Schwartzer Jared J, Ricci Lesley A, Melloni Richard H
Behavioral Neuroscience Program, Department of Psychology, 125 Nightingale Hall, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, United States.
Behav Brain Res. 2009 May 16;199(2):257-62. doi: 10.1016/j.bbr.2008.11.048. Epub 2008 Dec 6.
Chronic anabolic-androgenic steroid (AAS) treatment during adolescence facilitates offensive aggression in male Syrian hamsters (Mesocricetus auratus). Serotonin (5-HT) modulates aggressive behavior and has been shown to be altered after chronic treatment with AAS. Furthermore, 5-HT type 2 receptors have been implicated in the control of aggression. For example, treatment with 5-HT(2A) receptor antagonists suppress the generation of the offensive aggressive phenotype. However, it is unclear whether these receptors are sensitive to adolescent AAS exposure. The current study assessed whether treatment with AAS throughout adolescence influenced the immunohistochemical localization of 5-HT(2A) in areas of the hamster brain implicated in the control of aggression. Hamsters were administered AAS (5.0 mg/kg) each day throughout adolescence, scored for offensive aggression, and then examined for differences in 5-HT(2A)-immunoreactivity (5-HT(2A)-ir). When compared with non-aggressive oil-treated controls, aggressive AAS-treated hamsters showed significant increases in 5-HT(2A)-ir fibers in the lateral portion of the anterior hypothalamus (LAH). Further analysis revealed that AAS treatment also produced a significant increase in the number of cells expressing 5-HT(2A)-ir in the LAH. Together, these results support a role for altered 5-HT(2A) expression and further implicate the LAH as a central brain region important in the control of adolescent AAS-induced offensive aggression.
青春期期间长期使用合成代谢雄激素类固醇(AAS)会促进雄性叙利亚仓鼠(金仓鼠)的攻击性。血清素(5-HT)调节攻击行为,并且已证实在长期使用AAS治疗后会发生改变。此外,5-HT 2型受体与攻击行为的控制有关。例如,用5-HT(2A)受体拮抗剂治疗可抑制攻击性攻击表型的产生。然而,尚不清楚这些受体是否对青春期AAS暴露敏感。当前的研究评估了整个青春期使用AAS治疗是否会影响仓鼠大脑中与攻击行为控制有关区域的5-HT(2A)免疫组织化学定位。在整个青春期,每天给仓鼠注射AAS(5.0毫克/千克),对其攻击性进行评分,然后检查5-HT(2A)免疫反应性(5-HT(2A)-ir)的差异。与未注射AAS的非攻击性对照相比,接受AAS治疗的攻击性仓鼠下丘脑前部外侧(LAH)的5-HT(2A)-ir纤维显著增加。进一步分析表明,AAS治疗还使LAH中表达5-HT(2A)-ir的细胞数量显著增加。总之,这些结果支持5-HT(2A)表达改变所起的作用,并进一步表明LAH是控制青春期AAS诱导的攻击性攻击的重要中枢脑区。