TY - JOUR
T1 - Low-calorie sweetener d-psicose promotes hydrogen peroxide-mediated apoptosis in c2c12 myogenic cells favoring skeletal muscle cell injury
AU - WEI, ZHEN JIE
AU - SUN, LU
AU - LI, YU LIN
AU - MUHAMMAD, JIBRAN SUALE H.
AU - WANG, YING
AU - FENG, QIAN WEN
AU - ZHANG, YAN ZHUO
AU - INADERA, HIDEKUNI
AU - CUI, ZHENG GUO
AU - WU, CHENG AI
N1 - Publisher Copyright:
© 2021 Spandidos Publications. All rights reserved.
PY - 2021/7
Y1 - 2021/7
N2 - Diet and exercise are the most effective approaches used to induce weight loss. D-psicose is a low-calorie sweetener that has been shown to reduce weight in obese individuals. However, the effect of D-psicose on muscle cells under oxidative stress, which is produced during exercise, requires further investigation. The present study aimed to determine the effects of D-psicose on C2C12 myogenic cells in vitro. Hydrogen peroxide (H2O2) was used to stimulate the generation of intracellular reactive oxygen species (RO S) in muscle cells to mimic exercise conditions. Cell viability was analyzed using a MTT assay and flow cytometry was used to analyze the levels of apoptosis, mitochondrial membrane potential (MMP), the generation of RO S and the cell cycle distribution following treatment. Furthermore, protein expression levels were analyzed using western blotting and cell proliferation was determined using a colony formation assay. The results of the present study revealed that D-psicose alone exerted no toxicity on C2C12 mouse myogenic cells. However, in the presence of low-dose (100 μM) H2O2-induced RO S, D-psicose induced C2C12 cell injury and significantly decreased C2C12 cell viability in a dose-dependent manner. In addition, the levels of apoptosis and the generation of RO S increased, while the MMP decreased. MAPK family molecules were also activated in a dose-dependent manner following treatment. Notably, the combined treatment induced G2/M phase arrest and reduced the proliferation of C2C12 cells. In conclusion, the findings of the present study suggested that D-psicose may induce toxic effects on muscle cells in a simulated exercise situation by increasing RO S levels, activating the MAPK signaling pathway and disrupting the MMP.
AB - Diet and exercise are the most effective approaches used to induce weight loss. D-psicose is a low-calorie sweetener that has been shown to reduce weight in obese individuals. However, the effect of D-psicose on muscle cells under oxidative stress, which is produced during exercise, requires further investigation. The present study aimed to determine the effects of D-psicose on C2C12 myogenic cells in vitro. Hydrogen peroxide (H2O2) was used to stimulate the generation of intracellular reactive oxygen species (RO S) in muscle cells to mimic exercise conditions. Cell viability was analyzed using a MTT assay and flow cytometry was used to analyze the levels of apoptosis, mitochondrial membrane potential (MMP), the generation of RO S and the cell cycle distribution following treatment. Furthermore, protein expression levels were analyzed using western blotting and cell proliferation was determined using a colony formation assay. The results of the present study revealed that D-psicose alone exerted no toxicity on C2C12 mouse myogenic cells. However, in the presence of low-dose (100 μM) H2O2-induced RO S, D-psicose induced C2C12 cell injury and significantly decreased C2C12 cell viability in a dose-dependent manner. In addition, the levels of apoptosis and the generation of RO S increased, while the MMP decreased. MAPK family molecules were also activated in a dose-dependent manner following treatment. Notably, the combined treatment induced G2/M phase arrest and reduced the proliferation of C2C12 cells. In conclusion, the findings of the present study suggested that D-psicose may induce toxic effects on muscle cells in a simulated exercise situation by increasing RO S levels, activating the MAPK signaling pathway and disrupting the MMP.
KW - Apoptosis
KW - D-psicose
KW - MAPK signaling pathway
KW - Muscle cell
KW - Reactive oxygen species
UR - http://www.scopus.com/inward/record.url?scp=85107892908&partnerID=8YFLogxK
U2 - 10.3892/MMR.2021.12175
DO - 10.3892/MMR.2021.12175
M3 - 学術論文
C2 - 34080650
AN - SCOPUS:85107892908
SN - 1791-2997
VL - 24
JO - Molecular Medicine Reports
JF - Molecular Medicine Reports
IS - 1
M1 - 12175
ER -