Evidence for a circadian rhythm of susceptibility to retinal light damage

被引:0
|
作者
Vaughan, DK [1 ]
Nemke, JL
Fliesler, SJ
Darrow, RM
Organisciak, DT
机构
[1] Univ Wisconsin, Dept Biol & Microbiol, Oshkosh, WI 54901 USA
[2] St Louis Univ, Sch Med, Dept Ophthalmol, Inst Eye, St Louis, MO USA
[3] St Louis Univ, Sch Med, Dept Pharmacol & Physiol Sci, St Louis, MO USA
[4] Wright State Univ, Sch Med, Dept Biochem & Mol Biol, Dayton, OH USA
关键词
D O I
10.1562/0031-8655(2002)075<0547:EFACRO>2.0.CO;2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study investigated a possible circadian rhythm of light damage susceptibility in photoreceptors of both cyclic light-reared and dark-reared rats. A single exposure to intense green light was administered, beginning either in the early light period, the late light period or the dark period. In some animals exposed in the dark period, the synthetic antioxidant dimethylthiourea was administered before or after the onset of intense light exposure. Retinas were examined either immediately after exposure or after 2 weeks of recovery in darkness. Rod outer segment length and outer nuclear layer thickness measurements were used to assess light damage, along with qualitative analysis of swelling and disruption of the outer retinal layers. In all animals, retinal light damage was the most severe when intense light exposure began during the dark period. However, this severe damage was significantly reduced by pretreatment with the antioxidant. In a separate set of unexposed animals, fluctuations in plasma adrenocorticotropic hormone (ACTH) and corticosterone concentrations followed the same time course, regardless of the light regime during rearing. Our data support the notion or a circadian rhythm of light damage susceptibility that peaks in the dark period and yet can be modulated by the exogenous administration of an antioxidant.
引用
收藏
页码:547 / 553
页数:7
相关论文
共 50 条
  • [1] Morphological study of a circadian rhythm of retinal light damage.
    Nemke, JL
    Vaughan, DK
    Fliesler, SJ
    Darrow, R
    Organisciak, DT
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2001, 42 (04) : S628 - S628
  • [2] Factors underlying circadian dependent susceptibility to light induced retinal damage
    Grewal, R
    Organisciak, D
    Wong, P
    RETINAL DEGENERATIVE DISEASES, 2006, 572 : 411 - 416
  • [3] Circadian regulated genes underlying retinal susceptibility and resistance to light-induced damage
    Ziesel, Alison C.
    Organisciak, Daniel T.
    Chrenek, Micah A.
    Wong, Paul
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2014, 55 (13)
  • [4] Circadian-dependent retinal light damage in rats
    Organisciak, DT
    Darrow, RM
    Barsalou, L
    Kutty, RK
    Wiggert, B
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (12) : 3694 - 3701
  • [5] CIRCADIAN SUSCEPTIBILITY RHYTHM TO HALOPERIDOL
    TAKAGI, A
    NAGAYAMA, H
    NISHIWAKI, K
    SAKURAI, Y
    TAKAHASHI, R
    JAPANESE JOURNAL OF PHARMACOLOGY, 1978, 28 : P49 - P49
  • [6] Blue light disrupts the circadian rhythm and create damage in skin cells
    Dong, K.
    Goyarts, E. C.
    Pelle, E.
    Trivero, J.
    Pernodet, N.
    INTERNATIONAL JOURNAL OF COSMETIC SCIENCE, 2019, 41 (06) : 558 - 562
  • [7] Rhodopsin and circadian dependent retinal light damage in transgenic rats
    Organisciak, DT
    Darrow, RM
    Barsalou, L
    Bicknell, IR
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1999, 40 (04) : S226 - S226
  • [8] CIRCADIAN SUSCEPTIBILITY RHYTHM OF THE RAT TO ALLOXAN
    HERNANDEZ, RE
    KUHL, JFW
    HALBERG, E
    HALBERG, F
    SHIOTSUKA, RN
    HAUS, E
    CHRONOBIOLOGIA, 1978, 5 (04) : 369 - 378
  • [9] STUDIES ON CIRCADIAN SUSCEPTIBILITY RHYTHM TO HALOPERIDOL
    NAGAYAMA, H
    TAKAGI, A
    SAKURAI, Y
    YOSHIMOTO, S
    NISHIWAKI, K
    TAKAHASHI, R
    FOLIA PHARMACOLOGICA JAPONICA, 1978, 74 (08) : 951 - 957
  • [10] MURINE CIRCADIAN SUSCEPTIBILITY RHYTHM TO CYCLOPHOSPHAMIDE
    HAUS, E
    FERNANDES, G
    KUHL, JFW
    YUNIS, EJ
    LEE, JK
    HALBERG, F
    CHRONOBIOLOGIA, 1974, 1 (03) : 270 - 277