Micro-Current Stimulation Can Modulate the Adipogenesis Process by Regulating the Insulin Signaling Pathway in 3T3-L1 Cells and ob / ob Mice.
Hana LeeJin-Ho LeeDoyong KimDonghyun HwangMinjoo LeeHalim ChungTack-Joong KimHan Sung KimPublished in: Life (Basel, Switzerland) (2023)
Obesity is a disease in which fat is abnormally or excessively accumulated in the body, and many studies have been conducted to overcome it with various techniques. In this study, we evaluated whether micro-current stimulation (MCS) can be applied to prevent obesity by regulating the adipogenesis through 3T3-L1 cells and ob / ob mice. To specify the intensity of MCS, Oil Red O staining was conducted with various intensities of MCS. Based on these, subsequent experiments used 200 and 400 μA for the intensity of MCS. The expressions of insulin signaling pathway-related proteins, including phosphorylation of IGF-1 and IR, were decreased in all MCS groups, and in turn, downstream signals such as Akt and ERK were decreased. In addition, MCS reduced the nucleus translocation of PPAR-γ and decreased the protein expression of C/EBP-α. In the ob / ob mouse model, MCS reduced body weight gain and abdominal adipose tissue volume. In particular, the concentration of triglycerides in serum was also decreased. Taken together, our findings showed that MCS inhibited lipid accumulation by regulating insulin signaling in 3T3-L1, and it was effective at reducing body weight and adipose tissue volume in ob / ob mice. These suggest that MCS may be a useful treatment approach for obesity.
Keyphrases
- high fat diet induced
- insulin resistance
- adipose tissue
- signaling pathway
- weight gain
- induced apoptosis
- type diabetes
- pi k akt
- metabolic syndrome
- cell cycle arrest
- weight loss
- high fat diet
- body weight
- mouse model
- body mass index
- cell proliferation
- glycemic control
- skeletal muscle
- birth weight
- cell death
- endoplasmic reticulum stress
- epithelial mesenchymal transition
- fatty acid
- case control
- physical activity
- drug induced
- flow cytometry
- protein kinase