Acta Pharmacologica Sinica (2009) 30: 805-817; doi: 10.1038/aps.2009.48

 
Original Article
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Kinetics of desensitization and recovery from desensitization for human α4β2-nicotinic acetylcholine receptors stably expressed in SH-EP1 cells
 

Kewei D YU1, Qiang LIU1, Jie WU1, *, Ronald J LUKAS2, *

 

1Division of Neurology and 2Division of Neurobiology, Barrow Neurological Institute, Phoenix , AZ 85013 , USA

 

Aim: Studies were conducted to define the kinetics of the onset of and recovery from desensitization for human α4β2-nicotinic acetylcholine receptors (nAChR) heterologously expressed in the SH-EP1 human epithelial cell line.

Methods:
Whole-cell patch clamp recordings were performed to evaluate α4β2-nAChR currents.

Results: Application of 0.1 µmol/L nicotine or 1 mmol/L acetylcholine (ACh) for 1 s or longer induced two phases, with time constants of ~70 and ~700 ms, for the onset of α4β2-nAChR desensitization.  For a given duration of agonist exposure, recovery from desensitization induced by nicotine was slower than recovery from ACh-induced desensitization.  Comparisons with published reports indicate that time constants for the recovery of α4β2-nAChRs from desensitization are smaller than those for the recovery of human muscle-type nAChRs[1] from desensitization produced by the same concentrations and durations of exposure to an agonist.  Moreover, the extent of human α4β2-nAChR desensitization and rate of recovery are the same, regardless of whether they are measured using whole-cell recording or based on published findings[2] using isotopic ion flux assays; this equality demonstrates the equivalent legitimacy of these techniques in the evaluation of nAChR desensitization.  Perhaps most significantly, recovery from desensitization also was best fit to a biphasic process.  Regardless of whether it was fit to single or double exponentials, however, half-times for recovery from desensitization grew progressively longer with an increased duration of agonist exposure during the desensitizing pulse.

Conclusion: These findings indicate the existence of α4β2-nAChRs in many distinctive states of desensitization, as well as the induction of progressively deeper states of desensitization with the increased duration of agonist exposure.
 

 

Keywords: acetylcholine; nicotinic acetylcholine receptors; patch-clamp techniques; SH-EP1 cells

 

This project, part of which was conducted in the Charlotte and Harold Simensky Neurochemistry of Alzheimer’s Disease Laboratory, was funded by the Arizona Disease Control Research Commission (9730 and 9615), the National Institutes of Health (NIH NS40417 and DA015389), the Roberta and Gloria Wallace Foundation, the Marjorie Newsome and Sandra Solheim Aiken fund, and the Men’s and Women’s Boards of the Barrow Neurological Foundation.

We thank J Brek EATON for cell maintenance and plating for electrophysiological studies and Dr Raphael GRUENER and Marsha SEGERBERG for critical readings of the manuscript.

 

* Correspondence to Dr Ronald J LUKAS or Prof Jie WU.
Email rlukas@chw.edu or Jie.Wu@chw.edu
Received 2009-02-16     Accepted 2009-03-17

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