TY - JOUR
T1 - The chemotherapeutic oxaliplatin alters voltage-gated Na+ channel kinetics on rat sensory neurons
AU - Adelsberger, Helmuth
AU - Quasthoff, Stefan
AU - Grosskreutz, Julian
AU - Lepier, Alexandra
AU - Eckel, Florian
AU - Lersch, Christian
PY - 2000/10/6
Y1 - 2000/10/6
N2 - The chemotherapeutic oxaliplatin causes a sensory-motor neuropathy with predominantly hyperpathic symptoms. The mechanism underlying this hyperexcitability was investigated using rat sensory nerve preparations, dorsal root ganglia and hippocampal neurons. Oxaliplatin resulted in an increase of the amplitude and duration of compound action potentials. It lengthened the refractory period of peripheral nerves suggesting an interaction with voltage-gated Na+ channels. Application of oxaliplatin to dorsal root ganglion neurons resulted in an increase of the Na+ current, a block of the maximal amplitude and a shift of the voltage-response relationship towards more negative membrane potentials. The effect was detectable on 13 of 18 tested cells. This observation, together with the absence of any effect on Na+ currents of hippocampal neurons, suggests that the interaction of oxaliplatin is restricted to one or more channel subtypes. The effect of oxaliplatin could be antagonised by the Na+ channel blocker carbamazepine which could be used to reduce side effects of oxaliplatin therapy in patients. Copyright (C) 2000 Elsevier Science B.V.
AB - The chemotherapeutic oxaliplatin causes a sensory-motor neuropathy with predominantly hyperpathic symptoms. The mechanism underlying this hyperexcitability was investigated using rat sensory nerve preparations, dorsal root ganglia and hippocampal neurons. Oxaliplatin resulted in an increase of the amplitude and duration of compound action potentials. It lengthened the refractory period of peripheral nerves suggesting an interaction with voltage-gated Na+ channels. Application of oxaliplatin to dorsal root ganglion neurons resulted in an increase of the Na+ current, a block of the maximal amplitude and a shift of the voltage-response relationship towards more negative membrane potentials. The effect was detectable on 13 of 18 tested cells. This observation, together with the absence of any effect on Na+ currents of hippocampal neurons, suggests that the interaction of oxaliplatin is restricted to one or more channel subtypes. The effect of oxaliplatin could be antagonised by the Na+ channel blocker carbamazepine which could be used to reduce side effects of oxaliplatin therapy in patients. Copyright (C) 2000 Elsevier Science B.V.
UR - http://www.scopus.com/inward/record.url?scp=0034613403&partnerID=8YFLogxK
U2 - 10.1016/S0014-2999(00)00667-1
DO - 10.1016/S0014-2999(00)00667-1
M3 - Journal articles
C2 - 11011028
AN - SCOPUS:0034613403
SN - 0014-2999
VL - 406
SP - 25
EP - 32
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
IS - 1
ER -