Mechanism and Prevention of Female Stress Urinary Incontinence

女性压力性尿失禁的发病机制及预防

• 批准号: 8531905
• 负责人: TOM F LUE
• 金额: $ 36.91万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-04-01 至 2014-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8531905
• 关键词: Adverse effects; Affect; Animal Model; Applications Grants; Basal lamina; Biological Preservation; Birth; Birth trauma; Blood Vessels; Cells; Chronic; Collagen; Collagen Fiber; Contracts; Coughing; Development; Doxycycline; Elastases; Elastic Fiber; Elastin; Epithelium; Estrogen Therapy; Estrogens; Event; Exercise; Extracellular Matrix; Extravasation; Female; Fiber; Functional disorder; Goals; Grant; Histocytochemistry; Image; Incontinence; Individual; Inflammation; Inflammatory; Intervention; Ischemia; Knockout Mice; Knowledge; Laboratories; Lead; Leukocyte Elastase; Life; MMP2 gene; Matrix Metalloproteinase Inhibitor; Matrix Metalloproteinases; Measures; Mediating; Medical; Metalloproteases; Modeling; Molecular; Molecular Biology Techniques; Morphology; Mucous Membrane; Muscle; Muscle Cells; Myosin Light Chains; Nerve; Operative Surgical Procedures; Ovariectomy; Paper; Pathogenesis; Pilot Projects; Prevention; Preventive; Protein-Lysine 6-Oxidase; Publishing; Quality of life; ROCK-I; Rattus; Recruitment Activity; Reperfusion Injury; Reticulin; Saline; Schwann Cells; Simulate; Smooth Muscle; Smooth Muscle Myocytes; Sneezing; Somatotropin; Sphincter; Stress Urinary Incontinence; Striated Muscles; Surgical sutures; System; Testing; Tissues; Translating; United States; Urethra; Urine; Vagina; Vaginal delivery procedure; Woman; Work; alpha-adrenergic receptor; beta Aminopropionitrile; clinical application; extracellular; fibulin; hormone therapy; inhibitor/antagonist; middle age; neuromuscular; neutrophil; older women; pressure; prevent; public health relevance; receptor expression; relating to nervous system; repaired; resilience; urinary

DESCRIPTION (provided by applicant): Stress urinary incontinence affects millions of women in the United States and has substantial negative effects on quality of life. There is currently no effective preventive or medical option for stress urinary incontinence (SUI) other than surgical elevation of the urethra with sutures or a synthetic sling. Our current grant has confirmed that treatment with estrogen increase the chances of incontinence in our animal model of simulated birth trauma. The mechanisms underlying this increase in incontinence appeared to include perturbations of urethral alpha adrenergic receptor expression, changes in expression of the cellular messengers RhoA, ROCK-I, ROCK-II, and phosphorylated myosin light chain (pMLC), and reduction in urethral collagen I and elastic fiber content. In an attempt to develop preventive measures for SUI, we noted that early administration of growth hormone significantly reduced the incontinence rate in our animal model. Preservation of elastic and collagen fibers in the urethra was the factor most strongly associated with reduction of incontinence. Since the neuromuscular contributions to continence have already been extensively studied, in this renewal application we propose to study the contribution of the extracellular collagen and elastic fibers to the normal function of the urethra. For these studies we will use living cell/tissue imaging and molecular biology technique. In addition, we will test a safe and inexpensive strategy to prevent incontinence as well as develop a long-term, chronic incontinence model to test treatment options. Our goal is to translate the knowledge obtained in our laboratory to clinical applications for women suffering from SUI. PUBLIC HEALTH RELEVANCE: Urinary leakage with coughing, sneezing or exercise (aka stress urinary incontinence, SUI) is a common medical problem in middle-aged and older women. In our current study, we determined that disruption of elastic and collagen fibers in the urethra is strongly associated with urine leakage in an animal model of SUI. This grant proposal will study means to stop birth-trauma mediated disruption of collagen and elastic fibers before it takes place and/or enhance repair of these fibers.

描述（由申请人提供）：压力性尿失禁影响着美国数百万女性，对生活质量有重大负面影响。目前对于压力性尿失禁（SUI）没有有效的预防或医疗选择，除了用缝线或合成吊带手术抬高尿道。我们目前的资助已经证实，在我们模拟产伤的动物模型中，雌激素治疗增加了失禁的机会。尿失禁增加的潜在机制似乎包括尿道α肾上腺素能受体表达的扰动，细胞信使RhoA、ROCK-I、ROCK-II和磷酸化肌球蛋白轻链（pMLC）表达的变化，以及尿道胶原蛋白I和弹性纤维含量的减少。在尝试开发SUI的预防措施时，我们注意到在我们的动物模型中，早期给予生长激素显著降低了尿失禁率。保留尿道中的弹性和胶原纤维是与尿失禁减少最密切相关的因素。由于神经肌肉对尿道的贡献已经被广泛研究，在这个更新的应用中，我们建议研究细胞外胶原和弹性纤维对尿道正常功能的贡献。对于这些研究，我们将使用活细胞/组织成像和分子生物学技术。此外，我们还将测试一种安全、廉价的预防尿失禁的策略，并开发一种长期的慢性尿失禁模型来测试治疗方案。我们的目标是将我们实验室获得的知识转化为临床应用，用于患有SUI的女性。 公共卫生相关性：伴随咳嗽、打喷嚏或运动的尿漏（又名压力性尿失禁，SUI）是中老年女性常见的医疗问题。在我们目前的研究中，我们确定了在SUI的动物模型中，尿道中弹性和胶原纤维的破坏与尿液渗漏密切相关。这项拨款提案将研究如何在发生之前阻止出生创伤介导的胶原蛋白和弹性纤维的破坏和/或增强这些纤维的修复。

项目成果

Urethral musculature and innervation in the female rat.

• DOI: 10.1002/nau.22722
• 发表时间: 2016-03
• 期刊: Neurourology and urodynamics
• 影响因子: 2
• 作者: Zhang X;Alwaal A;Lin G;Li H;Zaid UB;Wang G;Wang L;Banie L;Ning H;Lin CS;Guo Y;Zhou L;Lue TF
• 通讯作者: Lue TF