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嘌呤受体激动剂对大鼠膀胱肥厚平滑肌的影响。

Effects of purinoceptor agonists on smooth muscle from hypertrophied rat urinary bladder.

作者信息

Sjuve R, Ingvarson T, Arner A, Uvelius B

机构信息

Department of Physiology and Biophysics, Lund University, Sweden.

出版信息

Eur J Pharmacol. 1995 Mar 24;276(1-2):137-44. doi: 10.1016/0014-2999(95)00027-i.

Abstract

Tension responses induced by the purinoceptor agonists ATP and the stable ATP analogue alpha, beta-methylene ATP were investigated in isolated muscle strips from normal and hypertrophic urinary bladders from the rat. Hypertrophy was induced by a partial ligation of the urethra giving an increase in mean bladder weight from 65 mg to 300 mg. Activation with ATP and alpha, beta-methylene ATP caused phasic, concentration-dependent, contractions. The sensitivity to ATP was about 100-fold lower than that for alpha, beta-methylene ATP. The force of the contractions induced by the purinoceptor agonists was significantly lower in the hypertrophied bladder compared to the controls. The kinetics of the ATP-induced responses was studied by photolytic release of ATP from caged-ATP in intact fibre bundles. The rate of contraction following photolytic release of ATP was slower, and the force amplitude lower, in the hypertrophic preparations compared to the controls. The results suggest changes in the purinoceptor function or in the responses of the contractile system to transient increases in intracellular Ca2+ in the hypertrophic bladder.

摘要

研究了嘌呤受体激动剂ATP和稳定的ATP类似物α,β-亚甲基ATP在正常和肥大大鼠膀胱分离肌条中诱导的张力反应。通过部分结扎尿道诱导肥大,使膀胱平均重量从65毫克增加到300毫克。ATP和α,β-亚甲基ATP激活引起相位性、浓度依赖性收缩。对ATP的敏感性比对α,β-亚甲基ATP的敏感性低约100倍。与对照组相比,嘌呤受体激动剂诱导的肥大膀胱收缩力明显更低。通过在完整纤维束中从笼状ATP光解释放ATP来研究ATP诱导反应的动力学。与对照组相比,肥大制剂中ATP光解释放后的收缩速率较慢,力幅较低。结果表明,肥大膀胱中嘌呤受体功能或收缩系统对细胞内Ca2+瞬时增加的反应发生了变化。

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