Translational selenium nanotherapeutics counter-acts multiple risk factors to improve surgery-induced cognitive impairment

神经炎症 术后认知功能障碍 氧化应激 神经保护 药理学 活性氧 医学 发病机制 炎症 认知 化学 生物信息学 神经科学 内科学 心理学 生物 生物化学
作者
Xiaosheng Liang,Ting Liu,Linpeng Li,Jieli Li,Shufang Li,Ke Zeng,Chao Song,Tianfeng Chen,Yi Ming Zou
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:441: 135984-135984 被引量:14
标识
DOI:10.1016/j.cej.2022.135984
摘要

Postoperative cognition dysfunction (POCD) describes a condition of persistent deficits in attention, learning and memory following surgery. The mechanisms of POCD are far from being understood and the therapeutic strategies are limit. Surgery-induced oxidative stress and peripheral inflammation form a feedforward loop and eventually resulted in neuroinflammation, which underpin the pathogenesis of POCD. Therefore, the reactive oxygen species (ROS) homeostasis are tightly regulated by detoxifying enzymes, most of which are recognized as selenoproteins. The putative neuroprotective function of this trace element was investigated in this study using aged mice with POCD. Herein we demonstrate a facile strategy by using chemically-synthesized lentinan-functionalized selenium nanoparticles (LNT-SeNPs) that could be simply obtained in large scale and display high antioxidative and anti-inflammatory activities, to treat POCD. As expected, we found that, dietary supplements of LNT-SeNPs were effectively ingested and increased the levels of detoxifying selenoproteins in both serum and hippocampus of our aged mice. Behavioral assessments showed that LNT-SeNPs significantly improved the surgery-induced cognitive dysfunction, by alleviating surgery-induced oxidative stress and pro-inflammatory cytokine expression. In addition, dietary supplementation of LNT-SeNPs might protect central nervous system (CNS) function by improving gut microbiome and intestinal barrier function. Collectively, our results suggest that the use of translational LNT-SeNPs could be further developed as potent strategy for therapy of surgery-induced cognitive impairment.
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