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3-巯基吡啶甲酸,一种糖异生抑制剂。

3-mercaptopicolinic acid, an inhibitor of gluconeogenesis.

作者信息

DiTullio N W, Berkoff C E, Blank B, Kostos V, Stack E J, Saunders H L

出版信息

Biochem J. 1974 Mar;138(3):387-94. doi: 10.1042/bj1380387.

Abstract
  1. 3-Mercaptopicolinic acid (SK&F 34288) inhibited gluconeogenesis in vitro, with lactate as substrate, in rat kidney-cortex and liver slices. 2. In perfused rat livers, gluconeogenesis was inhibited when lactate, pyruvate or alanine served as substrate, but not with fructose, suggesting pyruvate carboxylase or phosphoenolpyruvate carboxylase as the site of inhibition. No significant effects were evident in O(2) consumption, hepatic glycogen, urea production, or [lactate]/[pyruvate] ratios. 3. A hypoglycaemic effect was evident in vivo in starved and alloxan-diabetic rats, starved guinea pigs and starved mice, but not in 4h-post-absorptive rats. 4. In the starved rat the hypoglycaemia was accompanied by an increase in blood lactate. 5. A trace dose of [(14)C]lactate in vivo was initially oxidized to a lesser extent in inhibitor-treated rats, but during 90min the total CO(2) evolved was slightly greater. The total amount of the tracer oxidized was not significantly different from that in the controls.
摘要
  1. 3-巯基吡啶甲酸(SK&F 34288)在体外以乳酸为底物时,可抑制大鼠肾皮质和肝切片中的糖异生作用。2. 在灌注的大鼠肝脏中,当以乳酸、丙酮酸或丙氨酸为底物时,糖异生作用受到抑制,但以果糖为底物时则不受影响,这表明丙酮酸羧化酶或磷酸烯醇丙酮酸羧化酶是抑制位点。在氧气消耗、肝糖原、尿素生成或[乳酸]/[丙酮酸]比值方面未观察到显著影响。3. 在饥饿的大鼠、四氧嘧啶糖尿病大鼠、饥饿的豚鼠和饥饿的小鼠体内,该物质具有明显的降血糖作用,但在吸收后4小时的大鼠中则没有。4. 在饥饿的大鼠中,低血糖伴随着血乳酸的增加。5. 体内微量的[(14)C]乳酸最初在抑制剂处理的大鼠中氧化程度较低,但在90分钟内释放的总二氧化碳量略多。示踪剂氧化的总量与对照组无显著差异。

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