Journal of Neuroscience, Vol 11, 2821-2828, Copyright © 1991 by Society for Neuroscience
Compensatory elevation of acetylcholine synthesis in vivo by cholinergic neurons surviving partial lesions of the septohippocampal pathway
PA Lapchak, DJ Jenden and F Hefti
Division of Neurogerontology, Andrus Gerontology Center, University of Southern California, Los Angeles 90089.
The present study characterized the effects of partial destruction of the
cholinergic septohippocampal pathway on transmitter functions of surviving
cholinergic neurons in the hippocampus. Partial and full fimbrial
transections were performed, and 3 weeks after lesioning, cholinergic
functions were assessed in vivo and in vitro. Hippocampal ChAT activity and
the capacity of hippocampal slices to synthesize [3H]ACh in vitro decreased
by 35% and 45%, respectively, following partial fimbrial lesions and by 68%
and 85%, respectively, following full fimbrial lesions. [3H]ACh release
from hippocampal slices in vitro was decreased by 57% and 87%,
respectively, following partial and full fimbrial lesions. Partial lesions
decreased high-affinity choline uptake into hippocampal synaptosomes by
52%. In contrast to the significant reductions in cholinergic parameters
measured in vitro after partial fimbrial lesions, such partial lesions did
not significantly alter in vivo measures of hippocampal cholinergic
function. Levels of endogenous ACh and choline measured in the hippocampus
following partial lesions were similar to that of control values. Also, the
hippocampal content of newly synthesized [2H4]ACh and the [2H4]ACh
synthesis rate were not significantly different from control values.
However, following full fimbrial lesions, in vivo measures of hippocampal
cholinergic function were decreased to a degree similar to that observed in
vitro. Hippocampal levels of endogenous ACh and [2H4]ACh and the synthesis
rate for [2H4]ACh were decreased by 73%, 72%, and 83%, respectively. These
results suggest that, following partial destruction of afferent cholinergic
fibers that innervate the hippocampal formation, residual cholinergic
neurons are able to upregulate their capacity to synthesize and store ACh
in vivo, thus compensating for lesion-induced losses of cholinergic
neurons.(ABSTRACT TRUNCATED AT 250 WORDS)