Folia Neuropathologica

Abstract

3/2023 vol. 61
Original paper

The protective effect of Wnt3a on inflammatory response in oxygen-glucose deprivation/reoxygenation (OGD/R) astrocyte model

  1. Department of Neurology, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, China
  2. Department of Neurology, Huizhou Central People’s Hospital, Huizhou City, Guangdong, China
  3. Department of Neurology, Peking University Shenzhen Hospital, Shenzhen, Guangdong, China
  4. Department of Clinical Psychology, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, China
  5. Department of Special Medical Center, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, China
  6. Department of Stomatology, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, Guangdong, China
  7. Department of Laboratory Medicine, Zhongshan City People’s Hospital, Zhongshan, Guangdong, China
Folia Neuropathol 2023; 61 (3): 242-248
Online publish date: 2023/08/04
View full text
Confronting perimenopausal women’s knowledge of coronary heart disease with their health behaviours. Controversial role of hormone replacement therapy in the protection of coronary heart disease
Involving in the immune response after cerebral infarction, astrocytes could secrete large amounts of pro- and anti-inflammatory factors. The aim of this study is to investigate the effect of Wnt3a intervention on the inflammatory response of oxygen-glucose deprivation (OGD) followed by reoxygenation (OGD/R) astrocyte model, and to provide a new target for immunoprotective treatment of cerebral infarction. We constructed the OGD/R rat astrocyte model, the astrocytes were treated by different concentrations of glucose (25, 50, 100 mM) intervened with/without Wnt3a (25 µg/ml). Microscope was used to observe the cell survival in rat astrocytes. The relative expression of inflammatory factors (TNF-a, IL-6, HIF-a) in rat astrocytes was detected by qRT-PCR. The expression of inflammatory factors such as TNF-a, IL-6 and HIF-a in rat astrocytes was increased after OGD/R treatment. The Wnt3a intervention promoted cell survival and decreased the expression of inflammatory factors in rat astrocytes induced by OGD/R. There is a neuroprotective effect that Wnt3a intervention could reduce inflammatory response in the OGD/R rat astrocyte model.
Share
without publication fees