Role of G‐proteins in muscarinic receptor inward and outward currents in rabbit jejunal smooth muscle.
- 1 August 1990
- journal article
- research article
- Published by Wiley in The Journal of Physiology
- Vol. 427 (1) , 395-419
- https://doi.org/10.1113/jphysiol.1990.sp018178
Abstract
1. Single smooth muscle cells obtained by enzymic dispersion of the longitudinal muscle layer of rabbit jejunum were held under voltage clamp using patch pipettes and membrane currents measured. The effects of carbachol or caffeine applied externally were examined in cells dialysed with normal pipette solutions or with a solution containing heparin (which blocks receptors for D‐myo‐inositol 1,4,5‐trisphosphate, InsP3), guanosine 5‐O‐(gamma‐thio)triphosphate (GTP gamma S) or guanosine 5‐O‐(beta‐thio)diphosphate (GDP beta S). 2. Outward current in response to application of carbachol or caffeine was considered to represent the opening of calcium‐activated potassium channels in response to a localized rise in the free ionized calcium concentration occasioned by the rapid discharge of stored calcium (Ca) by these agents. 3. Heparin included in the pipette solution blocked outward current to muscarinic receptor activation by carbachol but not that to caffeine, suggesting that receptor‐evoked discharge of stored cellular Ca is caused by InsP3 action. However, heparin did not affect muscarinic‐receptor inward current. 4. After dialysis with 0.1‐0.5 mM‐GTP gamma S, carbachol inward current was evoked in two out of three of the cells; after dialysis with 0.1‐0.2 mM‐GTP gamma S for an average of 7.7 min it was 80% of the normal response; after dialysis for an average of 8.6 min with 0.5 mM‐GTP gamma S it was 31% of the normal response. In contrast, 0.1 mM‐GTP gamma S reduced caffeine outward current by 93% after an average 4.5 min dialysis and spontaneous transient outward currents (STOCs) were abolished in 2.9 min on average. 5. Carbachol inward current (at ‐40 or ‐50 mV) and carbachol outward current (at 0 mV) in responding cells were reduced only by half after 8‐10 min dialysis with 1 mM‐GDP beta S which has been shown in portal vein cells to antagonize the depletion of Ca stores by intracellular GTP gamma S (Komori & Bolton, 1989). After 8‐10 min dialysis with 5 mM‐GDP beta S outward current was 27% of normal. However, if GDP beta S was present, outward current generally could not be evoked by a second application of carbachol. 6. The discharge of Ca stores by dialysis with 0.1 mM‐GTP gamma S was prevented completely by heparin included in the pipette solution, suggesting that activation of a G‐protein associated with phospholipase C (PLC) enzyme accelerates PLC activity. InsP3 production and depletion of Ca stores.(ABSTRACT TRUNCATED AT 400 WORDS)This publication has 25 references indexed in Scilit:
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