Abstract
The ionophore ionomycin produced concentration-dependent (5 x 10-9 to 5 x 10-6 M) contractions in guinea-pig ileal longitudinal smooth muscle. Responses were dependent on extracellular Ca2+, consistent with the known role of this Ca2+ source in supporting excitation-contraction coupling to a variety of stimulants in this tissue. Responses were insensitive to atropine (10-6 M) but were dependent upon extracellular Na+ and were completely blocked by low concentrations of the Ca2+-channel antagonists nicardipine, YC-93 (5 x 10-7 M), and D-600 (5 x 10-6 M). The behaviour of ionomycin is very similar to that shown by A 23187 in this tissue. Ionomycin, like A 23187, can apparently activate D-600 sensitive Ca2+ channels in the guinea-pig intestinal smooth muscle rather than simply translocating Ca2+ EXT.
| Original language | English |
|---|---|
| Pages (from-to) | 535-538 |
| Number of pages | 4 |
| Journal | Canadian Journal of Physiology and Pharmacology |
| Volume | 61 |
| Issue number | 5 |
| DOIs | |
| State | Published - 1983 |
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