In the present paper; we discuss the diversity of nicotinic receptors
(nAChRs) expressed in hippocampal neurons and their functional propert
ies. Three distinct types of whole-cell currents can be identified in
hippocampal neurons by brief application of nicotinic agonists. These
currents, which are referred to as types IA, II and III, were distingu
ished pharmacologically on the basis of their differential sensitiviti
es to various nicotinic agonists and antagonists, and functionally on
the basis of their rectification properties and rundown. Most of the h
ippocampal neurons show type IA current in response to nicotinic agoni
sts, and the single channels that account for these currents in additi
on to having a very short open time and a high conductance, have a hig
h Ca2+ permeability and inactivate very fast. Based on the comparison
of the properties of the nicotinic currents elicited in hippocampal ne
urons with those elicited by activation of nAChRs transiently expresse
d in oocytes, we have concluded that type IA currents may be subserved
by alpha 7-bearing nAChRs, type II currents by alpha 4 beta 2 nAChRs,
and type III currents by alpha 3 beta 4 nAChRs. Indeed in-situ hybrid
ization shows that mRNAs coding for alpha 7, alpha 4 and beta 2 nAChR
subunits are present in hippocampal neurons. These findings altogether
have given new insights for the studies of neurophysiological process
es and neuropathological conditions in which neuronal nAChRs may be im
plicated.