1974
DOI: 10.1016/0006-8993(74)90285-6
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Microelectrode study of projections from the amygdaloid complex to the nucleus accumbens in the cat

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Cited by 26 publications
(8 citation statements)
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“…Basolateral amygdala inactivation reduced both the discriminative stimulus- and non-discriminative stimulus-induced excitation of ipsilateral NAc core neurons, consistent with the proposed BLA–NAc flow of information. Accordingly and replicating reviewed electrophysiological findings (Ito et al, 1974; Powell et al, 1968; Sato, 1977; Yim and Mogenson, 1982), electrical stimulation of the BLA rapidly excited 16% of ipsilateral NAc neurons. More compelling, BLA-evoked NAc neurons in the ipsilateral hemisphere were disproportionately the same ones that were excited by the discriminative stimulus, and most of these had monosynaptic-like BLA-evoked latencies (4–20 ms; Ambroggi et al, 2008).…”
Section: Functional Significance Of Amygdala–ventrostriatal Pathwayssupporting
confidence: 52%
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“…Basolateral amygdala inactivation reduced both the discriminative stimulus- and non-discriminative stimulus-induced excitation of ipsilateral NAc core neurons, consistent with the proposed BLA–NAc flow of information. Accordingly and replicating reviewed electrophysiological findings (Ito et al, 1974; Powell et al, 1968; Sato, 1977; Yim and Mogenson, 1982), electrical stimulation of the BLA rapidly excited 16% of ipsilateral NAc neurons. More compelling, BLA-evoked NAc neurons in the ipsilateral hemisphere were disproportionately the same ones that were excited by the discriminative stimulus, and most of these had monosynaptic-like BLA-evoked latencies (4–20 ms; Ambroggi et al, 2008).…”
Section: Functional Significance Of Amygdala–ventrostriatal Pathwayssupporting
confidence: 52%
“…In the years since Dr. Nauta’s survey, others substantiated the existence of direct amygdalostriatal pathways, including anatomical (Cowan et al, 1965; De Olmos and Ingram, 1972; Ishikawa et al, 1969; Knook, 1966; Krettek and Price, 1978) and electrophysiological (Gloor, 1955a; Ito et al, 1974; Powell et al, 1968; Sato, 1977) evidence of an amygdaloid projection to the NAc via the stria terminalis. These studies, including those enabled by the recently developed tract-tracing methods of anterograde transport of tritiated amino acids (Krettek and Price, 1978) and retrograde labeling (Groenewegen et al, 1980; Newman and Winans, 1980), supported the hypothesis that amygdala projections to the ventral striatum, including the ventral putamen, NAc, and olfactory tubercle, arise from the BLA and basomedial amygdala (BMA).…”
Section: Identification Of Amygdalostriatal Projectionsmentioning
confidence: 99%
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“…This conclusion is consistent with the pattern of amygdala to NAS projection recently described using retrograde transport of wheat germ agglutinin (Phillipson and Griffiths, 1985). Amygdala stimulation-evoked spikes have been recorded previously in the rat (Yim and Mogenson, 1982), in the cat (Ito et al, 1974) and following stimulation of the stria terminalis in the rabbit (DeFrance et al, 1980). However, these past electrophysiological studies did not assess the topographical distribution of NAS cell responsiveness.…”
Section: Discussionmentioning
confidence: 95%
“…Similar to other striatal tissue, many of the efferent fibers terminate in the diencephalon or the pallidal complex, with projections reaching the stria terminalis, preoptic region, nucleus parataenialis, nucleus mediodorsalis thalami, lateral habenular nucleus, substantia nigra-ventral tegmental area, the lateral hypothalamus, cingulum, thalamus, globus pallidus, and subpallidal region [9,17,75,105,106,107,108,109]. There also appear to be projections to the amygdala [110,111] and septum [9,112,113,114], although this is not a universal finding [19] (fig. 1b).…”
Section: Efferentsmentioning
confidence: 99%