Literature DB >> 8728483

Presence of the voltage-gated potassium channels sensitive to charybdotoxin in inhibitory presynaptic terminals of cultured rat hippocampal neurons.

T Ohno-Shosaku1, I Kim, S Sawada, C Yamamoto.   

Abstract

To determine whether the charybdotoxin-sensitive subtypes of voltage-gated K+ channels (Kv1.2 and Kv1.3) exist in inhibitory pre-synaptic terminals, effects of K+ channel blockers including TEA, charybdotoxin (ChTX), iberiotoxin (IbTX), kaliotoxin (KTX) and margatoxin (MgTX) on the inhibitory transmission were examined with cultured rat hippocampal neurons. Monosynaptic inhibitory postsynaptic currents (IPSCs) evoked by electrical stimulation of single presynaptic neurons were recorded from the whole-cell clamped postsynaptic neurons. In the presence of TEA, application of ChTX greatly increased the amplitude of IPSCs. A specific maxi-K+ channel blocker IbTX failed to augment IPSCs. KTX and MgTX, both of which block Kv1.3 but not Kv1.2, mimicked the facilitating effect of ChTX. In the absence of TEA, application of ChTX increased the IPSC amplitude significantly, while IbTX was without effect. These results indicate that the ChTX-sensitive subtypes of voltage-gated K+ channels, most likely Kv1.3, contribute to the repolarization of action potentials at presynaptic terminals of hippocampal inhibitory neurons, and that the ChTX-induced facilitation of the transmission can be explained by its effects on the Kv channels rather than maxi-K+ channels.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8728483     DOI: 10.1016/0304-3940(96)12518-0

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  6 in total

1.  Kv1.3 channels regulate synaptic transmission in the nucleus of solitary tract.

Authors:  Angelina Ramirez-Navarro; Patricia A Glazebrook; Michelle Kane-Sutton; Caroline Padro; David D Kline; Diana L Kunze
Journal:  J Neurophysiol       Date:  2011-03-23       Impact factor: 2.714

2.  Increased Kv1 channel expression may contribute to decreased sIPSC frequency following chronic inhibition of NR2B-containing NMDAR.

Authors:  Shuijin He; Li-Rong Shao; W Bradley Rittase; Suzanne B Bausch
Journal:  Neuropsychopharmacology       Date:  2012-01-04       Impact factor: 7.853

3.  Endogenous animal toxin-like human β-defensin 2 inhibits own K(+) channels through interaction with channel extracellular pore region.

Authors:  Weishan Yang; Jing Feng; Fang Xiang; Zili Xie; Guoyi Zhang; Jean-Marc Sabatier; Zhijian Cao; Wenxin Li; Zongyun Chen; Yingliang Wu
Journal:  Cell Mol Life Sci       Date:  2014-09-20       Impact factor: 9.261

4.  Large conductance calcium-activated potassium channels: their expression and modulation of glutamate release from nerve terminals isolated from rat trigeminal caudal nucleus and cerebral cortex.

Authors:  Irene Samengo; Diego Currò; Vincenzo Barrese; Maurizio Taglialatela; Maria Martire
Journal:  Neurochem Res       Date:  2014-03-26       Impact factor: 3.996

5.  Granzyme B-induced neurotoxicity is mediated via activation of PAR-1 receptor and Kv1.3 channel.

Authors:  Tongguang Wang; Myoung-Hwa Lee; Elliot Choi; Carlos A Pardo-Villamizar; Sung Bin Lee; In Hong Yang; Peter A Calabresi; Avindra Nath
Journal:  PLoS One       Date:  2012-08-29       Impact factor: 3.240

6.  Effect of synthetic aβ peptide oligomers and fluorinated solvents on Kv1.3 channel properties and membrane conductance.

Authors:  Maria I Lioudyno; Matteo Broccio; Yuri Sokolov; Suhail Rasool; Jessica Wu; Michael T Alkire; Virginia Liu; J Ashot Kozak; Philip R Dennison; Charles G Glabe; Mathias Lösche; James E Hall
Journal:  PLoS One       Date:  2012-04-26       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.