TY - JOUR
T1 - Nonivamide enhances miRNA let-7d expression and decreases adipogenesis PPARγ expression in 3T3-L1 cells
AU - Rohm, Barbara
AU - Holik, Ann Katrin
AU - Kretschy, Nicole
AU - Somoza, Mark M.
AU - Ley, Jakob P.
AU - Widder, Sabine
AU - Krammer, Gerhard E.
AU - Marko, Doris
AU - Somoza, Veronika
N1 - Publisher Copyright:
© 2015 Wiley Periodicals, Inc.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - Red pepper and its major pungent principle, capsaicin (CAP), have been shown to be effective anti-obesity agents by reducing energy intake, enhancing energy metabolism, decreasing serum triacylglycerol content, and inhibiting adipogenesis via activation of the transient receptor potential cation channel subfamily V member 1 (TRPV1). However, the binding of CAP to the TRPV1 receptor is also responsible for its pungent sensation, strongly limiting its dietary intake. Here, the effects of a less pungent structural CAP-analog, nonivamide, on adipogenesis and underlying mechanisms in 3T3-L1 cells were studied. Nonivamide was found to reduce mean lipid accumulation, a marker of adipogenesis, to a similar extent as CAP, up to 10.4% (P < 0.001). Blockage of the TRPV1 receptor with the specific inhibitor trans-tert-butylcyclohexanol revealed that the anti-adipogenic activity of nonivamide depends, as with CAP, on TRPV1 receptor activation. In addition, in cells treated with nonivamide during adipogenesis, protein levels of the pro-adipogenic transcription factor peroxisome-proliferator activated receptor γ (PPARγ) decreased. Results from miRNA microarrays and digital droplet PCR analysis demonstrated an increase in the expression of the miRNA mmu-let-7d-5p, which has been associated with decreased PPARγ levels. J. Cell. Biochem. 116: 1153-1163, 2015.
AB - Red pepper and its major pungent principle, capsaicin (CAP), have been shown to be effective anti-obesity agents by reducing energy intake, enhancing energy metabolism, decreasing serum triacylglycerol content, and inhibiting adipogenesis via activation of the transient receptor potential cation channel subfamily V member 1 (TRPV1). However, the binding of CAP to the TRPV1 receptor is also responsible for its pungent sensation, strongly limiting its dietary intake. Here, the effects of a less pungent structural CAP-analog, nonivamide, on adipogenesis and underlying mechanisms in 3T3-L1 cells were studied. Nonivamide was found to reduce mean lipid accumulation, a marker of adipogenesis, to a similar extent as CAP, up to 10.4% (P < 0.001). Blockage of the TRPV1 receptor with the specific inhibitor trans-tert-butylcyclohexanol revealed that the anti-adipogenic activity of nonivamide depends, as with CAP, on TRPV1 receptor activation. In addition, in cells treated with nonivamide during adipogenesis, protein levels of the pro-adipogenic transcription factor peroxisome-proliferator activated receptor γ (PPARγ) decreased. Results from miRNA microarrays and digital droplet PCR analysis demonstrated an increase in the expression of the miRNA mmu-let-7d-5p, which has been associated with decreased PPARγ levels. J. Cell. Biochem. 116: 1153-1163, 2015.
KW - 3T3-L1 ADIPOGENESIS
KW - CELL DIFFERENTIATION
KW - LIPID ACCUMULATION
KW - PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR)
KW - TRPV1
KW - microRNA
KW - trans-tert-BUTYLCYCLOHEXANOL
UR - https://www.scopus.com/pages/publications/84926635120
U2 - 10.1002/jcb.25052
DO - 10.1002/jcb.25052
M3 - Article
C2 - 25704235
AN - SCOPUS:84926635120
SN - 0730-2312
VL - 116
SP - 1153
EP - 1163
JO - Journal of Cellular Biochemistry
JF - Journal of Cellular Biochemistry
IS - 6
ER -