KIOM-4 Protects against oxidative Stress-Induced Mitochondrial Damage in Pancreatic β-cells via its Antioxidant Effects

被引:8
|
作者
Kang, Kyoung Ah [1 ]
Kim, Jin Sook [2 ]
Zhang, Rui [1 ]
Piao, Mei Jing [1 ]
Maeng, Young Hee [1 ]
Kang, Mi Young [3 ]
Lee, In Kyung [4 ,5 ]
Kim, Bum Joon [4 ,5 ]
Hyun, Jin Won [1 ]
机构
[1] Jeju Natl Univ, Sch Med, Jeju Si 690756, South Korea
[2] Korea Inst Oriental Med, Div Tradit Korean Med Integrated Res, Diabet Complicat Res Ctr, Taejon, South Korea
[3] Chosun Univ, DNA Repair Ctr, Dept Biomat, Kwangju, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Microbiol, Seoul, South Korea
[5] Seoul Natl Univ, Coll Med, Caner Res Inst, Seoul, South Korea
关键词
SUPEROXIDE-DISMUTASE; RAT-LIVER; APOPTOSIS; HONOKIOL; MAGNOLOL; INHIBITION; TECTORIGENIN; ACTIVATION; ISOFLAVONE; MECHANISM;
D O I
10.1093/ecam/neq007
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The protective effect of KIOM-4, a mixture of plant extracts, was examined against streptozotocin (STZ)-induced mitochondrial oxidative stress in rat pancreatic beta-cells (RINm5F). KIOM-4 scavenged superoxide and hydroxyl radicals generated by xanthine/xanthine oxidase and Fenton reaction (FeSO4/H2O2), respectively, in a cell-free chemical system. In addition, a marked increase in mitochondrial reactive oxygen species (ROS) was observed in STZ-induced diabetic cells; this increase was attenuated by KIOM-4 treatment. Mitochondrial manganese superoxide dismutase (Mn SOD) activity and protein expression were down-regulated by STZ treatment and up-regulated by KIOM-4 treatment. In addition, NF-E2 related factor 2 (Nrf2), a transcription factor for Mn SOD, was up-regulated by KIOM-4. KIOM-4 prevented STZ-induced mitochondrial lipid peroxidation, protein carbonyl and DNA modification. Moreover, KIOM-4 treatment restored the loss of mitochondrial membrane potential (Delta psi) that was induced by STZ treatment, and inhibited the translocation of cytochrome c from the mitochondria to the cytosol. In addition, KIOM-4 treatment elevated the level of ATP, succinate dehydrogenase activity and insulin level, which were reduced by STZ treatment. These results suggest that KIOM-4 exhibits a protective effect through its antioxidant effect and the attenuation of mitochondrial dysfunction in STZ-induced diabetic cells.
引用
收藏
页码:1 / 11
页数:11
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