A comparative study of several serotonin receptor antagonists on basal and stimulus induced release of insulin and glucagon in the intact rat. |
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Authors: | G F Bryce J H Jacoby |
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Affiliation: | 1. Department of Cell Biology, Roche Research Center, Hoffman-La Roche Inc., Nutley, N.J. 07110, USA;1. Department of Pharmacology, New Jersey Medical School, College of Medicine and Dentistry of New Jersey, Newark, N.J. 07103, USA |
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Abstract: | Several commonly used serotonin receptor antagonists were studied for their ability to influence basal plasma insulin and glucagon (using 30K antibody) levels as well as the response of these hormones to a glucose or arginine challenge administered systematically to overnight fasted rats. Cyproheptadine, in contrast to other antagonists employed, induced large increases of insulin, glucagon and glucose, although this hyperinsulinemia was of a smaller magnitude when compared with hormone levels observed during an equivalent hyperglycemia resulting from glucose administration. The pancreatic response to a glucose load (increased insulin and decreased glucagon release) and an arginine load (increased insulin and glucagon release) were prevented by cyproheptadine pretreatment. Basal insulin levels were bot consistently altered by methysergide or cinanserin and were slightly elevated by metergoline. Basal glucagon levels were unaffected by these drugs. These three agents potentiated the insulinotropic effect of an arginine load whereas only metergoline exerted a similar effect on the response to glucose loading. Glucagon release in response to these stimuli was not significantly altered by drug pretreatment. |
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