Literature DB >> 9885957

Effects of aging on lens transmittance and retinal input to the suprachiasmatic nucleus in golden hamsters.

Y Zhang1, G C Brainard, P C Zee, L H Pinto, J S Takahashi, F W Turek.   

Abstract

Old animals are less sensitive by almost an order of magnitude to the phase-shifting effects of a low intensity light pulse on the locomotor activity rhythm and the associated induction of immediate early genes in the circadian clock. The transmittance of energy from 200 to 700 nm through the excised lens of the eyes of young and old golden hamsters was measured to determine if an age-related difference exists in the transmittance of light. There is only a small decrease (8-50%) in transmittance, with the magnitude being dependent upon wavelength. No significant differences were detected between young and old animals in the retinal innervation of the suprachiasmatic nucleus (SCN). These results support the hypothesis that the observed decrease in sensitivity to light in the aged circadian system occurs within the SCN itself and/or retino-hypothalamic tract photoreceptors.

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Mesh:

Year:  1998        PMID: 9885957     DOI: 10.1016/s0304-3940(98)00887-8

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  16 in total

1.  Responsiveness of the aging circadian clock to light.

Authors:  S Benloucif; K Green; M L'Hermite-Balériaux; S Weintraub; L F Wolfe; P C Zee
Journal:  Neurobiol Aging       Date:  2005-11-23       Impact factor: 4.673

2.  Decreased sensitivity to phase-delaying effects of moderate intensity light in older subjects.

Authors:  Jeanne F Duffy; Jamie M Zeitzer; Charles A Czeisler
Journal:  Neurobiol Aging       Date:  2006-04-18       Impact factor: 4.673

Review 3.  Aging in the circadian system: considerations for health, disease prevention and longevity.

Authors:  Erin M Gibson; Wilbur P Williams; Lance J Kriegsfeld
Journal:  Exp Gerontol       Date:  2008-05-23       Impact factor: 4.032

4.  Visual adaptations in a diurnal rodent, Octodon degus.

Authors:  G H Jacobs; J B Calderone; J A Fenwick; K Krogh; G A Williams
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2003-04-05       Impact factor: 1.836

Review 5.  The circadian clock and pathology of the ageing brain.

Authors:  Anna A Kondratova; Roman V Kondratov
Journal:  Nat Rev Neurosci       Date:  2012-03-07       Impact factor: 34.870

6.  Age-related changes in neurochemical components and retinal projections of rat intergeniculate leaflet.

Authors:  Felipe P Fiuza; Kayo D A Silva; Renata A Pessoa; André L B Pontes; Rodolfo L P Cavalcanti; Raquel S Pires; Joacil G Soares; Expedito S Nascimento Júnior; Miriam S M O Costa; Rovena C G J Engelberth; Jeferson S Cavalcante
Journal:  Age (Dordr)       Date:  2015-12-30

Review 7.  The circadian timing system: a recent addition in the physiological mechanisms underlying pathological and aging processes.

Authors:  Elvira Arellanes-Licea; Ivette Caldelas; Dalia De Ita-Pérez; Mauricio Díaz-Muñoz
Journal:  Aging Dis       Date:  2014-01-09       Impact factor: 6.745

8.  Voluntary exercise can strengthen the circadian system in aged mice.

Authors:  T L Leise; M E Harrington; P C Molyneux; I Song; H Queenan; E Zimmerman; G S Lall; S M Biello
Journal:  Age (Dordr)       Date:  2013-01-23

Review 9.  Aging and Circadian Rhythms.

Authors:  Jeanne F Duffy; Kirsi-Marja Zitting; Evan D Chinoy
Journal:  Sleep Med Clin       Date:  2015-09-15

10.  Circadian clock resetting in the mouse changes with age.

Authors:  Stephany M Biello
Journal:  Age (Dordr)       Date:  2009-12
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