Peroxisome proliferator‐activated receptor gamma participates in the acquisition of brain ischemic tolerance induced by ischemic preconditioning via glial glutamate transporter 1 in vivo and in vitro

• Published in: Journal of neurochemistry Vol. 151; no. 5; pp. 608 - 625
• Main Authors: Zhao, Cong‐Cong, Jiang, Meng‐Yang, Zhang, Ling‐Yan, Hu, Yu‐Yan, Hu, Zhen‐Jie, Zhang, Meng‐Yue, Qi, Jie, Su, A‐Chou, Lou, Nan, Xian, Xiao‐Hui, Zhang, Jing‐Ge, Li, Wen‐Bin, Zhang, Min
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01.12.2019
• Subjects: Astrocytes; astrocyte‐neuron co‐cultures; Brain; brain ischemic tolerance; Cortex; Deprivation; Glial fibrillary acidic protein; GLT‐1; Glutamic acid transporter; Hippocampus; Image acquisition; Immunofluorescence; Ischemia; ischemic preconditioning; Neuroprotection; PPARγ; Preconditioning; rat; Rodents; siRNA; ischemic preconditioning; astrocyte-neuron co-cultures; rat; PPARγ; GLT-1; brain ischemic tolerance
• ISSN: 0022-3042; 1471-4159; 1471-4159
• DOI: 10.1111/jnc.14824

Glial glutamate transporter 1 (GLT‐1) plays a vital role in the induction of brain ischemic tolerance (BIT) by ischemic preconditioning (IPC). However, the mechanism still needs to be further explained. The aim of this study was to investigate whether peroxisome proliferator‐activated receptor gamma (PPARγ) participates in regulating GLT‐1 during the acquisition of BIT induced by IPC. Initially, cerebral IPC induced BIT and enhanced PPARγ and GLT‐1 expression in the CA1 hippocampus in rats. The ratio of nuclear/cytoplasmic PPARγ was also increased. At the same time, the up‐regulation of PPARγ expression in astrocytes in the CA1 hippocampus was revealed by double immunofluorescence for PPARγ and glial fibrillary acidic protein. Then, the mechanism by which PPARγ regulates GLT‐1 was studied in rat cortical astrocyte‐neuron cocultures. We found that IPC [45 min of oxygen glucose deprivation (OGD)] protected neuronal survival after lethal OGD (4 h of OGD), which usually leads to neuronal death. The activation of PPARγ occurred earlier than the up‐regulation of GLT‐1 in astrocytes after IPC, as determined by western blot and immunofluorescence. Moreover, the preadministration of the PPARγ antagonist T0070907 or PPARγ siRNA significantly attenuated GLT‐1 up‐regulation and the neuroprotective effects induced by IPC in vitro. Finally, the effect of the PPARγ antagonist on GLT‐1 expression and BIT was verified in vivo. We observed that the preadministration of T0070907 by intracerebroventricular injection dose‐dependently attenuated the up‐regulation of GLT‐1 and BIT induced by cerebral IPC in rats. In conclusion, PPARγ participates in regulating GLT‐1 during the acquisition of BIT induced by IPC. Cover Image for this issue: doi: 10.1111/jnc.14532. Open Science: This manuscript was awarded with the Open Materials Badge For more information see: https://cos.io/our-services/open-science-badges/ Ischemic preconditioning (IPC) could induce neuron ischemic tolerance. During this process, IPC activated PPARγ in astrocytes, then the activation of PPARγ triggered the up‐regulation of GLT‐1 and contributed to the induction of neuroprotection by IPC in vivo and in vitro. It could be concluded that astrocytic PPARγ participates in the induction of neuron ischemic tolerance by IPC via regulating GLT‐1. Cover Image for this issue: doi: 10.1111/jnc.14532.