Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 May:60:150-160.
doi: 10.1016/j.neuro.2016.12.005. Epub 2016 Dec 19.

Consequences of acute Nav1.1 exposure to deltamethrin

Affiliations

Consequences of acute Nav1.1 exposure to deltamethrin

T F James et al. Neurotoxicology. 2017 May.

Abstract

Background: Pyrethroid insecticides are the most popular class of insecticides in the world, despite their near-ubiquity, their effects of delaying the onset of inactivation of voltage-gated sodium (Nav) channels have not been well-evaluated in all the mammalian Nav isoforms.

Objective: Here we compare the well-studied Nav1.6 isoforms to the less-understood Nav1.1 in their responses to acute deltamethrin exposure.

Methods: We used patch-clamp electrophysiology to record sodium currents encoded by either Nav1.1 or Nav1.6 channels stably expressed in HEK293 cells. Protocols evaluating both resting and use-dependent modification were employed.

Results: We found that exposure of both isoforms to 10μM deltamethrin significantly potentiated persistent and tail current densities without affecting peak transient current densities, and only Nav1.1 maintained these significant effects at 1μM deltamethrin. Window currents increased for both as well, and while only Nav1.6 displayed changes in activation slope and V1/2 of steady-state inactivation for peak currents, V1/2 of persistent current activation was hyperpolarized of ∼10mV by deltamethrin in Nav1.1 cells. Evaluating use-dependence, we found that deltamethrin again potentiated persistent and tail current densities in both isoforms, but only Nav1.6 demonstrated use-dependent enhancement, indicating the primary deltamethrin-induced effects on Nav1.1 channels are not use-dependent.

Conclusion: Collectively, these data provide evidence that Nav1.1 is indeed vulnerable to deltamethrin modification at lower concentrations than Nav1.6, and this effect is primarily mediated during the resting state.

General significance: These findings identify Nav1.1 as a novel target of pyrethroid exposure, which has major implications for the etiology of neuropsychiatric disorders associated with loss of Nav1.1-expressing inhibitory neurons.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Representative traces of HEK-Nav1.1 (A) or HEK-Nav1.6 (B) cells in DMSO or deltamethrin-treated conditions in response to an evoked step-wise protocol (schematic under traces). With DMSO in black, Panels C and D depict a current-voltage relationship for Nav1.1 and Nav1.6, respectively, showing deltamethrin treatment in blue for Nav1.1 and green for Nav1.6. Summary bar graphs comparing peak current densities at −10 mV for all three concentrations are shown below the I–V graphs. Voltage-dependencies of activation and steady-state inactivation are depicted for Nav1.1 (E) and Nav1.6 (F); control curves are represented with dashed lines. Window currents are depicted where activation and steady-state inactivation curves overlap, which is indicated with shaded areas—gray for DMSO and colors for deltamethrin. Error bars indicate SEM. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 2
Fig. 2
Representative traces of persistent currents and tail currents (insets) are shown for HEK-Nav1.1 cells (A) and HEK-Nav1.6 cells (B) with deltamethrin shown in blue and green, respectively. Current-voltage relationships are shown for Nav1.1 and Nav1.6 persistent currents (C, D, respectively) and for Nav1.1 and Nav1.6 tail currents (E, F, respectively). Circles represent 10 μM or 0.1% final DMSO concentration; triangles represent 1 μM or 0.01% final DMSO concentration, and diamonds indicate 0.1 μM or 0.001% final DMSO concentration. Error bars indicate SEM. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 3
Fig. 3
Current-voltage relationship for Nav1.1 (A) and Nav1.6 (B) depicting DMSO control peak currents (black squares) and deltamethrin persistent currents (colored circles). Concentration-dependent effect of deltamethrin as percentage of deltamethrin modified channels shown in C, with Nav1.1 represented in blue and Nav1.6 in green. Error bars indicate SEM. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 4
Fig. 4
Representative traces of: A) Use-dependent stimulation protocols, B) HEK-Nav1.1 cells treated with DMSO (black) or 10 μM deltamethrin (blue), C) HEK-Nav1.6 cells treated with DMSO (black) or 10 μM deltamethrin (green). Below traces are summary bar graphs for both stimulation frequencies representing: D) Peak current density, E) Tail current density, F) Peak current density modification, G) Tail current density modification, H) Persistent current density, I) Fraction of available current, J) Peak current modification, K) Total charge. Error bars indicate SEM. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Similar articles

Cited by

References

    1. Berkowicz SR, Featherby TJ, Qu Z, Giousoh A, Borg NA, Heng JI, et al. Brinp1 (−/−) mice exhibit autism-like behaviour, altered memory, hyperactivity and increased parvalbumin-positive cortical interneuron density. Mol. Autism. 2016;7:22. - PMC - PubMed
    1. Breckenridge CB, Holden L, Sturgess N, Weiner M, Sheets L, Sargent D, et al. Evidence for a separate mechanism of toxicity for the Type I and the Type II pyrethroid insecticides. Neurotoxicology. 2009;30(Suppl. 1):S17–31. - PubMed
    1. Catterall WA, Goldin AL, Waxman SG. International Union of Pharmacology: XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels. Pharmacol. Rev. 2005;57(4):397–409. - PubMed
    1. Catterall WA, Dib-Hajj S, Meisler MH, Pietrobon D. Inherited neuronal ion channelopathies: new windows on complex neurological diseases. J. Neurosci. 2008;28(46):11768–11777. - PMC - PubMed
    1. Catterall WA. From ionic currents to molecular review mechanisms: the structure and function of voltage-gated sodium channels. Neuron. 2000;26:13–25. - PubMed

MeSH terms

LinkOut - more resources