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长期饥饿期间的氨基酸代谢。

Amino acid metabolism during prolonged starvation.

作者信息

Felig P, Owen O E, Wahren J, Cahill G F

出版信息

J Clin Invest. 1969 Mar;48(3):584-94. doi: 10.1172/JCI106017.

Abstract

Plasma concentration, splanchnic and renal exchange, and urinary excretion of 20 amino acids were studied in obese subjects during prolonged (5-6 wk) starvation. Splanchnic amino acid uptake was also investigated in postabsorptive and briefly (36-48 hr) fasted subjects.A transient increase in plasma valine, leucine, isoleucine, methionine, and alpha-aminobutyrate was noted during the 1st wk of starvation. A delayed, progressive increase in glycine, threonine, and serine occurred after the 1st 5 days. 13 of the amino acids ultimately decreased in starvation, but the magnitude of this diminution was greatest for alanine which decreased most rapidly during the 1st week of fasting. In all subjects alanine was extracted by the splanchnic circulation to a greater extent than all other amino acids combined. Brief fasting resulted in an increased arterio-hepatic venous difference for alanine due to increased fractional extraction. After 5-6 wk of starvation, a marked falloff in splanchnic alanine uptake was attributable to the decreased arterial concentration. Prolonged fasting resulted in increased glycine utilization by the kidney and in net renal uptake of alanine. It is concluded that the marked decrease in plasma alanine is due to augmented and preferential splanchnic utilization of this amino acid in early starvation resulting in substrate depletion. Maintenance of the hypoalaninemia ultimately serves to diminish splanchnic uptake of this key glycogenic amino acid and is thus an important component of the regulatory mechanism whereby hepatic gluconeogenesis is diminished and protein catabolism is minimized in prolonged fasting. The altered renal extraction of glycine and alanine is not due to increased urinary excretion but may be secondary to the increased rate of renal gluconeogenesis observed in prolonged starvation.

摘要

在肥胖受试者长期(5 - 6周)饥饿期间,研究了20种氨基酸的血浆浓度、内脏和肾脏交换以及尿排泄情况。还对吸收后和短期(36 - 48小时)禁食的受试者的内脏氨基酸摄取进行了研究。饥饿第1周时,血浆缬氨酸、亮氨酸、异亮氨酸、蛋氨酸和α - 氨基丁酸出现短暂升高。在最初5天后,甘氨酸、苏氨酸和丝氨酸出现延迟的、逐渐增加的情况。13种氨基酸在饥饿时最终减少,但丙氨酸减少的幅度最大,在禁食第1周时下降最快。在所有受试者中,内脏循环对丙氨酸的提取程度高于所有其他氨基酸提取程度之和。短期禁食导致丙氨酸的肝动脉 - 肝静脉差值增加,这是由于提取分数增加所致。饥饿5 - 6周后,内脏丙氨酸摄取显著下降归因于动脉浓度降低。长期禁食导致肾脏对甘氨酸的利用增加以及肾脏对丙氨酸的净摄取增加。得出的结论是,血浆丙氨酸的显著降低是由于在饥饿早期内脏对这种氨基酸的利用增加且具有优先性,导致底物耗竭。低丙氨酸血症的维持最终有助于减少内脏对这种关键生糖氨基酸的摄取,因此是调节机制的一个重要组成部分,通过该机制,在长期禁食时肝脏糖异生减少,蛋白质分解代谢降至最低。肾脏对甘氨酸和丙氨酸提取的改变并非由于尿排泄增加,而是可能继发于长期饥饿时观察到的肾脏糖异生速率增加。

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