In the cat, gastric lipase secretion was equally but weakly stimulated by pentagastrin, a major stimulant of acid secretion, and by carbamylcholine, a major stimulant of pepsin secretion. Lipase was also stimulated by fresh liver, which induces a large blood gastrin release and not by canned food, which is a poor gastrin releaser. Lipase output always preceded that of acid an pepsin. Lipase was not correlated with acid and pepsin secretion while acid and pepsin were well correlated during all stimulations but not in basal state. Lipase is co-localized with pepsin in the chief cells but is also present in pepsin-free cells, the mucus surface cells of the fundus and the antrum. The distribution of lipase explains the lack of correlation between pepsin and lipase as already mentioned. However, our data show that lipase secretion is under the control of gastric stimulants and might play a role in the gastric initiation of pancreatic meal lipolysis.
In natural conditions young rabbit nurses once a day and therefore ingests the whole of his daily caloric intake during a single meal. The present work investigates glucose homeostasis during perinatal period in young rabbit by assessing blood glucose and glycogen stores before and after one single meal. Ponderal data, glycogen and blood metabolites were determined in 1-4 day- and 17-21 day-old rabbits before suckling and at different times (1, 3, 6, 9, 24, 48, 72 h) after controlled suckling. In "young" and "old" rabbits hepatic glycogen stores were exhausted after 48 and 72 h of fast. Within the first hours following milk ingestion, muscle and carcass glycogen did not vary until 9 h in the "young" and until 24 h in the "old" without notable variation of glycemia. From 24 to 72 h young rabbits were in a fasting period with low hepatic glycogen and a decrease of muscle and carcass glycogen, but glycaemia decreased only slightly at 48 and 72 h in "young" and at 72 h in "old" As blood alanine was decreased, it appears that gluconeogenesis was effective and that alanine-glucose and Cori cycles were operating in these conditions.
The stress of anaesthesia and of sampling on the concentrations of blood metabolites and tissue glycogen content was studied in awake, anaesthetized and decapitated young rabbits 1-2 days old ("young") and 17-18 days old ("old"), 24 h after the last controlled suckling. Stress of sampling and anaesthesia was particularly evidenced by high blood lactate observed for the three protocols in young rabbits and to a lesser extent in old animals. Decapitation appeared as the less aggressive procedure for blood lactate assessment in "young" and "old" rabbits. In "young" rabbits, blood glucose was not significantly modified by the mode of blood sampling while in "old" rabbits blood glucose was significantly lower in awake than in anaesthetized animals. Muscle and liver glycogen content data were not significantly different between the three protocols in old and young rabbits. From a comparison of these results with those found in adult animals in various species, it appears that blood puncture in awake "young" and "old" rabbits is a suitable procedure for determining the majority of blood metabolites except lactate in "young" animals.
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