Literature DB >> 8282970

Selecting animal models of human aging: inbred strains often exhibit less biological uniformity than F1 hybrids.

J P Phelan1, S N Austad.   

Abstract

Most gerontological research is conducted using inbred strains of animals in an attempt to maximize phenotypic uniformity within experiments and thus increase the experimenter's statistical power to detect treatment effects. However, for a wide range of phenotypic traits, F1 hybrids between inbred strains are considerably less variable than the parental inbred strains themselves. Therefore, the use of F1 hybrids is preferable for many research applications. In this article, we discuss the sources of phenotypic variability and explain why F1 hybrids are often less variable than inbred strains; we review the empirical literature illustrating the large range of species and traits for which this is true; and finally we suggest how this finding suggests that F1 hybrids may often be superior animal models for studying the aging process and how to manipulate it.

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Year:  1994        PMID: 8282970     DOI: 10.1093/geronj/49.1.b1

Source DB:  PubMed          Journal:  J Gerontol        ISSN: 0022-1422


  24 in total

1.  Life extension by diet restriction and N-acetyl-L-cysteine in genetically heterogeneous mice.

Authors:  Kevin Flurkey; Clinton M Astle; David E Harrison
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2010-09-05       Impact factor: 6.053

2.  Naturally occurring osteoarthritis in male mice with an extended lifespan.

Authors:  Dave Ewart; Lindsey Harper; Amy Gravely; Richard A Miller; Cathy S Carlson; Richard F Loeser
Journal:  Connect Tissue Res       Date:  2019-09-18       Impact factor: 3.417

3.  Normal aging involves modulation of specific inflammatory markers in the rat retina and choroid.

Authors:  Jena J Steinle; Sheena Sharma; Christopher P Smith; Lisa S McFayden-Ketchum
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2009-01-30       Impact factor: 6.053

4.  Aging in inbred strains of mice: study design and interim report on median lifespans and circulating IGF1 levels.

Authors:  Rong Yuan; Shirng-Wern Tsaih; Stefka B Petkova; Caralina Marin de Evsikova; Shuqin Xing; Michael A Marion; Molly A Bogue; Kevin D Mills; Luanne L Peters; Carol J Bult; Clifford J Rosen; John P Sundberg; David E Harrison; Gary A Churchill; Beverly Paigen
Journal:  Aging Cell       Date:  2009-04-09       Impact factor: 9.304

5.  Age-associated increase in cleaved caspase 3 despite phosphorylation of IGF-1 receptor in the rat retina.

Authors:  Youde Jiang; Robert J Walker; Jena J Steinle
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2009-08-20       Impact factor: 6.053

6.  Not Your Father's, or Mother's, Rodent: Moving Beyond B6.

Authors:  Richard A Miller
Journal:  Neuron       Date:  2016-09-21       Impact factor: 17.173

7.  Getting to compliance in forced exercise in rodents: a critical standard to evaluate exercise impact in aging-related disorders and disease.

Authors:  Jennifer C Arnold; Michael F Salvatore
Journal:  J Vis Exp       Date:  2014-08-22       Impact factor: 1.355

8.  Spatial reference memory in normal aging Fischer 344 × Brown Norway F1 hybrid rats.

Authors:  Joseph A McQuail; Michelle M Nicolle
Journal:  Neurobiol Aging       Date:  2014-07-03       Impact factor: 4.673

9.  Aging reveals a role for nigral tyrosine hydroxylase ser31 phosphorylation in locomotor activity generation.

Authors:  Michael F Salvatore; Brandon S Pruett; Sandy L Spann; Charles Dempsey
Journal:  PLoS One       Date:  2009-12-23       Impact factor: 3.240

10.  Rapamycin fed late in life extends lifespan in genetically heterogeneous mice.

Authors:  David E Harrison; Randy Strong; Zelton Dave Sharp; James F Nelson; Clinton M Astle; Kevin Flurkey; Nancy L Nadon; J Erby Wilkinson; Krystyna Frenkel; Christy S Carter; Marco Pahor; Martin A Javors; Elizabeth Fernandez; Richard A Miller
Journal:  Nature       Date:  2009-07-08       Impact factor: 49.962

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