首页> 外文期刊>Neuropsychopharmacology >Overexpression of corticotropin-releasing factor in the nucleus accumbens enhances the reinforcing effects of nicotine in intact?female versus male?and ovariectomized female rats
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Overexpression of corticotropin-releasing factor in the nucleus accumbens enhances the reinforcing effects of nicotine in intact?female versus male?and ovariectomized female rats

机译:核心尿蛋白酶释放因子的过度表达增强了尼古丁在完整的增强效果?雌性与雄性α和卵巢切除的雌性大鼠

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This study assessed the role of stress systems in the nucleus accumbens (NAc) in promoting sex differences in the reinforcing effects of nicotine. Intravenous self-administration (IVSA) of various doses of nicotine was compared following overexpression of corticotropin-releasing factor (CRF) in the NAc of female and male rats. Ovariectomized (OVX) females were also included to assess the role of ovarian hormones in promoting nicotine reinforcement. Rats received intra-NAc administration of an adeno-associated vector that overexpressed CRF (AAV2/5-CRF) or green fluorescent protein (AAV2/5-GFP). All rats were then given extended access (23?h/day) to an inactive and an active lever that delivered nicotine. Separate groups of rats?received intra-NAc AAV2/5-CRF and saline IVSA. Rats were also allowed to nose-poke for food and water during IVSA testing. At the end of the study, the NAc was dissected and rt-qPCR methods were used to estimate CRF overexpression and changes in CRF receptors (CRFr1, CRFr2) and the CRF receptor internalizing protein, β-arrestin2 (Arrb2). Overexpression of CRF in the NAc increased nicotine IVSA to a larger extent in intact female versus male and OVX females. Food intake was increased to a larger extent in intact and OVX females as compared to males. The increase in CRF gene expression was similar across all groups; however, in females, overexpression of CRF resulted in a larger increase in CRFr1 and CRFr2 relative to males. In males, overexpression of CRF produced a larger increase in Arrb2 than females, suggesting greater CRF receptor internalization. Our results suggest that stress systems in the NAc promote the reinforcing effectiveness of nicotine in female rats in an ovarian hormone-dependent manner.
机译:该研究评估了应力系统在核心尿嘧啶(NAC)中的作用促进尼古丁增强作用的性差异。在雌性和雄性大鼠的NAC中的皮质甾醇释放因子(CRF)过表达后,比较各种剂量的尼古丁的静脉内自我管理(IVSA)。还包括卵巢切除术(OVX)女性,以评估卵巢激素在促进尼古丁增强方面的作用。大鼠接受NAC内酰上施用过表达CRF(AAV2 / 5-CRF)或绿色荧光蛋白(AAV2 / 5-GFP)的腺相关载体。然后将所有大鼠延长进入(23Ω·h /天)递送到无效和递送尼古丁的活性杆。单独的大鼠组?接受NAC内AAV2 / 5-CRF和盐水IVSA。在IVSA测试期间,大鼠也可用于食物和水的鼻子。在研究结束时,解剖NAC,使用RT-QPCR方法来估计CRF过表达和CRF受体(CRFR1,CRFR2)和CRF受体内化蛋白,β-ArcketIn2(ARRB2)的变化。在NAC中CRF的过度表达在完整的女性与雄性和OVX女性中增加了尼古丁IVSA至更大程度。与雄性相比,食物摄入量增加至更大程度的完整和OVX女性。所有群体中CRF基因表达的增加相似;然而,在雌性中,CRF的过度表达导致CRFR1和CRFR2相对于雄性的增加较大。在雄性中,CRF的过度表达比女性在ARRB2增加,表明更大的CRF受体内化。我们的研究结果表明,NAC中的应力系统以卵巢激素依赖性方式促进尼古丁在雌性大鼠中的增强效果。

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