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Enhanced effect of limb remote ischemic postconditioning combined with paeoniflorin on alleviating cerebral ischemic injury via neutrophil NADPH pathway.

Authors :
Wu, Qi
Que, Wenxuan
Zhang, Jiangwei
Chen, Xun
Wang, Min
Kou, Junping
Chen, Gangling
Source :
Brain Research Bulletin. Aug2024, Vol. 214, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Limb remote ischemic postconditioning (LRIP) and paeoniflorin (PF) both can ameliorate cerebral ischemia reperfusion (I/R) injury. At present, whether LRIP combined with PF can achieve better therapeutic effect is unknown. This study explored the alleviating effect and mechanism of LRIP in combination with PF on cerebral I/R injury in rats. Middle cerebral artery occlusion (MCAO) surgery was performed on rats except Sham group. Then PF (2.5 mg/kg, 5 mg/kg, 10 mg/kg) was administrated by intraperitoneal injection 10 min before the start of reperfusion. LRIP was operated on the left femoral artery at 0 h of reperfusion. Behavioral testing was used to assess neurological impairment, while TTC staining was used to examine infarct volume. Protein expression of MyD88, TRAF6, p38-MAPK and phosphorylation of p47phox in neutrophils from rat peripheral blood were tested by Western blot. Rat bone marrow neutrophils were extracted and incubated for 24 h with serum from rats after LRIP combined with PF. p38 MAPK inhibitor group was administrated SB203580 while the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase inhibitor group was administrated Apocynin. Neutrophils were stimulated by fMLP (10 μM). Reactive oxygen species (ROS) production and protein expression of MyD88, TRAF6, p38 MAPK, and p47phox (ser 304 and ser 345) were detected. LRIP combined with PF (5 mg/kg) reduced cerebral infarct volume, ameliorated neurological deficit score (NDS), decreased fMLP-stimulated ROS release and downregulated the protein expression of MyD88, TRAF6, p38-MAPK and phosphorylation of p47phox (ser 304 and ser 345) in neutrophils. The protective effect of LRIP combined with PF on cerebral I/R injury was better than either alone. Taken together, we provided solid evidence to demonstrate that the combination of LRIP and PF had potential to alleviate cerebral I/R injury, which was regulated by MyD88-TRAF6-p38 MAPK pathway and neutrophil NADPH oxidase pathway. [Display omitted] • The protective effect of LRIP combined with PF on cerebral I/R injury is better than either alone. • LRIP combined with PF downregulate MyD88/TRAF6/p38-MAPK pathway in rat peripheral blood neutrophils. • In vitro , LRIP combined with PF serum downregulate MyD88/TRAF6/p38-MAPK pathway in bone marrow neutrophils. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03619230
Volume :
214
Database :
Academic Search Index
Journal :
Brain Research Bulletin
Publication Type :
Academic Journal
Accession number :
177885914
Full Text :
https://doi.org/10.1016/j.brainresbull.2024.111006