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Mechanisms of Renal Vasodilation by Relaxin

松弛素舒张肾血管的机制

基本信息

批准号：
7895648
负责人：
Kirk P Conrad
金额：
$ 18.66万
依托单位：
UNIVERSITY OF FLORIDA
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-08-01 至 2013-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7895648
关键词：
Address Affect Animals Antibodies Applications Grants Arginine Arteries Blood Circulation Blood Vessels Blood Volume Blood flow Cardiovascular system Communication Conscious Coupling Cyclic Peptides Data Development Disease Effectiveness Endothelin Endothelium Exploratory/Developmental Grant Female Fetal Growth Fetal Growth Retardation Filtration First Pregnancy Trimester Funding Mechanisms G-Protein-Coupled Receptors Gelatinase A Gelatinase B Gelatinases Gene Targeting Genes Goals Heating Hormones Hour Human In Vitro Incubated Kidney Knock-out Knockout Mice Knowledge Laboratories Leucine Link Location Matrix Metalloproteinase Inhibitor Matrix Metalloproteinases Mediating Metalloproteases Modeling Molecular Mus Mutant Strains Mice NG-Nitroarginine Methyl Ester Names Nitric Oxide Ovarian hormone Ovary Oxides Pathology Pathway interactions Patient currently pregnant Peptides Physiological Population Pre-Eclampsia Pregnancy Pregnant Women Protein Tyrosine Kinase Rattus Relaxation Relaxin Renal Blood Flow Renal Circulation Research Risk Role SU 5416 Signal Pathway Signal Transduction Staging Testing Therapeutic Therapeutic Agents Tissues Vascular Endothelial Growth Factor Receptor Vascular Endothelial Growth Factors Vascular Smooth Muscle Vascular resistance Vasodilation Vasodilator Agents Wild Type Mouse Work arginine methyl ester blood flow measurement endothelin-converting enzyme human subject in vivo Model inhibitor/antagonist insight instrument male mimetics mouse model neutralizing antibody novel peptide hormone phosphoramidon pregnant pressure prevent public health relevance receptor relaxin receptor renal artery research study response subcutaneous

项目摘要

DESCRIPTION (provided by applicant): The ovarian hormone, relaxin, is an important signal causing profound renal and systemic vasodilation, as well as increased arterial compliance in the maternal circulation during normal pregnancy. These changes are important for both initiating and accommodating increased maternal blood volume and flow that, in turn, support fetal growth. When circulating relaxin is deficient in pregnancy, renal and systemic arterial adaptations are compromised. Given its prominent role in the arterial changes of normal pregnancy, it is important to understand the mechanisms of relaxin action in the vasculature. Such understanding has the potential to explain dysregulation of vasodilation and arterial compliance during preeclampsia in which fetal growth is frequently compromised. Ultimately, vasodilation by relaxin depends on endothelial nitric oxide that relaxes the underlying vascular smooth muscle. The overarching hypothesis of this grant proposal is that the vasodilatory actions of relaxin hinge on bi-directional communication between the vascular smooth muscle and the endothelium. Preliminary data indicate that the major relaxin receptor, Lgr7, mediates the renal vasodilatory and arterial compliances changes of relaxin. Surprisingly, however, further preliminary results show substantially more Lgr7 receptor in vascular smooth muscle than endothelium. Thus, the first Hypothesis and Specific Aim address whether it is the Lgr7 receptor in the vascular smooth muscle that mediates the renal vasodilatory and arterial compliances changes of relaxin. Mice with conditional knock-out of the Lgr7 from the vascular smooth muscle will be generated, in order to test whether the renal vasodilatory and arterial compliance changes of relaxin are abolished in these mice. The second Hypothesis and Specific Aim address the molecular intermediate(s) stimulated by relaxin in the vascular smooth muscle that, in turn, communicate with the endothelium. In this respect, new and exciting preliminary data implicate vascular endothelial growth factor. As well, the second Hypothesis and Specific Aim address the molecular intermediate(s) stimulated in the endothelium leading to increased NO activity. These Hypotheses and Specific Aims will be interrogated by studying the function of small renal and subcutaneous arteries isolated from mice and humans, respectively, as well as renal blood flow and arterial pressure in conscious mice. This project is ideally suited to the R21 funding mechanism because it is exploratory, testing a novel mechanistic model of relaxin action in the renal circulation, proposes a new methodological approach to testing this mechanistic model in vivo that is in need of development (targeted gene knock-out mice), and last, but not least, will facilitate the therapeutic application of relaxin (or relaxin mimetic) as a vasodilator and modifier of arterial compliance. Indeed, the fundamental importance of relaxin in the cardiovascular adaptations of normal pregnancy holds promise for the effectiveness of pharmacologic manipulation of relaxin signaling in conditions of pathophysiological cardiovascular dysregulation in pregnancy. PUBLIC HEALTH RELEVANCE: A hormone from the ovary called relaxin is a key signal that acts on blood vessels to increase maternal blood flow during normal pregnancy that is important to support fetal growth. We propose to find out how relaxin affects blood vessels to cause this change. It is important to understand the mechanisms of action of relaxin in blood vessels for two main reasons: (i) it will help us understand abnormal pregnancy such as preeclampsia in which the major problem is decreased maternal blood flow, and (ii) it is necessary for potential use of relaxin as a therapeutic agent to treat various blood vessel diseases in the pregnant and nonpregnant populations.

描述（由申请方提供）：卵巢激素松弛素是一种重要信号，可引起严重的肾脏和全身血管舒张，以及正常妊娠期间母体循环中动脉顺应性增加。这些变化对于启动和适应增加的母体血容量和血流量都很重要，这反过来又支持胎儿生长。当怀孕期间循环松弛素缺乏时，肾脏和全身动脉的适应性就会受到损害。鉴于其在正常妊娠的动脉变化中的重要作用，了解松弛素在血管中的作用机制是很重要的。这种理解有可能解释先兆子痫期间血管舒张和动脉顺应性失调，其中胎儿生长经常受到影响。最终，松弛素的血管舒张作用依赖于内皮一氧化氮，内皮一氧化氮使血管平滑肌松弛。这项拨款提案的首要假设是松弛素的血管舒张作用取决于血管平滑肌和内皮之间的双向通讯。初步数据表明，主要的松弛素受体，Lgr 7，介导的肾血管舒张和动脉的顺应性的变化松弛素。然而，令人惊讶的是，进一步的初步结果显示，血管平滑肌中的Lgr 7受体比内皮多得多。因此，第一个假设和具体目标解决是否是血管平滑肌中的Lgr 7受体介导松弛素的肾血管舒张和动脉顺应性变化。将产生从血管平滑肌中条件性敲除Lgr 7的小鼠，以测试松弛素的肾血管舒张和动脉顺应性变化在这些小鼠中是否被消除。第二个假设和具体目标涉及血管平滑肌中松弛素刺激的分子中间体，而血管平滑肌反过来又与内皮通讯。在这方面，新的和令人兴奋的初步数据牵连血管内皮生长因子。此外，第二个假设和具体目标涉及在内皮中刺激的分子中间体，导致NO活性增加。将通过研究分别从小鼠和人分离的小肾动脉和皮下动脉的功能以及清醒小鼠的肾血流量和动脉压来探讨这些假设和特定目的。该项目非常适合R21资助机制，因为它是探索性的，测试了肾循环中松弛素作用的新机制模型，提出了一种新的方法学方法来测试需要开发的体内机制模型（靶向基因敲除小鼠），最后，但并非最不重要的，将促进松弛素（或松弛素模拟物）作为血管扩张剂和动脉顺应性调节剂的治疗应用。事实上，松弛素在正常妊娠的心血管适应中的根本重要性为松弛素信号传导在妊娠中的病理生理性心血管失调的条件下的药理学操纵的有效性提供了希望。公共卫生相关性：来自卵巢的一种叫做松弛素的激素是一种关键信号，它作用于血管，在正常妊娠期间增加母体血流量，这对支持胎儿生长很重要。我们建议找出松弛素是如何影响血管导致这种变化的。了解松弛素在血管中的作用机制很重要，主要有两个原因：（i）它将帮助我们了解异常妊娠，如先兆子痫，其中主要问题是母体血流量减少，以及（ii）松弛素作为治疗剂在妊娠和非妊娠人群中治疗各种血管疾病的潜在用途是必要的。