Disregulation of Potassium Channels in Menopausal Hot Flashes

更年期潮热时钾通道失调

• 批准号: 7431568
• 负责人: Jon E Levine
• 金额: $ 6.07万
• 依托单位: NORTHWESTERN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-06-01 至 2009-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7431568
• 关键词: Address; Age; Aging; Agonist; Anesthetics; Animal Model; Bioinformatics; Biological Assay; Body Temperature; Brain; Brain region; Cardiovascular system; Cells; Development; Disease; Esthesia; Estrogen Receptors; Estrogens; Excision; Family; Fire - disasters; Generations; Heart Rate; Heating; Hormone replacement therapy; Hormones; Hot flushes; Hypothalamic structure; Immunohistochemistry; In Situ Hybridization; Inhalant dose form; Investigation; Ion Channel; Life; Location; Malignant Neoplasms; Medical; Membrane Potentials; Menopausal hot flushes; Menopause; Messenger RNA; Molecular; Monitor; Mus; Neuraxis; Neurons; Numbers; Organism; Ovary; Pain; Perimenopause; Peripheral; Pharmaceutical Preparations; Physiologic Thermoregulation; Physiological; Physiology; Play; Postmenopause; Potassium; Potassium Channel; Preoptic Areas; Proteins; Quality of life; Regulation; Rest; Risk; Role; Skin Temperature; Source; Sweat; Symptoms; System; Tail; Tandem Pore Domain Potassium Channels; Temperature; Testing; Thinking; Time; Tissues; Vasodilation; Vasodilation disorder; Vasomotor; Withdrawal; Woman; Work; aging population; day; design; immunocytochemistry; improved; in vivo; insight; neuroprotection; response; tissue/cell culture

DESCRIPTION (provided by applicant): The hot flash, an abrupt sensation of heat, is the most common medical complaint among peri- and post-menopausal women. Peripherally, hot flashes are characterized by vasodilation, increased heart rate, and perspiration. The expression of the hot flash is correlated with lowered levels of circulating estrogen at the onset of menopause or surgical removal of the ovaries. Estrogen receptors are widely distributed throughout the central nervous system and the cardiovascular system. Within the central nervous system estrogen receptors are prominently expressed in the preoptic area (POA) of the hypothalamus - the location of temperature sensitive neurons associated with thermoregulation. It is thought that hot flashes are caused by a disturbance of normal thermoregulation brought on by the loss of estrogen; however, the underlying molecular, cellular, and physiological mechanism is unknown. Recently, a new family of ion channels, the background leak potassium channels or two-pore domain potassium (K2P) channels has been identified through the use of bioinformatics. In cell and tissue culture systems these channels have been shown to contribute the establishment of the resting membrane potential of cells. Activation of K2P channels causes hyperpolarization of cells resulting in inhibition of firing. Although some of the channels have been associated with temperature sensitivity, sensitivity to pain, response to inhalant anesthetics, and neuroprotection, the physiological functions of most of these channels in living organisms have yet to be established. It is hypothesized herein that estrogen regulates the expression of K2P channels in the central nervous system and that the withdrawal of estrogen results in a decrease in the number or activity of these channels. This reduction would depolarize neurons leading to greater excitability and the induction of hot flashes. The work proposed in this application will use a functional bioassay, radiotelemetric monitoring of tail skin temperature from estrogen deficient and replete mice, to monitor the effects of drugs that activate and inhibit K2P channels in a whole animal model. Immunohistochemistry will be used to determine whether or not the proteins are expressed in the same cells as estrogen receptors. Expression of the messenger RNAs for the channels will be quantified using real time-PCR and in situ hybridization. Although this application will investigate the role of K2P channels in generating hot flashes, increasing our understanding of the physiological functions of these channels may provide insight into mechanisms of other age-associated diseases associated with hyperexcitability of the central nervous system. Hot flashes are the most common medical complaint among peri- and post-menopausal women. Currently, the most commonly used treatment to alleviate hot flash symptoms is hormone replacement therapy (HRT). Unfortunately, HRT is associated with several risks, including an increase in hormone dependent cancers, leading many to seek other treatments. The cellular and molecular mechanisms that cause hot flashes are unknown. The work proposed in this application is designed to investigate the underlying cellular and molecular mechanisms responsible for hot flashes, leading to the development of safe and effective treatments.

描述（由申请人提供）：潮热，一种突然的热感，是绝经期和绝经后妇女最常见的医学症状。在外围，潮热的特征是血管舒张，心率加快和出汗。潮热的表达与更年期开始或卵巢手术切除时循环雌激素水平降低有关。雌激素受体广泛分布于中枢神经系统和心血管系统。在中枢神经系统中，雌激素受体在下丘脑的视前区（POA）显著表达，这是与体温调节相关的温度敏感神经元的位置。据认为，潮热是由雌激素的丧失引起的正常体温调节紊乱引起的；然而，潜在的分子、细胞和生理机制尚不清楚。近年来，利用生物信息学的方法发现了一类新的离子通道，即背景漏钾通道或双孔域钾通道。在细胞和组织培养系统中，这些通道已被证明有助于建立细胞的静息膜电位。K2P通道的激活引起细胞的超极化，从而抑制放电。虽然一些通道与温度敏感性、疼痛敏感性、吸入麻醉剂反应和神经保护有关，但大多数这些通道在生物体中的生理功能尚未确定。本文假设雌激素调节中枢神经系统中K2P通道的表达，雌激素的停用导致这些通道的数量或活性降低。这种减少会使神经元去极化，导致更大的兴奋性和潮热的诱导。本申请中提出的工作将使用功能性生物测定，对雌激素缺乏和雌激素充足的小鼠的尾部皮肤温度进行无线电遥测监测，以监测激活和抑制K2P通道的药物对整个动物模型的影响。免疫组织化学将用于确定这些蛋白是否与雌激素受体在相同的细胞中表达。通道信使rna的表达将通过实时pcr和原位杂交进行定量。虽然这项应用将研究K2P通道在潮热产生中的作用，但增加我们对这些通道生理功能的理解可能会为其他与中枢神经系统高兴奋性相关的年龄相关疾病的机制提供见解。潮热是围绝经期和绝经后妇女最常见的疾病。目前，缓解潮热症状最常用的治疗是激素替代疗法（HRT）。不幸的是，HRT与几种风险相关，包括激素依赖性癌症的增加，导致许多人寻求其他治疗方法。引起潮热的细胞和分子机制尚不清楚。在本应用程序中提出的工作旨在研究导致潮热的潜在细胞和分子机制，从而开发安全有效的治疗方法。