Arterial glucagon levels are elevated in fed pancreatectomised pigs and the source was sought by measuring the hormone in arterial, portal, hepatic and renal venous blood, and in gut tissues. Pigs which were starved for 48 hours (basal) were compared with sham operated or pancreatectomised pigs which were fed or starved for 7 days post operatively. Feeding of sham operated pigs caused a uniform increase in IRG 3485, while starvation resulted in a decreased portal IRG 7000. Pancreatectomy was associated with a uniform decrease in portal IRG 3485 and increase of IRG 7000 regardless of nutritional status. Hepatic and renal extraction of 23-26% was noted in fed animals (IRG 3485 in sham operated; IRG 7000 in pancreatectomised). In all starved pigs, hepatic and renal extraction were reduced to zero. The gastric and caecal mucosa and the pancreas contained most of IRG 3485. Gastric and caecal levels were increased after feeding of either group of animals, while fasting caused a marked increase in pancreatic IRG 3485 and a decrease in ileal IRG 7000. These studies demonstrate a direct effect of sustained nutritional status upon the distribution of glucagon in plasma and gastro intestinal tissues.

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Arterial glucagon levels are elevated in fed pancreatectomised pigs and the source was sought by measuring the hormone in arterial, portal, hepatic and renal venous blood, and in gut tissues. Pigs which were starved for 48 hours (basal) were compared with sham operated or pancreatectomised pigs which were fed or starved for 7 days post operatively. Feeding of sham operated pigs caused a uniform increase in IRG 3485, while starvation resulted in a decreased portal IRG 7000.

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Extraction of rat submaxillary salivary glands and ileal mucosa yielded a single immunoreactive glucagon component of 25,000 daltons and a major peak of approximately 9,000 daltons respectively. Eviscerated rats with and without functional livers were found to have decreased, but persistent levels of immunoreactive glucagon and total immunoreactive glucagon, as measured with a pancreatic specific and cross reacting antiserum respectively. Gel filtration of serum samples on Sephadex G-50 fine and G-200 superfine demonstrated that there was no measurable 3485, 9000 or 25,000 dalton glucagon immunoreactivity.

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Glucagon immunoreactivity (IRG) was measured in plasma of 8 duodenopancreatectomized patients with antiserum 30-K. Arginine infusions failed to raise plasma IRG, whereas in control subjects IRG rose 3-fold. Column chromatography revealed that the basal IRG measured in these plasmas was not due to glucagon (molecular weight 3485) but to other plasma factors, mainly of high molecular weight.

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