1. Academic Validation
  2. Resveratrol glycoside mediates microglial endoplasmic reticulum stress to mitigate LPS-induced sepsis-associated cognitive dysfunction

Resveratrol glycoside mediates microglial endoplasmic reticulum stress to mitigate LPS-induced sepsis-associated cognitive dysfunction

  • Behav Brain Res. 2023 Feb 20;443:114326. doi: 10.1016/j.bbr.2023.114326.
Yi Yin 1 Guoguang Lv 2 Wang Zhang 2 Jing Yuan 2 Yakun Yang 2 Yushui Wang 1 Shuai Liu 1 Shan Wang 1 Bin Yan 2 Hai Bo 3 Chaoqun Ye 4
Affiliations

Affiliations

  • 1 Department of Rehabilitation, Air Force Medical Center, Beijing 100142, China.
  • 2 PLA Rocket Force Characteristic Medical Center, Beijing 100088, China.
  • 3 Department of Military Training Medicines, Logistics University of Chinese People's Armed Police Force, Tianjin 300162, China. Electronic address: bohaixd@126.com.
  • 4 Department of Rehabilitation, Air Force Medical Center, Beijing 100142, China. Electronic address: yechaoqun24@163.com.
Abstract

Background: As a common complication of sepsis, sepsis-associated encephalopathy (SAE) is characterized by diffuse brain dysfunction and neurological damage and closely associated with long-term cognitive dysfunction. The dysregulated host response triggered by neurotoxicity of microglia is an important cause of diffuse brain dysfunction in SAE. Resveratrol glycoside has anti-inflammatory and antioxidant effects. However, there is no evidence whether resveratrol glycoside could alleviate SAE.

Methods: LPS administration was used to induce SAE in mice. Step-down test (SDT) and Morris water maze test (MWM) were performed to evaluate the cognitive function of mice with SAE. Western blot and immunofluorescence were used to reveal the endoplasmic reticulum stress (ERS) regulation. Microglia cell line BV-2 was used to validate the effect of resveratrol glycoside on LPS-stimulated ERS in vitro.

Results: Compared with the control group, LPS-stimulated mice had decreased cognitive function, but this phenomenon was well reversed by resveratrol glycoside administration, in which the SDT assay showed longer retention time, both in short-term memory (STM) and long-term memory (LTM). Western blot indicated that the expression of ER stress-related protein PERK/CHOP in LPS-stimulated mice were significantly increased, while that in the resveratrol glycoside-treated group were relieved. Furthermore, Immunofluorescence revealed resveratrol glycoside mainly worked on microglia in mediating the ER stress, in which the expression of PERK/CHOP were significantly inhibited in resveratrol glycoside group mice. In vitro, BV2 showed consistent results with the aforementioned.

Conclusion: Resveratrol glycoside could alleviate the cognitive dysfunction caused by LPS-induced SAE, mainly by inhibiting the ER stress and maintaining the homeostasis of ER function of microglia.

Keywords

Cognitive dysfunction; Endoplasmic reticulum stress; LPS; Microglia; Resveratrol glycoside; Septic-associated encephalopathy.

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