Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz

Stroke is a common cause of brain injury and contributes to significant mortality worldwide. Intracerebral hemorrhage (ICH) remains the least treatable stroke and is characterized by hematoma (HT) expansion and perihematomal (PHT) damage. Tumor necrosis factor-α (TNF-α) activation underlies PHT dama...

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Main Author: Abd. Aziz, Noor Azliza Wani
Format: Thesis
Language:English
Published: 2021
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Online Access:https://ir.uitm.edu.my/id/eprint/53664/1/53664.pdf
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id my-uitm-ir.53664
record_format uketd_dc
institution Universiti Teknologi MARA
collection UiTM Institutional Repository
language English
advisor Iezhitsa, Igor (Prof Dr.)
topic Materia medica
Materia medica
Pharmaceutical chemistry
spellingShingle Materia medica
Materia medica
Pharmaceutical chemistry
Abd. Aziz, Noor Azliza Wani
Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz
description Stroke is a common cause of brain injury and contributes to significant mortality worldwide. Intracerebral hemorrhage (ICH) remains the least treatable stroke and is characterized by hematoma (HT) expansion and perihematomal (PHT) damage. Tumor necrosis factor-α (TNF-α) activation underlies PHT damage in ICH. TNF-α triggers apoptosis and necroptosis by increasing caspase-3 (CASP3) and receptor-interacting protein kinase 3 (RIPK3) respectively. None of the current therapy protects PHT. The only definite treatment is by evacuation of HT, which often results in incomplete recovery from HT-induced secondary injury. In view of the neuroprotective effects of trans-resveratrol (RV), we investigated the effects of RV on brain injury induced by collagenase (COL) in Sprague-Dawley rats. The objective of this study was to elucidate the neuroprotective effect and mechanisms of action of RV, with an insight on the role of adenosine A1 receptor (A1R), against COL-induced ICH in rats. In this study, rats were separated into 5 groups: (i) control, (ii) sham-operated rats, (iii) ICH rats pretreated with vehicle (0.1% DMSO saline, i.c.v.), (iv) ICH rats pretreated with RV (4 nmol, i.c.v.), and (v) ICH rats pretreated with RV (4 nmol) and the A1R antagonist, DPCPX (8 nmol, i.c.v.). Thirty minutes after pretreatment, ICH was induced by intrastriatal injection of COL (0.04 U). Forty-eight hours after ICH, rats were subjected to a variety of neurological and neurobehavioural tests and the brain tissues were processed for gross, histological and biochemical analyses. Sections of brain tissue were examined for HT volume through gross morphometry, while morphological features, midline shift, damaged area and neuronal density through histopathological examination using H&E and neuronal nuclei (NeuN) immunostaining. This study revealed that pretreatment with RV reduced HT volume, damaged area and neuronal depletion. DPCPX abolished effects by RV on damaged area and neuronal depletion. Overall, our data demonstrated that RV resolved HT and preserved PHT, while A1R is involved in the neuroprotective effects by RV in PHT. In the next part of our study, mechanisms of neuroprotection by RV against COL-induced PHT damage in rats was elucidated. Homogenate of PHT brain tissues were examined for expression of TNF-α, CASP3 and RIPK3 activity using ELISA, while A1R, mitogen-activated protein kinase P38 (MAPK P38), heat shock protein (Hsp90), brain-derived neurotrophic factor (BDNF) and tropomyosin-related kinase B (TrkB) expression using RT-qPCR. It was observed that pretreatment with RV restored the expression of TNF-α, CASP3, RIPK3, A1R and Hsp90, and increased transcriptional activity of BDNF/TrkB. DPCPX abolished effects by RV on CASP3, RIPK3, A1R, Hsp90 and BDNF. Overall, our data demonstrated that A1R is involved in the antiapoptotic and antinecroptotic effects by RV in PHT via upregulation of BDNF. The final study was done to evaluate the sensorimotor function of rats using neurological severity score, tail flick, open field, grip strength and rotarod tests. This part of study demonstrated that RV protected against signs of neurological deficit including general locomotor, forelimb activity and motor coordination, and partially preserved behavioural activities. DPCPX abolished the effects of RV. This data demonstrated that A1R is involved in the effects by RV against COL-induced neurological and neurobehavioural deficits in rats. In conclusion, this study demonstrates involvement of A1R in the mechanisms of neuroprotection by RV by inhibiting CASP3-dependent apoptosis and RIPK3-dependent necroptosis in PHT area, probably via the cross talk between A1R and BDNF/TrkB pathway.
format Thesis
qualification_name Doctor of Philosophy (PhD.)
qualification_level Doctorate
author Abd. Aziz, Noor Azliza Wani
author_facet Abd. Aziz, Noor Azliza Wani
author_sort Abd. Aziz, Noor Azliza Wani
title Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz
title_short Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz
title_full Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz
title_fullStr Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz
title_full_unstemmed Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz
title_sort mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / noor azliza wani abd. aziz
granting_institution Universiti Teknologi MARA
granting_department Faculty of Medicine
publishDate 2021
url https://ir.uitm.edu.my/id/eprint/53664/1/53664.pdf
_version_ 1783734876997943296
spelling my-uitm-ir.536642022-03-25T02:14:27Z Mechanisms of resveratrol-induced neuroprotection in rats with intracerebral hemorrhage: insight on the role of adenosine / Noor Azliza Wani Abd. Aziz 2021-02 Abd. Aziz, Noor Azliza Wani Materia medica Pharmacognosy. Pharmaceutical substances (Plant, animal, and inorganic) Pharmaceutical chemistry Stroke is a common cause of brain injury and contributes to significant mortality worldwide. Intracerebral hemorrhage (ICH) remains the least treatable stroke and is characterized by hematoma (HT) expansion and perihematomal (PHT) damage. Tumor necrosis factor-α (TNF-α) activation underlies PHT damage in ICH. TNF-α triggers apoptosis and necroptosis by increasing caspase-3 (CASP3) and receptor-interacting protein kinase 3 (RIPK3) respectively. None of the current therapy protects PHT. The only definite treatment is by evacuation of HT, which often results in incomplete recovery from HT-induced secondary injury. In view of the neuroprotective effects of trans-resveratrol (RV), we investigated the effects of RV on brain injury induced by collagenase (COL) in Sprague-Dawley rats. The objective of this study was to elucidate the neuroprotective effect and mechanisms of action of RV, with an insight on the role of adenosine A1 receptor (A1R), against COL-induced ICH in rats. In this study, rats were separated into 5 groups: (i) control, (ii) sham-operated rats, (iii) ICH rats pretreated with vehicle (0.1% DMSO saline, i.c.v.), (iv) ICH rats pretreated with RV (4 nmol, i.c.v.), and (v) ICH rats pretreated with RV (4 nmol) and the A1R antagonist, DPCPX (8 nmol, i.c.v.). Thirty minutes after pretreatment, ICH was induced by intrastriatal injection of COL (0.04 U). Forty-eight hours after ICH, rats were subjected to a variety of neurological and neurobehavioural tests and the brain tissues were processed for gross, histological and biochemical analyses. Sections of brain tissue were examined for HT volume through gross morphometry, while morphological features, midline shift, damaged area and neuronal density through histopathological examination using H&E and neuronal nuclei (NeuN) immunostaining. This study revealed that pretreatment with RV reduced HT volume, damaged area and neuronal depletion. DPCPX abolished effects by RV on damaged area and neuronal depletion. Overall, our data demonstrated that RV resolved HT and preserved PHT, while A1R is involved in the neuroprotective effects by RV in PHT. In the next part of our study, mechanisms of neuroprotection by RV against COL-induced PHT damage in rats was elucidated. Homogenate of PHT brain tissues were examined for expression of TNF-α, CASP3 and RIPK3 activity using ELISA, while A1R, mitogen-activated protein kinase P38 (MAPK P38), heat shock protein (Hsp90), brain-derived neurotrophic factor (BDNF) and tropomyosin-related kinase B (TrkB) expression using RT-qPCR. It was observed that pretreatment with RV restored the expression of TNF-α, CASP3, RIPK3, A1R and Hsp90, and increased transcriptional activity of BDNF/TrkB. DPCPX abolished effects by RV on CASP3, RIPK3, A1R, Hsp90 and BDNF. Overall, our data demonstrated that A1R is involved in the antiapoptotic and antinecroptotic effects by RV in PHT via upregulation of BDNF. The final study was done to evaluate the sensorimotor function of rats using neurological severity score, tail flick, open field, grip strength and rotarod tests. This part of study demonstrated that RV protected against signs of neurological deficit including general locomotor, forelimb activity and motor coordination, and partially preserved behavioural activities. DPCPX abolished the effects of RV. This data demonstrated that A1R is involved in the effects by RV against COL-induced neurological and neurobehavioural deficits in rats. In conclusion, this study demonstrates involvement of A1R in the mechanisms of neuroprotection by RV by inhibiting CASP3-dependent apoptosis and RIPK3-dependent necroptosis in PHT area, probably via the cross talk between A1R and BDNF/TrkB pathway. 2021-02 Thesis https://ir.uitm.edu.my/id/eprint/53664/ https://ir.uitm.edu.my/id/eprint/53664/1/53664.pdf text en public phd doctoral Universiti Teknologi MARA Faculty of Medicine Iezhitsa, Igor (Prof Dr.)