Coleman R A
Br J Pharmacol. 1980 Jul;69(3):359-66. doi: 10.1111/j.1476-5381.1980.tb07022.x.
1 To test the possibility that adenosine receptors exist within the trachea of the guinea-pig, an attempt has been made to identify a compound with adenosine antagonist activity in this tissue.2 Quinidine, phentolamine, phenoxybenzamine, 2-2'-pyridylisatogen tosylate (PIT) and caffeine were tested for antagonism of spasmolytic responses to adenosine, adenosine 5'-triphosphate (ATP) and adenine on the guinea-pig isolated trachea.3 Quinidine (10 and 25 mug/ml), phentolamine (10 and 30 mug/ml) and phenoxybenzamine (10 mug/ml) had little or no effect on response to adenosine, ATP and adenine. PIT (21 mug/ml) potentiated responses to adenosine, ATP and adenine by an unexplained mechanism.4 Caffeine (25 mug/ml) partially relaxed the trachea and inhibited spasmolytic responses to both adenosine and ATP, but not to adenine, isoprenaline, aminophylline or prostaglandin E(2) (PGE(2)).5 A number of compounds related to caffeine (xanthine, hypoxanthine, theophylline and theobromine) were tested for adenosine antagonist activity. Xanthine (300 mug/ml) and hypoxanthine (300 mug/ml) did not relax the trachea or antagonize spasmolytic responses to adenosine. Both theophylline (10 mug/ml) and theobromine (30 mug/ml) partially relaxed the trachea; theophylline, but not theobromine, antagonized spasmolytic responses to adenosine.6 pA(2) values for caffeine and theophylline as antagonists of adenosine were 4.3 and 4.7 respectively. However, the slopes of the Schild plot regressions were significantly less than 1.0 for both compounds.7 Four compounds, adenine, AH 8883, M30966 and ICI 63197, which like caffeine and theophylline, have phosphodiesterase inhibitory activity were tested for adenosine antagonist activity in the trachea. Adenine and AH 8883 had no effect and M30966 and ICI 63197 caused significant potentiation.8 The effects of caffeine and theophylline were also investigated on the non-adrenergic inhibitory response to nerve stimulation (NAIR). Both caffeine (100 mug/ml, n = 4) and theophylline (30 mug/ml, n = 4) enhanced the NAIR (20 Hz) while virtually abolishing matched responses to exogenous adenosine.9 The results support the existence of adenosine receptors in the guinea-pig trachea.
为了验证豚鼠气管中是否存在腺苷受体,已尝试在该组织中鉴定具有腺苷拮抗剂活性的化合物。
对奎尼丁、酚妥拉明、酚苄明、2-2'-吡啶异吲哚啉对甲苯磺酸盐(PIT)和咖啡因进行了测试,以观察它们对豚鼠离体气管中腺苷、5'-三磷酸腺苷(ATP)和腺嘌呤的解痉反应的拮抗作用。
奎尼丁(10和25微克/毫升)、酚妥拉明(10和30微克/毫升)和酚苄明(10微克/毫升)对腺苷、ATP和腺嘌呤的反应几乎没有影响。PIT(21微克/毫升)通过一种不明机制增强了对腺苷、ATP和腺嘌呤的反应。
咖啡因(25微克/毫升)使气管部分松弛,并抑制对腺苷和ATP的解痉反应,但对腺嘌呤、异丙肾上腺素、氨茶碱或前列腺素E2(PGE2)无此作用。
对一些与咖啡因相关的化合物(黄嘌呤、次黄嘌呤、茶碱和可可碱)进行了腺苷拮抗剂活性测试。黄嘌呤(300微克/毫升)和次黄嘌呤(300微克/毫升)未使气管松弛,也未拮抗对腺苷的解痉反应。茶碱(10微克/毫升)和可可碱(30微克/毫升)均使气管部分松弛;茶碱可拮抗对腺苷的解痉反应,而可可碱则无此作用。
咖啡因和茶碱作为腺苷拮抗剂的pA2值分别为4.3和4.7。然而,这两种化合物的Schild图回归斜率均显著小于1.0。
对四种与咖啡因和茶碱一样具有磷酸二酯酶抑制活性的化合物——腺嘌呤、AH 8883、M30966和ICI 63197——进行了气管中腺苷拮抗剂活性测试。腺嘌呤和AH 8883无作用,M30966和ICI 63197则引起显著增强。
还研究了咖啡因和茶碱对神经刺激的非肾上腺素能抑制反应(NAIR)的影响。咖啡因(100微克/毫升,n = 4)和茶碱(30微克/毫升,n = 4)均增强了NAIR(20赫兹),同时几乎消除了对外源性腺苷的相应反应。
结果支持豚鼠气管中存在腺苷受体。