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α4β2 Nicotinic acetylcholine receptors, willing if able
Author(s) -
Papke Roger L
Publication year - 2010
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.2010.00868.x
Subject(s) - cytisine , receptor , agonist , acetylcholine receptor , nicotinic agonist , partial agonist , nicotine , chemistry , population , biophysics , neuroscience , pharmacology , hek 293 cells , ion channel , acetylcholine , microbiology and biotechnology , biology , biochemistry , medicine , environmental health
Li and Steinbach apply nonstationary noise analysis to the whole‐cell current responses of low sensitivity α4β2 nAChR stably‐expressed in HEK cells. These receptors represent one of the most important nAChR subtypes in brain, and also one of the most difficult to study in native tissues. They found the activating properties of the full agonists ACh and nicotine to be similar with regard to P open and single channel conductance, whereas the weak α4β2 partial agonist cytisine caused channels to open with low probability but increased single channel conductance. When optimally stimulated by either of the full agonists, approximately 80% of the available receptors opened at the peak of the response. However, comparisons of whole‐cell current to estimates of total cell surface receptors, indicated that only about 7% of the total receptor population can be activated. These observations provide important and intriguing new pieces of the brain nicotine receptor puzzle.