Melatonin ameliorates simulated-microgravity-induced mitochondrial dysfunction and lipid metabolism dysregulation in hepatocytes.
Yue XiongChiyuan MaQin LiWenya ZhangHuashan ZhaoPeigen RenKe ZhangXiaohua LeiPublished in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology (2023)
The liver is an essential multifunctional organ, which constantly communicates with nearly all tissues. It has raised the concern that microgravity exposure can lead to liver dysfunction and metabolic syndromes. However, molecular mechanisms and intervention measures of the adverse effects of microgravity on hepatocytes are limited. In this study, we utilized the random positioning machine culture system to investigate the adverse effects on hepatocytes under simulated microgravity (SMG). Our results showed that SMG impaired hepatocyte viability, causing cell cycle arrest and apoptosis. Compared to normal gravity, it also triggered lipid accumulation, elevated triglyceride (TG) and ROS levels, and impaired mitochondria function in hepatocytes. Furthermore, RNA sequencing results showed that SMG upregulated genes implicated in lipid metabolisms, including PPARγ, PLIN2, CD36, FABPs, etc. Importantly, all these defects can be suppressed by melatonin, a potent antioxidant secreted by the pineal gland, suggesting its potential use of therapeutic intervention.
Keyphrases
- cell cycle arrest
- cell death
- liver injury
- drug induced
- oxidative stress
- randomized controlled trial
- pi k akt
- fatty acid
- anti inflammatory
- gene expression
- adverse drug
- drug delivery
- high glucose
- signaling pathway
- reactive oxygen species
- insulin resistance
- genome wide
- mouse model
- type diabetes
- cancer therapy
- emergency department
- adipose tissue
- transcription factor
- dna methylation
- endothelial cells
- cell proliferation
- electronic health record
- nk cells
- stress induced
- low density lipoprotein