Tranberg K G
Am J Physiol. 1979 Dec;237(6):E509-18. doi: 10.1152/ajpendo.1979.237.6.E509.
The hepatic uptake of unlabeled insulin (5--50 mU/kg) was determined in 45 nondiabetic patients without hepatic disease. Thirty patients were studied at normoglycemia and 15 at moderate steady hyperglycemia, induced by intraportal infusion of 80 or 200 mg glucose per h and per kg. The first pass fractional hepatic uptake of insulin (FH) was estimated by comparing the results after a portal and a peripheral infusion of unlabeled insulin in each patient. It varied negatively with the amount of insulin given, decreasing about 50% after a tenfold increase in dose. FH was markedly smaller during steady hyperglycemia than at normoglycemia, regardless of insulin dose. For low doses (5--10 mU/kg), giving insulin concentrations within the physiological range, FH was 0.43 (5 mU/kg) and 0.40 (10 mU/kg) at normoglycemia and 0.16 (10 mU/kg) at hyperglycemia. FH did not vary with the fasting or the glucose-stimulated, endogenous insulin levels recorded before insulin infusion. It is suggested that glucose is more important than insulin in modulating the fractional hepatic uptake of insulin.
在45例无肝脏疾病的非糖尿病患者中测定了未标记胰岛素(5-50 mU/kg)的肝脏摄取情况。30例患者在正常血糖水平下进行研究,15例患者在中度持续高血糖状态下进行研究,通过每小时每千克门静脉输注80或200 mg葡萄糖诱导产生高血糖。通过比较每位患者门静脉输注和外周静脉输注未标记胰岛素后的结果,估算胰岛素的首过肝脏摄取分数(FH)。FH与给予的胰岛素量呈负相关,剂量增加10倍后降低约50%。无论胰岛素剂量如何,持续高血糖期间的FH均明显低于正常血糖水平时。对于低剂量(5-10 mU/kg),即给予生理范围内的胰岛素浓度,正常血糖时FH为0.43(5 mU/kg)和0.40(10 mU/kg),高血糖时为0.16(10 mU/kg)。FH与胰岛素输注前记录的空腹或葡萄糖刺激的内源性胰岛素水平无关。提示在调节胰岛素的肝脏摄取分数方面,葡萄糖比胰岛素更重要。