Differential effects of Tityus bahiensis scorpion venom on tetrodotoxin-sensitive and tetrodotoxin-resistant sodium currents.

Neurotox Res

Departamento de Fisiologia e Biofísica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil.

Published: January 2011

We examined modification of sodium channel gating by Tityus bahiensis scorpion venom (TbScV), and compared effects on native tetrodotoxin-sensitive and tetrodotoxin-resistant sodium currents from rat dorsal root ganglion neurons and cardiac myocytes. In neurons, TbScV dramatically reduced the rate of sodium current inactivation, increased current amplitude, and caused a negative shift in the voltage-dependence of activation and inactivation of tetrodotoxin-sensitive channels. Enhanced activation of modified sodium channels was independent of a depolarizing prepulse. We identified two components of neuronal tetrodotoxin-resistant current with biophysical properties similar to those described for NaV1.8 and NaV1.9. In contrast to its effects on neuronal tetrodotoxin-sensitive current, TbScV caused a small decrease in neuronal tetrodotoxin-resistant sodium current amplitude and the gating modifications described above were absent. A third tetrodotoxin-resistant current, NaV1.5 recorded in rat cardiac ventricular myocytes, was inhibited approximately 50% by TbScV, and the remaining current exhibited markedly slowed activation and inactivation. In conclusion, TbScV has very different effects on different sodium channel isoforms. Among the neuronal types, currents resistant to tetrodotoxin are also resistant to gating modification by TbScV. The cardiac tetrodotoxin-resistant current has complex sensitivity that includes both inhibition of current amplitude and slowing of activation and inactivation.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12640-009-9144-8DOI Listing

Publication Analysis

Top Keywords

tetrodotoxin-resistant sodium
12
current amplitude
12
activation inactivation
12
tetrodotoxin-resistant current
12
current
9
tityus bahiensis
8
bahiensis scorpion
8
scorpion venom
8
tetrodotoxin-sensitive tetrodotoxin-resistant
8
sodium currents
8

Similar Publications

Drug discovery targeting Na1.8: Structural insights and therapeutic potential.

Curr Opin Chem Biol

December 2024

Beijing Frontier Research Center for Biological Structures, State Key Laboratory of Membrane Biology, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China; Institute of Bio-Architecture and Bio-Interactions (IBABI), Shenzhen Medical Academy of Research and Translation (SMART), Guangming District, Shenzhen 518107, Guangdong Province, China; Institute of Chemical Biology, Shenzhen Bay Laboratory, Guangming District, Shenzhen 518132, Guangdong Province, China. Electronic address:

Voltage-gated sodium (Na) channels are crucial in transmitting action potentials in neurons. The tetrodotoxin-resistant subtype Na1.8 is predominantly expressed in the peripheral nervous system, offering a unique opportunity to design selective inhibitors for pain relief.

View Article and Find Full Text PDF
Article Synopsis
  • NaV1.8 and NaV1.9 are sodium channels crucial for pain signaling in sensory neurons, affecting how pain stimuli are processed and transmitted.
  • Mutations in the genes encoding these channels (SCN10A and SCN11A) can lead to various pain-related disorders, including small fiber neuropathy and congenital insensitivity to pain.
  • Researchers created double knockout mice to study the effects of losing both sodium channels, finding moderate pain behavior impairment and valuable insights for exploring human pain-related genetic variants.
View Article and Find Full Text PDF

Peripheral nerve injury (PNI), typically caused by traumatic accidents or medical events, is currently one of the most common diseases that leads to limb disability. After PNI, tetrodotoxin-resistant voltage-gated sodium channel Nav1.8 is upregulated at the lesion site.

View Article and Find Full Text PDF

Cl-dependent amplification of excitatory synaptic potentials at distal dendrites revealed by voltage imaging.

Sci Adv

August 2024

Department of Biophysics, Graduate School of Science, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan.

The processing of synaptic signals in somatodendritic compartments determines neuronal computation. Although the amplification of excitatory signals by local voltage-dependent cation channels has been extensively studied, their spatiotemporal dynamics in elaborate dendritic branches remain obscure owing to technical limitations. Using fluorescent voltage imaging throughout dendritic arborizations in hippocampal pyramidal neurons, we demonstrate a unique chloride ion (Cl)-dependent remote computation mechanism in the distal branches.

View Article and Find Full Text PDF

Multiple approaches have targeted voltage-gated sodium (Nav) channels for analgesia. In this issue of the JCI, Shin et al. identified a peptide aptamer, NaViPA1, carrying a short polybasic motif flanked by serine residues in a structurally disordered region of loop 1 in tetrodotoxin-sensitive (TTX-S) but not tetrodotoxin-resistant (TTX-R) channels.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!