Neuroprotection by Trans-Resveratrol in Rats with Intracerebral Hemorrhage: Insights into the Role of Adenosine A1 Receptors

• Published in: Journal of Neuropathology and Experimental Neurology
• Main Author: Abd. Aziz N.A.W.; Iezhitsa I.; Agarwal R.; Bakar N.S.; Abd. Latiff A.; Ismail N.M.
• Format: Article
• Language: English
• Published: Oxford University Press 2022
• Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-85134720623&doi=10.1093%2fjnen%2fnlac047&partnerID=40&md5=ece319b2a91a675498d02e8eaeeab141

Given the neuroprotective effects of trans-resveratrol (RV), this study aimed to investigate the involvement of the adenosine A1 receptor (A1R) in RV-mediated neuroprotection in a rat intracerebral hemorrhage (ICH) model induced by intrastriatal injection of collagenase. Rats were divided into 5 groups: (1) control, (2) sham-operated, (3) ICH pretreated with vehicle, (4) ICH pretreated with RV, and (5) ICH pretreated with RV and the A1R antagonist DPCPX. At 48 hours after ICH, the rats were subjected to neurological testing. Brain tissues were assessed for neuronal density and morphological features using routine and immunohistochemical staining. Expression of tumor necrosis factor-α (TNF-α), caspase-3, and RIPK3 proteins was examined using ELISA. A1R, MAPK P38, Hsp90, TrkB, and BDNF genes were examined using RT-qPCR. RV protected against neurological deficits and neuronal depletion, restored the expression of TNF-α, CASP3, RIPK3, A1R, and Hsp90, and increased BDNF/TrkB. DPCPX abolished the effects of RV on neurological outcomes, neuronal density, CASP3, RIPK3, A1R, Hsp90, and BDNF. These data indicate that the neuroprotection by RV involves A1R and inhibits CASP3-dependent apoptosis and RIPK3-dependent necroptosis in the perihematoma region; this is likely to be mediated by crosstalk between A1R and the BDNF/TrkB pathway. © The Author(s) 2022.Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. All rights reserved.