Natural products with minor side effects have been reported to be an effective adjuvant therapy for glucose and lipid metabolism disorders. Chrysin, a flavone, has a wide range of physiological effects, such as antioxidant, anti-inflammatory, anti-diabetes, anti-hyperlipidemia, and hepatoprotective. This study was designed to explore the effects and mechanism of chrysin on metabolic syndrome using insulin-resistant HepG2 cells and HFD/STZ-induced C57BL/6J mice. The results indicated that chrysin significantly decreased insulin resistance, oxidative stress, inflammation, and liver injury. In addition, chrysin improved glycogen synthesis and fatty acid oxidation and inhibited gluconeogenesis and fatty acid synthesis by regulating GSK3β, G6Paes, PEPCK, SREBP1, FAS, and ACC1. Furthermore, the results of western blot and real-time PCR experiments demonstrated that chrysin modulated glucose and lipid metabolism through the AMPK/PI3K/AKT signaling pathway. Treatment with the AMPK inhibitor verified that AMPK activation is positively correlated with chrysin activity on glycolipid metabolism. This study confirms that chrysin is a potential treatment for glucose and lipid metabolism disorders.

Nonalcoholic fatty liver disease (NAFLD) is a metabolic syndrome, whose main characteristics are excessive lipid accumulation and oxidative stress. Major royal jelly proteins (MRJPs) is a kind of water-soluble protein, which is abundant in royal jelly (RJ). The aim of this study was to evaluate the effect of MRJPs on lipid accumulation and oxidative stress of liver cells. Here, we first optimized the conditions for extracting MRJPs from RJ and identified the extraction effect and product by SDS-PAGE. Then, we used oleic acid (OA) of 1.0 mM to induce hepatocytes for 24 hr to establish a stable cell models of lipid accumulation, and we found that pre-administration (24 hr) of MRJPs (0.2, 0.5, and 1.0 g/L) could significantly reduce the lipid drop content and triglyceride level in the model cells, and simultaneously reduce the alanine aminotransferase and aspertate aminotransferase levels in the cell culture supernatant. In addition, pre-incubation (24 hr) with MRJPs (0.2, 0.5, and 1.0 g/L) could restore superoxide dismutase (SOD) level and mitochondrial membrane potential as compared with OA group. Furthermore, MRJPs administration significantly upregulated the expression of Silent Information Regulator 2 Associated Protein 3, mitochondrial superoxide dismutase (SOD2), and cytochrome c oxidase subunit IV in OA-treated HepG2 cells. The study for the first time provides evidences on the lipid-lowering effect of MRJPs at the cellular level, which can further provide support for the development and application of polypeptide drugs in the future, and can also provide a choice for the prevention and treatment of liver metabolic diseases represented by NAFLD. PRACTICAL APPLICATION: Our study proved that MRJPs had substantial preventing effect on OA-induced lipid accumulation and mitochondrial dysfunction in HepG2 cells. This research can further provide theoretical support for the development and application of peptide drugs in the future. Besides, it can not only further broaden our understanding of NAFLD and other diseases, but also provide ideas for research on oxidative stress and lipid accumulation in the body.

Eugenol is a representative methoxyphenol derived from the pyrolysis of lignin containing a branched alkene group. Its concentration in the atmosphere is equivalent to guaiacol and syringol. In this present paper, the gas phase reaction mechanisms and kinetic parameters of eugenol with hydroxyl radicals (OH) and ozone molecules (O3) were calculated at the M06-2×/6-311+G(3df,2p)//M06-2×/6-311+G(d,p) level. There are two distinct reaction types between eugenol and OH. In particular, Path2 is most favorable in the OH additions, whereas IM16 is most advantageous in H atom abstraction pathways. OH additions have more advantages than H abstraction reactions. Thus, the comprehensive and detailed reaction schemes for the further reactions of IM2 were presented. The main products generated by IM2 are methyl (Z)-3-(2-formylpenta-1,4-dien-1-yl)-2-hydroxyoxirane-2-carboxylate (P2B-4), 2-methoxy-2-oxoacetic acid (P2B-10), 2-allylmalealdehyde (P2B-11) and other carbonyl or carboxyl compounds. As for the reaction of eugenol with O3, the cycloaddition reactions and subsequent oxidative degradation processes were also explored, which yielded the most dominant product 2-(4-hydroxy-3-methoxyphenyl) acetaldehyde (P8-1). The reaction constants of the primary reactions for eugenol with OH and O3 under the temperature range of 225- 375 K were successively calculated by POLYRATE and MESMER program. At 298 K and 1 atm, the respective rate coefficients are 5.91 × 10-11 and 5.48 × 10-16 cm3 molecule-1 s-1 and the corresponding atmospheric lifetimes are 4.70 h and 0.72 h. The short lifetimes suggest that once eugenol enters the atmosphere, it is likely to be rapidly degraded. This work aims to provide theoretical guidance for the photochemical reaction mechanisms of eugenol with OH and O3, and present a reference for more experimental researches.