1978
DOI: 10.1152/ajpendo.1978.235.4.e387
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Secretory effects of VIP on isolated perfused porcine pancreas.

Abstract: We studied the secretion of insulin, glucagon, and the exocrine secretion of the isolated perfused porcine pancreas in response to vasoactive intestinal polypeptide (VIP) in concentrations ranging from 30 to 18,750 pmol/liter at various concentrations of glucose in the perfusion medium. VIP stimulated the insulin and glucagon secretion in a dose-dependent manner. The response pattern was critically dependent on the glucose concentration. In the presence of a glucose concentration of 7.5 mmol/liter, VIP enhance… Show more

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Cited by 43 publications
(28 citation statements)
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“…The level of cholecystokinin also increased ; in its sulfated octapeptide form this product is a regulatory peptide of pancreatic enzyme secretion in pigs (Jensen et al, 19811 Chayvialle et al (1980). It is known that VIP is mainly a neurotransmitter (Larsson et al, 1978) and that in pigs it has less effect on pancreatic secretion than does secretin (Jensen et al, 1978b). According to Fahrenkrug (1979), local reflexes may initiate VIP-mediated increases in blood flow.…”
mentioning
confidence: 99%
“…The level of cholecystokinin also increased ; in its sulfated octapeptide form this product is a regulatory peptide of pancreatic enzyme secretion in pigs (Jensen et al, 19811 Chayvialle et al (1980). It is known that VIP is mainly a neurotransmitter (Larsson et al, 1978) and that in pigs it has less effect on pancreatic secretion than does secretin (Jensen et al, 1978b). According to Fahrenkrug (1979), local reflexes may initiate VIP-mediated increases in blood flow.…”
mentioning
confidence: 99%
“…This allowed a classification of VIP-secretin receptors into three subtypes: (1) VlP-preferring receptors; (2) high-affinity secretin receptors, and (3) low-affinity secretin receptors. The properties of secretin at high-affinity secretin receptors were likely to reflect a contribution of membranes from centroacinar and duct cells.Secretin and vasoactive intestinal peptide (VIP) stimulate the pancreatic exocrine secre tion with variable relative efficacy and po tency in several animal species [6,12,13,19,21], The predominant response is, in general, a water and bicarbonate hypersecretion that originates, at least partially, from centroaci nar and duct cells [7], In rat and guinea pig, secretin and VIP also elicit the secretion of hydrolases in vriro [5,24,26] indicating an added direct effect of both peptides on pan creatic acinar cells.The VIP-secretin receptors of pancreatic acinar cells from guinea pig have been exten sively characterized [4,10,25]. 'VIP-preferring receptors' are distinct from 'secretin-pre ferring receptors' and appear to be associated with the secretory effect of both peptides [ 10].…”
mentioning
confidence: 99%
“…Thus VIP may exert its action by release from nerve terminals, and the VIP level in the venous plasma may represent an overflow (Jensen et al, 1978). The VIP level in the venous plasma in the anaesthetized and atropinized cat was raised up 0.27 nm after vagus nerve stimulation , and this level induced a moderate increase in pancreatic juice flow in the isolated and perfused kitten pancreas.…”
Section: Discussionmentioning
confidence: 97%