Am. Svensson et al., PANCREATIC-ISLET BLOOD-FLOW IN THE RAT AFTER ADMINISTRATION OF ISLET AMYLOID POLYPEPTIDE OR CALCITONIN-GENE-RELATED PEPTIDE, Diabetes, 43(3), 1994, pp. 454-458
Citations number
36
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
Anesthetized male Sprague-Dawley rats (350-400 g) were injected intrav
enously with either 0.1, 1, 15, or 25 nmol rat islet amyloid polypepti
de (IAPP), 65 or 650 pmol rat calcitonin gene-related peptide (CGRP),
or saline alone. IAPP at the two highest doses decreased the mean arte
rial blood pressure (BP), increased blood glucose concentrations, and
decreased serum insulin concentrations. CGRP at both doses decreased t
he BP but did not affect the blood glucose concentrations. The blood f
low to the whole pancreas, pancreatic islets, adrenal glands, colon, d
uodenum, liver, and kidney was measured with a microsphere technique 3
0 min after administration of IAPP and 3 min after injection of CGRP.
The two higher doses of IAPP (15 and 25 nmol) markedly reduced the who
le pancreatic blood flow, whereas the islet blood flow remained unaffe
cted. This resulted in an increase in the fraction of whole pancreatic
blood flow diverted through the islets from similar to 10 to 17%. No
blood flow changes in the pancreas or the islets were observed when 0.
1 or 1 nmol IAPP was injected. CGRP at both doses caused a decrease in
both whole pancreatic and islet blood flow. No changes in fractional
islet blood flaw were observed, despite similar effects on mean arteri
al BP as observed after IAPP injections. Neither adrenal, duodenal, co
lonic, hepatic, skeletal muscle, nor renal blood flow were significant
ly affected by any of the concentrations of IAPP used, whereas 650 pmo
l CGRP decreased both duodenal and colonic blood flow. We conclude tha
t IAPP and CGRP have different effects on pancreatic islet blood flow
and that IAPP may be of importance for islet blood flow regulation.