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- W1994441628 abstract "Blockers selective for different potassium (K + ) channels were examined for their ability to reverse inhibition of electrically evoked contractions of longitudinal muscle-myenteric plexus (lm-mp) by adenosine analogs. Cyclohexyl adenosine (CHA) was selected for these studies, since it effectively inhibited contraction (EC 50 33 nM). 4-aminopyridine (4-AP) antagonized the inhibition by the adenosine analog, but also stimulated contraction by itself. α- and γ-dendrotoxin produced the most profound reversal of CHA-induced inhibition, while producing a minimal contraction alone. Other blockers produced only nominal reversal of the CHA-induced inhibition. These results suggest that inhibition by CHA is mediated via activation of and α- and γ-dendrotoxin-sensitive K + channel." @default.
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- W1994441628 date "1995-04-01" @default.
- W1994441628 modified "2023-09-26" @default.
- W1994441628 title "Ability of some K+ channel blockers to reverse inhibition of electrically evoked contractions of longitudinal muscle-myenteric plexus" @default.
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- W1994441628 doi "https://doi.org/10.1016/0167-4889(94)00223-2" @default.
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