Your browser doesn't support javascript.
loading
Electroacupuncture attenuates middle cerebral artery occlusion-induced learning and memory impairment by regulating microglial polarization in hippocampus.
Wen, Qiong; Zha, Fubing; Shan, Linlin; Zhang, Shaohua; Xiao, Peng; Zhang, Chunxia; Yu, Haibo; Wang, Yulong.
  • Wen Q; The Fourth Clinical Medical College of Guangzhou University of Chinese Medicine, Shenzhen, China.
  • Zha F; Department of Rehabilitation, Shenzhen Dapeng New District Nanao People's Hospital, Shenzhen, China.
  • Shan L; Department of Rehabilitation, The First Affiliated Hospital, Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China.
  • Zhang S; Department of Rehabilitation, The First Affiliated Hospital, Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China.
  • Xiao P; Department of Rehabilitation, Shenzhen Dapeng New District Nanao People's Hospital, Shenzhen, China.
  • Zhang C; Department of Rehabilitation, Shenzhen Dapeng New District Nanao People's Hospital, Shenzhen, China.
  • Yu H; Department of Rehabilitation, Shenzhen Dapeng New District Nanao People's Hospital, Shenzhen, China.
  • Wang Y; The Fourth Clinical Medical College of Guangzhou University of Chinese Medicine, Shenzhen, China.
Int J Neurosci ; : 1-13, 2024 Feb 14.
Article en En | MEDLINE | ID: mdl-38315119
ABSTRACT

BACKGROUND:

As a traditional medical therapy, electroacupuncture (EA) has been demonstrated to have beneficial effects on ischemic stroke-induced cognitive impairment. However, the underlying mechanism is largely unclear.

METHODS:

Adult rats received occlusion of the middle cerebral artery and reperfusion (MCAO/R) to establish the ischemic stroke model. Morris water maze test was performed following EA stimulation at the GV20, PC6, and KI1 acupoints in rats to test the learning and memory ability. Western blot, immunofluorescent staining, and enzyme-linked immunosorbent assay were conducted to assess the cellular and molecular mechanisms.

RESULTS:

EA stimulation attenuated neurological deficits. In the Morris water maze test, EA treatment ameliorated the MCAO/R-induced learning and memory impairment. Moreover, we observed that MCAO/R induced microglial activation and polarization in the ischemic hippocampus, whereas, EA treatment dampened microglial activation and inhibited M1 microglial polarization but enhanced M2 microglial polarization. EA treatment inhibited the increased expression of proinflammatory cytokines and enhanced the increased expression of anti-inflammatory cytokines. Finally, we found that EA treatment dampened microglial p38 mitogen-activated protein kinase (MAPK) phosphorylation.

CONCLUSION:

Collectively, our data suggested that EA treatment ameliorated cognitive impairment induced by MCAO/R and the underlying mechanism may be p38-mediated microglia polarization and neuroinflammation.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article