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Título: | Bupivacaine effects on hkv1.5 channels are dependent on extracellular pH |
Autor: | Longobardo, Mónica; González, Teresa CSIC ORCID; Caballero, Ricardo; Delpón, Eva; Tamargo, Juan; Valenzuela, Carmen CSIC ORCID CVN | Fecha de publicación: | 2001 | Editor: | Nature Publishing Group Wiley-Blackwell |
Citación: | British Journal of Pharmacology 134(2): 359-369 (2001) | Resumen: | Bupivacaine-induced cardiotoxicity increases in hypoxic and acidotic conditions. We have analysed the effects of R(+)bupivacaine on hKv1.5 channels stably expressed in Ltk− cells using the whole-cell patch-clamp technique, at three different extracellular pH (pHo), 6.5, 7.4 and 10.0. Acidification of the pHo from 7.4 to 6.5 decreased 4 fold the potency of R(+)bupivacaine to block hKv1.5 channels. At pHo 10.0, the potency of the drug increased ∼2.5 fold. Block induced by R(+)bupivacaine at pHo 6.5, 7.4 and 10.0, was voltage- and time-dependent in a manner consistent with an open state block of hKv1.5 channels. At pHo 6.5, but not at pHo 7.4 or 10.0, R(+)bupivacaine increased by 95±3 % (n=6; P<0.05) the hKv1.5 current recorded at −10 mV, likely due to a drug-induced shift of the midpoint of activation (ΔV=−8.5±1.4 mV; n=7). R(+)bupivacaine development of block exhibited an ‘instantaneous’ component of block at the beginning of the depolarizing pulse, which averaged 12.5±1.8% (n=5) and 4.6±1.6% (n=6), at pHo 6.5 and 7.4, respectively, and that was not observed at pHo 10.0. It is concluded that: (a) alkalinization of the pHo increases the potency of block of R(+)bupivacaine, and (b) at pHo 6.5, R(+)bupivacaine induces an ‘agonist effect’ of hKv1.5 current when recorded at negative membrane potentials | Versión del editor: | http://dx.doi.org/10.1038/sj.bjp.0704251 | URI: | http://hdl.handle.net/10261/79862 | DOI: | 10.1038/sj.bjp.0704251 | Identificadores: | doi: 10.1038/sj.bjp.0704251 issn: 0007-1188 e-issn: 1476-5381 |
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