Université de Lyon, F-69373, Lyon, France.
Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jun 3;43:40-8. doi: 10.1016/j.pnpbp.2012.11.015. Epub 2012 Dec 8.
The neurobiological mechanisms underlying the pathophysiology and therapeutics of bipolar disorder are still unknown. In recent years, protein kinase C (PKC) has emerged as a potential key player in mania. To further investigate the role of this signaling system in mood regulation, we examined the effects of PKC modulators in behavioral tests modeling several facets of bipolar disorder and in adult hippocampal cell proliferation in rats. Our results showed that a single injection of the PKC inhibitors tamoxifen (80 mg/kg, i.p.) and chelerythrine (3 mg/kg, s.c.) attenuated amphetamine-induced hyperlocomotion and decreased risk-taking behavior, supporting the efficacy of PKC blockade in acute mania. Moreover, chronic exposure to tamoxifen (10 mg/kg/day, i.p., for 14 days) or chelerythrine (0.3 mg/kg/day, s.c., for 14 days) caused depressive-like behavior in the forced swim test, and resulted in a reduction of cell proliferation in the dentate gyrus of the hippocampus. Finally, we showed that, contrary to the PKC inhibitors, the PKC activator phorbol 12-myristate 13-acetate (PMA) enhanced risk-taking behavior and induced an antidepressant-like effect. Taken together, these findings support the involvement of PKC in regulating opposite facets of bipolar disorder, and emphasize a major role for PKC in this disease.
双相障碍的病理生理学和治疗学的神经生物学机制仍不清楚。近年来,蛋白激酶 C(PKC)已成为躁狂症的潜在关键因素。为了进一步研究该信号系统在情绪调节中的作用,我们研究了 PKC 调节剂在模拟双相障碍多个方面的行为测试中的作用,以及在成年海马细胞增殖中的作用。我们的结果表明,单次注射 PKC 抑制剂他莫昔芬(80mg/kg,ip)和 Chelerythrine(3mg/kg,sc)可减弱安非他命诱导的过度活跃,并降低冒险行为,支持 PKC 阻断在急性躁狂中的疗效。此外,慢性暴露于他莫昔芬(10mg/kg/天,ip,14 天)或 Chelerythrine(0.3mg/kg/天,sc,14 天)导致强迫游泳试验中的抑郁样行为,并导致海马齿状回细胞增殖减少。最后,我们表明,与 PKC 抑制剂相反,PKC 激活剂佛波醇 12-肉豆蔻酸 13-乙酸酯(PMA)增强了冒险行为,并诱导了抗抑郁样作用。总之,这些发现支持 PKC 参与调节双相障碍的相反方面,并强调 PKC 在这种疾病中的主要作用。