Daily Oral Administration of Protease-Treated Royal Jelly Protects Against Denervation-Induced Skeletal Muscle Atrophy.
Tomohiko ShirakawaAki MiyawakiTakuma MatsubaraNobuaki OkumuraHideto OkamotoNaoya NakaiThira RojasawasthienKazumasa MorikawaAsako InoueAkino GotoAyako WashioToshiyuki TsujisawaTatsuo KawamotoShoichiro KokabuPublished in: Nutrients (2020)
Honeybees produce royal jelly (RJ) from their cephalic glands. Royal jelly is a source of nutrition for the queen honey bee throughout its lifespan and is also involved in fertility and longevity. Royal jelly has long been considered beneficial to human health. We recently observed that RJ delayed impairment of motor function during aging, affecting muscle fiber size. However, how RJ affects skeletal muscle metabolism and the functional component of RJ is as of yet unidentified. We demonstrate that feeding mice with RJ daily prevents a decrease in myofiber size following denervation without affecting total muscle weight. RJ did not affect atrophy-related genes but stimulated the expression of myogenesis-related genes, including IGF-1 and IGF receptor. Trans-10-hydroxy-2-decenoic acid (10H2DA) and 10-hydroxydecanoic acid (10HDAA), two major fatty acids contained in RJ. After ingestion, 10H2DA and 10HDAA are metabolized into 2-decenedioic acid (2DA) and sebacic acid (SA) respectively. We found that 10H2DA, 10HDAA, 2DA, and SA all regulated myogenesis of C2C12 cells, murine myoblast cells. These novel findings may be useful for potential preventative and therapeutic applications for muscle atrophy disease included in Sarcopenia, an age-related decline in skeletal muscle mass and strength.
Keyphrases
- skeletal muscle
- human health
- induced apoptosis
- physical activity
- insulin resistance
- umbilical cord
- risk assessment
- cell cycle arrest
- binding protein
- mesenchymal stem cells
- body mass index
- climate change
- pi k akt
- poor prognosis
- transcription factor
- endoplasmic reticulum stress
- bone marrow
- weight gain
- high fat diet induced
- signaling pathway
- endothelial cells
- cell proliferation
- young adults
- high glucose
- diabetic rats
- childhood cancer