rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
1
|
pubmed:dateCreated |
1988-9-20
|
pubmed:abstractText |
Isolated mouse islets were used to identify the muscarinic receptor subtype present in pancreatic B-cells. We thus compared the inhibitory potencies of atropine (non-specific), of pirenzepine (specific for M1 receptors) and of compound AF-DX 116 (specific for cardiac M2 receptors) on acetylcholine-induced insulin release, 86Rb+ efflux and 45Ca2+ efflux. The three antagonists inhibited all effects of acetylcholine, but EC50 values were markedly different: atropine = 1.5-5 nM, pirenzepine = 0.6-1.7 microM and AF-DX 116 = 1.7-11 microM. The results did not suggest that the various effects of ACh could result from the activation of different subtypes of receptors. It is concluded that muscarinic receptors of pancreatic B-cells belong to an M2 subtype distinct from the cardiac M2 receptors.
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0014-5793
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
236
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
89-92
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:3042468-Acetylcholine,
pubmed-meshheading:3042468-Animals,
pubmed-meshheading:3042468-Atropine,
pubmed-meshheading:3042468-Calcium,
pubmed-meshheading:3042468-Female,
pubmed-meshheading:3042468-Insulin,
pubmed-meshheading:3042468-Islets of Langerhans,
pubmed-meshheading:3042468-Mice,
pubmed-meshheading:3042468-Pirenzepine,
pubmed-meshheading:3042468-Potassium,
pubmed-meshheading:3042468-Receptors, Muscarinic,
pubmed-meshheading:3042468-Rubidium Radioisotopes
|
pubmed:year |
1988
|
pubmed:articleTitle |
The muscarinic receptor subtype in mouse pancreatic B-cells.
|
pubmed:affiliation |
Unité de Diabétologie et Nutrition, University of Louvain, Faculty of Medicine, Brussels, Belgium.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|