The significance of altered gluconeogenesis in surgical catabolism.
The significance of altered gluconeogenesis in surgical catabolism.
复制标题
糖异生改变在手术分解代谢中的重要性。
DOI:
10.1097/00005373-197508000-00013
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发表时间:
1975
期刊:
影响因子:
--
通讯作者:
J. Kinney
中科院分区:
文献类型:
--
作者:
F. Gump;C. Long;J. Geiger;J. Kinney
Supported by the National Institute of General Medical Sciences, Grant GM 14546-08. Presented at the Thirty-fourth Annual Session of the American Association for the Surgery of Trauma, 17–19 October 1974, Hot Springs, Virginia. Address for reprints: Frank E. Gump, MD, De-these patients had elective operations rather than traumatic injuries, but were selected for the study because they developed major septic complications resulting in fever, weight loss, and a negative nitrogen balance. All caloric intake including IV glucose was terminated at midnight on the day before the study. Hepatic vein catheterization was carried out with a No. 7 Goodale-Lubin catheter in-serted into an exposed right antecubital vein. The catheter was advanced to a large right hepatic vein under fluoroscopic control. The catheter tip was wedged and then withdrawn 2–4 cm until free flow of blood was obtained. An arterial needle was inserted into the femoral artery. Estimated splanchnic blood flow (ESBF) was measured by the continuous infusion technique (3) with indocyanine green dye (4), The dye was infused at a rate of 0.3 mg/min/M* BSA follow-ing a 5-mg priming dose.After the catheters were in place the patient was placed in a head canopy for continuous measurement of oxygen consumption and CO, production (19). Finally, simultaneous arterial and hepatic venous blood samples were ob-tained for blood glucose, blood urea nitrogen, 20 amino acids, and indocyanine green concentration. Samples were drawn at zero, 15, and 30 minutes during the half-hour study period. The patients were considered to be in a steady state during this time period. Arterio-hepatic venous differences for glucose, urea, and indocyanine green were calculated from the means of the three arterial and hepatic venous samples, but only one arterial and one hepatic venous sample was analyzed for the 20 amino acids. The uptake or release of any substrate was then