Scholpa Natalie E, Briggs Sherri B, Wagner John J, Cummings Brian S
Departments of Pharmaceutical and Biomedical Sciences (N.E.S., B.S.C.) and Physiology and Pharmacology (S.B.B., J.J.W.), University of Georgia, Athens, Georgia.
Departments of Pharmaceutical and Biomedical Sciences (N.E.S., B.S.C.) and Physiology and Pharmacology (S.B.B., J.J.W.), University of Georgia, Athens, Georgia
J Pharmacol Exp Ther. 2016 Apr;357(1):56-65. doi: 10.1124/jpet.115.230888. Epub 2016 Jan 20.
This study investigated the functional role of cyclin-dependent kinase inhibitor 1a (Cdkn1a or p21) in cocaine-induced responses using a knockout mouse model. Acute locomotor activity after cocaine administration (15 mg/kg, i.p.) was decreased in p21(-/-) mice, whereas cocaine-induced place preference was enhanced. Interestingly, κ-opioid-induced place aversion was also significantly enhanced. Concentration-dependent analysis of locomotor activity in response to cocaine demonstrated a rightward shift in the p21(-/-) mice. Pretreatment with a 5-hydroxytryptamine receptor antagonist did not alter the enhancement of cocaine-induced conditioned place preference in p21(-/-) mice, indicating a lack of involvement of serotonergic signaling in this response. Cocaine exposure increased p21 expression exclusively in the ventral sector of the hippocampus of rodents after either contingent or noncontingent drug administration. Increased p21 expression was accompanied by increased histone acetylation of the p21 promoter region in rats. Finally, increased neurogenesis in the dorsal hippocampus of p21(-/-) mice was also observed. These results show that functional loss of p21 altered the acute locomotor response to cocaine and the conditioned responses to either rewarding or aversive stimuli. Collectively, these findings demonstrate a previously unreported involvement of p21 in modulating responses to cocaine and in motivated behaviors.
本研究使用基因敲除小鼠模型,探究了细胞周期蛋白依赖性激酶抑制剂1a(Cdkn1a或p21)在可卡因诱导反应中的功能作用。给予可卡因(15毫克/千克,腹腔注射)后,p21基因敲除小鼠的急性运动活性降低,而可卡因诱导的位置偏爱增强。有趣的是,κ-阿片受体诱导的位置厌恶也显著增强。对可卡因反应的运动活性进行浓度依赖性分析表明,p21基因敲除小鼠的剂量反应曲线向右移动。用5-羟色胺受体拮抗剂预处理并未改变p21基因敲除小鼠中可卡因诱导的条件性位置偏爱的增强,表明该反应中缺乏5-羟色胺能信号传导的参与。无论是在偶然还是非偶然给药后,可卡因暴露均仅在啮齿动物海马体腹侧区增加p21表达。在大鼠中,p21表达增加伴随着p21启动子区域组蛋白乙酰化增加。最后,在p21基因敲除小鼠的背侧海马体中也观察到神经发生增加。这些结果表明,p21的功能丧失改变了对可卡因的急性运动反应以及对奖赏或厌恶刺激的条件反应。总的来说,这些发现证明了p21在调节对可卡因的反应和动机行为方面有先前未报道的作用。