Afferent Mechanisms of Pelvic Hypersensitivity
Afferent Mechanisms of Pelvic Hypersensitivity
批准号:
8706856
负责人:
MICHAEL S GOLD
金额:
$58.95万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-19 至 2016-07-31
关键词:
AddressAreaAttenuatedBehavioralBladderCNS processingChronicColorectalCutaneousDevelopmentDiseaseElectric StimulationExhibitsFecesFrequenciesFunctional disorderGastroenterologistGynecologistHabitsHyperalgesiaHypersensitivityInflammationInflammatoryInterstitial CystitisIntestinesIrritable Bowel SyndromeLocal AnestheticsLocal anesthesiaMaintenanceMusNerveNeuronsNociceptorsOrganPainPain DisorderPathologyPathway interactionsPatientsPelvic PainPelvisPersonsProcessRectal AdministrationRecurrenceRelative (related person)ResearchRoleSigns and SymptomsSpinal GangliaStimulusStretchingSymptomsTimeTissuesUrologistVisceralVisceral AfferentsVisceral painWomanchronic abdominal painchronic painintravesicalnerve supplyrectalresearch studyresponse
中文摘要
描述(由申请人提供):患有慢性腹部和盆腔疼痛疾病的患者在胃肠科医生、泌尿科医生和妇科医生那里寻求缓解的患者中占很大比例。两种常见的盆腔疾病,膀胱疼痛综合征(PBS)和肠易激综合征(IBS),其特征是膀胱/排便习惯改变(例如,尿急、尿频,肠易激综合征中大便一致性)、疼痛和过敏。这些患者通常表现出明显较低的刺激反应阈值(例如,膀胱术,直肠膨胀),抱怨在正常器官功能期间敏感性增加,并且在躯体转诊区域表现出压痛增加,此外,体积扩大。有趣的是,PBS和IBS在没有明显的病理生物学原因的情况下存在,因此被定性为“功能性”。人们普遍认为功能障碍反映了中枢神经系统加工的改变,但大量证据表明,持续的传入驱动显著地导致了复发性的、无法解释的疼痛和超敏反应。本建议的目的是确定疼痛和超敏反应产生的机制,并将其作为制定更明智和更成功的管理策略的必要步骤。目的1:在膀胱和结直肠的腰椎内脏神经和盆腔神经的电生理实验中,表征机械敏感和不敏感传入神经的比例。7目的2:在行为实验中评估器官超敏反应,然后在超敏小鼠膀胱和结直肠中测定膀胱和结直肠机械不敏感传入神经(MIAs)的比例。我们假设,与正常对照相比,过敏小鼠器官中mia的比例将显著降低。目的3:确定机械敏感和不敏感的膀胱和结肠背根神经节神经元在腰椎和盆腔神经通路中的“化学型”。我们假设mia和机械敏感传入神经之间、不同机械敏感传入神经之间以及器官之间的化学型存在显著差异。
英文摘要
DESCRIPTION (provided by applicant): Persons with chronic abdominal and pelvic pain disorders comprise a large proportion of patients seeking relief from gastroenterologists, urologists and gynecologists. Two common pelvic disorders, painful bladder syndrome (PBS) and irritable bowel syndrome (IBS), are characterized by altered bladder/bowel habits (e.g., urge, frequency and, in IBS, stool consistency), pain and hypersensitivity. These patients typically exhibit significantly lower response thresholds to provocative stimuli (e.g., cystometry, rectal distension), complain of increased sensitivity during normal organ function, and exhibit increased tenderness in areas of somatic referral which, in addition, are expanded in size. Interestingly, PBS and IBS exist in the absence of an apparent pathobiological cause and are thus characterized as 'functional.' It is widely assumed that functional disorders reflect altered CNS processing, but considerable evidence suggests that persistent afferent drive contributes significantly to the recurrent, unexplained pain and hypersensitivity that characterize them. The objective of this proposal is to determine the mechanisms by which pain and hypersensitivity arise and is maintained as a necessary step in developing better informed and more successful management strategies. The Aims include: 7 Aim 1: characterize the proportions of mechano-sensitive and insensitive afferents in electrophysiological experiments in the both the lumbar splanchnic and pelvic nerve innervations of the bladder and colorectum. 7 Aim 2: evaluate organ hypersensitivity in behavioral experiments, after which the proportions of bladder and colorectal mechanically insensitive afferents (MIAs) will be determined in bladder and colorectum removed from hypersensitive mice. We hypothesize the proportions of MIAs will be significantly reduced in organs from hypersensitive mice relative to normal controls. 7 Aim 3: identify the 'chemotypes' of mechano-sensitive and insensitive bladder and colorectal dorsal root ganglion neurons in both the lumbar splanchnic and pelvic nerve pathways. We hypothesize that there are significant differences in chemotype between MIAs and mechanosensitive afferents as well as between different mechanosensitive afferents and, further, between organs.
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DOI:
10.1111/nmo.12455
发表时间:
2014-12
期刊:
Neurogastroenterology and motility
影响因子:
3.5
作者:
[La JH, Gebhart GF]
通讯作者:
Gebhart GF
Novel method to assess axonal excitability using channelrhodopsin-based photoactivation.
使用基于视紫红质的光激活评估轴突兴奋性的新方法。
DOI:
10.1152/jn.00982.2014
发表时间:
2015
期刊:
Journal of neurophysiology
影响因子:
2.5
作者:
[Zhu,Yi, Feng,Bin, Schwartz,EricaS, Gebhart,GF, Prescott,StevenA]
通讯作者:
Prescott,StevenA
Distribution across tissue layers of extrinsic nerves innervating the mouse colorectum - an in vitro anterograde tracing study.
支配小鼠结肠直肠的外在神经的组织层分布——一项体外顺行追踪研究。
DOI:
10.1111/nmo.12419
发表时间:
2014
期刊:
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society
影响因子:
--
作者:
[Brumovsky,PabloR, La,Jun-Ho, Gebhart,GeraldF]
通讯作者:
Gebhart,GeraldF
DOI:
10.1523/jneurosci.5114-12.2013
发表时间:
2013-06-05
期刊:
The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子:
--
作者:
[Feng B, Kiyatkin ME, La JH, Ge P, Solinga R, Silos-Santiago I, Gebhart GF]
通讯作者:
Gebhart GF
Nociceptive and inflammatory mediator upregulation in a mouse model of chronic prostatitis.
慢性前列腺炎小鼠模型中的伤害性和炎症介质上调。
DOI:
10.1097/j.pain.0000000000000201
发表时间:
2015-08
期刊:
Pain
影响因子:
7.4
作者:
[Schwartz ES, Xie A, La JH, Gebhart GF]
通讯作者:
Gebhart GF
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