Show simple item record

‘Accelerated aging’: a primrose path to insight?

dc.contributor.authorMiller, Richard A.en_US
dc.date.accessioned2010-06-01T19:56:09Z
dc.date.available2010-06-01T19:56:09Z
dc.date.issued2004-04en_US
dc.identifier.citationMiller, Richard A. (2004). "‘Accelerated aging’: a primrose path to insight?." Aging Cell 3(2): 47-51. <http://hdl.handle.net/2027.42/73065>en_US
dc.identifier.issn1474-9718en_US
dc.identifier.issn1474-9726en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/73065
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15038817&dopt=citationen_US
dc.description.abstractOrganism envy afflicts most researchers who work on aging in mice; how frustrating it is to see the worm and fly biologists nail down milestone after milestone, citation after citation! Surely genetic trickery can produce mice that age in a comparable jiffy? Alas, our near-total ignorance of what times the aging process makes it hard to guess what genes to tweak, if indeed aging can be mimicked a presto . Building a case that a given short-lived mutant ages quickly is a steep and thorny path, requiring more than just plucking a symptom here and there from a list of things that sometimes go wrong in old people or old mice. The hallmark of aging is that a lot goes wrong more or less at the same time, in 2-year-old mice, 10-year-old dogs and 70-year-old people. Finding ways to damage one or two systems in a 6-week or 6-month-old mouse is not too hard to do, but the implications of such studies for improved understanding of aging per se are at best indirect and at worst imaginary and distracting.en_US
dc.format.extent111292 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing, Ltd.en_US
dc.rights© Blackwell Publishing Ltd/Anatomical Society of Great Britain and Ireland 2004en_US
dc.subject.otherSegmental Agingen_US
dc.subject.otherSkepticismen_US
dc.subject.otherLongevityen_US
dc.subject.otherMouse Modelsen_US
dc.subject.otherMutantsen_US
dc.subject.otherPathologyen_US
dc.title‘Accelerated aging’: a primrose path to insight?en_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology and Geriatrics Center, University of Michigan, Ann Arbor VA Medical Center, Ann Arbor, MI 48103, USAen_US
dc.identifier.pmid15038817en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/73065/1/j.1474-9728.2004.00081.x.pdf
dc.identifier.doi10.1111/j.1474-9728.2004.00081.xen_US
dc.identifier.sourceAging Cellen_US
dc.identifier.citedreferenceAustad SN, Fischer KE ( 1991 ) Mammalian aging, metabolism, and ecology: evidence from the bats and marsupials. J. Gerontol.: Biol. Sci. 46, B47 – B53.en_US
dc.identifier.citedreferenceBartke A, Wright JC, Mattison JA, Ingram DK, Miller RA, Roth GS ( 2001 ) Extending the lifespan of long-lived mice. Nature 414, 412.en_US
dc.identifier.citedreferenceBluher M, Kahn BB, Kahn CR ( 2003 ) Extended longevity in mice lacking the insulin receptor in adipose tissue. Science 299, 572 – 574.en_US
dc.identifier.citedreferenceBrown WT ( 1991 ) Genetic diseases of premature aging as models of senescence. Annu. Rev. Gerontol. Geriatrics 10, 23 – 42.en_US
dc.identifier.citedreferenceChaffey A ( 2003 ) Double dactyls. http://www.stinky.com/dactyl/dactyl.html #description. 28 November 2003.en_US
dc.identifier.citedreferenceFlurkey K, Papaconstantinou J, Miller RA, Harrison DE ( 2001 ) Lifespan extension and delayed immune and collagen aging in mutant mice with defects in growth hormone production. Proc. Natl Acad. Sci. USA 98, 6736 – 6741.en_US
dc.identifier.citedreferenceGershon D ( 1979 ) Current status of age altered enzymes: alternative mechanisms. Mechanisms Ageing Dev. 9, 189 – 196.en_US
dc.identifier.citedreferenceHarrison DE ( 1994 ) Potential misinterpretations using models of accelerated aging. J. Gerontol.: Biol. Sci. 49, B245 – B000.en_US
dc.identifier.citedreferenceHasty P, Campisi J, Hoeijmakers J, van Steeg H, Vijg J ( 2003 ) Aging and genome maintenance: lessons from the mouse? Science 299, 1355 – 1359.en_US
dc.identifier.citedreferenceHerrera E, Samper E, Martin-Caballero J, Flores JM, Lee HW, Blasco MA ( 1999 ) Disease states associated with telomerase deficiency appear earlier in mice with short telomeres. EMBO J. 18, 2950 – 2960.en_US
dc.identifier.citedreferenceHolzenberger M, Dupont J, Ducos B, Leneuve P, Geloen A, Even PC, Cervera P and Le Bouc Y. ( 2003 ) IGF-1 receptor regulates lifespan and resistance to oxidative stress in mice. Nature 421, 182 – 187.en_US
dc.identifier.citedreferenceIkeno Y, Bronson RT, Hubbard GB, Lee S, Bartke A ( 2003 ) Delayed occurrence of fatal neoplastic diseases in ames dwarf mice: correlation to extended longevity. J. Gerontol. Series. A. -Biol. Sci. Med. Sci. 58, 291 – 296.en_US
dc.identifier.citedreferenceKinney BA, Coschigano KT, Kopchick JJ, Steger RW, Bartke A ( 2001a ) Evidence that age-induced decline in memory retention is delayed in growth hormone resistant GH-R.-KO (Laron) mice. Physiol. Behav. 72, 653 – 660.en_US
dc.identifier.citedreferenceKinney BA, Meliska CJ, Steger RW, Bartke A ( 2001b ) Evidence that Ames dwarf mice age differently from their normal siblings in behavioral and learning and memory parameters. Horm. Behav. 39, 277 – 284.en_US
dc.identifier.citedreferenceKuro-o M, Matsumura Y, Aizawa H, Kawaguchi H, Suga T, Utsugi T, Ohyama Y, Kurabayashi M, Kaname T, Kume E, Iwasaki H, Lida A, Shiraki-lida T, Nishikawa S, Nagai R and Nabeshima YI. ( 1997 ) Mutation of the mouse klotho gene leads to a syndrome resembling ageing. Nature 390, 45 – 51.en_US
dc.identifier.citedreferenceLi Y, Huang TT, Carlson EJ, et al. ( 1995 ) Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. Nat. Genet. 11, 376 – 381.en_US
dc.identifier.citedreferenceMiller RA ( 2001 ) Genetics of increased longevity and retarded aging in mice. In Handbook of the Biology of Aging ( Masoro EJ, Austad SN, eds). San Diego, CA: Academic Press, pp. 369 – 395.en_US
dc.identifier.citedreferenceMiller RA, Austad SN ( 1999 ) Large animals in the fast lane. Science 285, 199.en_US
dc.identifier.citedreferenceMiller RA, Harper JM, Dysko RC, Durkee SJ, Austad SN ( 2002 ) Longer life spans and delayed maturation in wild-derived mice. Exp. Biol. Med. 227, 500 – 508.en_US
dc.identifier.citedreferenceOlshansky SJ, Carnes BA, Cassel C ( 1990 ) In search of Methuselah: estimating the upper limits to human longevity. Science 250, 634 – 640.en_US
dc.identifier.citedreferenceSilberberg R ( 1972 ) Articular aging and osteoarthritis in dwarf mice. Path. Microbiol. 38, 417 – 430.en_US
dc.identifier.citedreferenceSmith GS, Walford RL ( 1977 ) Influence of the main histocompatibility complex on aging in mice. Nature 270, 727 – 729.en_US
dc.identifier.citedreferenceTakeshita S, Hosokawa M, Irino M, et al. ( 1982 ) Spontaneous age-associated amyloidosis in senescence-accelerated mouse (SAM). Mechanisms Ageing Dev. 20, 13 – 23.en_US
dc.identifier.citedreferenceTyner SD, Venkatachalam S, Choi J, et al. ( 2002 ) p53 mutant mice that display early ageing-associated phenotypes. Nature 415, 45 – 53.en_US
dc.identifier.citedreferenceUmezawa M, Hosokawa M, Kohno A, Ishikawa S, Kitagawa K, Takeda T ( 1993 ) Dietary soybean protein compared with casein retards senescence in the senescence accelerated mouse. J. Nutr. 123, 1905 – 1912.en_US
dc.identifier.citedreferenceZimmerman JA, Malloy V, Krajcik R, Orentreich N ( 2003 ) Nutritional control of aging. Exp. Gerontol. 38, 47 – 52.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.