• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

神经完整或慢性脊髓横断大鼠膀胱条中,毒蕈碱对递质释放促进作用的频率依赖性

Frequency dependence of muscarinic facilitation of transmitter release in urinary bladder strips from neurally intact or chronic spinal cord transected rats.

作者信息

Somogyi G T, Zernova G V, Yoshiyama M, Yamamoto T, de Groat W C

机构信息

Department of Pharmacology, University of Pittsburgh, Pennsylvania 15261, USA.

出版信息

Br J Pharmacol. 1998 Sep;125(2):241-6. doi: 10.1038/sj.bjp.0702041.

DOI:10.1038/sj.bjp.0702041
PMID:9786494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1565611/
Abstract
  1. Electrical stimulation evoked release of 3H-noradrenaline (NA) and 14C-acetylcholine (ACh), as well as neurally evoked contractions were measured at various (1-40 Hz, 100 shocks) stimulation frequencies in bladder strips from neurally intact (NI) and spinal cord transected (SCT) rats. 2. The frequency response curves for ACh and NA release were shifted to the left in SCT bladder strips as compared to NI bladder strips. 3. Atropine (1 microM) depressed ACh release in NI bladder strips at high frequency stimulation (10 and 40 Hz) but not at low frequency stimulation (2-5 Hz). However, in SCT bladders, atropine depressed ACh release both at low and high frequencies of stimulation, indicating that muscarinic facilitation occurs at lower frequencies. 4. Atropine depressed the release of NA in NI bladders at only 40 Hz stimulation, but depressed release at all frequencies in SCT bladders. 5. The amplitude of neurally evoked contractions of bladder strips from NI rats was enhanced as the frequency of stimulation was increased from 1 to 40 Hz (80 shocks). The frequency response curve was shifted to the left in SCT bladders. Atropine blocked the neurally evoked contractions in SCT bladder strips to a greater extent than the contractions in NI strips indicating a cholinergic dominance in the SCT bladders. 6. Maximal contractile force of SCT bladder strips evoked by neural stimulation at 20 Hz 10 shocks and 80 shocks was significantly lower than that of NI bladder strips, whereas the release of ACh was significantly higher in SCT than NI bladders indicating a postjunctional defect in the SCT preparations. 7. It is suggested that presynaptic muscarinic facilitatory mechanisms are upregulated in the cholinergic and adrenergic nerve terminals in SCT bladders leading to a larger relative contractile response at lower frequencies of stimulation (2-5 Hz). Thus the hyperreflexic bladder occurring after spinal cord injury may be due in part to an enhancement of transmitter release at bladder postganglionic nerve terminals.
摘要
  1. 在来自神经完整(NI)和脊髓横断(SCT)大鼠的膀胱条上,于不同刺激频率(1 - 40 Hz,100次电击)下测量电刺激诱发的3H - 去甲肾上腺素(NA)和14C - 乙酰胆碱(ACh)释放以及神经诱发的收缩。2. 与NI膀胱条相比,SCT膀胱条中ACh和NA释放的频率响应曲线向左移动。3. 阿托品(1 microM)在高频刺激(10和40 Hz)时抑制NI膀胱条中的ACh释放,但在低频刺激(2 - 5 Hz)时不抑制。然而,在SCT膀胱中,阿托品在低频和高频刺激时均抑制ACh释放,表明毒蕈碱促进作用在较低频率时发生。4. 阿托品仅在40 Hz刺激时抑制NI膀胱中的NA释放,但在所有频率下均抑制SCT膀胱中的NA释放。5. 随着刺激频率从1增加到40 Hz(80次电击),NI大鼠膀胱条神经诱发收缩的幅度增强。SCT膀胱中的频率响应曲线向左移动。阿托品在SCT膀胱条中比在NI条中更大程度地阻断神经诱发的收缩,表明SCT膀胱中胆碱能占主导地位。6. 神经刺激在20 Hz、10次电击和80次电击时诱发的SCT膀胱条的最大收缩力明显低于NI膀胱条,而SCT中ACh的释放明显高于NI膀胱,表明SCT制剂中存在接头后缺陷。7. 提示SCT膀胱中胆碱能和肾上腺素能神经末梢的突触前毒蕈碱促进机制上调,导致在较低刺激频率(2 - 5 Hz)时产生更大的相对收缩反应。因此,脊髓损伤后出现的反射亢进膀胱可能部分归因于膀胱节后神经末梢递质释放的增强。

相似文献

1
Frequency dependence of muscarinic facilitation of transmitter release in urinary bladder strips from neurally intact or chronic spinal cord transected rats.神经完整或慢性脊髓横断大鼠膀胱条中,毒蕈碱对递质释放促进作用的频率依赖性
Br J Pharmacol. 1998 Sep;125(2):241-6. doi: 10.1038/sj.bjp.0702041.
2
Change in muscarinic modulation of transmitter release in the rat urinary bladder after spinal cord injury.脊髓损伤后大鼠膀胱中递质释放的毒蕈碱调节变化
Neurochem Int. 2003 Jul;43(1):73-7. doi: 10.1016/s0197-0186(02)00193-6.
3
M1 muscarinic receptor-induced facilitation of ACh and noradrenaline release in the rat bladder is mediated by protein kinase C.毒蕈碱M1受体诱导大鼠膀胱中乙酰胆碱和去甲肾上腺素释放的促进作用由蛋白激酶C介导。
J Physiol. 1996 Oct 1;496 ( Pt 1)(Pt 1):245-54. doi: 10.1113/jphysiol.1996.sp021681.
4
Prejunctional facilitatory alpha 1-adrenoceptors in the rat urinary bladder.大鼠膀胱中的接头前易化性α1肾上腺素能受体
Br J Pharmacol. 1995 Apr;114(8):1710-6. doi: 10.1111/j.1476-5381.1995.tb14961.x.
5
M1 muscarinic receptor-mediated facilitation of acetylcholine release in the rat urinary bladder.M1毒蕈碱受体介导大鼠膀胱中乙酰胆碱释放的促进作用。
J Physiol. 1994 Oct 1;480 ( Pt 1)(Pt 1):81-9. doi: 10.1113/jphysiol.1994.sp020342.
6
Role of L- and N-type Ca2+ channels in muscarinic receptor-mediated facilitation of ACh and noradrenaline release in the rat urinary bladder.L型和N型钙通道在毒蕈碱受体介导的大鼠膀胱乙酰胆碱和去甲肾上腺素释放促进中的作用
J Physiol. 1997 Mar 15;499 ( Pt 3)(Pt 3):645-54. doi: 10.1113/jphysiol.1997.sp021957.
7
Loss of caveolin-1 expression is associated with disruption of muscarinic cholinergic activities in the urinary bladder.小窝蛋白-1表达缺失与膀胱毒蕈碱胆碱能活性破坏有关。
Neurochem Int. 2004 Dec;45(8):1185-93. doi: 10.1016/j.neuint.2004.06.016.
8
Plasticity of non-adrenergic non-cholinergic bladder contractions in rats after chronic spinal cord injury.慢性脊髓损伤后大鼠非肾上腺素能非胆碱能膀胱收缩的可塑性。
Brain Res Bull. 2011 Aug 10;86(1-2):91-6. doi: 10.1016/j.brainresbull.2011.06.001. Epub 2011 Jun 13.
9
Receptor activated bladder and spinal ATP release in neurally intact and chronic spinal cord injured rats.神经功能正常和慢性脊髓损伤大鼠中受体激活的膀胱和脊髓ATP释放
Neurochem Int. 2007 Jan;50(2):345-50. doi: 10.1016/j.neuint.2006.09.002. Epub 2006 Oct 25.
10
Effect of cryoinjury on the contractile parameters of bladder strips: a model of impaired detrusor contractility.冷冻损伤对膀胱条收缩参数的影响:逼尿肌收缩功能受损的模型。
Brain Res Bull. 2002 Oct 15;59(1):23-8. doi: 10.1016/s0361-9230(02)00833-x.

引用本文的文献

1
Pathophysiology of Overactive Bladder and Pharmacologic Treatments Including β3-Adrenoceptor Agonists -Basic Research Perspectives.膀胱过度活动症的病理生理学及包括β3肾上腺素能受体激动剂在内的药物治疗——基础研究视角
Int Neurourol J. 2024 Feb;28(Suppl 1):12-33. doi: 10.5213/inj.2448002.001. Epub 2024 Feb 29.
2
Nerve transfer for restoration of lower motor neuron-lesioned bladder function. Part 1: attenuation of purinergic bladder smooth muscle contractions.用于恢复下运动神经元损伤膀胱功能的神经移植。第1部分:嘌呤能膀胱平滑肌收缩的减弱
Am J Physiol Regul Integr Comp Physiol. 2021 Jun 1;320(6):R885-R896. doi: 10.1152/ajpregu.00299.2020. Epub 2021 Mar 24.
3
The role of the mucosa in modulation of evoked responses in the spinal cord injured rat bladder.黏膜在调制脊髓损伤大鼠膀胱诱发反应中的作用。
Neurourol Urodyn. 2018 Jun;37(5):1583-1593. doi: 10.1002/nau.23512. Epub 2018 Feb 10.
4
Bladder smooth muscle strip contractility as a method to evaluate lower urinary tract pharmacology.膀胱平滑肌条收缩性作为评估下尿路药理学的一种方法。
J Vis Exp. 2014 Aug 18(90):e51807. doi: 10.3791/51807.
5
Changes in nerve-mediated contractility of the lower urinary tract in a mouse model of premature ageing.早衰小鼠模型下尿路神经介导收缩性的变化
Br J Pharmacol. 2014 Apr;171(7):1687-705. doi: 10.1111/bph.12567.
6
Diabetic plasticity of non-adrenergic non-cholinergic and P2X-mediated rat bladder contractions.糖尿病大鼠非肾上腺素能非胆碱能和 P2X 介导的膀胱收缩的可塑性。
Brain Res Bull. 2013 Jun;95:40-5. doi: 10.1016/j.brainresbull.2013.03.006. Epub 2013 Apr 2.
7
Excitatory and Inhibitory Influence of Pathways in the Pelvic Nerve on Bladder Activity in Rats with Bladder Outlet Obstruction.膀胱出口梗阻大鼠盆腔神经通路对膀胱活动的兴奋和抑制作用
Low Urin Tract Symptoms. 2009 Jun;1(1):51-55. doi: 10.1111/j.1757-5672.2009.00004.x.
8
Plasticity of non-adrenergic non-cholinergic bladder contractions in rats after chronic spinal cord injury.慢性脊髓损伤后大鼠非肾上腺素能非胆碱能膀胱收缩的可塑性。
Brain Res Bull. 2011 Aug 10;86(1-2):91-6. doi: 10.1016/j.brainresbull.2011.06.001. Epub 2011 Jun 13.
9
Activation of cholinergic receptors blocks non-adrenergic non-cholinergic contractions in the rat urinary bladder.胆碱能受体的激活可阻断大鼠膀胱中的非肾上腺素能非胆碱能收缩。
Brain Res Bull. 2008 Dec 16;77(6):420-6. doi: 10.1016/j.brainresbull.2008.07.011. Epub 2008 Aug 26.
10
The neural control of micturition.排尿的神经控制。
Nat Rev Neurosci. 2008 Jun;9(6):453-66. doi: 10.1038/nrn2401.