Hyperexcitability and reduced low threshold potassium currents in auditory neurons of mice lacking the channel subunit Kv1.1

被引:114
作者
Brew, HM
Hallows, JL
Tempel, BL
机构
[1] Univ Washington, Sch Med, Virginia Merrill Bloedel Hearing Res Ctr, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Otolaryngol Head & Neck Surg, Seattle, WA 98195 USA
[3] Univ Washington, Sch Med, Dept Pharmacol, Seattle, WA 98195 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2003年 / 548卷 / 01期
关键词
D O I
10.1113/jphysiol.2002.035568
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A low voltage-activated potassium current, I-KL, is found in auditory neuron types that have low excitability and precisely preserve the temporal pattern of activity present in their presynaptic inputs. The gene Kcna1 codes for Kv1.1 potassium channel Subunits, which combine in expression systems to produce channel tetramers with properties similar to those of I-KL, including sensitivity to dendrotoxin (DTX). Kv1.1 is strongly expressed in neurons with I-KL, including auditory neurons of the medial nucleus of the trapezoid body (MNTB). We therefore decided to investigate how the absence of Kv1.1 affected channel properties and function in MNTB neurons from mice lacking Kcna1. We used the whole cell version of the patch clamp technique to record from MNTB neurons in brainstem slices from Kcna1-null (-/-) mice and their wild-type (+/+) and heterozygous (+/-) littermates. There was an IKL in voltage-damped -/- MNTB neurons, but it was about half the amplitude of the IKL in +/+ neurons, with otherwise similar properties. Consistent with this, -/- MNTB neurons were more excitable than their +/+ counterparts; they fired more than twice as many action potentials (APs) during current steps, and the threshold current amplitude required to generate an AP was roughly halved. +/- MNTB neurons had excitability and IKL amplitudes identical to the +/+ neurons. The IKL remaining in -/- neurons was blocked by DTX, suggesting the underlying channels contained subunits Kv1.2 and/or Kv1.6 (also DTX-sensitive). DTX increased excitability further in the already hyperexcitable -/- MNTB neurons, suggesting that -/- IKL limited excitability despite its reduced amplitude in the absence of Kv1.1. subunits.
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页码:1 / 20
页数:20
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