Department of Biomedical Sciences, College of Graduate Studies, Midwestern University, Glendale, AZ 85308, USA.
Department of Physiology, College of Graduate Studies, Midwestern University, Glendale, AZ 85308, USA.
Molecules. 2020 Apr 30;25(9):2100. doi: 10.3390/molecules25092100.
(1) Background: Diet-induced obesity inhibits hepatic carnitine biosynthesis. Herein, the effects of high-fat (HF) and high-sugar (HFHS) feeding and exercise training (ET) on renal carnitine biosynthesis and uptake were determined. (2) Methods: Male C57BL/6J mice were assigned to the following groups: lean control (standard chow), HFHS diet, and HFHS diet with ET. ET consisted of 150 min of treadmill running per week for 12 weeks. Protein levels of γ-butyrobetaine hydroxylase (γ-BBH) and organic cation transporter-2 (OCTN2) were measured as markers of biosynthesis and uptake, respectively. (3) Results: HFHS feeding induced an obese diabetic state with accompanying hypocarnitinemia, reflected by decreased free carnitine levels in plasma and kidney. This hypocarnitinemia was associated with decreased γ-BBH (30%) and increased OCTN2 levels (50%). ET failed to improve the obesity and hyperglycemia, but improved insulin levels and prevented the hypocarnitinemia. ET increased protein levels of γ-BBH, whereas levels of OCTN2 were decreased. Peroxisome proliferator-activated receptor-alpha content was not changed by the HFHS diet or ET. (4) Conclusions: Our results indicate that ET prevents the hypocarnitinemia induced by HFHS feeding by increasing carnitine biosynthesis in kidney. Increased expression of OCTN2 with HFHS feeding suggests that renal uptake was stimulated to prevent carnitine loss.
(1) 背景:饮食诱导的肥胖会抑制肝脏肉碱生物合成。本文旨在研究高脂肪(HF)和高糖(HFHS)喂养以及运动训练(ET)对肾脏肉碱生物合成和摄取的影响。(2) 方法:雄性 C57BL/6J 小鼠被分为以下几组:瘦对照组(标准饲料)、HFHS 饮食组和 HFHS 饮食加 ET 组。ET 包括每周 150 分钟的跑步机跑步,持续 12 周。γ-丁羟丁酸羟化酶(γ-BBH)和有机阳离子转运体-2(OCTN2)的蛋白水平分别作为生物合成和摄取的标志物进行测量。(3) 结果:HFHS 喂养导致肥胖型糖尿病状态,伴随低肉碱血症,表现为血浆和肾脏中游离肉碱水平降低。这种低肉碱血症与 γ-BBH 降低(约 30%)和 OCTN2 升高(约 50%)有关。ET 虽然不能改善肥胖和高血糖,但可以改善胰岛素水平并预防低肉碱血症。ET 增加了肾脏中 γ-BBH 的蛋白水平,而 OCTN2 的水平则降低。过氧化物酶体增殖物激活受体-α的含量不受 HFHS 饮食或 ET 的影响。(4) 结论:我们的结果表明,ET 通过增加肾脏肉碱生物合成来预防 HFHS 喂养引起的低肉碱血症。HFHS 喂养时 OCTN2 的表达增加表明肾脏摄取受到刺激以防止肉碱丢失。