Neural Regeneration Research ›› 2014, Vol. 9 ›› Issue (10): 1079-1088.doi: 10.4103/1673-5374.133171

Previous Articles    

Attenuated inhibition of medium spiny neurons participates in the pathogenesis of childhood depression

Dandan Liu, Linghan Hu, Junqi Zhang, Ping Zhang, Shengtian Li   

  1. Bio-X Institutes, Shanghai Jiao Tong University, Shanghai, China
  • Received:2014-04-11 Online:2014-05-26 Published:2014-05-26
  • Contact: Shengtian Li, M.D., Ph.D., Bio-X Institutes, Shanghai Jiao Tong University, Shanghai 200240, China, lstian@sjtu.edu.cn.
  • Supported by:

    This study was supported by the National Natural Science Foundation of China, No. 31271198 and 81121001; grants from the Shanghai Committee of Science and Technology, No. 11ZR1415900; and the State Key Laboratory of Medical Neurobiology, Fudan University, No. 10-12.

Abstract:

Accumulating evidence suggests that the nucleus accumbens, which is involved in mechanisms of reward and addiction, plays a role in the pathogenesis of depression and in the action of antidepressants. In the current study, intraperitoneal injection of nomifensine, a dopamine reuptake inhibitor, decreased depression-like behaviors in the Wistar Kyoto rat model of depression in the sucrose-preference and forced swim tests. Nomifensine also reduced membrane excitability in medium spiny neurons in the core of the nucleus accumbens in the childhood Wistar Kyoto rats as evaluated by electrophysiological recording. In addition, the expression of dopamine D2-like receptor mRNA was downregulated in the nucleus accumbens, striatum and hippocampus of nomifensine-treated childhood Wistar Kyoto rats. These experimental findings indicate that impaired inhibition of medium spiny neurons, mediated by dopamine D2-like receptors, may be involved in the formation of depression-like behavior in childhood Wistar Kyoto rats, and that nomifensine can alleviate depressive behaviors by reducing medium spiny neuron membrane excitability.

Key words: nerve regeneration, brain injury, neurophysiology, MSNs, dopamine D2-like receptors, childhood depression, Wistar Kyoto rats, nucleus accumbens, excitatory inhibition, neural plasticity, nomifensine, NSFC grant, neural regeneration