Suppr超能文献

NIH 小鼠代谢表型中心:集中表型分析的力量。

NIH Mouse Metabolic Phenotyping Centers: the power of centralized phenotyping.

机构信息

Division of Diabetes, Endocrinology and Metabolic Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, 6707 Democracy Blvd, Rm. 787, MSC 5460, Bethesda, MD 20892-5460, USA.

出版信息

Mamm Genome. 2012 Oct;23(9-10):623-31. doi: 10.1007/s00335-012-9425-z. Epub 2012 Sep 1.

Abstract

The Mouse Metabolic Phenotyping Centers (MMPCs) were founded in 2001 by the National Institutes of Health (NIH) to advance biomedical research by providing the scientific community with standardized, high-quality phenotyping services for mouse models of diabetes, obesity, and their complications. The intent is to allow researchers to take optimum advantage of the many new mouse models produced in labs and in high-throughput public efforts. The six MMPCs are located at universities around the country and perform complex metabolic tests in intact mice and hormone and analyte assays in tissues on a fee-for-service basis. Testing is subsidized by the NIH in order to reduce the barriers for mouse researchers. Although data derived from these tests belong to the researcher submitting mice or tissues, these data are archived after publication in a public database run by the MMPC Coordinating and Bioinformatics Unit. It is hoped that data from experiments performed in many mouse models of metabolic diseases, using standard protocols, will be useful in understanding the nature of these complex disorders. The current areas of expertise include energy balance and body composition, insulin action and secretion, whole-body and tissue carbohydrate and lipid metabolism, cardiovascular and renal function, and metabolic pathway kinetics. In addition to providing services, the MMPC staff provides expertise and advice to researchers, and works to develop and refine test protocols to best meet the community's needs in light of current scientific developments. Test technology is disseminated by publications and through annual courses.

摘要

小鼠代谢表型中心(MMPC)成立于 2001 年,由美国国立卫生研究院(NIH)创立,旨在通过为糖尿病、肥胖症及其并发症的小鼠模型提供标准化、高质量的表型服务,推动生物医学研究。其目的是让研究人员能够充分利用实验室和高通量公共努力中产生的许多新的小鼠模型。这 6 个 MMPC 分布在全国各地的大学,根据服务收费的方式,在完整的小鼠中进行复杂的代谢测试,并在组织中进行激素和分析物的检测。NIH 对测试进行补贴,以降低对小鼠研究人员的障碍。虽然这些测试的数据属于提交小鼠或组织的研究人员,但在 MMPC 协调和生物信息学部门运行的公共数据库中发表后,这些数据会被存档。人们希望使用标准协议在许多代谢疾病的小鼠模型中进行的实验数据,将有助于理解这些复杂疾病的性质。目前的专业领域包括能量平衡和身体成分、胰岛素作用和分泌、全身和组织碳水化合物和脂质代谢、心血管和肾功能以及代谢途径动力学。除了提供服务外,MMPC 工作人员还为研究人员提供专业知识和建议,并努力开发和完善测试方案,以根据当前科学发展,最好地满足社区的需求。测试技术通过出版物和年度课程进行传播。

相似文献

1
NIH Mouse Metabolic Phenotyping Centers: the power of centralized phenotyping.
Mamm Genome. 2012 Oct;23(9-10):623-31. doi: 10.1007/s00335-012-9425-z. Epub 2012 Sep 1.
3
NIH experiment in centralized mouse phenotyping: the Vanderbilt experience and recommendations for evaluating glucose homeostasis in the mouse.
Am J Physiol Endocrinol Metab. 2009 Oct;297(4):E849-55. doi: 10.1152/ajpendo.90996.2008. Epub 2009 Jul 28.
5
Trans-NIH neuroscience initiatives on mouse phenotyping and mutagenesis.
Mamm Genome. 2001 Aug;12(8):575-81. doi: 10.1007/s00335-001-4005-7.
6
The future of Cochrane Neonatal.
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.
7
An action plan for mouse genomics.
Nat Genet. 1999 Jan;21(1):73-5. doi: 10.1038/5012.
8
9
The mutant mouse resource and research center (MMRRC) consortium: the US-based public mouse repository system.
Mamm Genome. 2024 Dec;35(4):524-536. doi: 10.1007/s00335-024-10070-3. Epub 2024 Sep 20.
10

引用本文的文献

3
Conserved immunomodulatory transcriptional networks underlie antipsychotic-induced weight gain.
Transl Psychiatry. 2021 Jul 22;11(1):405. doi: 10.1038/s41398-021-01528-y.
5
Recommended housing densities for research mice: filling the gap in data-driven alternatives.
FASEB J. 2019 Mar;33(3):3097-3111. doi: 10.1096/fj.201801972R. Epub 2018 Dec 6.
6
Network Modules of the Cross-Species Genotype-Phenotype Map Reflect the Clinical Severity of Human Diseases.
PLoS One. 2015 Aug 24;10(8):e0136300. doi: 10.1371/journal.pone.0136300. eCollection 2015.
7
Blastocyst genotyping for quality control of mouse mutant archives: an ethical and economical approach.
Transgenic Res. 2015 Oct;24(5):921-7. doi: 10.1007/s11248-015-9897-1. Epub 2015 Jul 16.
8
A review of standardized metabolic phenotyping of animal models.
Mamm Genome. 2014 Oct;25(9-10):497-507. doi: 10.1007/s00335-014-9532-0. Epub 2014 Sep 9.
9
Approach to assessing determinants of glucose homeostasis in the conscious mouse.
Mamm Genome. 2014 Oct;25(9-10):522-38. doi: 10.1007/s00335-014-9533-z. Epub 2014 Jul 30.
10

本文引用的文献

1
Hyperinsulinemic-euglycemic clamps in conscious, unrestrained mice.
J Vis Exp. 2011 Nov 16(57):3188. doi: 10.3791/3188.
4
Standard operating procedures for describing and performing metabolic tests of glucose homeostasis in mice.
Dis Model Mech. 2010 Sep-Oct;3(9-10):525-34. doi: 10.1242/dmm.006239. Epub 2010 Aug 16.
5
Assessment of feeding behavior in laboratory mice.
Cell Metab. 2010 Jul 7;12(1):10-7. doi: 10.1016/j.cmet.2010.06.001.
6
Identification of body fat mass as a major determinant of metabolic rate in mice.
Diabetes. 2010 Jul;59(7):1657-66. doi: 10.2337/db09-1582. Epub 2010 Apr 22.
7
The intestinal lymph fistula model--a novel approach to study ghrelin secretion.
Am J Physiol Gastrointest Liver Physiol. 2010 Mar;298(3):G474-80. doi: 10.1152/ajpgi.00367.2009. Epub 2009 Dec 31.
8
NIH experiment in centralized mouse phenotyping: the Vanderbilt experience and recommendations for evaluating glucose homeostasis in the mouse.
Am J Physiol Endocrinol Metab. 2009 Oct;297(4):E849-55. doi: 10.1152/ajpendo.90996.2008. Epub 2009 Jul 28.
9
Long chain fatty acid uptake in vivo: comparison of [125I]-BMIPP and [3H]-bromopalmitate.
Lipids. 2008 Aug;43(8):703-11. doi: 10.1007/s11745-008-3183-4. Epub 2008 May 15.
10
Glucose metabolism in vivo in four commonly used inbred mouse strains.
Diabetes. 2008 Jul;57(7):1790-9. doi: 10.2337/db07-1615. Epub 2008 Apr 8.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验