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酮症性低血糖的发病机制(作者译)

[Pathogenesis of ketotic hypoglycemia (author's transl)].

作者信息

Ploier R, Tulzer W, Sommer R

出版信息

Padiatr Padol. 1979;14(1):53-61.

PMID:418997
Abstract

4 children with ketotic hypoglycemia (KH) showed during a fasting period over 24 hours significant higher decreases of serum alanine levels than normal controls. Insulin induced hypoglycemia was followed by only minimal increase of urine epinephrine secretion, while all controls showed more than 6 times higher increases. 2-desoxy-glucose-tests were pathological in all cases with KH. One can speculate, that there is a connection between the reduced availability of alanine and the adrenal medullary hyporesponsiveness. Epinephrine stimulates glycogenolysis in muscle cells. Lack of epinephrine reduces pyruvate production and subsequently alanine synthesis. Alanine however is essential for gluconeogenesis in liver cells especially during starvation. After some days administration of diazoxide the 2-desoxy-glucose-test was normalised in all patients. This observation could probably be of some interest in therapy of KH.

摘要

4名酮症低血糖(KH)患儿在超过24小时的禁食期内,血清丙氨酸水平的下降幅度明显高于正常对照组。胰岛素诱导的低血糖仅使尿肾上腺素分泌略有增加,而所有对照组的增加幅度则高出6倍以上。所有KH病例的2-脱氧葡萄糖试验均呈病理性。可以推测,丙氨酸可用性降低与肾上腺髓质反应性降低之间存在联系。肾上腺素刺激肌肉细胞中的糖原分解。肾上腺素缺乏会减少丙酮酸生成,进而减少丙氨酸合成。然而,丙氨酸对于肝细胞中的糖异生至关重要,尤其是在饥饿期间。给予二氮嗪几天后,所有患者的2-脱氧葡萄糖试验均恢复正常。这一观察结果可能对KH的治疗具有一定意义。

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