2. Academic Validation
  3. Pharmacological inhibition of the cGAS-STING pathway suppresses microglia pyroptosis in sepsis-associated encephalopathy

Pharmacological inhibition of the cGAS-STING pathway suppresses microglia pyroptosis in sepsis-associated encephalopathy

  • J Neuroinflammation. 2025 Jul 9;22(1):176. doi: 10.1186/s12974-025-03507-2.
Qing-Quan Zeng # 1,  Yang Qi # 2,  Hui Yu # 3,  Ying Xu 1,  Jin-Xing Chen 1,  You-Wei Zheng 1,  Gui-Fei Zhang 1,  Qiao-Ling Zhang 1,  Yan-Hua Zheng 1,  Jing Guo 1,  Zi-Hong Zhao 1,  Fa-Sheng Wang 4,  Gui-Lin Jin 5 6
Affiliations

Affiliations

  • 1 Department of Pharmacology, School of Pharmacy, Fujian Medical University, Fuzhou, Fujian, 350108, P. R. China.
  • 2 Department of Pharmacy, 900th Hospital of PLA Joint Logistic Support Force, Fuzhou, 350025, China.
  • 3 Department of Pharmacy, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.
  • 4 Department of Orthopedics, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China. wfshine@foxmail.com.
  • 5 Department of Pharmacology, School of Pharmacy, Fujian Medical University, Fuzhou, Fujian, 350108, P. R. China. jinguilin0611@163.com.
  • 6 Fujian Key Laboratory of Drug Target Discovery and Structural and Functional Research, Fuzhou, Fujian, China. jinguilin0611@163.com.
  • # Contributed equally.
PMID: 40634978 DOI: 10.1186/s12974-025-03507-2
Abstract

Sepsis-associated encephalopathy (SAE) presents significant challenges in clinical management due to its association with cognitive impairments and high mortality rates. This study aims to elucidate the molecular mechanisms underlying microglial Pyroptosis and the stimulator of interferon genes (STING) signaling pathway in SAE, with a focus on identifying potential therapeutic targets. Employing the cecal ligation and puncture (CLP) model - the gold-standard polymicrobial sepsis model that faithfully replicates human sepsis progression - in C57BL/6J mice, we assessed the effects of various pharmacological agents, including the Pyroptosis inhibitor dimethyl fumarate (DMF), the STING inhibitor C176, and the mitochondrial protectant idebenone, on cognitive and behavioral outcomes in SAE mice. Results indicated that DMF significantly prevented microglial Pyroptosis, reduced inflammatory cytokine levels in the hippocampus, thereby enhancing survival rates and cognitive function. Additionally, inhibition of microglial Pyroptosis through C176 effectively inhibited the STING signaling pathway, consequently reducing microglial Pyroptosis and ameliorating behavioral symptoms associated with SAE. Furthermore, idebenone was observed to exert mitochondrial protection and inhibit STING-mediated Pyroptosis of microglia, leading to an improvement in behavioral symptoms in the SAE model. In conclusion, our findings underscore the pivotal roles of Pyroptosis and the STING signaling pathway in the pathophysiology of SAE, suggesting that targeting these mechanisms may provide promising therapeutic avenues for improving cognitive recovery in sepsis patients. Future studies should focus on elucidating the underlying molecular mechanisms and exploring their clinical viability in the management of SAE.

Graphical Abstract:

Supplementary Information: The online version contains supplementary material available at 10.1186/s12974-025-03507-2.

Keywords

Microglia; Pyroptosis; STING; Sepsis; Sepsis-associated encephalopathy.

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