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7 subunit to multiple subtypes of nicotinic receptors in embryonic chick sympathetic neurones
7 subunit of the neuronal nicotinic acetylcholine receptor (nAChR) family have demonstrated that this
-bungarotoxin (
-BgTx)-binding neuronal receptor can participate in ACh-gated channels. Heterologous expression studies reveal that
7 subunits form homomeric channels of unusually high Ca2+ permeability. However, the physiological role of the
7 subunit in native neuronal nAChR channels is less clear.
7 subunit contributes to the function of at least three subtypes of native nAChR expressed by embryonic chick sympathetic neurones. These subtypes are functionally distinct from heterologously expressed homomeric
7 nAChRs as well as homomeric-like currents described in studies of hippocampal and parasympathetic neurones.
7 nAChRs in their sensitivity to block by
7 subunit-specific antagonists:
-BgTx and methyllycaconitine (MLA). While MLA blocks 60 % of the macroscopic ACh response,
-BgTx inhibits a small component of the macroscopic current described by slow-on and slow-off kinetics.
7 subunit by antisense oligonucleotide treatment eliminates the susceptibility of the nAChRs to block by both MLA and
-BgTx.
-BgTx-sensitive
7-containing nAChRs have a small unitary conductance (18 pS), brief open time kinetics and relatively low open probability (Po). MLA-sensitive
7 nAChRs are characterized by a conductance of ~35 pS, intermediate burst duration, and a relatively high Po.
7 antisense treatment is characterized by a unitary conductance of 50 pS and prolonged opening duration.
7-containing nAChRs are distinct heteromeric complexes that include other
and/or
nAChR subunits.
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