Candesartan Mitigates Perioperative Neurocognitive Disorders by Modulating Hypertension-Linked Neuroinflammatory Factor.

Journal: Neurochemical research
Published Date:

Abstract

Perioperative neurocognitive disorders (PND) are linked to neuroinflammation, a key factor in hypertension, but their causal relationship is underexplored. This study aims to investigate whether hypertension is a risk factor for PND, identify related neuroinflammatory targets, and determine if the angiotensin receptor blockers (ARBs) candesartan can improve cognitive function in PND mouse models by modulating these targets. This study identified hypertension as a risk factor for cognitive dysfunction (OR = 1.0767, P = 0.0057) through Mendelian randomization (MR) analysis. Subsequently, bioinformatics techniques were employed to identify the neuroinflammatory targets associated with hypertension for ARBs. Differential analysis revealed Bdkrb1, Ccr1, and Thbs1 were PND biomarkers associated with hypertension, confirmed by machine learning and receiver operating characteristic (ROC) analysis (area under the curve (AUC) > 0.9). Immune infiltration showed Thbs1 positively correlated with MoDC cells (r = 0.70), while Bdkrb1 negatively correlated with Plasma cells (r = -0.75). In the PND mouse model, we assessed whether candesartan could inhibit the onset of neuroinflammation by modulating the targets identified through our screening process. Molecular experiments, including RT-qPCR, Western blotting, immunofluorescence, and ELISA, analyzed gene expression and neuroinflammatory changes in the hippocampus. In a PND mouse model, candesartan improved cognitive function, reducing escape latency and increasing spontaneous alternation rates. Molecular analysis demonstrated candesartan downregulated Bdkrb1 and Ccr1 expression while upregulating Thbs1 in the hippocampus. Additionally, candesartan reduced IL-1β, IL-6, TNF-α levels and microglial activation, highlighting its anti-inflammatory and neuroprotective effects in PND. In conclusion, candesartan improved cognitive function in PND mice by modulating Bdkrb1, Ccr1, and Thbs1, reducing neuroinflammation, and targeting hippocampal immune responses, highlighting its therapeutic potential for PND.

Authors

  • Zhenyu Wu
    Department of Biomedical Informatics, The Ohio State University, Columbus, OH 43210, USA.
  • Yuqing Li
    Deep Space Exploration Research Center, 47822Harbin Institute of Technology, Harbin, China.
  • Taowu Gong
    Guizhou Provincial Key Laboratory for Brain Science and Brain Disease Prevention and Control, Zunyi, Guizhou Province, China.
  • Jia Li
    Zhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan Tsuihang New District, Guangdong, 528400, PR China; School of Pharmacy, Zunyi Medical University, Zunyi, 563000, PR China; National Center for Drug Screening, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, PR China.
  • Pengcheng Zhao
    School of Life Science, Northwestern Polytechnical University, Xi'an, 710072, China.
  • Xufang Huo
    Department of Anesthesiology, The Affiliated Baiyun Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China.
  • Yuhang Zhu
    Department of Radiology, China-Japan Union Hospital of Jilin University, Changchun, 130033, P.R. China.
  • Qingfan Zeng
    Department of Anesthesiology, The Affiliated Baiyun Hospital of Guizhou Medical University, Guiyang, Guizhou Province, China. 445483296@qq.com.