Abstract

To establish a method detecting the expression of vanilloid receptor type 1 (VR1) and explore the physiological role of VR1 as a possible bio-target molecule of formaldehyde (FA), VR1 <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">+</sup> -HEK293 (human embryonic kidney, HEK) cell model was constructed using the VRl-cDNA plasmid through the molecular cloning and transfection technology. And then, testing of capsaicin and FA-induced cell death rate in transfected VR1 <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">+</sup> - HEK293 cells were carried out. The Results showed that VR1 was functionally expressed in VR1 <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">+</sup> -HEK293 cell model, and measurement of VR1 <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">+</sup> -HEK293 cell death rate should be an available and effective method, which can be applied in detecting the VR1 expression in cells in vitro; activated VR1 by FA could be blocked by capsazepine (CPZ), a specific antagonist of VR1, suggesting that VR1 may be the possible bio-target molecule of FA and related to the development of FA-induced airway irritant effect and neurogenic inflammation.

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