Journal
BIOMEDICINES
Volume 8, Issue 6, Pages -Publisher
MDPI
DOI: 10.3390/biomedicines8060155
Keywords
Tf2; sodium channel; Na(V)1.3; Na(V)1.9; scorpion; toxin
Categories
Funding
- Australian National Health and Medical Research Council (NMHRC) [APP1162503]
- NHMRC - Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [APP1139961, LA2740/3-1, 363055819/GRK2415, 368482240/GRK2416]
- Interdisciplinary Centre for Clinical Research within the faculty of Medicine at the RWTH Aachen University [IZKF TN1-8/IA 532008]
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Na(V)1.3 is a subtype of the voltage-gated sodium channel family. It has been implicated in the pathogenesis of neuropathic pain, although the contribution of this channel to neuronal excitability is not well understood. Tf2, a beta-scorpion toxin previously identified from the venom of Tityus fasciolatus, has been reported to selectively activate Na(V)1.3. Here, we describe the activity of synthetic Tf2 and assess its suitability as a pharmacological probe for Na(V)1.3. As described for the native toxin, synthetic Tf2 (1 mu M) caused early channel opening, decreased the peak current, and shifted the voltage dependence of Na(V)1.3 activation in the hyperpolarizing direction by -11.3 mV, with no activity at Na(V)1.1, Na(V)1.2, and Na(V)1.4-Na(V)1.8. Additional activity was found at Na(V)1.9, tested using the hNav1.9_C4 chimera, where Tf2 (1 mu M) shifted the voltage dependence of activation by -6.3 mV. In an attempt to convert Tf2 into an Na(V)1.3 inhibitor, we synthetized the analogue Tf2[S14R], a mutation previously described to remove the excitatory activity of related beta-scorpion toxins. Indeed, Tf2[S14R](10 mu M) had reduced excitatory activity at Na(V)1.3, although it still caused a small -5.8 mV shift in the voltage dependence of activation. Intraplantar injection of Tf2 (1 mu M) in mice caused spontaneous flinching and swelling, which was not reduced by the Na(V)1.1/1.3 inhibitor ICA-121431 nor in Na(V)1.9(-/-) mice, suggesting off-target activity. In addition, despite a loss of excitatory activity, intraplantar injection of Tf2[S14R](10 mu M) still caused swelling, providing strong evidence that Tf2 has additional off-target activity at one or more non-neuronal targets. Therefore, due to activity at Na(V)1.9 and other yet to be identified target(s), the use of Tf2 as a selective pharmacological probe may be limited.
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