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RI-INBRE > Research Core > Molecular Toxicology > Steven Symington

Steven Symington

Characterization of Pyrethroids on Human Voltage-Sensitive Calcium Channels (2009 - Present)

Investigator:  Steven Symington, Salve Regina University
Mentor
:
  J. Marshall Clark, University of Massachusetts - Amherst 

Abstract:  Pyrethroids are widely used insecticides, especially in urban environments, to protect agricultural commodities and control vectors of human diseases. It is well established that pyrethroids modulate voltage-sensitive sodium channels; however, recent evidence suggests that voltage-sensitive calcium and chloride channels are also inhibited. Furthermore, pyrethroids modulate voltage-sensitive calcium channels at concentrations that elicit the in vivo acute neurotoxic symptoms of intoxication. The goal of this study is to determine relative indices of toxicity for pyrethroids on various human voltage-sensitive calcium channels expressed in vitro and validate the in vivo actions of pyrethroids. Xenopus oocytes, injected with human voltage-sensitive calcium channels cRNA, will be used to determine the direct and comparative action of pyrethroids on these channels. The specific aims of the present proposal are; 1) To examine the structure activity relationship of pyrethroids on the characteristics of human voltage-sensitive calcium channels. 2) To determine pyrethroid relative indices of toxicity on human voltage-sensitive calcium channels.

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RI-INBRE Newsletter Fall 2009

RI-INBRE Newsletter Fall 2009

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Important Dates

RI-INBRE Calendar


12/3//09 - Shahram Khademi, Ph.D, University of Iowa - "The structure and mechanism of ammonia channels"


12/4/09 - 4th Annual BioNES Meeting, Roger Williams University, Bristol, RI


1/29/10 - RI-INBRE Research Fellows Meeting & Faculty Retreat, Providence College, Providence, RI


3/1/10 - Application Deadline for the 2010 Summer Undergraduate Research Fellowships


6/16/10 - 6/18/10 National IDeA Symposium of Biomedical Research Excellence, Bethesda, MD

 Supported by grant #  P20RR016457 from:

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