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Role of gap junctions and EETs in endothelium‐dependent hyperpolarization of porcine coronary artery
Author(s) -
Edwards G,
Thollon C,
Gardener M J,
Félétou M,
Vilaine J P,
Vanhoutte P M,
Weston A H
Publication year - 2000
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0703188
Subject(s) - iberiotoxin , bradykinin , apamin , hyperpolarization (physics) , charybdotoxin , ouabain , chemistry , medicine , vascular smooth muscle , endothelium , substance p , endocrinology , gap junction , biophysics , vasodilation , membrane potential , potassium channel , biochemistry , smooth muscle , biology , stereochemistry , intracellular , neuropeptide , receptor , organic chemistry , nuclear magnetic resonance spectroscopy , sodium
The effects of endothelium‐derived hyperpolarizing factor (EDHF: elicited using substance P or bradykinin) were compared with those of 11,12‐EET in pig coronary artery. Smooth muscle cells were usually impaled with microelectrodes through the adventitial surface. Substance P (100 n M ) and 11,12‐EET (11,12‐epoxyeicosatrienoic acid; 3 μ M ) hyperpolarized endothelial cells in intact arteries. These actions were unaffected by 100 n M iberiotoxin but were abolished by charybdotoxin plus apamin (each 100 n M ). Substance P (100 n M ) and bradykinin (30 n M ) hyperpolarized intact artery smooth muscle; Substance P had no effect after endothelium removal. 11,12‐EET hyperpolarized de‐endothelialized vessels by 12.6±0.3 mV, an effect abolished by 100 n M iberiotoxin. 11,12‐EET hyperpolarized intact arteries by 18.6±0.8 mV, an action reduced by iberiotoxin, which was ineffective against substance P. Hyperpolarizations to 11,12‐EET and substance P were partially inhibited by 100 n M charybdotoxin and abolished by further addition of 100 n M apamin. 30 μ M barium plus 500 n M ouabain depolarized intact artery smooth muscle but responses to substance P and bradykinin were unchanged. 500 μ M gap 27 markedly reduced hyperpolarizations to substance P and bradykinin which were abolished in the additional presence of barium plus ouabain. Substance P‐induced hyperpolarizations of smooth muscle cells immediately below the internal elastic lamina were unaffected by gap 27, even in the presence of barium plus ouabain. In pig coronary artery, 11,12‐EET is not EDHF. Smooth muscle hyperpolarizations attributed to ‘EDHF’ are initiated by endothelial cell hyperpolarization involving charybdotoxin‐ (but not iberiotoxin) and apamin‐sensitive K + channels. This may spread electrotonically via myoendothelial gap junctions but the involvement of an unknown endothelial factor cannot be excluded.British Journal of Pharmacology (2000) 129 , 1145–1154; doi: 10.1038/sj.bjp.0703188