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低柠檬酸合酶活性与葡萄糖不耐受和脂毒性相关。

Low Citrate Synthase Activity Is Associated with Glucose Intolerance and Lipotoxicity.

作者信息

Alhindi Yosra, Vaanholt Lobke M, Al-Tarrah Mustafah, Gray Stuart R, Speakman John R, Hambly Catherine, Alanazi Bader S, Gabriel Brendan M, Lionikas Arimantas, Ratkevicius Aivaras

机构信息

Clinical Pharmacy Department, Pharmacy Collage, Umm Al-Qura University, Makkah, Saudi Arabia.

Institute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, UK.

出版信息

J Nutr Metab. 2019 Mar 3;2019:8594825. doi: 10.1155/2019/8594825. eCollection 2019.

DOI:10.1155/2019/8594825
PMID:30944739
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6421790/
Abstract

Citrate synthase (CS) is a key mitochondrial enzyme. The aim of this study was to test the hypothesis that low CS activity impairs the metabolic health of mice fed a high fat diet (HFD) and promotes palmitate-induced lipotoxicity in muscle cells. C57BL/6J (B6) mice and congenic B6.A-(rs3676616-D10Utsw1)/KjnB6 (B6.A), a strain which carries the A/J allele of CS on the B6 strain background, were fed HFD (45% kcal from fat) for 12 weeks. C2C12 mouse muscle cells were used to investigate effects of CS knockdown on cell viability and signalling after incubation in 0.8 mM palmitate. CS activity, but not that of -hydroxyacyl-coenzyme-A dehydrogenase was lower in the gastrocnemius muscle and heart of B6.A mice compared to B6 mice ( < 0.001). During HFD feeding, glucose tolerance of mice decreased progressively and to a greater extent in B6.A females compared to B6 females, with males showing a similar trend. Body weight and fat gain did not differ between B6.A and B6 mice. After an 18 h incubation in 0.8 mM palmitate C2C12 muscle cells with ∼50% shRNA mediated reduction in CS activity showed lower ( < 0.001) viability and increased ( < 0.001) levels of cleaved caspase-3 compared to the scramble shRNA treated C2C12 cells. A/J strain variant of CS is associated with low enzyme activity and impaired metabolic health. This could be due to impaired lipid metabolism in muscle cells.

摘要

柠檬酸合酶(CS)是一种关键的线粒体酶。本研究的目的是验证以下假设:低CS活性会损害高脂饮食(HFD)喂养小鼠的代谢健康,并促进棕榈酸酯诱导的肌肉细胞脂毒性。将C57BL/6J(B6)小鼠和同基因B6.A-(rs3676616-D10Utsw1)/KjnB6(B6.A)小鼠(该品系在B6品系背景上携带CS的A/J等位基因)喂食HFD(脂肪提供45%千卡热量)12周。使用C2C12小鼠肌肉细胞研究CS敲低对在0.8 mM棕榈酸酯中孵育后的细胞活力和信号传导的影响。与B6小鼠相比,B6.A小鼠腓肠肌和心脏中的CS活性较低,但β-羟酰基辅酶A脱氢酶的活性没有差异(P<0.001)。在HFD喂养期间,小鼠的葡萄糖耐量逐渐降低,与B6雌性小鼠相比,B6.A雌性小鼠的葡萄糖耐量下降幅度更大,雄性小鼠也呈现类似趋势。B6.A小鼠和B6小鼠之间的体重和脂肪增加没有差异。在0.8 mM棕榈酸酯中孵育18小时后,与经乱序shRNA处理的C2C12细胞相比,CS活性经约50%的shRNA介导降低的C2C12肌肉细胞显示出较低的活力(P<0.001)和增加的裂解型半胱天冬酶-3水平(P<0.001)。CS的A/J品系变体与低酶活性和受损的代谢健康相关。这可能是由于肌肉细胞中的脂质代谢受损所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/d264c0fa1be9/JNME2019-8594825.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/359743f248bf/JNME2019-8594825.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/7180fd787b9d/JNME2019-8594825.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/9e771ecd20d5/JNME2019-8594825.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/f22709ad6fe2/JNME2019-8594825.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/d8ec1f1848c8/JNME2019-8594825.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/1406cc2450f8/JNME2019-8594825.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/d264c0fa1be9/JNME2019-8594825.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/359743f248bf/JNME2019-8594825.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/7180fd787b9d/JNME2019-8594825.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/9e771ecd20d5/JNME2019-8594825.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/f22709ad6fe2/JNME2019-8594825.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/d8ec1f1848c8/JNME2019-8594825.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/1406cc2450f8/JNME2019-8594825.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ef0/6421790/d264c0fa1be9/JNME2019-8594825.007.jpg

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