Portal glucose delivery stimulates muscle but not liver protein metabolism.
Portal glucose delivery stimulates muscle but not liver protein metabolism.
复制标题
门脉葡萄糖输送刺激肌肉但不刺激肝脏蛋白质代谢。
DOI：
10.1152/ajpendo.00140.2012
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发表时间：
2012
期刊：
影响因子：
--
通讯作者：
Moore,MaryCourtney
中科院分区：
文献类型：
--
作者：
Kraft,Guillaume;Coate,KatieC;Dardevet,Dominique;Farmer,Ben;Donahue,EPatrick;Williams,PhillipE;Cherrington,AlanD;Moore,MaryCourtney
Portal vein glucose delivery (the portal glucose signal) stimulates glucose uptake and glycogen storage by the liver, whereas portal amino acid (AA) delivery (the portal AA signal) induces an increase in protein synthesis by the liver. During a meal, both signals coexist and may interact. In this study, we compared the protein synthesis rates in the liver and muscle in response to portal or peripheral glucose infusion during intraportal infusion of a complete AA mixture. Dogs were surgically prepared with hepatic sampling catheters and flow probes. After a 42-h fast, they underwent a 3-h hyperinsulinemic (4× basal) hyperglucagonemic (3× basal) hyperglycemic (≈160 mg/dl) hyperaminoacidemic (hepatic load 1.5× basal; delivered intraportally) clamp (postprandial conditions). Glucose was infused either via a peripheral (PeG;n= 7) or the portal vein (PoG;n= 8). Protein synthesis was assessed with a primed, continuous [14C]leucine infusion. Net hepatic glucose uptake was stimulated by portal glucose infusion (+1 mg·kg−1·min−1,P< 0.05) as expected, but hepatic fractional AA extraction and hepatic protein synthesis did not differ between groups. There was a lower arterial AA concentration in the PoG group (−19%,P< 0.05) and a significant stimulation (+30%) of muscle protein synthesis associated with increased expression of LAT1 and ASCT2 AA transporters and p70S6 phosphorylation. Concomitant portal glucose and AA delivery enhances skeletal muscle protein synthesis compared with peripheral glucose and portal AA delivery. These data suggest that enteral nutrition support may have an advantage over parenteral nutrition in stimulating muscle protein synthesis.
