Dl. Ridley et al., Differential effects of chronic drug treatment on alpha 3*and alpha 7 nicotinic receptor binding sites, in hippocampal neurones and SH-SY5Y cells, BR J PHARM, 133(8), 2001, pp. 1286-1295
1 The aim of this study was to compare the effects of chronic treatment (fo
r 4 or 7 days) with nicotinic drugs and 20 mM KCl on numbers of surface alp
ha7 nicotinic AChR, identified by [I-125]-alpha bungarotoxin (alpha -Bgt) b
inding, in primary hippocampal cultures and SH-SY5Y cells. Numbers of alpha
3* nicotinic AChR were also examined in SH-SY5Y cells, using [H-3]-epibatid
ine, which is predicted to label the total cellular population of predomina
ntly alpha3 beta2* nicotinic AChR under the conditions used.
2 All the nicotinic agonists examined. the antagonists d-tubocurarine and m
ethyllycaconitine, and KCl, upregulated[I-125]-alpha Bgt binding sites by 2
0-60% in hippocampal neurones and, where examined. SH-SY5Y cells.
3 Upregulation of [I-125]-alpha -Bgt binding sites by KCl was prevented by
co-incubation with the L-type Ca2+ channel blocker verapamil or the Ca2+-ca
lmodulin dependent kinase II (CaM-kinase II) inhibitor KN-62. Upregulation
of [I-125]-alpha -Bgt binding sites by nicotine or 3,[(4-dimethylamino) cin
namylidene] anabaseine maleate (DMAC) was insensitive to these agents.
4 [H-3]-Epibatidine binding sites in SH-SY5Y cells were not affected by KCI
but were upregulated in a verapamil-insensitive manner by nicotine and DMA
C. KN-62 itself provoked a 2 fold increase in [H-3]-epibatidine binding. Th
e inactive analogue KN-04 had no effect, suggesting that CaM-kinase II play
s a role in regulating numbers of alpha3* nicotinic AChR.
5 These data indicate that numbers of alpha3* and alpha7 nicotinic AChR are
modulated differently. Nicotinic agonists and KCI upregulate alpha7 nicoti
nic AChR through distinct cellular mechanisms, the latter involving L-type
Ca2+ channels and CaM-kinase II. In contrast, alpha3* nicotinic AChR are no
t upregulated by KCI. This difference may reflect the distinct physiologica
l roles proposed for alpha7 nicotinic AChR.