Adiponectin receptor agonist AdipoRon alleviates memory impairment in the hippocampus of septic mice

IF 2.6 3区 心理学 Q2 BEHAVIORAL SCIENCES
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引用次数: 0

Abstract

Sepsis-associated encephalopathy (SAE) is a common and severe clinical feature of sepsis; however, therapeutic approaches are limited because of the unclear pathogenesis. Adiponectin receptor agonist (AdipoRon) is a small-molecule agonist of the adiponectin receptor that exhibits anti-inflammatory and memory-improving effects in various diseases. In the present study, we established lipopolysaccharide (LPS)-induced mice models of SAE and found that Adiponectin receptor 1 (AdipoR1) was significantly decreased in the hippocampus. Administration of AdipoRon improves memory impairment, mitigates synaptic damage, and alleviates neuronal death. Furthermore, AdipoRon reduces the number of microglia. More importantly, AdipoRon promotes the phosphorylation of adenosine 5 '-monophosphate activated protein kinase (pAMPK). In conclusion, AdipoRon is protective against SAE-induced memory decline and brain injury in the SAE models via activating the hippocampal adenosine 5 '-monophosphate activated protein kinase (AMPK).

脂肪连接素受体激动剂 AdipoRon 可减轻脓毒症小鼠海马体的记忆损伤。
败血症相关脑病(SAE)是败血症的一种常见且严重的临床特征;然而,由于发病机制不明确,治疗方法受到限制。脂联素受体激动剂(AdipoRon)是一种小分子脂联素受体激动剂,在多种疾病中具有抗炎和改善记忆的作用。在本研究中,我们建立了脂多糖(LPS)诱导的小鼠 SAE 模型,发现海马中的脂肪素受体 1(AdipoR1)明显减少。服用 AdipoRon 可改善记忆损伤,减轻突触损伤,缓解神经元死亡。此外,AdipoRon 还能减少小胶质细胞的数量。更重要的是,AdipoRon 能促进 5'-单磷酸腺苷活化蛋白激酶(pAMPK)的磷酸化。总之,AdipoRon 可通过激活海马 5'-单磷酸腺苷激活蛋白激酶(AMPK),防止 LPS 诱导的小鼠模型出现与 SAE 相关的记忆衰退和脑损伤。
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来源期刊
Behavioural Brain Research
Behavioural Brain Research 医学-行为科学
CiteScore
5.60
自引率
0.00%
发文量
383
审稿时长
61 days
期刊介绍: Behavioural Brain Research is an international, interdisciplinary journal dedicated to the publication of articles in the field of behavioural neuroscience, broadly defined. Contributions from the entire range of disciplines that comprise the neurosciences, behavioural sciences or cognitive sciences are appropriate, as long as the goal is to delineate the neural mechanisms underlying behaviour. Thus, studies may range from neurophysiological, neuroanatomical, neurochemical or neuropharmacological analysis of brain-behaviour relations, including the use of molecular genetic or behavioural genetic approaches, to studies that involve the use of brain imaging techniques, to neuroethological studies. Reports of original research, of major methodological advances, or of novel conceptual approaches are all encouraged. The journal will also consider critical reviews on selected topics.
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