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Endothelin-1 and pancreatic islet vasculature: studies in vivo and on isolated, vascularly perfused pancreatic islets
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Medical Cell Biology.
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2007 (English)In: American Journal of Physiology. Endocrinology and Metabolism, ISSN 0193-1849, E-ISSN 1522-1555, Vol. 292, no 6, E1616-E1623 p.Article in journal (Refereed) Published
Abstract [en]

Endothelin-1 (ET-1) is a potent endothelium-derived vasoconstrictor, which also stimulates insulin release. The aim of the present study was to evaluate whether exogenously administered ET-1 affected pancreatic islet blood flow in vivo in rats and the islet arteriolar reactivity in vitro in mice. Furthermore, we aimed to determine the ET-receptor subtype that was involved in such responses. When applying a microsphere technique for measurements of islet blood perfusion in vivo, we found that ET-1 (5 nmol/kg) consistently and markedly decreased total pancreatic and especially islet blood flow, despite having only minor effects on blood pressure. Neither endothelin A (ET(A)) receptor (BQ-123) nor endothelin-B (ET(B)) receptor (BQ-788) antagonists, alone or in combination, could prevent this reduction in blood flow. To avoid confounding interactions in vivo, we also examined the arteriolar vascular reactivity in isolated, perfused mouse islets. In the latter preparation, we demonstrated a dose-dependent constriction in response to ET-1. Administration of BQ-123 prevented this, whereas BQ-788 induced a right shift in the response. In conclusion, the pancreatic islet vasculature is highly sensitive to exogenous ET-1, which mediates its effect mainly through ET(A) receptors.

Place, publisher, year, edition, pages
2007. Vol. 292, no 6, E1616-E1623 p.
Keyword [en]
Adrenal Glands/blood supply, Animals, Arterioles/physiology, Blood Glucose/metabolism, Blood Pressure/drug effects, Colon/blood supply, Drug Synergism, Duodenum/blood supply, Endothelin-1/*pharmacology, Insulin/blood, Islets of Langerhans/*blood supply, Male, Mice, Mice; Inbred C57BL, Oligopeptides/pharmacology, Pancreas/blood supply, Peptides; Cyclic/pharmacology, Piperidines/pharmacology, Rats, Rats; Sprague-Dawley, Receptor; Endothelin A/antagonists & inhibitors, Receptor; Endothelin B/antagonists & inhibitors, Regional Blood Flow/drug effects, Vasoconstriction
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Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-11911DOI: 10.1152/ajpendo.00640.2006ISI: 000247939100014PubMedID: 17284574OAI: oai:DiVA.org:uu-11911DiVA: diva2:39680
Available from: 2007-11-06 Created: 2007-11-06 Last updated: 2017-12-11Bibliographically approved

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Lai, En YinBodin, BirgittaAndersson, ArnePettersson, UlrikaHansell, PeterJansson, Leif

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