Inhibition of insulin secretion via distinct signaling pathways in alpha2-adrenoceptor knockout mice
Author(s) -
M Peterhoff,
Andreas Sieg,
Marc Brede,
CM Chao,
Lutz Hein,
Susanne Ullrich
Publication year - 2003
Publication title -
european journal of endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.897
H-Index - 148
eISSN - 1479-683X
pISSN - 0804-4643
DOI - 10.1530/eje.0.1490343
Subject(s) - medicine , endocrinology , adenylyl cyclase , forskolin , pertussis toxin , alpha (finance) , secretion , insulin , islet , receptor , biology , g protein , agonist , gs alpha subunit , gi alpha subunit , chemistry , construct validity , nursing , patient satisfaction
Adrenaline inhibits insulin secretion through activation of alpha(2)-adrenoceptors (ARs). These receptors are linked to pertussis toxin-sensitive G proteins. Agonist binding leads to inhibition of adenylyl cyclase, inhibition of Ca(2+) channels and activation of K(+) channels. Recently, three distinct subtypes of alpha(2)-AR were described, alpha(2A)-AR, alpha(2B)-AR and alpha(2C)-AR. At present, it is unknown which of these alpha(2)-AR subtype(s) may regulate insulin secretion. We used mice deficient in alpha(2)-ARs to analyze the coupling and role of individual alpha(2)-AR subtypes in insulin-secreting beta cells.
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