Mesolimbic dopamine system and its modulation by vitamin D in a chronic mild stress model of depression in the rat
•Active form of vitamin D selectively reduced anhedonic effect of chronic mild stress (CMS) induced-depression-like behavior dose dependently in rat.•Vitamin D did not affect the anxiety-like behavior in CMS rats.•Vitamin D restored the Dopamine transporter, DAT, protein expression after significant...
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Veröffentlicht in: | Behavioural brain research 2019-01, Vol.356, p.156-169 |
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Sprache: | eng |
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Zusammenfassung: | •Active form of vitamin D selectively reduced anhedonic effect of chronic mild stress (CMS) induced-depression-like behavior dose dependently in rat.•Vitamin D did not affect the anxiety-like behavior in CMS rats.•Vitamin D restored the Dopamine transporter, DAT, protein expression after significant decline following the CMS in rat. This effect was similar to or higher than anti-depressant fluoxetine.
Depression, a common mood disorder, involves anhedonia and defects in reward circuits and mesolimbic dopamine transmission in the striatum and nucleus accumbens (NAc). Active vitamin-D, (1,25-(OH)2 vitamin-D3), exerts protective and regulatory effects on the brain dopamine system. In this study, key depression-like symptoms were induced in rats by chronic mild-stress (CMS) and the comparative effect of treatment with 1,25-(OH)2 vitamin-D3 (5, 10 μg/kg, or vehicle; i.p., twice weekly) or fluoxetine (5 mg/kg or vehicle, i.p., daily) on anhedonic behavior, locomotor activity and anxiety-like behavior was examined using sucrose preference test (SPT), open field test (OFT) and novel object exploration test (NOT), respectively. We also measured serum corticosterone levels and dopamine transporter-immunoreactivity (DAT-ir) levels in NAc shell and core. CMS exposure for 3 weeks was followed by a SPT and thereafter CMS was continued for 5 weeks, along with vitamin-D or fluoxetine treatment and further testing, which was concluded with another SPT. Vitamin-D treatment enhanced sucrose preference (P |
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ISSN: | 0166-4328 1872-7549 |
DOI: | 10.1016/j.bbr.2018.08.020 |