Zheng Cai-Xia, Lu Min, Guo Ya-Bi, Zhang Feng-Xia, Liu Hua, Guo Feng, Huang Xiao-Lin, Han Xiao-Hua
Department of Rehabilitation Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China.
Department of Rehabilitation Medicine, Xiangyang Central Hospital, Hubei College of Arts and Science, Xiangyang, Hubei Province, China.
Evid Based Complement Alternat Med. 2016;2016:7893710. doi: 10.1155/2016/7893710. Epub 2016 Oct 18.
Electroacupuncture (EA) has shown protective effects on cognitive decline. However, the underlying molecular mechanisms are ill-understood. The present study was undertaken to determine whether the cognitive function was ameliorated in cerebral hypoperfusion rats following EA and to investigate the role of PKA/CREB pathway. We used a rat 2-vessel occlusion (2VO) model and delivered EA at Baihui (GV20) and Dazhui (GV14) acupoints. Morris water maze (MWM) task, electrophysiological recording, Golgi silver stain, Nissl stain, Western blot, and real-time PCR were employed. EA significantly (1) ameliorated the spatial learning and memory deficits, (2) alleviated long-term potentiation (LTP) impairment and the reduction of dendritic spine density, (3) suppressed the decline of phospho-CREB (pCREB) protein, brain-derived neurotrophic factor (BDNF) protein, and microRNA132 (miR132), and (4) reduced the increase of p250GAP protein of 2VO rats. These changes were partially blocked by a selective protein kinase A (PKA) inhibitor, N-[2-(p-bromocinnamylamino)ethyl]-5-isoquinoline-sulfonamide (H89), suggesting that the PKA/CREB pathway is potentially involved in the effects of EA. Moreover, any significant damage to the pyramidal cell layer of CA1 subregion was absent. These results demonstrated that EA could ameliorate learning and memory deficits and alleviate hippocampal synaptic plasticity impairment of cerebral hypoperfusion rats, potentially mediated by PKA/CREB signaling pathway.
电针已显示出对认知衰退的保护作用。然而,其潜在的分子机制尚不清楚。本研究旨在确定电针治疗后脑缺血大鼠的认知功能是否得到改善,并探讨蛋白激酶A(PKA)/环磷腺苷反应元件结合蛋白(CREB)信号通路的作用。我们采用大鼠双侧颈总动脉结扎(2VO)模型,并在百会(GV20)和大椎(GV14)穴位进行电针治疗。采用 Morris 水迷宫(MWM)实验、电生理记录法、高尔基银染法、尼氏染色法、蛋白质免疫印迹法及实时荧光定量聚合酶链反应(PCR)。电针显著:(1)改善空间学习和记忆缺陷;(2)减轻长时程增强(LTP)损伤及树突棘密度降低;(3)抑制磷酸化 CREB(pCREB)蛋白、脑源性神经营养因子(BDNF)蛋白及微小RNA132(miR132)的下降;(4)降低 2VO 大鼠 p250GAP 蛋白的升高。这些变化部分被选择性蛋白激酶 A(PKA)抑制剂 N-[2-(对溴肉桂酰胺基)乙基]-5-异喹啉磺酰胺(H89)阻断,提示 PKA/CREB 信号通路可能参与电针的作用机制。此外,CA1 亚区锥体细胞层未见明显损伤。这些结果表明,电针可改善脑缺血大鼠的学习记忆缺陷,减轻海马突触可塑性损伤,其机制可能与 PKA/CREB 信号通路有关。