Transgenic analysis of CNS melanocortin receptors
CNS 黑皮质素受体的转基因分析
基本信息
- 批准号:6721187
- 负责人:
- 金额:$ 14.68万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2002
- 资助国家:美国
- 起止时间:2002-04-01 至 2004-05-31
- 项目状态:已结题
- 来源:
- 关键词:bioenergeticsbiological signal transductioncentral nervous systemdisease /disorder proneness /riskgene expressiongene targetinggenetic recombinationgenetic regulationgenetically modified animalshypothalamuslaboratory mouseleptinmolecular geneticsneuronsneuropeptide receptorneurophysiologyobesityproopiomelanocortinreceptor expressionrecombinasethyrotropin releasing hormonetransfection
项目摘要
DESCRIPTION: (provided by applicant) Obesity is the most common nutritional
disorder in the United States and, in adults, the reduction in lifespan
associated with obesity can be attributed to the development of Type II
diabetes mellitus as well as cardiovascular disorders including stroke,
hypertension and heart disease. Advances in our understanding of underlying
mechanisms that can cause energy imbalances have been aided by studies that
focus on both the adipocyte and the brain. The recent discovery that disruption
of melanocortin signaling in the CNS is the cause of obesity in the yellow
obese mouse has led to the verification of a similar pathway that exists in
humans, as well as the identification of mutations in the melanocortin 4
receptor (MC4-R) and proopiomelanocortin (POMC) genes causing human disease. In
the CNS, neurons that express melanocortin receptors (MC4-R and/or MC3-R) are
regulated by separate and independent populations of neurons originating in the
arcuate nucleus of the hypothalamus (ARC), which express precursors for either
a melanocortin agonist (POMC) or a naturally occurring antagonist
(agouti-related protein or AGRP). Both POMC and AGRP neurons express receptors
for leptin. While MC4-R deficient animals recapitulate agouti-induced obesity
syndrome, little is known about the neuroendocrine circuits involved with
melanocortin control of energy balance through this receptor. Since
melanocortin receptors are expressed throughout the CNS, the immediate goals of
this project are to test the overall hypothesis that hypothalamic and not
brainstem expression of MC4-R governs melanocortin control of energy balance,
and the specific hypotheses that expression of MC4-R in hypothalamic
thyrotropin-releasing hormone (TRH) and melanin-concentrating hormone (MCH)
neurons is required for normal weight homeostasis. Conditions for optimal
regulation of CNS transgene expression in adult mice using an adenovirus and
cre/lox technology will also be established. However, the long-term goal of
this proposal is to develop animal models to define the neural circuitry by
which a-MSH, AGRP, and CNS melanocortin receptors regulate feeding behaviour,
thermogenesis, and cardiovascular control. To this end, MC4-R expression in the
CNS will be modulated using cre recombinase.
描述:(由申请人提供)肥胖是最常见的营养
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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ROBERT A KESTERSON其他文献
ROBERT A KESTERSON的其他文献
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{{ truncateString('ROBERT A KESTERSON', 18)}}的其他基金
Loss of NF1 drives hormone dependent mammary carcinogenesis in a rat model with intact immune system
在具有完整免疫系统的大鼠模型中,NF1的缺失会导致激素依赖性乳腺癌发生
- 批准号:
10642882 - 财政年份:2022
- 资助金额:
$ 14.68万 - 项目类别:
UAB Pilot Center for Precision Animal Modeling (C-PAM) - Disease Modeling Unit
UAB 精密动物建模试点中心 (C-PAM) - 疾病建模单位
- 批准号:
10477314 - 财政年份:2020
- 资助金额:
$ 14.68万 - 项目类别:
UAB Pilot Center for Precision Animal Modeling (C-PAM) - Disease Modeling Unit
UAB 精密动物建模试点中心 (C-PAM) - 疾病建模单位
- 批准号:
10260619 - 财政年份:2020
- 资助金额:
$ 14.68万 - 项目类别:
UAB High Throughput DNA AutoGenPrep 965
UAB 高通量 DNA AutoGenPrep 965
- 批准号:
7794043 - 财政年份:2010
- 资助金额:
$ 14.68万 - 项目类别:
Transgenic analysis of CNS melanocortin receptors
CNS 黑皮质素受体的转基因分析
- 批准号:
6473178 - 财政年份:2002
- 资助金额:
$ 14.68万 - 项目类别:
Transgenic analysis of CNS melanocortin receptors
CNS 黑皮质素受体的转基因分析
- 批准号:
6837819 - 财政年份:2002
- 资助金额:
$ 14.68万 - 项目类别:
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