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논문 기본 정보

자료유형
학술저널
저자정보
Dae Yun Seo (Inje University) 배준현 (인하대학교) Didi Zhang (Xiang Minzu University) Wook Song (Seoul National University) Hyo-Bum Kwak (Inha University) Jun-Won Heo (Inha University) Su-Jeen Jung (Seoil University) 윤형록 (인제대학교) Tae Nyun Kim (Inje University) Sang Ho Lee (Dong-A University) Amy Hyein Kim (Inje University) Dae Hoon Jeong (Inje University) Hyoung Kyu Kim (Inje University) 한진 (인제대학교)
저널정보
대한생화학·분자생물학회 BMB Reports BMB Reports 제54권 제11호
발행연도
2021.11
수록면
575 - 580 (6page)

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Cisplatin is widely known as an anti-cancer drug. However,the effects of cisplatin on mitochondrial function and autophagyrelatedproteins levels in the skeletal muscle are unclear. Thepurpose of this study was to investigate the effect of differentdoses of cisplatin on mitochondrial function and autophagy-relatedprotein levels in the skeletal muscle of rats. Eight-weekoldmale Wistar rats (n = 24) were assigned to one of threegroups; the first group was administered a saline placebo (CON,n = 10), and the second and third groups were given 0.1mg/kg body weight (BW) (n = 6), and 0.5 mg/kg BW (n = 8)of cisplatin, respectively. The group that had been administered0.5 mg cisplatin exhibited a reduced BW, skeletal muscletissue weight, and mitochondrial function and upregulated levelsof autophagy-related proteins, including LC3II, Beclin 1, andBNIP3. Moreover, this group had a high LC3 II/I ratio in theskeletal muscle; i.e., the administration of a high dose of cisplatindecreased the muscle mass and mitochondrial functionand increased the levels of autophagy-related proteins. Theseresults, thus, suggest that reducing mitochondrial dysfunctionand autophagy pathways may be important for preventing skeletalmuscle atrophy following cisplatin administration.

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