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10周促红细胞生成素治疗对健康男性脂质氧化无影响。

No effect of 10 weeks erythropoietin treatment on lipid oxidation in healthy men.

作者信息

Risikesan Jeyanthini, Nellemann Birgitte, Christensen Britt, Jørgensen Jens Otto Lunde, Nielsen Søren

机构信息

Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.

Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.

出版信息

Endocr Connect. 2020 Dec;9(12):1148-1155. doi: 10.1530/EC-20-0305.

Abstract

Studies indicate that erythropoietin (EPO) has effect on lipid and energy metabolism; however, the impact of EPO on lipid oxidation in vivo has not been well documented. Here, we evaluate whether long-term erythropoiesis-stimulating agent (ESA) treatment affects the oxidation of plasma very low-density lipoprotein triglycerides (VLDL-TG) fatty acids (FA), plasma free fatty acids (FFA) and non-plasma (residual) FA in healthy, young, sedentary men. Infusion of [1-14C]VLDL-TG and [9,10-3H]palmitate was used in combination with indirect calorimetry to assess resting lipid fuel utilization and kinetics, and resting energy expenditure (REE) before and after 10 weeks of ESA exposure compared with placebo. REE increased significantly during ESA compared with placebo (P = 0.023, RM-ANOVA). Oxidation rates of VLDL-TG FA, FFA, and residual FA remained unchanged during ESA compared with placebo. The relative contribution of the lipid stores was greatest for FFA (47.1%) and the total lipid oxidation rate and was not significantly different between ESA and placebo-treated subjects. We conclude that long-term ESA treatment of healthy young men increases REE but does not alter the oxidation rates of plasma and non-plasma FA sources.

摘要

研究表明,促红细胞生成素(EPO)对脂质和能量代谢有影响;然而,EPO对体内脂质氧化的影响尚未有充分的文献记载。在此,我们评估长期促红细胞生成刺激剂(ESA)治疗是否会影响健康、年轻、久坐男性血浆极低密度脂蛋白甘油三酯(VLDL-TG)脂肪酸(FA)、血浆游离脂肪酸(FFA)和非血浆(残余)FA的氧化。输注[1-14C]VLDL-TG和[9,10-3H]棕榈酸酯,并结合间接量热法,以评估ESA暴露10周前后与安慰剂相比的静息脂质燃料利用和动力学以及静息能量消耗(REE)。与安慰剂相比,ESA治疗期间REE显著增加(P = 0.023,重复测量方差分析)。与安慰剂相比,ESA治疗期间VLDL-TG FA、FFA和残余FA的氧化率保持不变。脂质储备对FFA的相对贡献最大(47.1%),且总脂质氧化率在ESA治疗组和安慰剂治疗组之间无显著差异。我们得出结论,长期对健康年轻男性进行ESA治疗可增加REE,但不会改变血浆和非血浆FA来源的氧化率。

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