This study compared the effects of endogenous (portal) insulin secretion versus peripheral insulin administration with subcutaneous or inhaled human insulin [INH; Exubera, insulin human (rDNA origin) inhalation powder] on glucose disposal in fasted dogs. In the control group, glucose was infused into the portal vein (Endo; n ϭ 6). In two other groups, glucose was infused portally, whereas insulin was administered peripherally by inhalation (n ϭ 13) or s.c. injection (n ϭ 6) with somatostatin and basal glucagon. In the Endo group, over the first 3 h, the arterial insulin concentration was twice that of the peripheral groups, whereas hepatic sinusoidal insulin levels were half as much.Although net hepatic glucose uptake was greatest in the Endo group, the peripheral groups demonstrated larger increases in nonhepatic glucose uptake so that total glucose disposal was greater in the latter groups. Compared with s.c. insulin action, glucose excursions were smaller and shorter, and insulin action was at least twice as great after INH. Thus, at the glucose dose and insulin levels chosen, peripheral insulin delivery was associated with greater whole-body glucose disposal than endogenous (portal) insulin secretion. INH administration resulted in increased insulin sensitivity in nonhepatic but not in hepatic tissues compared with s.c. delivery.Most patients with diabetes requiring insulin treatment rely on daily injections of insulin. Various alternatives to injectable insulin have been investigated, including insulin patches, pumps, oral formulations, and inhalation. Inhaled human insulin [INH; Exubera, insulin human (rDNA origin) inhalation powder] seems to be a promising alternative for effective, noninvasive insulin delivery to injection. It is approved in the United States and European Union for treatment of hyperglycemia in adults with diabetes mellitus.Insulin delivered by inhalation or s.c. administration enters directly into the peripheral circulation, exposing muscle, fat, and other nonhepatic tissues to relatively higher insulin concentrations than the liver (Cherrington et al., 2004). On the other hand, endogenously secreted insulin enters into the portal vein, exposing the liver to the highest concentrations of insulin. Because insulin has discrete effects on hepatic and nonhepatic tissues, it is important to understand how differences in the route of insulin appearance may affect glucose metabolism, both at the liver and other tissues. Therefore, one purpose of this study was to compare the effect of portal (endogenous) insulin delivery to the effect of insulin delivered peripherally (by inhalation or s.c. injection) on hepatic and nonhepatic glucose metabolism during a simulated oral glucose load.In addition, in clinical trials comparing INH with s.c. insulin (Humulin) delivered, INH reduced the postprandial glucose rise (0 -3 h) at least as effectively as Humulin, with less late (4 -5 h) glucose reduction below baseline (Skyler et al., 2005). Remarkably, compared with s.c. administration, insulin in...