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犬运动过程中肝脏谷氨酰胺代谢的调节

Regulation of hepatic glutamine metabolism during exercise in the dog.

作者信息

Halseth A E, Rhéaume N, Messina A B, Reed E K, Krishna M G, Flakoll P J, Lacy D B, Wasserman D H

机构信息

Department of Molecular Physiology and Biophysics, Diabetes Research and Training Center, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

出版信息

Am J Physiol. 1998 Oct;275(4):E655-64. doi: 10.1152/ajpendo.1998.275.4.E655.

Abstract

The goal of this study was to determine how liver glutamine (Gln) metabolism adapts to acute exercise in the 18-h-fasted dogs (n = 7) and in dogs that were glycogen depleted by a 42-h fast (n = 8). For this purpose, sampling (carotid artery, portal vein, and hepatic vein) and infusion (vena cava) catheters and Doppler flow probes (portal vein, hepatic artery) were implanted under general anesthesia. At least 16 days later an experiment, consisting of a 120-min equilibration period, a 30-min basal sampling period, and a 150-min exercise period was performed. At the start of the equilibration period, a constant-rate infusion of [5-15N]Gln was initiated. Arterial Gln flux was determined by isotope dilution. Gut and liver Gln release into and uptake from the blood were calculated by combining stable isotopic and arteriovenous difference methods. The results of this study show that 1) in the 18-h-fasted dog, approximately 10% and approximately 35% of the basal Gln appearance in arterial blood is due to Gln release from the gut and liver, respectively, whereas approximately 30% and approximately 25% of the basal Gln disappearance is due to removal by these tissues; 2) extending the fast to 42 h does not affect basal arterial Gln flux or the contribution of the gut to arterial Gln fluxes but decreases hepatic Gln release, causing a greater retention of gluconeogenic carbon by the liver; 3) moderate-intensity exercise increases hepatic Gln removal from the blood regardless of fast duration but does not affect the hepatic release of Gln; and 4) Gln plays an important role in channeling nitrogen into the ureagenic pathway in the basal state, and this role is increased by approximately 80% in response to exercise. These studies illustrate the quantitative importance of the splanchnic bed contribution to arterial Gln flux during exercise and the ability of the liver to acutely adapt to changes in metabolic requirements induced by the combined effects of fasting and exercise.

摘要

本研究的目的是确定禁食18小时的犬(n = 7)以及禁食42小时导致糖原耗竭的犬(n = 8)的肝脏谷氨酰胺(Gln)代谢如何适应急性运动。为此,在全身麻醉下植入采样(颈动脉、门静脉和肝静脉)和输注(腔静脉)导管以及多普勒血流探头(门静脉、肝动脉)。至少16天后进行一项实验,该实验包括120分钟的平衡期、30分钟的基础采样期和150分钟的运动期。在平衡期开始时,开始以恒定速率输注[5-¹⁵N]Gln。通过同位素稀释法测定动脉Gln通量。结合稳定同位素法和动静脉差值法计算肠道和肝脏向血液中释放Gln以及从血液中摄取Gln的量。本研究结果表明:1)在禁食18小时的犬中,动脉血中基础Gln出现量的约10%和约35%分别归因于肠道和肝脏释放的Gln,而基础Gln消失量的约30%和约25%归因于这些组织的清除;2)将禁食时间延长至42小时不影响基础动脉Gln通量或肠道对动脉Gln通量的贡献,但会减少肝脏Gln释放,导致肝脏对糖异生碳的保留增加;3)无论禁食时间长短,中等强度运动均会增加肝脏从血液中清除Gln的量,但不影响肝脏释放Gln;4)在基础状态下,Gln在将氮导入尿素生成途径中起重要作用,运动后这一作用增加约80%。这些研究说明了内脏床对运动期间动脉Gln通量贡献的定量重要性,以及肝脏对由禁食和运动的联合作用引起的代谢需求变化进行急性适应的能力。

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