[State of the insular apparatus in experimental thyrotoxicosis]. 1980

V I Kandror, and S N Arslanov, and P S Zavadskiĭ

The oral intravenous glucose tolerance tests revealed an increase in the rate of glucose utilization in rabbits fed high thyroidine doses. Hypoglycemia and hypoinsulinemia on fasting stomach, as well as a reduction of insulin reaction to intravenous glucose load were seen in such animals. A fall of insulin secretion in thyrotoxicosis is considered to be a compensatory reaction permitting glucose output from the liver to meet increased tissue demands in the oxidative substrates.

UI MeSH Term Description Entries
D006980 Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. Hyperthyroid,Primary Hyperthyroidism,Hyperthyroidism, Primary,Hyperthyroids
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
D007515 Islets of Langerhans Irregular microscopic structures consisting of cords of endocrine cells that are scattered throughout the PANCREAS among the exocrine acini. Each islet is surrounded by connective tissue fibers and penetrated by a network of capillaries. There are four major cell types. The most abundant beta cells (50-80%) secrete INSULIN. Alpha cells (5-20%) secrete GLUCAGON. PP cells (10-35%) secrete PANCREATIC POLYPEPTIDE. Delta cells (~5%) secrete SOMATOSTATIN. Islands of Langerhans,Islet Cells,Nesidioblasts,Pancreas, Endocrine,Pancreatic Islets,Cell, Islet,Cells, Islet,Endocrine Pancreas,Islet Cell,Islet, Pancreatic,Islets, Pancreatic,Langerhans Islands,Langerhans Islets,Nesidioblast,Pancreatic Islet
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
D005947 Glucose A primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is used therapeutically in fluid and nutrient replacement. Dextrose,Anhydrous Dextrose,D-Glucose,Glucose Monohydrate,Glucose, (DL)-Isomer,Glucose, (alpha-D)-Isomer,Glucose, (beta-D)-Isomer,D Glucose,Dextrose, Anhydrous,Monohydrate, Glucose
D005951 Glucose Tolerance Test A test to determine the ability of an individual to maintain HOMEOSTASIS of BLOOD GLUCOSE. It includes measuring blood glucose levels in a fasting state, and at prescribed intervals before and after oral glucose intake (75 or 100 g) or intravenous infusion (0.5 g/kg). Intravenous Glucose Tolerance,Intravenous Glucose Tolerance Test,OGTT,Oral Glucose Tolerance,Oral Glucose Tolerance Test,Glucose Tolerance Tests,Glucose Tolerance, Oral
D000078790 Insulin Secretion Production and release of insulin from PANCREATIC BETA CELLS that primarily occurs in response to elevated BLOOD GLUCOSE levels. Secretion, Insulin
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia

Related Publications

V I Kandror, and S N Arslanov, and P S Zavadskiĭ
January 1974, Problemy endokrinologii,
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
March 1975, Vrachebnoe delo,
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
January 1967, Stomatologiia,
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
January 1980, Voprosy onkologii,
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
June 1974, Arkhiv anatomii, gistologii i embriologii,
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
November 1969, Pediatriia,
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
January 1955, Zeitschrift fur Zellforschung und mikroskopische Anatomie (Vienna, Austria : 1948),
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
May 1975, Vrachebnoe delo,
V I Kandror, and S N Arslanov, and P S Zavadskiĭ
March 1976, Klinicheskaia meditsina,
Copied contents to your clipboard!