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Ability of Post-treatment Glycyrrhizic Acid to Mitigate Cerebral Ischemia/Reperfusion Injury in Diabetic Mice.

Abstract
BACKGROUND Diabetes aggravates cerebral ischemia/reperfusion (I/R) injury by increasing inflammatory reactions, but its specific mechanism is currently unclear. MATERIAL AND METHODS Diabetes was induced in mice with a high-fat diet combined with streptozotocin. These mice were subjected to transient middle cerebral artery occlusion (tMCAO) for 60 min, followed by reperfusion for 24-72 h and post-treatment glycyrrhizic acid (GA). Control and diabetic mice were randomly allocated to 8 groups of 18 mice each. Blood glucose, brain infarction, brain edema, and neurological function were monitored. Necrosis was determined by Nissl staining, loss of neurons by immunofluorescent (IF) staining for NeuN, and activation of inflammatory microglia by IF staining for Iba-1. Levels of HMGB1, TLR4, Myd88, and NF-kappaB mRNA and protein in ischemic brain were determined by qRT-PCR and western blotting, respectively, and serum concentrations of IL-1ß, IL-6, and TNF-alpha by ELISA. RESULTS Infarction volume, brain edema, and neurological function after tMCAO were significantly aggravated in diabetes, but ameliorated by post-treatment GA. GA also reduced neuronal loss and microglial activation. Cerebral Myd88 level showed a positive correlation with neurological scores. GA suppressed the expression of Myd88 and a proinflammatory pathway that included Myd88, HMGB1, TLR4, and NF-kappaB, as well as reducing serum concentrations of IL-1ß, IL-6, and TNF-alpha. CONCLUSIONS Post-treatment inhibited inflammatory responses and provided therapeutic benefits in diabetic mice with cerebral I/R injury, suggesting that GA may be a candidate drug to suppress cerebral I/R in diabetic patients.
AuthorsYuan Li, Na Yao, Ting Zhang, Fengying Guo, Xiangying Niu, Zhihui Wu, Shaozhang Hou
JournalMedical science monitor : international medical journal of experimental and clinical research (Med Sci Monit) Vol. 26 Pg. e926551 (Sep 28 2020) ISSN: 1643-3750 [Electronic] United States
PMID32981927 (Publication Type: Journal Article)
Chemical References
  • Glycyrrhizic Acid
Topics
  • Animals
  • Cerebrovascular Disorders (drug therapy, etiology, metabolism, pathology)
  • Diabetes Complications (drug therapy, metabolism)
  • Diabetes Mellitus, Experimental (drug therapy, metabolism, pathology)
  • Gene Expression Regulation (drug effects)
  • Glycyrrhizic Acid (pharmacology)
  • Male
  • Mice
  • Reperfusion Injury (drug therapy, etiology, metabolism, pathology)

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