Renal removal of glucagon and insulin after acute hepatic ischaemia in dogs. 1983

S Contini, and A Pezzarossa, and A Corradi, and C Scarpignato

The renal extraction of insulin and glucagon was studied in dogs subjected to temporary interruption of vascular perfusion of the liver. This was performed using hepatic artery occlusion after functional end-to-side portacaval anastomosis. The renal extraction of immunoreactive insulin and glucagon was studied by means of renal arterial-venous concentration differences with concurrent estimates of renal plasma flow and glomerular filtration rate. The degree of liver damage was reflected by dramatic increases of liver enzymes in the plasma after ischaemia and by hypoglycemia which developed in all the animals. Ninety minute occlusion of hepatic blood flow resulted in a dramatic reduction of renal plasma flow and glomerular filtration rate. Portacaval shunt alone had little effect on these parameters. Because hypoglycemia developed after hepatic insult, some animals were made hyperglycemic by intravenous infusion of glucose. In both (hypo- and hyperglycemic) groups of animals the percentage extraction of hormones by the kidney fell dramatically 60 minutes after the end of the hepatic ischaemia and this reduction persisted 180 min later. These data suggest that the impaired renal function may contribute to the increased plasma levels of islet hormones observed during acute hepatic failure.

UI MeSH Term Description Entries
D007328 Insulin A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1). Iletin,Insulin A Chain,Insulin B Chain,Insulin, Regular,Novolin,Sodium Insulin,Soluble Insulin,Chain, Insulin B,Insulin, Sodium,Insulin, Soluble,Regular Insulin
D007511 Ischemia A hypoperfusion of the BLOOD through an organ or tissue caused by a PATHOLOGIC CONSTRICTION or obstruction of its BLOOD VESSELS, or an absence of BLOOD CIRCULATION. Ischemias
D007668 Kidney Body organ that filters blood for the secretion of URINE and that regulates ion concentrations. Kidneys
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008297 Male Males
D001786 Blood Glucose Glucose in blood. Blood Sugar,Glucose, Blood,Sugar, Blood
D004285 Dogs The domestic dog, Canis familiaris, comprising about 400 breeds, of the carnivore family CANIDAE. They are worldwide in distribution and live in association with people. (Walker's Mammals of the World, 5th ed, p1065) Canis familiaris,Dog
D005260 Female Females
D005919 Glomerular Filtration Rate The volume of water filtered out of plasma through glomerular capillary walls into Bowman's capsules per unit of time. It is considered to be equivalent to INULIN clearance. Filtration Rate, Glomerular,Filtration Rates, Glomerular,Glomerular Filtration Rates,Rate, Glomerular Filtration,Rates, Glomerular Filtration
D005934 Glucagon A 29-amino acid pancreatic peptide derived from proglucagon which is also the precursor of intestinal GLUCAGON-LIKE PEPTIDES. Glucagon is secreted by PANCREATIC ALPHA CELLS and plays an important role in regulation of BLOOD GLUCOSE concentration, ketone metabolism, and several other biochemical and physiological processes. (From Gilman et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 9th ed, p1511) Glucagon (1-29),Glukagon,HG-Factor,Hyperglycemic-Glycogenolytic Factor,Proglucagon (33-61),HG Factor,Hyperglycemic Glycogenolytic Factor

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