首页> 外文期刊>American Journal of Physiology >Sensitization of pelvic afferent nerves in the in vitro rat urinary bladder-pelvic nerve preparation by purinergic agonists and cyclophosphamide pretreatment
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Sensitization of pelvic afferent nerves in the in vitro rat urinary bladder-pelvic nerve preparation by purinergic agonists and cyclophosphamide pretreatment

机译:嘌呤能激动剂和环磷酰胺预处理可敏化体外大鼠膀胱-盆腔神经制剂中的盆腔传入神经

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摘要

Effects of purinergic agonists (alpha,beta-meATP and ATP) and cyclophosphamide-induced cystitis on bladder afferent nerve (BAN) activity were studied in an in vitro bladder-pelvic nerve preparation. Distension of the bladder induced spontaneous bladder contractions that were accompanied by multiunit afferent firing. Intravesical administration of 40 and 130 muM alpha,beta-meATP increased afferent firing from 27 +- 3 to 53 +- 6 and 61 +- 2 spikes/s, respectively, but did not change the maximum amplitude of spontaneous bladder contractions. Electrical stimulation on the surface of the bladder elicited action potentials (AP) in BAN. alpha,beta-meATP decreased the voltage threshold from 9.0 +- 1.2 to 3.5 +- 0.5 V (0.15-ms pulse duration) and increased the area of the APs (82% at 80-V stimulus intensity). These effects were blocked by TNP-ATP (30 muM). ATP (2 mM) applied in the bath produced similar changes in BAN activity. These effects were blocked by bath application of PPADS (30 muM). Neither TNP-ATP nor PPADS affected BAN activity induced by distension of the bladder. Cystitis induced by pretreatment of the rats with cyclophosphamide (100 mg/kg ip) increased afferent firing in response to isotonic bladder distension (10-40 cmH_2O), decreased the threshold, and increased the area of evoked APs. The increase in afferent firing at 10 cmH_2O intravesical pressure was reduced 52% by PPADS. These results indicate that purinergic agonists acting on P2X receptors and cystitis induced by cyclophosphamide can increase excitability of the BANs.
机译:在体外膀胱-盆腔神经制剂中研究了嘌呤能激动剂(α,β-meATP和ATP)和环磷酰胺诱导的膀胱炎对膀胱传入神经(BAN)活性的影响。膀胱膨胀引起自发性膀胱收缩,并伴有多单位传入性放电。膀胱内给予40和130μMα,β-meATP可使传入放电分别从27±3增加到53±6和61±2尖峰/秒,但没有改变自发性膀胱收缩的最大幅度。膀胱表面的电刺激在BAN中引起动作电位(AP)。 α,β-meATP将电压阈值从9.0 +-1.2降低到3.5 +-0.5 V(0.15毫秒脉冲持续时间),并增加了AP的面积(在80 V刺激强度下为82%)。这些作用被TNP-ATP(30μM)阻断。浴液中的ATP(2 mM)产生了类似的BAN活性变化。这些作用被PPADS(30μM)的沐浴作用所阻断。 TNP-ATP和PPADS均不影响由膀胱扩张引起的BAN活性。用环磷酰胺(100 mg / kg ip ip)预处理大鼠诱发的膀胱炎,可响应等渗性膀胱扩张(10-40 cmH_2O)而增加传入放电,降低阈值,并增加诱发的AP面积。通过PPADS,在10 cmH_2O的膀胱内压力下传入放电的增加减少了52%。这些结果表明,作用于环磷酰胺诱导的P2X受体和膀胱炎的嘌呤能激动剂可以增加BAN的兴奋性。

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