DiscussionBoth AD and PD preclinical studies discussed here suggest a dysregulation of the SPM levels and their receptors in disease condition as compared to healthy individuals. In both conditions, several studies suggest a benefit from administration of SPMs in various models (Table 1). SPMs hold great promise for neuroprotection in AD by altering gene expression of pro-inflammatory genes, modulating macrophage function, serving as a biomarker for AD status, and promoting resolution of neuroinflammation. In PD, data from in vitro, in vivo, and observational studies suggest SPM are able to cross the blood-brain barrier, inhibit microglial activation and decrease induced markers of inflammation, possibly as a result of their ability to downregulate NFκB signaling pathways (Xu et al., 2013, 2017; Tian et al., 2015). Further, treatment with these lipid-derived mediators may improve behavioral deficit as a result of the protection of DA neurons and prevents the onset of PD by attenuating neuroinflammation
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Special pro-resolving mediator (SPM) actions in regulating gastrointestinal inflammation and gut mucosal immune responses