The fungicide tebuconazole modulates the sodium current of human NaV1.5 channels expressed in HEK293 cells

The fungicide Tebuconazole is a widely used pesticide in agriculture and may cause cardiotoxicity. In our present investigation the effect of Tebuconazole on the sodium current (I-Na) of human cardiac sodium channels (Na(V)1.5) was studied using a heterologous expression system and whole-cell patch-clamp techniques. Tebuconazole reduced the amplitude of the peak I-Na in a concentration- and voltage-dependent manner. At the holding potential of -120 mV the IC50 was estimated at 204.1 & PLUSMN; 34.3 & mu;M, while at -80 mV the IC50 was 0.3 & PLUSMN; 0.1 & mu;M. The effect of the fungicide is more pronounced at more depolarized potentials, indicating a state-dependent interaction. Tebuconazole caused a negative shift in the half-maximal inactivation voltage and delayed recovery from fast inactivation of I-Na. Also, it enhanced closed-state inactivation, exhibited use-dependent block in a voltage-dependent manner. Furthermore, Tebuconazole reduced the increase in late sodium current induced by the pyrethroid insecticide & beta;-Cyfluthrin. These results suggest that Tebuconazole can interact with Na(V)1.5 channels and modulate I-Na. The observed effects may lead to decreased cardiac excitability through reduced I-Na availability, which could be a new mechanism of cardiotoxicity to be attributed to the fungicide.

Automated summary

The fungicide Tebuconazole affects the sodium current of human cardiac sodium channels by reducing its amplitude in a concentration- and voltage-dependent manner. It alters the inactivation properties and recovery kinetics of the current, and enhances closed-state inactivation and use-dependent block. Furthermore, Tebuconazole reduces the increase in late sodium current induced by another insecticide. These findings suggest a new mechanism of cardiotoxicity attributed to Tebuconazole.