Eh. Bertram et Dx. Zhang, Thalamic excitation of hippocampal CA1 neurons: A comparison with the effects of CA3 stimulation, NEUROSCIENC, 92(1), 1999, pp. 15-26
CA1 is the major output area for the hippocampus, and current evidence show
s that it is excited primarily from ipsilateral and contralateral CA3 pyram
idal cells in the rat. Direct connections from the midline thalamic nuclei
to the hippocampus have been described anatomically, but the physiological
role of these connections has not been reported until the recent observatio
n that these inputs may have a mild excitatory effect (subthreshold for pop
ulation spikes). In this study, we report a more powerful excitatory effect
of thalamic stimulation on the response of the CA1 neurons in the urethane
-anesthetized rat. Electrical stimulation to the midline thalamus induced r
esponses similar to responses from stimulation of the contralateral hippoca
mpus (CA3), with well-developed field excitatory postsynaptic potentials an
d large population spikes. The latency of the CA1 response suggested that t
he thalamic connection was monosynaptic, and there was a laminar CA1 respon
se profile that depended on the site of stimulation (contralateral CA3 or t
halamus). In an initial examination of possible differences in the physiolo
gical effects of these two pathways on the CA1 region, we tested both sites
for long-term potentiation of CA1, for the effects of repetitive stimulati
on on CA1 responses (e.g., possible augmenting responses) and for the effec
t of paired-pulse stimulation. In these three measures, there were clear an
d statistically significant differences between the effects of CA3 and thal
amic stimulation on CA1 responses.
This study demonstrates that the well-described thalamic connection to the
hippocampus allows for the direct and powerful excitation of the CA1 region
. This thalamohippocampal connection bypasses the trisynaptic/commissural p
athway that has been thought to be the exclusive excitatory drive to CA1. I
n addition, preliminary data indicate that the thalamus and CA3 inputs have
different physiological effects on CA1 pyramidal cells. (C) 1999 IBRO. Pub
lished by Elsevier Science Ltd.