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电针对 LPS 诱导的神经炎症的预防作用是通过上调海马小胶质细胞中的 PICK-TLR4 复合物实现的。

Electroacupuncture prevents LPS- induced neuroinflammation via upregulation of PICK-TLR4 complexes in the microglia of hippocampus.

机构信息

The department of Anesthesiology and Operation Room, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

The department of Anesthesiology and Operation Room, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Brain Res Bull. 2021 Dec;177:295-304. doi: 10.1016/j.brainresbull.2021.10.010. Epub 2021 Oct 19.

Abstract

Sepsis-associated encephalopathy (SAE) is a common complication of sepsis caused by neuroinflammation. Electroacupuncture (EA) can be used to treat SAE, but the underlying mechanism is not clear. Lack of PICK1 further aggravates the inflammatory response in mice with sepsis. Therefore, we sought to investigate whether PICK1 is involved in the protective effects of electroacupuncture to SAE. In this study, mice were treated with EA after lipopolysaccharide (LPS) treatment. Behavioral tests; microglial activity of hippocampus; neuron survival and the inflammatory factors PICK1 and TLR4, as well as TLR4-related proteins, such as ERK, JNK, and P38, were assessed after EA treatment. PICK1, TLR4, and TLR4-related proteins, as well as PICK1-TLR4 complex levels were assessed in BV2 cells treated with LPS, PICK1 siRNA, or PICK1 polypeptide. The results indicated that EA could improve neurological assessment and reduce activation of microglial and TLR4 and expression of proinflammatory cytokines. EA also reduced the expression of TLR4 and phosphorylation of ERK/JNK/P38 while, increased the expression of PICK1 and TLR4 complexes. PICK1 knockdown further promoted the expression of TLR4 and phosphorylation of ERK/JNK/P38 in BV2 cells, but this effect was reversed by PICK1 polypeptides. These results suggest that EA may reduce neuroinflammation responses, decrease inflammatory factors, and finally, protect SAE by increasing the formation of PICK1-TLR4 complexes in microglia.

摘要

脓毒症相关性脑病(SAE)是由神经炎症引起的脓毒症的常见并发症。电针(EA)可用于治疗 SAE,但潜在机制尚不清楚。PICK1 的缺乏进一步加重了脓毒症小鼠的炎症反应。因此,我们试图研究 PICK1 是否参与电针对 SAE 的保护作用。在这项研究中,在脂多糖(LPS)处理后,用 EA 处理小鼠。进行行为测试;评估海马小胶质细胞的活性;神经元存活以及炎症因子 PICK1 和 TLR4,以及 TLR4 相关蛋白,如 ERK、JNK 和 P38;评估 LPS、PICK1 siRNA 或 PICK1 多肽处理的 BV2 细胞中的 PICK1、TLR4 和 TLR4 相关蛋白以及 PICK1-TLR4 复合物水平。结果表明,EA 可以改善神经评估,减少小胶质细胞和 TLR4 的激活以及促炎细胞因子的表达。EA 还降低了 TLR4 和 ERK/JNK/P38 的磷酸化表达,同时增加了 PICK1 和 TLR4 复合物的表达。PICK1 敲低进一步促进了 BV2 细胞中 TLR4 和 ERK/JNK/P38 的磷酸化表达,但这一作用被 PICK1 多肽逆转。这些结果表明,EA 可能通过增加小胶质细胞中 PICK1-TLR4 复合物的形成来减轻神经炎症反应,降低炎症因子,最终保护 SAE。

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