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The phospholipase C inhibitor U-73122 inhibits Ca2+ release from the intracellular sarcoplasmic reticulum Ca2+ store by inhibiting Ca2+ pumps in smooth muscle

MacMillan, D. and McCarron, J.G. (2010) The phospholipase C inhibitor U-73122 inhibits Ca2+ release from the intracellular sarcoplasmic reticulum Ca2+ store by inhibiting Ca2+ pumps in smooth muscle. British Journal of Pharmacology, 160 (6). 1295–1301. ISSN 0007-1188

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Abstract

The sarcoplasmic reticulum (SR) releases Ca2+ via inositol 1,4,5-trisphosphate receptors (IP3R) in response to IP3-generating agonists. Ca2+ release subsequently propagates as Ca2+ waves. To clarify the role of IP3 production in wave generation, the contribution of a key enzyme in the production of IP3 was examined using a phosphoinositide-specific phospholipase C (PI-PLC) inhibitor, U-73122. Single colonic myocytes were voltage-clamped in whole-cell configuration and cytosolic Ca2+ concentration ([Ca2+]cyto) measured using fluo-3. SR Ca2+ release was evoked either by activation of IP3Rs (by carbachol or photolysis of caged IP3) or ryanodine receptors (RyRs; by caffeine). U-73122 inhibited carbachol-evoked [Ca2+]cyto transients. The drug also inhibited [Ca2+]cyto increases, evoked by direct IP3R activation (by photolysis of caged IP3) and RyR activation (by caffeine), which do not require PI-PLC activation. U-73122 also increased steady-state [Ca2+]cyto and slowed the rate of Ca2+ removal from the cytoplasm. An inactive analogue of U-73122, U-73343, was without effect on either IP3R- or RyR-mediated Ca2+ release. U-73122 inhibited carbachol-evoked [Ca2+]cyto increases. However, the drug also reduced Ca2+ release when evoked by direct activation of IP3R or RyR, slowed Ca2+ removal and increased steady-state [Ca2+]cyto. These results suggest U-73122 reduces IP3-evoked Ca2+ transients by inhibiting the SR Ca2+ pump to deplete the SR of Ca2+ rather than by inhibiting PI-PLC.

Item type: Article
ID code: 25983
Keywords: phospholipase c, smooth muscle, calcium, pharmacology, U-73122, Therapeutics. Pharmacology, Pharmacology
Subjects: Medicine > Therapeutics. Pharmacology
Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
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Depositing user: Strathprints Administrator
Date Deposited: 16 Sep 2010 16:51
Last modified: 27 Mar 2014 08:53
URI: http://strathprints.strath.ac.uk/id/eprint/25983

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