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Abstract

Direct determination of acetylcholine release by radioimmunoassay and presence of presynaptic M1 muscarinic receptors in guinea pig ileum.

K Kawashima, K Fujimoto, T Suzuki and H Oohata
Journal of Pharmacology and Experimental Therapeutics March 1988, 244 (3) 1036-1039;
K Kawashima
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K Fujimoto
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T Suzuki
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H Oohata
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Abstract

Radioimmunoassay for acetylcholine (ACh) with a sensitivity of 10 pg/tube was applied to the direct determination of ACh output from the nerve endings in longitudinal muscle strips of guinea pig ileum. The strips were preincubated with an irreversible cholinesterase inhibitor and superfused with Krebs' solution under various experimental conditions. Pirenzepine (0.1-10 microM) and atropine (10-100 nM) produced an increase in electrically evoked ACh output through the inhibition of presynaptic muscarinic receptors. Contractile response to endogenous ACh released by electrical stimulation was enhanced by pirenzepine and atropine at lower concentrations, whereas the highest concentrations of pirenzepine (10 microM) and atropine (100 nM) caused a reduction in the enhanced contractile response and a significantly diminished response, respectively. These results demonstrate that the concentrations of pirenzepine and atropine, effective in inhibiting presynaptic muscarinic receptors, differ from those inhibiting postsynaptic muscarinic receptors and suggest the possibility that presynaptic M1 muscarinic receptors regulating ACh output may be present in the guinea pig ileum.

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Journal of Pharmacology and Experimental Therapeutics
Vol. 244, Issue 3
1 Mar 1988
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Abstract

Direct determination of acetylcholine release by radioimmunoassay and presence of presynaptic M1 muscarinic receptors in guinea pig ileum.

K Kawashima, K Fujimoto, T Suzuki and H Oohata
Journal of Pharmacology and Experimental Therapeutics March 1, 1988, 244 (3) 1036-1039;

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Abstract

Direct determination of acetylcholine release by radioimmunoassay and presence of presynaptic M1 muscarinic receptors in guinea pig ileum.

K Kawashima, K Fujimoto, T Suzuki and H Oohata
Journal of Pharmacology and Experimental Therapeutics March 1, 1988, 244 (3) 1036-1039;
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