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藻粉包埋虾青素预防性治疗,给药剂量相当于人体摄入量,可预防 LPS 诱导的大鼠认知障碍。

Preventive Treatment with Astaxanthin Microencapsulated with Spirulina Powder, Administered in a Dose Range Equivalent to Human Consumption, Prevents LPS-Induced Cognitive Impairment in Rats.

机构信息

Eurecat-Centre Tecnològic de Catalunya, Unitat de Nutrició i Salut, 43204 Reus, Spain.

Lubrizol Nutraceuticals, 08850 Gavà, Spain.

出版信息

Nutrients. 2023 Jun 23;15(13):2854. doi: 10.3390/nu15132854.

DOI:10.3390/nu15132854
PMID:37447181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10343420/
Abstract

Cognitive alterations are a common feature associated with many neurodegenerative diseases and are considered a major health concern worldwide. Cognitive alterations are triggered by microglia activation and oxidative/inflammatory processes in specific areas of the central nervous system. Consumption of bioactive compounds with antioxidative and anti-inflammatory effects, such as astaxanthin and spirulina, can help in preventing the development of these pathologies. In this study, we have investigated the potential beneficial neuroprotective effects of a low dose of astaxanthin (ASX) microencapsulated within spirulina (ASXSP) in female rats to prevent the cognitive deficits associated with the administration of LPS. Alterations in memory processing were evaluated in the Y-Maze and Morris Water Maze (MWM) paradigms. Changes in microglia activation and in gut microbiota content were also investigated. Our results demonstrate that LPS modified long-term memory in the MWM and increased microglia activation in the hippocampus and prefrontal cortex. Preventive treatment with ASXSP ameliorated LPS-cognitive alterations and microglia activation in both brain regions. Moreover, ASXSP was able to partially revert LPS-induced gut dysbiosis. Our results demonstrate the neuroprotective benefits of ASX when microencapsulated with spirulina acting through different mechanisms, including antioxidant, anti-inflammatory and, probably, prebiotic actions.

摘要

认知改变是许多神经退行性疾病的共同特征,被认为是全球主要的健康关注点。认知改变是由中枢神经系统特定区域的小胶质细胞激活和氧化/炎症过程引发的。摄入具有抗氧化和抗炎作用的生物活性化合物,如虾青素和螺旋藻,可以帮助预防这些病理的发生。在这项研究中,我们研究了低剂量虾青素(ASX)微胶囊化在螺旋藻内(ASXSP)对雌性大鼠的潜在有益的神经保护作用,以预防与 LPS 给药相关的认知缺陷。在 Y 迷宫和 Morris 水迷宫(MWM)范式中评估了记忆处理的改变。还研究了小胶质细胞激活和肠道微生物群含量的变化。我们的结果表明,LPS 改变了 MWM 中的长期记忆,并增加了海马体和前额叶皮层中小胶质细胞的激活。ASXSP 的预防性治疗改善了 LPS 引起的认知改变和两个脑区的小胶质细胞激活。此外,ASXSP 能够部分逆转 LPS 诱导的肠道菌群失调。我们的结果表明,当与螺旋藻一起微胶囊化时,虾青素具有神经保护作用,其作用机制包括抗氧化、抗炎,可能还有益生元作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/74c4d7850f78/nutrients-15-02854-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/25bb029489ba/nutrients-15-02854-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/b5f5114d5afd/nutrients-15-02854-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/e5bcde020744/nutrients-15-02854-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/b071b5686276/nutrients-15-02854-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/1dfc146d259b/nutrients-15-02854-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/74c4d7850f78/nutrients-15-02854-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/25bb029489ba/nutrients-15-02854-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/b5f5114d5afd/nutrients-15-02854-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/e5bcde020744/nutrients-15-02854-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/b071b5686276/nutrients-15-02854-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/1dfc146d259b/nutrients-15-02854-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5b3/10343420/74c4d7850f78/nutrients-15-02854-g005.jpg

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Redefining microglia states: Lessons and limits of human and mouse models to study microglia states in neurodegenerative diseases.重新定义小胶质细胞状态:人类和小鼠模型在研究神经退行性疾病中小胶质细胞状态方面的经验与局限
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