The role of mitochondrial autophagy activated NLRP3 inflammasome in postpartum depression-like behaviors induced by stress during pregnancy.

Abstract

Postpartum depression is a severe mental disorder affecting approximately 10% to 20% of women after childbirth, yet the physiological mechanism behind this is poorly understood. The NLRP3 inflammasome is pivotal in neuroinflammatory and neural disorders. It undergoes a dual modulation by mitochondrial autophagy during its activation phase, and its role in the occurrence and development of postpartum depression is worth exploring. A model of chronic stress during pregnancy in rats was established by subjecting the animals to chronic unpredictable mild stress (CUMS) starting from the third day of mating to evaluate the direct effect of pregnant stress on PPD and explore the mechanism. After rat model was established, the emotional function was observed by Open-field test (OFT), Sucrose preference test (SPT), Tail suspension test (TST), Forced swimming test (FST), mitophagy and NLRP3 inflammasome activation determined by ELISA and Western Blotting. The results showed that rats exposed to chronic stress during pregnancy exhibited postpartum depression-like behaviors such as anxiety, anhedonia, and despair. Significant neuronal damage from chronic stress was observed in the hippocampal CA1 region and the pyramidal cell layer of the prefrontal cortex, with disrupted mitochondrial structures. Accumulations of autophagosomes were found in the hippocampal CA1 region, and there was a decrease in mitochondrial membrane potential. The expression of NLRP3 inflammasome-related proteins and the expression of its downstream inflammatory cytokines IL-1β and IL-18 were both increased. Overall, our results highlighted that postpartum depression of chronic stress was closely associated with various stress factors experienced during pregnancy. During the onset and progression of PPD, stress led to impaired mitochondrial autophagy, and the incomplete clearance of damaged mitochondria activated the NLRP3 inflammasome, triggering an inflammatory response.