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   <subfield code="a">Evidence for M1 muscarinic cholinoceptors mediating facilitation of noradrenaline release in guinea-pig carotid artery</subfield>
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   <subfield code="c">[Miguel Casado, Jesús Marin, Mercedes Salaices]</subfield>
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   <subfield code="a">Summary: The muscarinic agonists acetylcholine (150 μmol/l), carbachol (1-10 μmol/l) and McN-A-343 (1-50 μmol/l, selective for M1 receptors) increased, in a concentration-dependent manner, the electrically-evoked tritium overflow from guinea-pig carotid arteries preincubated with [3H]-noradrenaline. The increase caused by acetylcholine was not modified by hexamethonium (300 μmol/l) but was reduced by the muscarinic receptor antagonists methylatropinium (0.5 and 1 nmol/l, nonselective), pirenzepine (1 and 5 μmol/l, M1-selective), methoctramine (1 and 5 μmol/l, M2-selective) and pfluoro-hexahydro-sila-difenidol (0.1-1 μmol/l, M3-selective). The order of potencies (expressed as negative logarithms of concentrations that reduced by 50% the facilitatory effect of acetylcholine) was: methylatropinium (9.93) &gt; pirenzepine (8.83) &gt; p-fluoro-hexahydro-siladifenidol (6.81) ≥ methoctramine (6.20). These results demonstrate the existence of facilitatory M1 receptors modulating noradrenaline release in blood vessels.</subfield>
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