Fig. 7.
Integrated pathways modulated by PFS through the gut-liver-muscle axis. Schematic representation illustrating the integrated signalling and metabolic pathways influenced by Perilla frutescens seed (PFS) supplementation. PFS enhanced microbial butyrate production in the gut. In the liver, PFS promoted hepatic synthesis of PUFAs via upregulation of ELOVL2 and FADS2, and modulated glycerophospholipid metabolism through suppression of PLA2G and LPCAT, resulting in reduced LysoPC(20:4) levels. Enhanced bile acid metabolism was characterised by increased GHDCA and CA, activating bile acid receptor TGR5 signalling. In immune-related pathways, PFS upregulated FcγR-mediated phagocytosis and T-cell receptor (TCR) signalling, while suppressing pro-inflammatory mediators (IL-1β, TNF-α) and enhancing anti-inflammatory cytokines (IL-10, TGF-β). The overall regulation of arachidonic acid metabolism and reinforcement of antioxidant defence collectively contribute to improved immune resilience and metabolic balance along the gut-liver-muscle axis. Red indicates upregulated elements, and blue indicates downregulated elements in response to PFS supplementation. CA: cholic acid; GHDCA: glycohyodeoxycholic acid; PUFAs: polyunsaturated fatty acids
