Ineffectiveness of 6,2′,4′-trimethoxyflavone in mitigating cerebral ischemia/reperfusion injury after post-reperfusion administration in rats
Chul-Woong Woo, Monica Young Choi, Hwon Heo, Yeon Ji Chae, Yu Sub Sung, Yoonseok Choi, Dong Cheol WooBackground
Pharmacological inhibition of aryl hydrocarbon receptor (AhR) activation after ischemia alleviates cerebral ischemia/reperfusion (IR) injury.
Purpose
To investigate whether AhR antagonist administration after reperfusion was also effective in attenuating cerebral IR injury.
Material and Methods
A total of 24 Sprague–Dawley rats were divided into the sham-operated group (no IR), control group (IR), and 6,2′,4′-trimethoxyflavone (TMF) group (IR + TMF administration), with 10 rats assigned to each group. Cerebral IR injury was induced by 60 min of middle cerebral artery occlusion followed by reperfusion. TMF (5 mg/kg) was used as the AhR antagonist and was administered intraperitoneally immediately after reperfusion. Cerebral IR injury was observed using magnetic resonance imaging (MRI) and neurobehavioral assessments at baseline, immediately after ischemia, and at 3 days after ischemia.
Results
On MRI, the TMF group showed no significant differences in relative apparent diffusion coefficient (ADC), T2, and fractional anisotropy (FA) values; midline shift value; and infarct volume. In terms of neurobehavioral function, factors such as grip strength, contralateral forelimb use, time to touch, and time to remove adhesive tape from the forepaw, were also not significantly different between the control and TMF groups.
Conclusion
This study demonstrated that AhR treatment after reperfusion had no noticeable effect on reducing cerebral IR injury in rats.