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首页> 外文期刊>American Journal of Physiology >Sprouting of substance P-expressing primary afferent central terminals and spinal micturition reflex NK1 receptor dependence after spinal cord injury
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Sprouting of substance P-expressing primary afferent central terminals and spinal micturition reflex NK1 receptor dependence after spinal cord injury

机译:脊髓损伤后表达P物质的初级传入中枢末梢的发芽和脊髓排尿反射NK1受体依赖性

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Sprouting of substance P-expressing primary afferent central terminals and spinal micturition reflex NK1 receptor dependence after spinal cord injury. Am J Physiol Regul Integr Comp Physiol 295: R2084-R2096, 2008. First published October 22, 2008; doi:10.1152/ajpregu.90653.2008.-The primary afferent neurotrans-mitter triggering the spinal micturition reflex after complete spinal cord injury (SCI) in the rat is unknown. Substance P detected immunohistochemically in the sacral parasympathetic nucleus was significantly higher in 12 SCI rats than in 12jspinaHy intact rats (P = 0.008), suggesting substance P as a plausible candidate for the primary afferent neurotransmitter. The effects of the tachykinin NK1 receptor antagonist L-733060 on the spinal micturition reflex were then determined by performing conscious cystometry in an additional 14 intact rats and 14 SCI rats with L-733060 (0.1-100 |xg) administered intrathecally at L6-S1. L-733060 was without effect in intact rats, but blocked the spinal micturition reflex in 10 of 14 SCI rats and increased the intermicturition interval in 2 of 4 others at doses ranging from 10 to 100 |xg. Both phasic and nonphasic voiding contractions, differentiated according to the presence of phasic external urethral sphincter (EUS) activity, were present in most SCI rats. Both types of contractions were blocked by high doses of L-733060. Interestingly, there was a relative decline in phasic voiding contractions at high doses as well as a decline in contraction amplitude in nonphasic voiding contractions. In other respects, cystometric variables were largely unaffected in either spinally intact or SCI rats. L-733060 did not affect tonic EUS activity at any dose except when the spinal micturition reflex was blocked and tonic activity was consequently lost. These experiments show that tachykinin action at spinal NK1 receptors plays a major role in the spinal micturition reflex in SCI rats
机译:脊髓损伤后发芽表达P物质的初级传入中枢终末和对排尿反射NK1受体的依赖性。 Am J Physiol Regul Integr Comp Physiol 295:R2084-R2096,2008年。2008年10月22日首次发布; doi:10.1152 / ajpregu.90653.2008.-大鼠完全脊髓损伤(SCI)后触发脊髓排尿反射的主要传入神经递质是未知的。 12副交感神经核中免疫组化检测到的P物质在12例SCI大鼠中明显高于在12 spinaHy完整大鼠中(P = 0.008),表明P物质是主要传入神经递质的合理候选者。然后通过对另外14只完整大鼠和14只SCI大鼠进行L6-733060(0.1-100 | xg)鞘内注射L6-S1进行有意识的膀胱测压,确定速激肽NK1受体拮抗剂L-733060对脊髓排尿反射的影响。 。 L-733060在完整大鼠中无作用,但在10至100μg的剂量下,阻断了14只SCI大鼠中10只的脊髓排尿反射,并增加了4只其他大鼠中2只的排尿间隔。在大多数SCI大鼠中都存在根据阶段性尿道括约肌(EUS)活性而区分的阶段性和非阶段性排尿收缩。两种类型的收缩都被高剂量的L-733060阻断。有趣的是,高剂量时的相洞性空洞收缩相对减少,而非相洞性空洞性收缩的收缩幅度下降。在其他方面,在脊髓完整或SCI大鼠中,膀胱测压变量基本不受影响。 L-733060在任何剂量下均不影响强直性EUS活性,除非脊髓排尿反射受阻,因而强直性活性丧失。这些实验表明速激肽对脊髓NK1受体的作用在SCI大鼠脊髓排尿反射中起主要作用

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