ArticleBritish journal of pharmacology1994
All-or-nothing responses to carbachol in single intestinal smooth muscle cells of rat.
Article in British journal of pharmacology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
6 citing papers in PubMed, 15 citations in OpenAlex.
- Chai-Qin-Cheng-Qi Decoction and Carbachol Improve Intestinal Motility by Regulating Protein Kinase C-Mediated CaEvidence-based complementary and alternative medicine : eCAM · 2017Article
- Clusters of specialized detector cells provide sensitive and high fidelity receptor signaling in the intact endothelium.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016Article
- Conversion of human fibroblasts to angioblast-like progenitor cells.Nature methods · 2013Article
- The properties of ryanodine-sensitive Ca(2+) release in mouse gastric smooth muscle cells.British journal of pharmacology · 2001Article
- Rise in cytosolic Ca2+ concentration induced by P2-purinoceptor activation in isolated myocytes from the rat gastrointestinal tract.British journal of pharmacology · 1996Article
- Ca2+ entry activated by emptying of intracellular Ca2+ stores in ileal smooth muscle of the rat.British journal of pharmacology · 1995Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. Concentration-response relationships for carbachol (CCh)-induced increases in the cytosolic calcium concentration ([Ca2+]i) and membrane currents were studied by use of fura-2 microfluorimetry and nystatin-perforated whole-cell recording in single smooth muscle cells isolated from rat intestine. 2. CCh produced an initial peak rise in [Ca2+]i followed by a small sustained rise. In individual cells, the peak rise in [Ca2+]i did not increase in amplitude even with increasing concentrations of CCh, though the threshold concentration varied in different cells. The initial peak rise in [Ca2+]i, but not the sustained rise, was due to the release of stored Ca2+, because it was unchanged after removal of external Ca2+ and the addition of nifedipine (1 microM) or La3+ (1 mM). 3. CCh elicited an outward and inward current in a cell dialyzed with a pipette solution containing KCl at a holding potential of -30 mV and with one containing NaCl at -60 mV, respectively. In individual cells, the amplitude of each current was similar in cells stimulated at over the threshold concentration of CCh, but the threshold was different among cells. 4. The percentage of cells showing Ca(2+)-transient responses to CCh at given concentrations was similar to those showing current responses and contractile responses. 5. In thin muscle bundles, a concentration-dependent contraction was evoked by CCh in the absence of external Ca2+. Its threshold was similar to those of Ca(2+)-transient and current responses in single cells. 6. These results suggest that CCh-induced release of stored Ca2+ takes place in an all-or-nothing fashion in individual cells of the rat intestinal smooth muscle.
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