Fagerli Eric, Jackson Charles W, Escobar Iris, Ferrier Fernando J, Perez Lao Efrain J, Saul Isabel, Gomez Jorge, Dave Kunjan R, Bracko Oliver, Perez-Pinzon Miguel A
Peritz Scheinberg Cerebral Vascular Disease Research Laboratories, University of Miami Leonard M. Miller School of Medicine, Miami, FL 33136, USA.
Department of Neurology, University of Miami Leonard M. Miller School of Medicine, Miami, FL 33136, USA.
Antioxidants (Basel). 2024 Aug 14;13(8):984. doi: 10.3390/antiox13080984.
Vascular cognitive impairment and dementia (VCID) is the second leading cause of dementia. There is currently no effective treatment for VCID. Resveratrol (RSV) is considered an antioxidant; however, our group has observed pleiotropic effects in stroke paradigms, suggesting more effects may contribute to mechanistic changes beyond antioxidative properties. The main goal of this study was to investigate if administering RSV twice a week could alleviate cognitive declines following the induction of a VCID model. Additionally, our aim was to further describe whether this treatment regimen could decrease cell death in brain areas vulnerable to changes in cerebral blood flow, such as the hippocampus and medial septum. We hypothesized RSV treatments in a mouse model of gradual cerebral hypoperfusion protect against cognitive impairment. We utilized gradual bilateral common carotid artery stenosis (GBCCAS) via the surgical implantation of ameroid constrictor devices. RSV treatment was administered on the day of implantation and twice a week thereafter. Cerebral perfusion was measured by laser speckle contrast imaging, and cognitive functions, including the recognition memory, the spatial working memory, and associative learning, were assessed by novel object recognition (NOR), Y-maze testing, and contextual fear conditioning (CFC), respectively. RSV treatment did not alleviate cerebral perfusion deficits but mitigated cognitive deficits in CFC and NOR after GBCCAS. Despite these deficits, no hippocampal pathology was observed; however, cholinergic cell loss in the medial septum was significantly increased after GBCCAS. This cholinergic cell loss was mitigated by RSV. This study describes a novel mechanism by which chronic RSV treatments protect against a VCID-induced cognitive decline through the preservation of cholinergic cell viability to improve memory performance.
血管性认知障碍和痴呆(VCID)是痴呆的第二大主要病因。目前尚无针对VCID的有效治疗方法。白藜芦醇(RSV)被认为是一种抗氧化剂;然而,我们团队在中风模型中观察到了多效性作用,这表明可能有更多作用促成了超出抗氧化特性的机制变化。本研究的主要目的是调查每周两次给予RSV是否能减轻VCID模型诱导后的认知衰退。此外,我们的目标是进一步描述这种治疗方案是否能减少在脑血流量变化易损脑区(如海马体和内侧隔区)的细胞死亡。我们假设在逐渐脑灌注不足的小鼠模型中进行RSV治疗可预防认知障碍。我们通过手术植入阿梅里德缩窄装置来实现双侧颈总动脉逐渐狭窄(GBCCAS)。在植入当天给予RSV治疗,此后每周两次。通过激光散斑对比成像测量脑灌注,并分别通过新物体识别(NOR)、Y迷宫测试和情境恐惧条件反射(CFC)评估包括识别记忆、空间工作记忆和联想学习在内的认知功能。RSV治疗并未缓解脑灌注不足,但减轻了GBCCAS后CFC和NOR中的认知缺陷。尽管存在这些缺陷,但未观察到海马体病理变化;然而,GBCCAS后内侧隔区的胆碱能细胞损失显著增加。RSV减轻了这种胆碱能细胞损失。本研究描述了一种新机制,即慢性RSV治疗通过保留胆碱能细胞活力来改善记忆表现,从而预防VCID诱导的认知衰退。