Laboratory for Molecular Biology and Endocrinology, VINCA Institute of Nuclear Sciences, University of Belgrade, PO Box-522-MBE090, 11001 Belgrade, Serbia.
Neuropharmacology. 2013 Jul;70:100-11. doi: 10.1016/j.neuropharm.2012.12.012. Epub 2013 Jan 23.
Chronic psychosocial isolation stress (CPSI) modulates glucocorticoid receptor (GR) functioning in Wistar male rat hippocampus (HIPPO) through alteration of nuclear GR phosphorylation and its upstream kinases signaling, which parallels animal depressive-like behavior. The current study investigated potential gender specificities regarding the effect of chronic therapy by an antidepressant fluoxetine (FLU) on GR signaling in HIPPO and depressive-like behavior in CPSI animals. FLU was administrated to female and male naïve or CPSI rats for 21 days and GR protein, its phosphorylation status and upstream kinases, as well as GR and BDNF mRNA were followed in HIPPO together with animal serum corticosterone (CORT) and depressive-like behavior. The results showed that CPSI increased immobility in males versus hyperactivity in females and disrupted nuclear pGR232-Cdk5 pathway and JNK signaling in a gender-specific way. In contrast, in both genders CPSI increased the nuclear levels of GR and pGR246 but decreased CORT and mRNA levels of GR and BDNF. Concomitant FLU normalized the depressive-like behavior and altered the nuclear pGR232-Cdk5 signaling in a gender-specific manner. In both females and males, FLU reversed the nuclear levels of GR and pGR246 without affecting CORT and GR mRNA levels. In contrast, FLU exhibited gender-specific effect on BDNF mRNA in CPSI animals, by increasing it in females, but not in males. In spite of normalization the total nuclear GR level upon FLU treatment in both gender, down-regulation of GR mRNA is possibly maintained through prevalence of pGR232 isoform only in males. The gender-specific alterations of pGR232-Cdk5 signaling and BDNF gene expression in HIPPO and normalization of depressive-like behavior upon FLU treatment distinguishes this signaling pathway as potential future antidepressant target for gender-specific therapy of stress related mood disorders.
慢性心理社会隔离应激(CPSI)通过改变核 GR 磷酸化及其上游激酶信号转导,调节 Wistar 雄性大鼠海马(HIPPO)中的糖皮质激素受体(GR)功能,这与动物抑郁样行为平行。本研究调查了慢性抗抑郁药氟西汀(FLU)治疗对 CPSI 动物 HIPPO 中 GR 信号转导和抑郁样行为的潜在性别特异性影响。FLU 被给予雌性和雄性的未处理或 CPSI 大鼠 21 天,并在 HIPPO 中跟踪 GR 蛋白、其磷酸化状态和上游激酶,以及动物血清皮质酮(CORT)和抑郁样行为。结果表明,CPSI 增加了雄性的不动性,而增加了雌性的多动性,并以性别特异性的方式破坏了核 pGR232-Cdk5 途径和 JNK 信号。相反,在两种性别中,CPSI 均增加了核 GR 和 pGR246 的水平,但降低了 CORT 和 GR 和 BDNF 的 mRNA 水平。同时,FLU 以性别特异性的方式使抑郁样行为正常化并改变了核 pGR232-Cdk5 信号。在雌性和雄性中,FLU 逆转了核 GR 和 pGR246 的水平,而不影响 CORT 和 GR mRNA 水平。相反,FLU 在 CPSI 动物中对 BDNF mRNA 表现出性别特异性效应,在雌性中增加,但在雄性中不增加。尽管在两种性别中,FLU 治疗后总核 GR 水平正常化,但仅在雄性中 pGR232 同工型的优势可能维持 GR mRNA 的下调。HIPPO 中 pGR232-Cdk5 信号和 BDNF 基因表达的性别特异性改变以及 FLU 治疗对抑郁样行为的正常化将这种信号通路区分出来,作为针对应激相关情绪障碍的性别特异性治疗的潜在未来抗抑郁靶标。