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Previous studies have shown that suicidal states are associated with various biochemical changes affecting neurotransmitter systems (i.e., serotonin, glutamate, -aminobutyric acid, and their signaling pathways) [8,9,10,11], the inflammatory response [12], hypothalamicpituitaryadrenal axis [13], and glial cell function/neurotrophic factors [14, 15]

In a murine model of IDD, the absence of PGRN accelerates the degenerative process, as evidenced by an increase in osteoblast markers, depletion of proteoglycans, and upregulation of inflammatory mediators (64)

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ROS signaling under metabolic stress: cross-talk between AMPK and AKT pathway

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