Vitamin K2 reprograms the multi-organ transcriptional landscape in mice with high-fat diet-induced obesity.

Vitamin K2 (VK2) shows promise as a nutritional intervention for obesity-related disorders, but its mechanisms of action in obesity and associated phenotypes are not yet fully understood. This study aims to elucidate the rescue effects of VK2 on multiple tissues during obesity. Twenty-eight 8-week-old male C57BL6/N mice are divided into four groups and fed a high-fat diet or normal diet for 16 weeks, receiving either menaquinone-7 (MK-7) or soybean oil solvent via gavage. RNA sequencing of brain, colon, muscle, heart, kidney, and liver tissues constructed a multi-organ transcriptional profile. The "rescue differentially expressed genes (DEGs)" are identified and tissue-tissue communication is analyzed. VK2 improves the biochemical profile in high-fat diet-induced obesity. Following VK2 intervention, the brain and kidneys exhibit more changes in autophagy, neurodegenerative diseases, energy metabolism, and immune response pathways. VK2 rescues over 10% of abnormally expressed genes, with most being fully restored. These rescue genes exhibit tissue-specific biological effects, including neuropeptide signaling and neuron ensheathment in the brain; triglyceride metabolism and carboxylic acid catabolism in the colon; microvillus organization and vascular permeability regulation in the heart; regulation of immune processes and collagen biosynthesis in the kidney; transforming growth factor-beta receptor signaling, iron transport and homeostasis in the liver; and muscle contraction, ATP transport, and filament sliding in the muscle. VK2 eliminates elevated ligand-receptor signals in immune response pathways and promotes the tissue-tissue signaling network to approach healthy control levels. VK2 significantly rescues the multi-organ transcriptome and restores tissue-specific pathways in high-fat diet-induced obese mice, providing the molecular mechanisms countering metabolic disorders.