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. 2008 Sep;30(2-3):135-45.
doi: 10.1007/s11357-008-9057-0. Epub 2008 May 30.

Wild-derived mouse stocks: an underappreciated tool for aging research

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Wild-derived mouse stocks: an underappreciated tool for aging research

James M Harper. Age (Dordr). 2008 Sep.

Abstract

Virtually all biomedical research makes use of a relatively small pool of laboratory-adapted, inbred, isogenic stocks of mice. Although the advantages of these models are many, there are a number of disadvantages as well. When studying a multifaceted process such as aging, the problems associated with using laboratory stocks are greatly inflated. On the other hand, wild-derived mouse stocks, loosely defined here as either wild-caught individuals or the recent progeny of wild-caught individuals, have much to offer to biogerontology research. Hence, the aims of this review are threefold: (1) to (re)acquaint readers with the pros and cons of using a typical inbred laboratory mouse model for aging research; (2) to reintroduce the notion of using wild-derived mouse stocks in aging research as championed by Austad, Miller and others for more than a decade, and (3) to provide an overview of recent advances in biogerontology using wild-derived mouse stocks.

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References

    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'DOI', 'value': '10.1016/j.exger.2004.09.005', 'is_inner': False, 'url': 'https://doi.org/10.1016/j.exger.2004.09.005'}, {'type': 'PubMed', 'value': '15664729', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/15664729/'}]}
    2. Argentino DP, Dominici FP, Munoz MC, Al-Regaiey K, Bartke A, Turyn D (2005) Effects of long-term caloric restriction on glucose homeostasis and on the first steps of the insulin signaling system in skeletal muscle of normal and Ames dwarf (Prop1df/Prop1df) mice. Exp Gerontol 40:27–35 - PubMed
    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'PubMed', 'value': '8297929', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/8297929/'}]}
    2. Austad S (1993a) The comparative perspective and choice of animal models in aging research. Aging Clin Exp Res 5:259–267 - PubMed
    1. None
    2. Austad SN (1993b) Retarded senescence in an insular population of Virginia opossums (Didelphis virginiana). J Zool 229:695–708
    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'DOI', 'value': '10.1046/j.1474-9728.2003.00053.x', 'is_inner': False, 'url': 'https://doi.org/10.1046/j.1474-9728.2003.00053.x'}, {'type': 'PubMed', 'value': '12934713', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/12934713/'}]}
    2. Austad SN, Kristan DM (2003) Are mice calorically restricted in nature? Aging Cell 2:201–207 - PubMed
    1. {'text': '', 'ref_index': 1, 'ids': [{'type': 'DOI', 'value': '10.1023/A:1022448532248', 'is_inner': False, 'url': 'https://doi.org/10.1023/a:1022448532248'}, {'type': 'PubMed', 'value': '12652183', 'is_inner': True, 'url': 'https://pubmed.ncbi.nlm.nih.gov/12652183/'}]}
    2. Bartke A, Chandrashekar V, Dominici F, Turyn D, Kinney B, Steger R, Kopchick JJ (2003) Insulin-like growth factor 1 (IGF-1) and aging: controversies and new insights. Biogerontology 4:1–8 - PubMed