Chronic light exposure alters serotonergic and orexinergic systems in the rat brain and reverses maternal separation-induced increase in orexin receptors in the prefrontal cortex

被引:5
|
作者
Dimatelis, J. J. [1 ]
Mtintsilana, A. [1 ]
Naidoo, V. [1 ]
Stein, D. J. [2 ,3 ]
Russell, V. A. [1 ]
机构
[1] Univ Cape Town, Dept Human Biol, Fac Hlth Sci, ZA-7925 Cape Town, South Africa
[2] Univ Cape Town, Dept Psychiat & Mental Hlth, Fac Hlth Sci, ZA-7925 Cape Town, South Africa
[3] Univ Cape Town, MRC Unit Anxiety & Stress Disorders, Fac Hlth Sci, ZA-7925 Cape Town, South Africa
基金
新加坡国家研究基金会;
关键词
Depression; Maternal separation; Chronic constant light; Dopamine; serotonin; Orexin; DEPRESSIVE-LIKE BEHAVIOR; CONSTANT LIGHT; ENERGY HOMEOSTASIS; ADRENAL-FUNCTION; DOPAMINE SYSTEM; STRESS; NUCLEUS; ANXIETY; REWARD; OREXIN/HYPOCRETIN;
D O I
10.1007/s11011-017-0123-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Maternal separation (MS) is a well-established rodent model of depression. Chronic constant light (CCL) treatment during adolescence has been shown to reverse the depression-like behaviour induced by MS. We aimed to further delineate the antidepressant effect of light by investigating the involvement of the dopaminergic, serotonergic and orexinergic systems. MS was used to induce changes in adult male Sprague-Dawley rats, some of whom were also treated with CCL for 3 weeks during adolescence. At P80, rats were decapitated and brain tissue collected for analysis of glutamate- and potassium-stimulated dopamine release in the nucleus accumbens (NAc) using an in vitro superfusion technique. Enzyme-linked immunosorbent assays were employed to measure 5-hydroxytryptamine (5-HT) levels in the hypothalamus and prefrontal cortex (PFC). Western blotting was used to measure orexin receptor 1 (OXR-1) and 2 (OXR-2) in the PFC. MS did not affect 5-HT levels in these rats. However, CCL increased hypothalamic 5-HT and reduced 5-HT levels in the PFC. CCL had opposite effects on OXR levels in the PFC of maternally separated and non-separated rats. MS increased OXR-1 and OXR-2 levels in the PFC, an effect that was normalized by CCL treatment. MS reduced glutamate-stimulated dopamine release in the NAc, an effect that was not reversed by CCL. The present results suggest that CCL treatment affects 5-HT and orexinergic systems in the MS model while not affecting the MS-induced decrease in dopamine release in the NAc. The reversal of changes in the orexinergic system may be of particular relevance to the antidepressant effect of CCL in depression.
引用
收藏
页码:433 / 441
页数:9
相关论文
共 6 条
  • [1] Chronic light exposure alters serotonergic and orexinergic systems in the rat brain and reverses maternal separation-induced increase in orexin receptors in the prefrontal cortex
    J. J. Dimatelis
    A. Mtintsilana
    V. Naidoo
    D. J. Stein
    V. A. Russell
    Metabolic Brain Disease, 2018, 33 : 433 - 441
  • [2] Chronic exposure to light reverses the effects of maternal separation on the rat prefrontal cortex
    Russel, V.
    Dimatelis, J.
    SOUTH AFRICAN JOURNAL OF PSYCHIATRY, 2013, 19 (03) : 122 - 123
  • [3] Chronic Exposure to Light Reverses the Effect of Maternal Separation on Proteins in the Prefrontal Cortex
    Dimatelis, J. J.
    Stein, D. J.
    Russell, V. A.
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2013, 51 (03) : 835 - 843
  • [4] Chronic Exposure to Light Reverses the Effect of Maternal Separation on Proteins in the Prefrontal Cortex
    J. J. Dimatelis
    D. J. Stein
    V. A. Russell
    Journal of Molecular Neuroscience, 2013, 51 : 835 - 843
  • [5] Maternal separation alters serotonergic transporter densities and serotonergic 1A receptors in rat brain
    Vicentic, A.
    Francis, D.
    Moffett, M.
    Lakatos, A.
    Rogge, G.
    Hubert, G. W.
    Harley, J.
    Kuhar, M. J.
    NEUROSCIENCE, 2006, 140 (01) : 355 - 365
  • [6] CHRONIC ETHANOL INDUCED INCREASE IN HMGB1 AND RAGE EXPRESSION IN PREFRONTAL CORTEX OF ADULT RAT BRAIN IS MEDIATED BY CB1 CANNABINOID RECEPTOR DEPENDEN
    Khatri, D.
    Laroche, G.
    Vetreno, R.
    Crews, F.
    Mukhopadhyay, S.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2016, 40 : 23A - 23A