Sobacı, Sanem2025-01-302025-01-302025-012025-012025-01-28https://hdl.handle.net/11693/115973Cataloged from PDF version of article.Includes bibliographical references (leaves 59-72).Endoplasmic reticulum (ER) stress plays a critical role in cellular homeostasis and is implicated in various neurodegenerative diseases. The inositol-requiring enzyme 1 (IRE1) is one of the arms of the unfolded protein response (UPR), which is activated in the presence of ER stress. IRE1 pathway activates c-Jun N-terminal kinase (JNK) downstream under prolonged stress. This thesis explores the activation of the IRE1 and JNK signaling pathways in the mouse cerebral cortex following DSS-induced colitis, focusing on their roles as markers of ER stress in the context of the gut-brain axis. While DSS-induced intestinal inflammation and ER stress are well-established, neurological effects remain less understood. Employing a murine model, the study explored ER stress markers in the cerebral cortex resulting from intestinal pathology. Despite evidence of DSS-triggered systemic inflammation and ER stress in intestinal tissues, our study revealed no significant differences in the expression levels of IRE1, p-IRE1, or the p-IRE1/IRE1, nor in JNK, p-JNK, or the p-JNK/JNK between the control and DSS-treated groups. Additionally, these results are supported with correlational and linear discriminant analyses (LDA). These findings suggest that acute DSS-induced colitis did not elicit a detectable ER stress response in the mouse cerebral cortex under the conditions used. Possible explanations include tissue-specific reactions to the ER stress, transient activation of the IRE1-JNK pathway that returned to baseline by the time of analysis, or potential survivor's bias. Despite its limitations, this thesis provides a novel investigation into the effects of DSS-induced colitis on ER stress in the cerebral cortex.xvi, 74 leaves : color illsutrations, charts ; 30 cm.Englishinfo:eu-repo/semantics/openAccessIRE1JNKER stressUPRDSS-induced colitisGut-brain axisThesisB022449