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Nongenomic bile acid on smooth muscle BK channels

平滑肌 BK 通道上的非基因组胆汁酸

基本信息

批准号：
7212256
负责人：
ALEX M. DOPICO
金额：
$ 17.02万
依托单位：
UNIVERSITY OF TENNESSEE HEALTH SCI CTR
依托单位国家：
美国
项目类别：
财政年份：
2004
资助国家：
美国
起止时间：
2004-05-01 至 2009-04-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7212256
关键词：
Acute Address Adverse effects Androgens Arteries Bile Acids Binding Blood Vessels Cell Nucleus Cells Cerebrovascular Disorders Cerebrum Chemical Structure Chemicals Chemosensitization Cholesterol Cloning Complement Complex Data Development Drug effect disorder Electrophysiology (science)Engineering Environment Estradiol Exposure to Functional disorder Future Genomics Goals Hormonal In Vitro Ion Channel Laboratories Lateral Lead Length Link Lithocholic Acid Measures Mediator of activation protein Membrane Methodology Modeling Molecular Molecular Biology Molecular Biology Techniques Muscle Muscle Cells Muscle Tonus Muscle relaxation phase Mutagenesis Other Finding Patch-Clamp Techniques Pharmaceutical Preparations Pharmacology Physiology Process Progesterone Protein Region Proteins Proteolipids Rattus Relaxation Resolution Role Smooth Muscle Steroids Testing Text Therapeutic Therapeutic Uses Thinking Tissues Vascular Diseases Vascular Smooth Muscle Vasodilation Vasodilator Agents Xenopus oocyte analog base cerebral artery cerebrovascular design experience in vitro Model in vivo insight large-conductance calcium-activated potassium channels non-genomic patch clamp research study response steroid metabolism

项目摘要

DESCRIPTION (provided by applicant): Previous data from our laboratory demonstrated that acute exposure to cholane derivatives (bile acids and synthetic analogs) increases the activity of large conductance, Ca2+-sensitive K+ (BK) channels in arterial smooth muscle. Activation of smooth muscle BK channels is thought to be a major mechanism underlying vasodilation caused by not only bile acid derivatives, but also other physiologically relevant steroids, such as estradiol, progesterone, and androgens. In contrast, others and we found that increased cholesterol levels lead to smooth muscle BK channel inhibition. The long-term goal of this proposal is to identify both the structural determinants in the steroid molecule and the channel protein regions that are responsible for steroid activation of BK channels. Combining methodologies from Electrophysiology (patch-clamp), Molecular Biology, and Pharmacology, we will specifically address: 1) which chemical determinants in the cholane derivative molecule are critical for activating smooth muscle BK channels; 2) which channel subunit (alpha vs. beta) is necessary/sufficient for cholane derivative action; 3) which protein regions in the channel subunits are responsible for conferring cholane sensitivity to the ion channel complex; 4) whether modulation of BK channel activity by cholane derivatives underlies smooth muscle relaxation caused by these steroids. We will answer these questions going from studies in isolated arteries to evaluate drug action on tissue physiology to studies that used engineered ion channel subunits expressed in Xenopus oocytes to address the more mechanistic aspects of the application. We will initially use the rat cerebral artery to freshly isolate both a resistive artery segment to measure changes in tone caused by steroids, and dissociated myocytes to probe steroid modulation of native BK channels. The same overall strategy can be applied to other relevant vessels in the future. We chose the rat cerebral artery/myocyte model because: a) the key role of BK channel activity as regulator of arterial tone was clearly demonstrated; b) we have experience studying the effect of modulators on the active/passive tone of isolated rat cerebral arteries; c) we have isolated, cloned and successfully expressed in Xenopus oocytes the pore forming subunit of the rat cerebral artery BK channel; d) the therapeutic need for new cerebral vasodilators that act on the smooth muscle itself, i.e., that can be effective in the absence of intact endothelial function. Pinpointing the molecular mechanisms involved in the steroid-cerebrovascular BK channel interaction will bring fundamental insight for the rationale design of steroidal vasodilators of potential therapeutic use, devoid of hormonal side effects.

描述（由申请人提供）：我们实验室以前的数据表明，急性暴露于胆烷衍生物（胆汁酸和合成类似物）会增加动脉平滑肌中大电导、Ca2+敏感K+ (BK)通道的活性。平滑肌BK通道的激活被认为是血管舒张的主要机制，不仅由胆汁酸衍生物引起，也由其他生理相关类固醇如雌二醇、黄体酮和雄激素引起。相比之下，其他人和我们发现胆固醇水平升高会导致平滑肌BK通道抑制。本提案的长期目标是确定类固醇分子中的结构决定因素和负责类固醇激活BK通道的通道蛋白区域。结合电生理学（膜片钳）、分子生物学和药理学的方法，我们将具体解决：1)胆烷衍生物分子中的哪些化学决定因素对激活平滑肌BK通道至关重要；2)哪个通道亚基（α与β）对于胆烷衍生物作用是必要/充分的；3)通道亚基中哪些蛋白质区域负责赋予胆碱对离子通道复合物的敏感性；4)胆烷衍生物是否对BK通道活性的调节是这些类固醇引起的平滑肌松弛的基础。我们将回答这些问题，从在孤立动脉中评估药物对组织生理学的作用的研究，到在非洲爪蟾卵母细胞中表达的工程离子通道亚基的研究，以解决应用的更多机制方面。我们将首先利用大鼠大脑动脉分离出一段新的抗阻动脉段来测量类固醇引起的张力变化，并分离出肌细胞来探测类固醇对天然BK通道的调节。未来，同样的整体策略也可以应用于其他相关船只。我们选择大鼠脑动脉/肌细胞模型是因为：a) BK通道活性作为动脉张力调节的关键作用已被清楚地证明；B)我们有经验研究调节剂对离体大鼠脑动脉主动/被动张力的影响；c)分离、克隆并在爪蟾卵母细胞中成功表达了大鼠脑动脉BK通道孔形成亚基；D)治疗需要对平滑肌本身起作用的新型脑血管扩张剂，也就是说，在没有完整内皮功能的情况下可以有效。明确类固醇-脑血管BK通道相互作用的分子机制将为潜在治疗用途的类固醇血管扩张剂的基本原理设计带来根本的见解，没有激素副作用。