Sepsis compromises post-ischemic stroke neurological recovery and is associated with sex differences

• Published in: Life sciences (1973) 2024-07, Vol.349, p.122721, Article 122721
• Main Authors: Joaquim, Larissa Silva, Steiner, Beatriz, Farias, Brenno, Machado, Richard Simon, Danielski, Lucineia Gainski, Mathias, Khiany, Stork, Solange, Lanzzarin, Everton, Novaes, Linerio, Bonfante, Sandra, Generoso, Jaqueline da Silva, Alano, Carolina Giassi, Lemos, Isabela, Dominguini, Diogo, Giustina, Amanda Della, Catalão, Carlos Henrique Rocha, Streck, Emilio Luiz, Giridharan, Vijayasree V, Dal-Pizzol, Felipe, Barichello, Tatiana, de Bitencourt, Rafael Mariano, Petronilho, Fabricia
• Format: Article
• Language: English
• Subjects: Animals; Brain Ischemia - complications; Brain Ischemia - metabolism; Female; Hippocampus - metabolism; Hippocampus - pathology; Infarction, Middle Cerebral Artery - complications; Infarction, Middle Cerebral Artery - metabolism; Infarction, Middle Cerebral Artery - pathology; Ischemic stroke; Ischemic Stroke - complications; Ischemic Stroke - metabolism; Ischemic Stroke - pathology; Male; Neuroinflammation; Oxidative Stress; Peroxidase - metabolism; Prefrontal Cortex - metabolism; Prefrontal Cortex - pathology; Rats; Rats, Wistar; Recovery of Function; sepsis; Sepsis - complications; Sepsis - metabolism; Sex Characteristics; Sex differences; Sex Factors
• ISSN: 0024-3205; 1879-0631; 1879-0631
• DOI: 10.1016/j.lfs.2024.122721

Infection is a complication after stroke and outcomes vary by sex. Thus, we investigated if sepsis affects brain from ischemic stroke and sex involvement. Male and female Wistar rats, were submitted to middle cerebral artery occlusion (MCAO) and after 7 days sepsis to cecal ligation and perforation (CLP). Infarct size, neuroinflammation, oxidative stress, and mitochondrial activity were quantified 24 h after CLP in the prefrontal cortex and hippocampus. Survival and neurological score were assessed up to 15 days after MCAO or 8 days after CLP (starting at 2 h after MCAO) and memory at the end. CLP decreased survival, increased neurological impairments in MCAO females. Early, in male sepsis following MCAO led to increased glial activation in the brain structures, and increased TNF-α and IL-1β in the hippocampus. All groups had higher IL-6 in both tissues, but the hippocampus had lower IL-10. CLP potentiated myeloperoxidase (MPO) in the prefrontal cortex of MCAO male and female. In MCAO+CLP, only male increased MPO and nitrite/nitrate in hippocampus. Males in all groups had protein oxidation in the prefrontal cortex, but only MCAO+CLP in the hippocampus. Catalase decreased in the prefrontal cortex and hippocampus of all males and females, and MCAO+CLP only increased this activity in males. Female MCAO+CLP had higher prefrontal cortex complex activity than males. In MCAO+CLP-induced long-term memory impairment only in females. The parameters evaluated for early sepsis after ischemic stroke show a worse outcome for males, while females are affected during long-term follow-up. [Display omitted]