Acacetin inhibits activation of microglia to improve neuroinflammation after subarachnoid hemorrhage through the PERK signaling pathway mediated autophagy

• Published in: Human & experimental toxicology 2024-01, Vol.43, p.9603271241251447-9603271241251447
• Main Authors: Liu, Ying, Tang, Jianhua, Hou, Yiwei, Li, Lu, Li, Wenna, Yu, Ling, Wang, Xue, Sui, Changbai
• Format: Article
• Language: English
• Subjects: Animals; Autophagy - drug effects; eIF-2 Kinase - metabolism; Flavones - pharmacology; Flavones - therapeutic use; Male; Microglia - drug effects; Microglia - metabolism; Neuroinflammatory Diseases - drug therapy; Rats; Rats, Sprague-Dawley; Signal Transduction - drug effects; Subarachnoid Hemorrhage - complications; Subarachnoid Hemorrhage - drug therapy; Subarachnoid Hemorrhage - metabolism
• ISSN: 0960-3271; 1477-0903
• DOI: 10.1177/09603271241251447

Purpose To explore the effect of acacetin on subarachnoid hemorrhage (SAH) and its possible mechanism. Methods SAH model of rat was established, and intraperitoneally injected with three doses of acacetin. To verify the role of PERK pathway, we used the CCT020312 (PERK inhibitor) and Tunicamycin (activators of endoplasmic reticulum stress). The SAH score, neurological function score, brain edema content, and Evans blue (EB) exudate were evaluated. Western blot was used to determine the expression of inflammation-associated proteins and PERK pathway. The activation of microglia was also determined through Iba-1 detection. TEM and immunofluorescence staining of LC3B were performed to observe the autophagy degree of SAH rats after acacetin. Tunel/NeuN staining, HE and Nissl’ staining were performed for neuronal damage. Results Acacetin increased the neurological function score, reduce brain water content, Evans blue exudation and SAH scores. The microglia in cerebral cortex were activated after SAH, while acacetin could inhibit its activation, and decreased the expression of TNF-α and IL-6 proteins. The pathological staining showed the severe neuronal damage and increased neuronal apoptosis after SAH, while acacetin could improve these pathological changes. We also visualized the alleviated autophagy after acacetin. The expression of Beclin1 and ATF4 proteins were increased, but acacetin could inhibit them. Acacetin also inactivated PERK pathway, which could improve the neuronal injury and neuroinflammation after SAH, inhibit the microglia activation and the overactivated autophagy through PERK pathway. Conclusion Acacetin may alleviate neuroinflammation and neuronal damage through PERK pathway, thus having the protective effect on EBI after SAH.