Yu Bo, Wang Xue, Wei Jin-xue, Ni Pei-yan, Liang Lin-hui, Zhao Lian-sheng, Ma Xiao-hong, Li Tao, Wang Ying-cheng
Sichuan Da Xue Xue Bao Yi Xue Ban. 2015 Jul;46(4):528-32, 610.
To investigate the effect of risperidone on the expression of brain-derived neurotrophic factor (BDNF) and its receptors, tyrosine kinase receptor (TrkB) and P75 neurotrophin receptor (P75NTR) in rat brain.
Sixteen SD rats were divided into two groups (n = 8 for each group). The rats in experimental group were treated with risperidone [0.25 mg/(kg · d)] for 14 d, while the control group was given placebo. Total RNA sample in prefrontal cortex, temporal cortex and hippocampus was extracted, and the expression of BDNF, TrkB and P75NTR mRNA were determined by quantitative real-time PCR.
The treatment of risperidone significantly up-regulated the expressions of BDNF and TrkB in prefrontal cortex, temporal cortex and hippocampus, while the expression of P75NTR was not significantly changed.
Risperidone upregulated BDNF-TrkB signaling, but not BDNF-P75NTR signaling, which may be helpful for the further pharmacological study of risperidone.
探讨利培酮对大鼠脑源性神经营养因子(BDNF)及其受体酪氨酸激酶受体(TrkB)和P75神经营养因子受体(P75NTR)表达的影响。
将16只SD大鼠分为两组(每组n = 8)。实验组大鼠给予利培酮[0.25 mg/(kg·d)]治疗14天,对照组给予安慰剂。提取前额叶皮质、颞叶皮质和海马的总RNA样本,采用实时定量PCR法检测BDNF、TrkB和P75NTR mRNA的表达。
利培酮治疗显著上调了前额叶皮质、颞叶皮质和海马中BDNF和TrkB的表达,而P75NTR的表达无明显变化。
利培酮上调BDNF-TrkB信号通路,但不上调BDNF-P75NTR信号通路,这可能有助于利培酮进一步的药理学研究。