Cerebral ischemia/reperfusion injury activates microglia, resident immune cells in the brain, and allows the infiltration of circulating immune cells into the ischemic lesions. Microglia play both exacerbating and protective roles in pathological processes and are thus often referred to as "double-edged swords." In ischemic brains, blood-borne macrophages play a role that is distinct from that of resident activated microglia. Recently, the metabolic alteration of immune cells in the pathogenesis of inflammatory disorders including cerebral infarction has become a critical target for investigation. We begin this review by describing the multifaceted functions of microglia in cerebral infarction. Next, we focus on the metabolic alterations that occur in microglia during pathological processes. We also discuss morphological changes that take place in the mitochondria, leading to functional disturbances, accompanied by alterations in microglial function. Moreover, we describe the involvement of the reactive oxygen species that are produced during aberrant metabolic activity. Finally, we discuss therapeutic strategies to ameliorate aggravative changes in metabolism. (C) 2020 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society.
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Department of Physiology,Shanghai University of Traditional Chinese MedicineDepartment of Physiology,Shanghai University of Traditional Chinese Medicine
FU Yan
YANG Pin
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Department of Physiology,Shanghai University of Traditional Chinese MedicineDepartment of Physiology,Shanghai University of Traditional Chinese Medicine
YANG Pin
ZHAO Yang
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Department of Physiology,Shanghai University of Traditional Chinese MedicineDepartment of Physiology,Shanghai University of Traditional Chinese Medicine
ZHAO Yang
XU Ying
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Department of Physiology,Shanghai University of Traditional Chinese MedicineDepartment of Physiology,Shanghai University of Traditional Chinese Medicine
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Univ Lille, CNRS, INSERM, CHU Lille,Inst Pasteur Lille,U1019,UMR 8204,CIIL, F-59000 Lille, FranceUPMC, Unite Immunophysiopathol Infect, CRNS URA 1961, Inst Pasteur, Paris, France
Shrivastava, Sandeep K.
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Dalko, Esther
Delcroix-Genete, Delphine
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Univ Lille, CNRS, INSERM, CHU Lille,Inst Pasteur Lille,U1019,UMR 8204,CIIL, F-59000 Lille, FranceUPMC, Unite Immunophysiopathol Infect, CRNS URA 1961, Inst Pasteur, Paris, France
Delcroix-Genete, Delphine
Herbert, Fabien
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Univ Lille, CNRS, INSERM, CHU Lille,Inst Pasteur Lille,U1019,UMR 8204,CIIL, F-59000 Lille, FranceUPMC, Unite Immunophysiopathol Infect, CRNS URA 1961, Inst Pasteur, Paris, France
Herbert, Fabien
Cazenave, Pierre-Andre
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UPMC, Unite Immunophysiopathol Infect, CRNS URA 1961, Inst Pasteur, Paris, FranceUPMC, Unite Immunophysiopathol Infect, CRNS URA 1961, Inst Pasteur, Paris, France
Cazenave, Pierre-Andre
Pied, Sylviane
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UPMC, Unite Immunophysiopathol Infect, CRNS URA 1961, Inst Pasteur, Paris, FranceUPMC, Unite Immunophysiopathol Infect, CRNS URA 1961, Inst Pasteur, Paris, France