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P2受体介导反应的温度依赖性。

Temperature dependency of P2 receptor-mediated responses.

作者信息

Ziganshin Airat U, Rychkov Alexey V, Ziganshina Lilia E, Burnstock Geoffrey

机构信息

Department of Pharmacology, Kazan State Medical University, Kazan, Russia.

出版信息

Eur J Pharmacol. 2002 Dec 5;456(1-3):107-14. doi: 10.1016/s0014-2999(02)02655-9.

Abstract

The P2 receptor-mediated responses of isolated guinea pig urinary bladder and vas deferens (P2X receptors) and taenia caeci (P2Y receptors) were registered at the three temperature conditions of 30, 37 and 42 degrees C. The contractile responses of both urinary bladder and vas deferens to a P2X receptor agonist alpha,beta-methylene ATP (alpha,beta-meATP; 0.01-30 microM) and to electrical field stimulation (1-64 Hz, 0.1 ms, supramaximal voltage) in the presence of atropine (0.1 microM) and phentolamine (1 microM) were markedly more prominent at a temperature of 30 degrees C than at 37 or 42 degrees C. Similarly, relaxation of carbachol-precontracted taenia caeci caused by electrical field stimulation (0.5-8 Hz, 0.1 ms, supramaximal voltage) temperature-dependently increased with decrease of temperature, while relaxation of this tissue by exogenous ATP (1-100 microM) was not affected by the temperature. A P2 receptor antagonist pyridoxalphosphate-6-azophenyl-2',4'-disulphonic acid (PPADS, 1-30 microM) at all three temperature conditions concentration-dependently antagonised contractile responses to alpha,beta-methylene ATP and electrical field stimulation in both urinary bladder and vas deferens. PPADS, even at the highest concentration tested (30 microM), had no effect on the relaxant responses of the taenia caeci either to electrical field stimulation or ATP and its action was not affected by the change of temperature. It is concluded from this study that the effectiveness of P2 receptor-mediated responses in guinea pig urinary bladder, vas deferens and taenia caeci increases by decrease of temperature.

摘要

在30、37和42摄氏度这三种温度条件下,记录了分离的豚鼠膀胱、输精管(P2X受体)和盲肠带(P2Y受体)的P2受体介导反应。在存在阿托品(0.1微摩尔)和酚妥拉明(1微摩尔)的情况下,膀胱和输精管对P2X受体激动剂α,β-亚甲基ATP(α,β-meATP;0.01 - 30微摩尔)以及电场刺激(1 - 64赫兹,0.1毫秒,超最大电压)的收缩反应在30摄氏度时比在37或42摄氏度时明显更显著。同样,电场刺激(0.5 - 8赫兹,0.1毫秒,超最大电压)引起的卡巴胆碱预收缩盲肠带的松弛随温度降低而呈温度依赖性增加,而外源性ATP(1 - 100微摩尔)对该组织的松弛作用不受温度影响。P2受体拮抗剂磷酸吡哆醛 - 6 - 偶氮苯基 - 2',4'-二磺酸(PPADS,1 - 30微摩尔)在所有三种温度条件下均浓度依赖性地拮抗膀胱和输精管对α,β-亚甲基ATP和电场刺激的收缩反应。PPADS即使在测试的最高浓度(30微摩尔)下,对盲肠带对电场刺激或ATP的松弛反应也没有影响,并且其作用不受温度变化的影响。从这项研究得出结论,豚鼠膀胱、输精管和盲肠带中P2受体介导反应的有效性随温度降低而增加。

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