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葡萄糖在人类新生儿内源性葡萄糖生成调节中的作用。

Role of glucose in the regulation of endogenous glucose production in the human newborn.

作者信息

Kalhan S C, Oliven A, King K C, Lucero C

出版信息

Pediatr Res. 1986 Jan;20(1):49-52. doi: 10.1203/00006450-198601000-00013.

Abstract

The role of plasma glucose concentration in the regulation of endogenous glucose production in the human newborn was examined by infusing glucose at 2.6-4.6 mg/kg . min as a continuous infusion to eight normal term appropriate for gestational age infants, five preterm, and six small for gestational age infants. All infants were healthy, had no overt clinical problems and were studied 6 h after their last feed. Glucose production rates were measured during the basal state and during glucose infusion by tracer dilution using [6,6(2)H2]glucose. The rate of glucose production during the basal state was similar in preterm and term appropriate for gestational age infants (appropriate for gestational age 3.53 +/- 0.32, preterm 3.49 +/- 0.38 mg/kg . min, mean +/- SD), while it was higher in the small for gestational age infants (4.25 +/- 0.98, p less than 0.03) as compared with appropriate for gestational age. During glucose infusion, the peak glucose concentration was related to the rate of glucose infusion. The endogenous glucose production rates during glucose infusion were variable in the three groups. However, a negative correlation between peak glucose concentration and endogenous glucose production rate was observed (r = 0.59, p = 0.006). The insulin response to glucose infusion was comparable in all infants. In addition, three small gestational age and one preterm infants, who had become hypoglycemic in the immediate newborn period, were studied while they were receiving parenteral glucose and their plasma glucose had stabilized at 55.5 +/- 10.25 mg/dl. Tracer kinetic studies showed persistence of endogenous glucose production in these infants even though they were receiving high rates of exogenous glucose infusion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过以2.6 - 4.6毫克/千克·分钟的速率持续输注葡萄糖,对8名足月适于胎龄、5名早产和6名小于胎龄的健康婴儿进行研究,以探讨血浆葡萄糖浓度在人类新生儿内源性葡萄糖生成调节中的作用。所有婴儿均健康,无明显临床问题,且在末次喂食后6小时进行研究。通过使用[6,6(2)H2]葡萄糖的示踪剂稀释法,在基础状态和葡萄糖输注期间测量葡萄糖生成率。基础状态下,早产和足月适于胎龄婴儿的葡萄糖生成率相似(适于胎龄3.53±0.32,早产3.49±0.38毫克/千克·分钟,均值±标准差),而小于胎龄婴儿的葡萄糖生成率高于适于胎龄婴儿(4.25±0.98,p<0.03)。葡萄糖输注期间,峰值葡萄糖浓度与葡萄糖输注速率相关。三组内源性葡萄糖生成率在葡萄糖输注期间各不相同。然而,观察到峰值葡萄糖浓度与内源性葡萄糖生成率呈负相关(r = 0.59,p = 0.006)。所有婴儿对葡萄糖输注的胰岛素反应相当。此外,对3名小于胎龄和1名早产婴儿进行了研究,这些婴儿在新生儿早期出现低血糖,当时他们正在接受肠外葡萄糖治疗,且血浆葡萄糖已稳定在55.5±10.25毫克/分升。示踪动力学研究表明,尽管这些婴儿接受高剂量的外源性葡萄糖输注,但仍存在内源性葡萄糖生成。(摘要截断于250字)

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