Am. Bratt et al., BEHAVIORAL AND NEUROCHEMICAL EFFECTS OF SUPERIOR CERVICAL GANGLIONECTOMY IN RATS WITH SEPTOHIPPOCAMPAL LESIONS, Experimental Brain Research, 102(3), 1995, pp. 429-444
This longitudinal study, extending over 12 months, assessed the behavi
oural and biochemical effects of hippocampal sympathetic ingrowth (HSI
) into the partially denervated hippocampus. Male Long-Evans rats rece
ived fimbria-fornix lesions (FIFO) or sham operations at 90 days of ag
e. At the same time half of the rats from each group sustained bilater
al ablation of the superior cervical ganglia (SCGX). A battery of beha
vioural tests, measuring spontaneous alternation, activity in the open
field and home cage, and radial-maze performance, were employed, star
ting after one very short (16 days) and one extended (216 days) postop
erative delay. Neurochemical analyses measuring choline acetyltransfer
ase (ChAT) activity, high-affinity choline (HACU) and noradrenaline up
take by hippocampal synaptosomes (HANU), hippocampal noradrenaline ([N
A]), serotonin ([5-HT]) and 5-hydroxyindoleacetic acid ([5-HIAA]) conc
entrations were carried out in a dorsal, a ''middle'' and a ventral re
gion of the hippocampus. Lesion of the FIFO induced a significant and
enduring deficit in radial-maze performance, in addition to a persiste
nt locomotor hyperactivity. ChAT and HACU were significantly depleted
in all three regions of the hippocampus at 12 months, and these defici
ts were negatively correlated with maze performance. SCGX in the prese
nce of the FIFO lesion significantly reduced [NA] in the middle region
of the hippocampus, as compared to SCGX rats, and contributed to a re
storation of lesion-induced depletions in [5-HT] and [5-HIAA] in the m
iddle and ventral hippocampal regions, whilst failing to elicit any be
havioural changes at either time point. It is concluded that if lesion
-induced HSI indeed occurred, as is suggested by neurochemical evidenc
e, it had no effect upon the observed behavioural deficits elicited by
transection of the FIFO in the rat.