EFFECT OF VAGAL AUTOTRANSPLANTATION AND BIFEMELANE HYDROCHLORIDE ON CHOLINERGIC MARKERS AND EVENT-RELATED POTENTIALS IN RATS WITH LESIONS OF THE NUCLEUS BASALIS MAGNOCELLULARIS
K. Ikeda et al., EFFECT OF VAGAL AUTOTRANSPLANTATION AND BIFEMELANE HYDROCHLORIDE ON CHOLINERGIC MARKERS AND EVENT-RELATED POTENTIALS IN RATS WITH LESIONS OF THE NUCLEUS BASALIS MAGNOCELLULARIS, Brain research, 688(1-2), 1995, pp. 171-183
In rats lesioned by injecting the ibotenic acid (8 mu g/site) into the
unilateral nucleus basalis magnocellularis (NBM), the effect of treat
ment with bifemelane hydrochloride (BIF) or autotransplantation of the
vagal nodosal ganglion was studied electrophysiologically by serial m
easurement of the event-related potential (ERP, P300) for 4 weeks. In
addition, the effects on cholinergic markers were assessed by determin
ing the specific binding of [H-3]QNB (quinuclidinyl benzilate) to the
muscarinic acetylcholine receptor (mAChR) as well as the activity of c
holine acetyltransferase (ChAT) and acetylcholinesterase (AChE). The P
300 latency was delayed and its amplitude remained low for 4 weeks in
NBM-lesioned rats. In contrast, a return to normal occurred after 2-3
weeks in rats given daily intraperitoneal injections of BIF (15 mg/kg)
and in autotransplanted rats. In lesioned rats, the cortical ChAT and
AChE activities on the affected side did not recover, but the postsyn
aptic receptor response was transiently activated soon after lesioning
. BIF increased specific mAChR binding (an early increase of affinity
and a subsequent increase of receptor density) as well as presynaptic
ChAT activity. Transplantation achieved the early activation of mAChR
binding (increased receptor density) and continuously increased ChAT a
ctivity. Thus, the postsynaptic compensatory receptor mechanism of den
ervation supersensitivity acted as an early response to the depression
of presynaptic cholinergic activity, but it could not improve the P30
0 response until the subsequent increase of cortical ChAT activity. Im
provement of P300 combined with cortical cholinergic recovery after no
dosal ganglion grafting or administration of BIF suggests that the neo
cortical ACh level may play an important role in regulating ERP.