Linked Life Data

8298800

Source:http://linkedlifedata.com/resource/pubmed/id/8298800

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1994-3-4
pubmed:abstractText
1. Effects were studied of 6-(3-dimethylaminopropionyl) forskolin (NKH477), a water-soluble forskolin derivative and of dibutyryl-cyclic AMP, a membrane-permeable cyclic AMP analogue on noradrenaline (NA)-induced Ca2+ mobilization in smooth muscle strips of the rabbit mesenteric artery. The intracellular concentration of Ca2+ ([Ca2+]i), isometric force and cellular concentration of inositol 1,4,5-trisphosphate (InsP3) were measured. 2. NA (10 microM) produced a phasic, followed by a tonic increase in both [Ca2+]i and force in a solution containing 2.6 mM Ca2+. NKH477 (0.01-0.3 microM) attenuated the phasic and the tonic increases in both [Ca2+]i and force induced by 10 microM NA, in a concentration-dependent manner. 3. In Ca(2+)-free solution containing 2 mM EGTA with 5.9 mM K+, NA (10 microM) produced only phasic increases in [Ca2+]i and force. NKH477 (0.01 microM) and dibutyryl-cyclic AMP (0.1 mM) each greatly inhibited these increases. 4. NA (10 microM) led to the production of InsP3 in intact smooth muscle strips and InsP3 (10 microM) increased Ca2+ in Ca(2+)-free solution after a brief application of Ca2+ in beta-escin-skinned smooth muscle strips. NKH477 (0.01 microM) or dibutyryl-cyclic AMP (0.1 mM) modified neither the NA-induced synthesis of InsP3 in intact muscle strips nor the InsP3-induced Ca2+ release in skinned strips. 5. In Ca(2+)-free solution, high K+ (40 and 128 mM) itself failed to increase [Ca2+]i but concentration-dependently enhanced the amplitude of the increase in [Ca2+]i induced by 10 microM NA with a parallel enhancement of the maximum rate of rise. The extent of the inhibition induced by NKH477 (0.01 microM)or dibutyryl-cyclic AMP (0.1 mM) on the NA-induced [Ca2+] increase was inversely related to the maximum rate of rise of [Ca2+], induced by NA in Ca2+-free solution containing various concentrations of K+. These results suggest that the increase in the rate of Ca2+ release induced by NA can conceal the inhibitory action on NA-induced Ca2+ mobilization of agents that increase cyclic AMP.6. Repetitive application of 10 JAM NA in Ca2+-free solution led to a disappearance of the NA-induced increase in [Ca2+]j, but NA could again increase [Ca2+], in Ca2+-free solution after a brief application of Ca2+ with 40 mM K+ ('Ca2+-loading'). The magnitude of this NA-induced increase in [Ca2+]i depended on the duration of the Ca2+-loading. With application of dibutyryl-cyclic AMP (0.1 mM) during the Ca2+-loading period, the loading duration required for the restoration of the maximum NA-response was shortened.7. Cyclopiazonic acid (10 microM, an inhibitor of Ca2+-ATPase at intracellular storage sites) attenuated the inhibitory action of dibutyryl-cyclic AMP on the NA-induced increase in [Ca2+], in Ca2+-free solution.When NA (10 microM) was applied twice for 30 s with a 10 min interval in Ca2+-free solution, the amplitude of response to the second application was about one third of the first response. With application of 0.1 mM dibutyryl-cyclic AMP during the first application of NA, the increase in [Ca2+], induced by the first application of NA was inhibited, but the response induced by the second was enhanced. These results suggest that dibutyryl-cyclic AMP enhances Ca2+ uptake into the NA-sensitive storage sites.8. We conclude that, in smooth muscle of the rabbit mesenteric artery, agents that increase cyclic AMP inhibit the NA-induced increase in [Ca2+] through an activation of Ca2+ uptake into the cellular storage sites.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-1318797, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-1328618, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-1387024, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-1706144, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-1786512, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-1834695, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2179606, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2191782, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-233130, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-233257, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2530215, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2547906, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2704996, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2836409, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2844859, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2847175, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2962783, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-2983811, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-3003053, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-3007748, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-3033708, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-3098964, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-3755550, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-3838314, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-6092518, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-6286950, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-6296369, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-6386811, http://linkedlifedata.com/resource/pubmed/commentcorrection/8298800-6410057
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0007-1188
pubmed:author
pubmed:issnType
Print
pubmed:volume
110
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1117-25
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
Effects of a water-soluble forskolin derivative (NKH477) and a membrane-permeable cyclic AMP analogue on noradrenaline-induced Ca2+ mobilization in smooth muscle of rabbit mesenteric artery.
pubmed:affiliation
Department of Pharmacology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't