U. Jurgens et al., C-FOS EXPRESSION DURING VOCAL MOBBING IN THE NEW-WORLD MONKEY SAGUINUS-FUSCICOLLIS, European journal of neuroscience, 8(1), 1996, pp. 2-10
In order to find brain areas involved in the vocal expression of emoti
on, we compared c-fos expression in three groups of saddle-back tamari
ns (Saguinus fuscicollis). One group, consisting of three animals, was
made to utter more than 800 mobbing calls by electrical stimulation o
f the periaqueductal grey of the midbrain (FAG). A second group, consi
sting of two animals, was stimulated in the FAG with the same intensit
y and for the same duration as the first group but at sites that did n
ot produce vocalization. These sites lay somewhat medial to the vocali
zation-eliciting sites. A third group, consisting of two animals, was
stimulated at vocalization-eliciting sites in the FAG but with an inte
nsity below vocalization threshold. Fos-like immunoreactivity that was
found in the vocalizing but not in the non-vocalizing animals was loc
ated in the dorsomedial and ventrolateral prefrontal cortex, anterior
cingulate cortex, ventrolateral premotor cortex, sensorimotor face cor
tex, insula, inferior parietal cortex, superior temporal cortex, claus
trum, entorhinal and parahippocampal cortex, basal amygdaloid nucleus,
anterior and dorsomedial hypothalamus, nucleus reuniens, lateral habe
nula, Edinger-Westphal nucleus, ventral and dorsolateral midbrain tegm
entum, nucleus cuneiformis, sagulum, pedunculopontine and laterodorsal
tegmental nuclei, ventral raphe, periambigual reticular formation and
solitary tract nucleus. For some of these structures (e.g. anterior c
ingulate cortex and periambigual reticular formation), there is eviden
ce also from electrical stimulation, lesioning and single-unit recordi
ng studies that they are involved in vocal control. For other structur
es (e.g. lateral habenula, Edinger-Westphal nucleus), the available ev
idence speaks against such a role. Fos activation in these cases is pr
obably related to non-vocal reactions accompanying the electrically el
icited vocalizations. A third group of structures consists of areas fo
r which a role in vocal control cannot be excluded but for which the p
resent study presents the first evidence for such a role (e.g. claustr
um and sagulum). These structures deserve further studies using more s
pecific methods.