用和ATP受体阻断作用是该化合物的独立特性。