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Biomedical subjects

G Glazer

Publications and source records attributed to G Glazer.

15 recordsLinked to original sources
PubMed1976

Prostaglandin release in canine acute haemorrhagic pancreatitis.

Acute haemorrhagic pancreatitis was induced in greyhound dogs by a bile salt/trypsin injection into the main pancreatic duct. Prostaglandin-like activity in the pancreatic venous blood, right atrial blood, and arterial blood was measured by bioassay. Activity rose significantly in the pancreatic venous blood of test dogs but not in controls. Chromatographic analysis of the peritoneal exudate from the dogs with pancreatitis showed high levels of prostaglandin E-like material (mean 43 ng/ml prostaglandin E2 equivalents). It seems likely that prostaglandins contribute to the induced pancreatitis.

Acute Disease↗
PubMed1976

Parallel secretion of digestive enzymes by the in vitro rabbit pancreas.

Nonparallel discharge of digestive enzymes by the in vitro rabbit pancreas has been previously reported and this observation has been used to challenge the mass transport theory of enzyme synthesis and secretion by the exocrine pancreas. The current investigation reexamines the pattern of enzyme secretion from the in vitro rabbit pancreas. Secretion of alpha-amylase, trypsinogen, and chymotrypsinogen was studied from the unstimulated gland and from glands stimulated with either methacholine, cholecystokinin-pancreozymin, or the active octapeptide of cholecystokinin-pancreozymin. In all cases, only parallel discharge of alpha-amlyse, trypsinogen, and chymotrypsinogen was noted. These observations are consistent with the mass-transport theory.

Amylases↗
PubMed1975

Glucose production in the newborn dog. I. Effects of glucagon in vivo.

Systemic glucose production rates were evaluated 4 hr after feeding in 14 newborn beagle dogs at ages between 1 and 5 days. After a prime injection of radioisotopic tracers, glucose production was determined during infusion of intermixed tracer [2-3H] glucose and [1-14C] glucose at a constant rate. Seven of the new born dogs served as controls throughout the 3-hr period of infusion, while seven of their littermates, infused simultaneously, received glucagon at a constant rate of 3.3 mug/min between 90 and 180 min of study. In control dogs, mean glucose production, determined by dilution of [2-3H] glucose, was 55 +/- 3 mumol/min-kg body weight. During the control period, their littermates produced glucose at a similar rate; however, glucagon infusion raised glucose production to 81 +/- 4 mumol/min-kg. The average glucose production rate estimated with [1-14C]glucose was 88% of that with 3H tracer during the initial control period and 77% during the glucagon injusion. In order to confirm that this discrepancy reflected the recycling of 14C and the early development of gluconeogenesis, and additional 14 new born dogs were infused with potential substrates for [14C] glucose. In separate studies, [U-14C] lactate, [3-14C] lactate, [U-14C] alanine, and [6-14C]- glucose were incorporated into glucose and [1-14C] glucose. Quantification of gluconeogenesis by simultaneous infusion of [6-3H] glucose and [3-14C] lactate in a 5-day-old dog demonstrated that 25% of the glucose produced originated from lactate, whereas 10% was incorporated into carbon 1. Thus, systemic glucose production was established rapidly in newborn dogs and responded to stimulation with glucagon. A significant proportion of the glucose originated from recycling via the gluconeogenic pathway.

Animals↗