Oxamate suppresses whole-body energy metabolism at rest and during exercise in mice by inhibiting fat oxidation and altering lactate dynamics.

Physical activity and nutrition Pub Date : 2025-06-01 Epub Date: 2025-06-30 DOI:10.20463/pan.2025.0011
Deunsol Hwang, Taeho Kim, Sunghwan Kyun, Inkwon Jang, Hun-Young Park, Sung-Woo Kim, Jin-Soo Han, Jae-Moo So, Chi-Ho Lee, Jonghoon Park, Kiwon Lim, Jisu Kim
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引用次数: 0

Abstract

Purpose: Oxamate is a well-known inhibitor of glycolysis. However, its broad inhibitory effects on whole-body energy metabolism in vivo have not been identified. Therefore, we aimed to investigate its effects on wholebody energy metabolism in mice.

Methods: Ten-week-old male ICR mice were used in this study. The resting metabolic rate was measured for 3 h immediately after the intraperitoneal injection of oxamate (750 mg/kg) using a metabolic chamber system. In addition, resting blood glucose and lactate concentrations were measured. Next, the metabolism during exercise (10-25 m/min) was measured for 30 min immediately after oxamate injection using a metabolic treadmill chamber system. Post-exercise blood lactate concentrations were measured immediately after exercise sessions.

Results: The resting respiratory exchange rate remained unchanged, but fat and carbohydrate oxidation and energy expenditure (p = 0.003, 0.049, and 0.002, respectively) were significantly suppressed following oxamate injection. While the resting blood glucose levels were significantly reduced (p = 0.002), the lactate levels were significantly elevated (p = 0.005). The respiratory exchange rate during exercise significantly increased by oxamate injection (p = 0.02). Although fat oxidation during exercise significantly reduced (p = 0.009), carbohydrate oxidation remained unchanged. Consequently, energy expenditure during exercise was significantly reduced (p = 0.024) and post-exercise blood lactate levels were significantly elevated (p = 0.005) by oxamate injection.

Conclusion: Oxamate suppressed whole-body energy metabolism by inhibiting fat oxidation and altering lactate dynamics in vivo. These results provide novel insights into the systemic metabolic effects of oxamate and highlight the need for further investigation of its impact under different physiological conditions.

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草酸酯通过抑制脂肪氧化和改变乳酸动力学来抑制小鼠休息和运动时的全身能量代谢。
目的:草酸酯是一种众所周知的糖酵解抑制剂。然而,其对体内全身能量代谢的广泛抑制作用尚未确定。因此,我们旨在研究其对小鼠全身能量代谢的影响。方法:选用10周龄雄性ICR小鼠。利用代谢室系统,在腹腔注射草酸酯(750 mg/kg)后立即测量静息代谢率3小时。此外,测量静息血糖和乳酸浓度。接下来,在注射草酸酯后立即使用代谢跑步机室系统测量运动期间(10-25 m/min)的代谢(30 min)。运动后立即测量血乳酸浓度。结果:注射草酸酯后,大鼠静息呼吸交换率不变,但脂肪和碳水化合物氧化及能量消耗明显受到抑制(p分别为0.003、0.049和0.002)。静息血糖水平显著降低(p = 0.002),乳酸水平显著升高(p = 0.005)。注射草酸酯显著提高运动时呼吸交换率(p = 0.02)。虽然运动期间脂肪氧化显著减少(p = 0.009),但碳水化合物氧化保持不变。因此,注射草酸酯能显著降低运动时的能量消耗(p = 0.024),显著提高运动后血乳酸水平(p = 0.005)。结论:草酸酯通过抑制体内脂肪氧化和改变体内乳酸动力学来抑制全身能量代谢。这些结果为了解草酸酯的全身代谢作用提供了新的见解,并强调了进一步研究其在不同生理条件下的影响的必要性。
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