Physiology of Calcium Appetite

钙食欲的生理学

• 批准号: 8015407
• 负责人: MICHAEL G TORDOFF
• 金额: $ 9.97万
• 依托单位: MONELL CHEMICAL SENSES CENTER
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-03-22 至 2011-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8015407
• 关键词: Address; Agonist; Behavioral; Brain; Breeding; Calcium; Calcium-Sensing Receptors; Candidate Disease Gene; Code; Computer Simulation; Congenic Strain; Consumption; Desire for food; Development; Dimerization; Disease; Electrophysiology (science); Embryo; Gene Expression; Gene Expression Profiling; Genes; Genetic; Genetic Polymorphism; Genome; Homeostasis; Human; Human Genome; Hypertension; Immunochemistry; Immunohistochemistry; In Situ Hybridization; Incidence; Ingestion; Lead; Link; Location; Magnesium; Methods; Minerals; Molecular Conformation; Mouse Strains; Mus; Obesity; Osteoporosis; Perception; Physiological; Physiology; Population; Premenstrual syndrome; Production; Proteins; Quantitative Trait Loci; Receptor Gene; Recommendation; Research; Saccharin; Signal Transduction; Site; Solutions; System; Taste Perception; Testing; Time; Tissues; Work; calcium intake; calcium metabolism; congenic; consomic; drinking; gene discovery; kidney cell; novel; preference; public health relevance; receptor; response; sweet receptor; sweet taste perception; treatment strategy

DESCRIPTION (provided by applicant): Low voluntary calcium intakes have been implicated in several diseases that afflict the U.S. population including osteoporosis, hypertension, obesity, and premenstrual syndrome. But despite many recommendations to increase calcium intake there has been almost no research to understand why calcium intakes are so low. This project will address this question by identifying and characterizing some of the physiological and genetic controls that underlie calcium consumption. Two aims are proposed in this renewal application. The first is to identify genes responsible for the consumption of calcium. In Aim 1.1, congenic and consomic mice will be bred in order to isolate small chromosomal fragments containing consumption-related genes. In Aim 1.2, candidate genes in each fragment will be assessed using a combination of in silico methods and gene expression studies. The second aim is to characterize the modes and sites of action of two genes that this project has already implicated in the control of calcium consumption; the calcium-sensing receptor, Casr, and the sweet taste receptor, Tas1r3. This will be done by comparing the receptor activity of a mouse strain that avoids calcium (the C57BL/6J or B6 strain) with a strain that drinks calcium avidly (the PWK/PhJ or PWK strain). The plan is to use an HEK cell expression system to compare the physiological responses of B6 and PWK forms of CaSR and T1R3 (Aim 2.1), in situ hybridization, real-time PCR, and immunochemistry to characterize the expression of the B6 and PWK forms of CaSR and T1R3 in taste tissue (Aim 2.2), and gustatory electrophysiology to determine the functional significance of any differences between the two strains in physiological response or location of CaSR and T1R3 (Aim 2.3). Aim 1 will lead to the discovery of genes involved in regulating the ingestion and metabolism of calcium. Aim 2 will test the possibility that a specific receptor or pair of receptors transduce calcium taste. Understanding the mechanisms underlying calcium perception is an important step toward answering the question of why calcium intakes are so low. Given the many similarities between the mouse and human genome, such studies in mice will have direct relevance for the control of calcium consumption by humans, and thus the many diseases associated with excess or insufficient calcium intake. PUBLIC HEALTH RELEVANCE: This project investigates the physiological and genetic controls of calcium intake and preference. Low calcium intakes are associated with several diseases including osteoporosis, hypertension and premenstrual syndrome. An understanding of how calcium consumption is controlled will lead to the development of effective strategies and treatments to increase calcium intake and thus reduce the incidence of these calcium- related diseases.

描述（由申请人提供）：自愿钙摄入量低与困扰美国人口的多种疾病有关，包括骨质疏松症、高血压、肥胖症和经前综合症。但是，尽管有许多增加钙摄入量的建议，但几乎没有研究来理解为什么钙摄入量如此之低。该项目将通过识别和表征钙消耗背后的一些生理和遗传控制来解决这个问题。本次续展申请提出了两个目标。首先是确定负责钙消耗的基因。在目标 1.1 中，将培育同源小鼠和同体小鼠，以分离含有消耗相关基因的小染色体片段。在目标 1.2 中，将结合计算机方法和基因表达研究来评估每个片段中的候选基因。第二个目标是描述该项目已经涉及钙消耗控制的两个基因的作用模式和位点；钙敏感受体 Casr 和甜味受体 Tas1r3。这将通过比较避免钙的小鼠品系（C57BL/6J 或 B6 品系）与大量喝钙的小鼠品系（PWK/PhJ 或 PWK 品系）的受体活性来完成。该计划是使用 HEK 细胞表达系统来比较 CaSR 和 T1R3 的 B6 和 PWK 形式的生理反应（目标 2.1），利用原位杂交、实时 PCR 和免疫化学来表征 B6 和 PWK 形式的表达味觉组织中 CaSR 和 T1R3 的变化（目标 2.2）和味觉电生理学，以确定两种菌株在生理反应或味觉位置方面的任何差异的功能意义CaSR 和 T1R3（目标 2.3）。目标 1 将发现参与调节钙摄入和代谢的基因。目标 2 将测试特定受体或一对受体转导钙味觉的可能性。了解钙感知的机制是回答钙摄入量为何如此低的问题的重要一步。鉴于小鼠和人类基因组之间有许多相似之处，此类小鼠研究将与人类钙消耗的控制直接相关，从而与钙摄入过量或不足相关的许多疾病具有直接相关性。公共健康相关性：该项目研究钙摄入量和偏好的生理和遗传控制。钙摄入量低与多种疾病有关，包括骨质疏松症、高血压和经前综合症。了解如何控制钙的消耗将有助于制定有效的策略和治疗方法来增加钙的摄入量，从而减少这些与钙相关的疾病的发病率。