Effects of Royal Jelly on Gut Dysbiosis and NAFLD in db / db Mice.
Genki KobayashiTakuro OkamuraSaori MajimaTakafumi SenmaruHiroshi OkadaEmi UshigomeNaoko NakanishiYuichiro NishimotoTakuji YamadaHideto OkamotoNobuaki OkumuraRyoichi SasanoYoshitaka HashimotoMichiaki FukuiPublished in: Nutrients (2023)
Royal jelly (RJ) is a naturally occurring substance synthesized by honeybees and has various health benefits. Herein, we focused on the medium-chain fatty acids (MCFAs) unique to RJ and evaluated their therapeutic efficacy in treating non-alcoholic fatty liver disease (NAFLD). We examined db / m mice that were exclusively fed a normal diet, db / db mice exclusively fed a normal diet, and db / db mice fed varying RJ quantities (0.2, 1, and 5%). RJ improved NAFLD activity scores and decreased gene expression related to fatty acid metabolism, fibrosis, and inflammation in the liver. RJ regulated innate immunity-related inflammatory responses in the small intestine and decreased the expression of genes associated with inflammation and nutrient absorption transporters. RJ increased the number of operational taxonomic units, the abundance of Bacteroides , and seven taxa, including bacteria that produce short-chain fatty acids. RJ increased the concentrations of RJ-related MCFAs (10-hidroxy-2-decenoic acid, 10-hydroxydecanoic acid, 2-decenedioic acid, and sebacic acid) in the serum and liver. These RJ-related MCFAs decreased saturated fatty acid deposition in HepG2 cells and decreased the gene expression associated with fibrosis and fatty acid metabolism. RJ and RJ-related MCFAs improved dysbiosis and regulated the expression of inflammation-, fibrosis-, and nutrient absorption transporter-related genes, thereby preventing NAFLD.
Keyphrases
- fatty acid
- gene expression
- oxidative stress
- dna methylation
- high fat diet induced
- healthcare
- transcription factor
- public health
- physical activity
- mental health
- metabolic syndrome
- insulin resistance
- liver fibrosis
- type diabetes
- microbial community
- climate change
- mesenchymal stem cells
- risk assessment
- diabetic nephropathy
- wild type
- antibiotic resistance genes