Nn. Doron et Je. Ledoux, Organization of projections to the lateral amygdala from auditory and visual areas of the thalamus in the rat, J COMP NEUR, 412(3), 1999, pp. 383-409
Projections to the amygdala from the auditory thalamus have been implicated
in the associative conditioning of fear responses to acoustic stimuli. Tha
lamo-amygdala auditory projections enter the amygdala via the lateral nucle
us (LA). It is well documented that these projections originate in the medi
al division (MGm) of the medial geniculate nucleus (MGN), the posterior int
ralaminar nucleus (PIN), and the suprageniculate nucleus (Sg). It is not kn
own, however, whether these thalamic projections terminate in a topographic
fashion within the LA. We therefore used several retrograde tract tracing
techniques to determine whether the terminations of thalamo-amygdala fibers
have a topographic organization within the LA. These tracers were injected
into various locations within the LA, and the distribution of the retrogra
dely labeled cells throughout the thalamus was analyzed. In general, rostra
l to caudal distinctions in the thalamus are maintained in the LA, such tha
t projections from throughout the MGN terminate in the anterior part of the
LA, whereas the caudal part of the MGN projects to the caudal part of the
LA. Furthermore, the density of cells that give rise to thalamo-amygdala pr
ojections varies within each thalamic nucleus along the rostro-caudal axis.
The patterns of thalamo-amygdala connectivity observed support previous pa
rcellation schemes that segregate the LA into dorsal, medial, and lateral a
reas, and suggest that the LA should be further divided into anterior and p
osterior parts. In addition to the well-known projections to the LA origina
ting from PIN, MGN, and Sg, we also found substantial projections from the
dorsal portion of the MGN (MGd) and the lateral posterior thalamic nucleus
(LP). These findings suggest that some of the functional segregation in the
thalamus may be preserved in the LA, and that the role of the MGd and LP i
n thalamo-amygdala transmission should be reconsidered. (C) 1999 Wiley-Liss
, Inc.