Control of motility in the internal anal sphincter
Control of motility in the internal anal sphincter
批准号:
8246415
负责人:
KATHLEEN D KEEF
金额:
$28.96万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-04-01 至 2014-03-31
关键词:
AddressAffectAnusBiochemicalCellsCircular layer of muscularis propria of anal canalDataDefecationDevelopmentDiagnosisDiseaseEffector CellEmploymentFecal IncontinenceFluorescence-Activated Cell SortingFunctional disorderGastrointestinal tract structureGene ExpressionGenerationsHealth Care CostsHealthcareInstitutionalizationInterstitial Cell of CajalIon ChannelMeasuresMembrane PotentialsMonkeysMorphologyMotorMusMuscle ContractionNerveNitroxidergic NervesPacemakersPathway interactionsPatternPeriodicityPlayProcessRegulationRelative (related person)RelaxationReportingRestRho-associated kinaseRoleSmooth Muscle MyocytesSocial isolationSorting - Cell MovementTRP channelTechniquesTissuesTransgenic MiceUnited Statescell motilityelectrical propertyinsightmouse modelnovel strategiespressurepreventpublic health relevanceresearch studyvoltage
中文摘要
描述(由申请人提供):内肛门括约肌(IAS)维持70%的肛门静息张力,这对维持大便失禁至关重要。收缩放松是排便的基本特征,这是由抑制性神经输入调节的。肛门张力降低和增加分别导致大便失禁和排便障碍。我们对维持IAS正常收缩机制的理解是有限的。最近的研究强调了Rho激酶通路的作用,但只有4篇报道研究了膜电位(Em)在胃肠道这一临床重要区域的调节中的作用。我们的初步数据表明,由Em调节的l型Ca2+通道(Cav1.2)是将Ca2+传递到收缩装置和确定IAS收缩活动模式的基础。初步实验还表明,Rho激酶对收缩的至少一部分调节可能涉及Em的变化。我们对IAS的免疫组织化学研究表明,Cajal间质细胞(ICC)密集分布在IAS的整个肌层中。然而,在IAS中,这些细胞对Em和电节律的贡献是未知的。因此,我们对这些研究的总体假设是,由于Em对Cav1.2活性的影响,IAS的收缩和抑制性运动神经引起的变化主要由Em调节,而ICC通过调节相邻SMCs中的Em在这一过程中发挥重要作用。为了检验这一假设,将在猴子和小鼠的IAS的孤立节段中测量Em和收缩。ICC和平滑肌细胞(SMC)也将从这些组织中分散出来,以评估离子通道活性,并使用荧光活化细胞分选(FACS)进行分类,以评估基因表达。Rho激酶通路将使用生化技术进行评估,氮能神经的分布及其与ICC和SMC的关系将使用免疫组织化学和免疫细胞化学技术确定。涉及新开发的转基因小鼠模型的新方法也将用于研究和消除ICC。IAS的功能失调导致严重的社会孤立、失业和制度化,并在美国榨取数十亿美元的医疗保健费用。尽管有这么大的卫生保健问题,IAS是胃肠道中研究最少的区域。这项拟议的研究将为控制肌肉收缩和肛门压力的机制提供新的见解。这些信息对于制定有助于预防、诊断和治疗IAS功能障碍的新战略至关重要。
英文摘要
DESCRIPTION (provided by applicant): The internal anal sphincter (IAS) maintains 70% of anal resting tone, which is critical for maintaining fecal continence. Relaxation of contraction is an essential feature of defecation, and this is regulated by input from inhibitory nerves. Reduced and increased anal tone contribute to fecal incontinence and defecatory disorders respectively. Our understanding of the mechanisms which maintain normal IAS contraction is limited. Recent studies have emphasized the role of the Rho kinase pathway, but there are only 4 reports which have investigated the role of membrane potential (Em) in the regulation of this clinically important region of the GI tract. Our preliminary data suggest that L-type Ca2+ channels (Cav1.2), regulated by Em, are fundamental to the delivery of Ca2+ to the contractile apparatus and for determining the pattern of contractile activity in the IAS. Preliminary experiments also suggest that at least a portion of the regulation of contraction by Rho kinase may involve changes in Em. Our immunohistochemical studies of the IAS have revealed that interstitial cells of Cajal (ICC) are densely distributed throughout the muscularis of the IAS. However, the contribution of these cells to Em and electrical rhythmicity in the IAS is unknown. Thus, our overall hypothesis for these studies is that contraction in the IAS and the changes elicited by inhibitory motor nerves is primarily regulated by Em due to its effects upon Cav1.2 activity and that ICC play an important role in this process by modulating Em in adjacent SMCs. To examine this hypothesis Em and contraction will be measured in isolated segments of the monkey and mouse IAS. ICC and smooth muscle cells (SMC) will also be dispersed from these tissues to evaluate ion channel activity and sorted using fluorescence activated cell sorting (FACS) to evaluate gene expression. The Rho kinase pathway will be assessed using biochemical techniques and the distribution of nitrergic nerves and their relationship to ICC and SMC will be determined using immmunohistochemical and immunocytochemical techniques. Novel approaches involving newly developed transgenic mice models will also be used to study and eliminate ICC. Dysfunction of the IAS leads to substantial social isolation, loss of employment, and institutionalization as well as extracting billions of dollars in health care costs in the United States. In spite of this large health care problem the IAS is the least studied region of the GI tract. The proposed study will provide new insights into the mechanisms which control muscle contraction and hence anal pressure. Such information is critical for developing new strategies to help prevent as well as diagnose and treat IAS dysfunction.
PUBLIC HEALTH RELEVANCE:
The internal anal sphincter (IAS) maintains 70% of resting anal pressure. Reduced and increased anal resting pressure contributes to fecal incontinence and defecatory disorders respectively. Dysfunction of the IAS leads to substantial social isolation, loss of employment, and institutionalization as well as extracting billions of dollars in health care costs in the United States. In spite of this large health care problem the IAS is the least studied region of the GI tract. The proposed study will provide new insights into the mechanisms which control muscle contraction and hence anal pressure. Such information is critical for developing new strategies to help prevent as well as diagnose and treat IAS dysfunction.
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Control of motility in the internal anal sphincter
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批准号:8961812
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项目类别:
-
资助金额:$43.39万
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财政年份:2010
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负责人:KATHLEEN D KEEF
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依托单位:
Control of motility in the internal anal sphincter
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批准号:8446206
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项目类别:
-
资助金额:$27.95万
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财政年份:2010
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负责人:KATHLEEN D KEEF
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依托单位:
Control of motility in the internal anal sphincter
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批准号:8049632
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项目类别:
-
资助金额:$28.96万
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财政年份:2010
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负责人:KATHLEEN D KEEF
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依托单位:
Tissue, Cell and Tissue Culture Core
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批准号:7413388
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项目类别:
-
资助金额:$27.14万
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财政年份:2007
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负责人:KATHLEEN D KEEF
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依托单位:
Tissue, Cell and Tissue Culture Core
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批准号:7235350
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项目类别:
-
资助金额:$27.14万
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财政年份:2006
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负责人:KATHLEEN D KEEF
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依托单位:
Tissue, Cell and Tissue Culture Core
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批准号:6801335
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项目类别:
-
资助金额:$26.2万
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财政年份:2004
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负责人:KATHLEEN D KEEF
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依托单位:
CORE--TISSUE, CELL AND TISSUE CULTURE LABORATORY
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批准号:6587862
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项目类别:
-
资助金额:$19.72万
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财政年份:2002
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负责人:KATHLEEN D KEEF
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依托单位:
CORE--TISSUE, CELL AND TISSUE CULTURE LABORATORY
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批准号:6448976
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项目类别:
-
资助金额:$18.5万
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财政年份:2001
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负责人:KATHLEEN D KEEF
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依托单位:
CORE--TISSUE, CELL AND TISSUE CULTURE LABORATORY
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批准号:6468909
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项目类别:
-
资助金额:$19.72万
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财政年份:2001
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负责人:KATHLEEN D KEEF
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依托单位:
CONTROL OF RECTOANAL MOTILITY
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批准号:6042647
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项目类别:
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资助金额:$17.32万
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财政年份:2000
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负责人:KATHLEEN D KEEF
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依托单位:
CONTROL OF RECTOANAL MOTILITY
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批准号:6637134
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项目类别:
-
资助金额:$18.92万
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财政年份:2000
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负责人:KATHLEEN D KEEF
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依托单位:
CORE--TISSUE, CELL AND TISSUE CULTURE LABORATORY
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批准号:6316597
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项目类别:
-
资助金额:$20.61万
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财政年份:2000
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负责人:KATHLEEN D KEEF
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依托单位:
CONTROL OF RECTOANAL MOTILITY
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批准号:6381245
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项目类别:
-
资助金额:$17.83万
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财政年份:2000
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负责人:KATHLEEN D KEEF
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依托单位:
CONTROL OF RECTOANAL MOTILITY
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批准号:6523731
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项目类别:
-
资助金额:$18.37万
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财政年份:2000
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负责人:KATHLEEN D KEEF
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依托单位:
CORE--TISSUE, CELL AND TISSUE CULTURE LABORATORY
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批准号:6105425
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项目类别:
-
资助金额:$20.61万
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财政年份:1999
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负责人:KATHLEEN D KEEF
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依托单位:
ENTERIC NEURAL CONTROL OF COLON
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批准号:2144609
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项目类别:
-
资助金额:$15.01万
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财政年份:1994
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负责人:KATHLEEN D KEEF
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依托单位:
ENTERIC NEURAL CONTROL OF COLON
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批准号:2016548
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项目类别:
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资助金额:$16.23万
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财政年份:1994
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负责人:KATHLEEN D KEEF
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依托单位:
ENTERIC NEURAL CONTROL OF COLON
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批准号:2144610
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项目类别:
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资助金额:$15.61万
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财政年份:1994
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负责人:KATHLEEN D KEEF
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依托单位:
KINASE REGULATION OF L TYPE CALCIUM CHANNELS
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批准号:6389061
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项目类别:
-
资助金额:$19.77万
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财政年份:1987
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负责人:KATHLEEN D KEEF
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依托单位:
ELECTROMECHANICAL COUPLING IN CORONARY ARTERY
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批准号:2219590
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项目类别:
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资助金额:$15.35万
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财政年份:1987
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负责人:KATHLEEN D KEEF
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依托单位:
海外基金