The circadian clock gene period extends healthspan in aging Drosophila melanogaster.

Natraj Krishnan, Doris Kretzschmar, Kuntol Rakshit, Eileen Chow, Jadwiga M. Giebultowicz

Research output: Contribution to journalArticle

75 Citations (Scopus)

Abstract

There is increasing evidence that aging is affected by biological (circadian) clocks - the internal mechanisms that coordinate daily changes in gene expression, physiological functions and behavior with external day/night cycles. Recent data suggest that disruption of the mammalian circadian clock results in accelerated aging and increased age-related pathologies such as cancer; however, the links between loss of daily rhythms and aging are not understood. We sought to determine whether disruption of the circadian clock affects lifespan and healthspan in the model organism Drosophila melanogaster. We examined effects of a null mutation in the circadian clock gene period (per(01)) on the fly healthspan by challenging aging flies with short-term oxidative stress (24h hyperoxia) and investigating their response in terms of mortality hazard, levels of oxidative damage, and functional senescence. Exposure to 24h hyperoxia during middle age significantly shortened the life expectancy in per(01) but not in control flies. This homeostatic challenge also led to significantly higher accumulation of oxidative damage in per(01) flies compared to controls. In addition, aging per(01) flies showed accelerated functional decline, such as lower climbing ability and increased neuronal degeneration compared to age-matched controls. Together, these data suggest that impaired stress defense pathways may contribute to accelerated aging in the per mutant. In addition, we show that the expression of per gene declines in old wild type flies, suggesting that the circadian regulatory network becomes impaired with age.

Original languageEnglish (US)
Pages (from-to)937-948
Number of pages12
JournalAging
Volume1
Issue number11
StatePublished - Nov 2009
Externally publishedYes

Fingerprint

Circadian Clocks
Drosophila melanogaster
Diptera
Genes
Hyperoxia
Biological Clocks
Gene Expression
Aptitude
Life Expectancy
Oxidative Stress
Pathology
Mutation
Mortality
Neoplasms

ASJC Scopus subject areas

  • Geriatrics and Gerontology

Cite this

Krishnan, N., Kretzschmar, D., Rakshit, K., Chow, E., & Giebultowicz, J. M. (2009). The circadian clock gene period extends healthspan in aging Drosophila melanogaster. Aging, 1(11), 937-948.

The circadian clock gene period extends healthspan in aging Drosophila melanogaster. / Krishnan, Natraj; Kretzschmar, Doris; Rakshit, Kuntol; Chow, Eileen; Giebultowicz, Jadwiga M.

In: Aging, Vol. 1, No. 11, 11.2009, p. 937-948.

Research output: Contribution to journalArticle

Krishnan, N, Kretzschmar, D, Rakshit, K, Chow, E & Giebultowicz, JM 2009, 'The circadian clock gene period extends healthspan in aging Drosophila melanogaster.', Aging, vol. 1, no. 11, pp. 937-948.
Krishnan N, Kretzschmar D, Rakshit K, Chow E, Giebultowicz JM. The circadian clock gene period extends healthspan in aging Drosophila melanogaster. Aging. 2009 Nov;1(11):937-948.
Krishnan, Natraj ; Kretzschmar, Doris ; Rakshit, Kuntol ; Chow, Eileen ; Giebultowicz, Jadwiga M. / The circadian clock gene period extends healthspan in aging Drosophila melanogaster. In: Aging. 2009 ; Vol. 1, No. 11. pp. 937-948.
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