高脂饮食性肥胖雌性LeeSung迷你猪线粒体功能和肾脏损伤的测定。

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Miao-Ju Chien, Sin-Jin Li, Shiu-Chung Wong, Chun-Hsien Chiang, Yuan-Yu Lin, Harry J Mersmann, Ching-Yi Chen
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引用次数: 2

摘要

本研究的目的是通过饮食诱导的肥胖迷你猪模型来研究线粒体功能与肾损伤之间的关系。饲喂高脂日粮6个月的母利成迷你猪出现肥胖、高血糖和血脂异常。HFD升高了与肾损伤相关的血浆生物标志物的水平,包括对称二甲基精氨酸、肌酐和尿素氮。hfd喂养的猪在小管和肾小球中观察到广泛的结构变化。与对照组相比,HFD肾脏中积累了大量的甘油三酯,而HFD肾脏中ATP水平和抗氧化能力均有所降低。此外,HFD改变了肾皮质线粒体相关蛋白的表达。综上所述,长期饲喂高脂饲料可导致Lee-Sung小型猪肥胖和肾损伤,并伴有肾皮质线粒体功能异常,提示其与肾脏疾病进展相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of mitochondrial functions and damage in kidney in female LeeSung minipigs with a high-fat diet-induced obesity.

The purpose of this study was to investigate the nexus between mitochondrial function and kidney injury by using a dietary-induced obese minipig model. Female Lee-Sung minipigs feeding a high-fat diet (HFD) for 6 months exhibited obesity, hyperglycaemia and dyslipidemia. HFD elevated the levels of plasma biomarkers related to renal injury, including symmetric dimethylarginine, creatinine and urea nitrogen. An extensive structural change in tubules and glomeruli was observed in HFD-fed pigs. A great amount of triacylglycerol was accumulated in HFD kidney compared to control kidney, whereas a reduction of ATP level and antioxidant capacity were exhibited in HFD kidney. Moreover, HFD altered the expressions of mitochondrial-related protein in renal cortex. To conclude, long-term HFD feeding to Lee-Sung minipigs induced obesity and kidney injury accompanied by abnormal mitochondrial functions in the renal cortex, suggesting an interrelationship with renal disease progression.

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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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