Effects of Guadipyr on voltage-gated calcium and potassium channels in central neurons of Helicoverpa armigera
Author of the article:GUAN Dan-Yang;JIANG Xiao-Wei;LI Qing-Ya;LIU Xiao;MA Yong-Qiang;CHEN Qiang;LI-Byarlay Hongmei
Author's Workplace:The Key Laboratory of Bioactive Materials of Ministry of Education, College of Life Sciences, Nankai University; Department of Applied Chemistry, China Agricultural University; Agricultural Research and Develop Program, Department of Agriculture and Life Science, Central State University
Key Words:Guadipyr; Helicoverpa armigera; voltage-gated calcium channels; voltage-gated potassium channels; Whole-cell Patch Clamp Technique
Abstract:
[Objectives] Guadipyr is a novel insecticide that has both
neonicotinoid and semicarbazone insecticidal activity. How it affects ion
channels and channel gating characteristics and functions is currently unknown. We examined the effects of Guadipyr on
voltage-gated calcium and potassium channels, and explored whether these
channels are potential targets for this pesticide. [Methods] The effects of
three concentrations (1, 10, and 100 μmol∙L-1) of Guadipyr on Ca2+and
K+ channels were studied using the patch clamp technique. [Results] All three concentrations of Guadipyr
significantly (P<0.05) shifted Ca2+ channel Ⅰ-Ⅴ and activation curves about 10-15 mV in the
negative direction. The inactivation curves of Ca2+ channels were
also shifted 5 mV towards the hyperpolarizing direction, which is a not
significant shift (P>0.05). The Ca2+ peak current was
significantly decreased by Guadipyr treatment relative to the control. The Ipeak decreased more slowly as the concentration of Guadipyr increased. The area of
window current increased the most (93.20%) following treatment with 1 μmol∙L-1 Guadipyr than by
treatment with 10 μmol∙L-1 and 100 μmol∙L-1. The number of Ca2+ channels activated increased after
Guadipyr treatment at a test voltage of ﹣60 mV to +10 mV. The K+ peak current decreased gradually when
Guadipyr was added to the external solution; the Ipeak decreased
more slowly as the Guadipyr concentration increased from 10 μmol∙L-1 to 100 μmol∙L-1. Ⅰ-Ⅴ curves declined and the activation of K+ channels
was shifted 8 mV towards the depolarizing direction, which was not significant
(P>0.05). This shows that K+ channels can be activated at
higher potentials by Guadipyr. [Conclusion] Guadipyr can effectively inhibit the Ipeak of the Ca2+and K+ channels, and shift the activation and
inactivation curves of these channels, thereby affecting the gating of Ca2+ channels and K+ channels. Therefore, Ca2+ and K+ channels in the central neurons of H. armigera are potential Guadipyr target
sites.