The present study examines the reactivity of the glial metabolic enzyme. gl
ycogen phosphorylase. within the amygdala and bed nucleus of the stria term
inalis. Reactivity for phosphorylase tr, the active form of glycogen phosph
orylase, was higher in all parts of the medial amygdaloid nucleus, in the m
edial division of the central amygdaloid nucelus, in the anterior amygdaloi
d area and in the bed nucleus of stria terminalis than in all parts of the
lateral amygdaloid nucleus, the anterior cortical amygdaloid nucleus, the p
osteromedial and posterolateral cortical amygdaloid nuclei, the intercalate
d nucleus of the amygdala, main part and the intercalated nuclei. A greater
degree of phosphorylase a reactivity was also observed in the basolateral
amygdaloid nucleus, anterior and posterior parts, and in the basomedial amy
gdaloid nucleus, anterior part, while other parts of these nuclei were less
reactive. Reactivity attributed to total glycogen phosphorylase enzyme, ph
osphorylase a + phosphorylase b activated by AMP, was higher and homogeneou
s across the amygdala. Phosphorylase cr patterns are likely to reflect diff
erences in the contribution of glycogenolysis to the metabolic support of c
ells in the amygdala acid bed nucleus of the stria terminalis. Possible rel
ationships to local neuronal activity and to differences in glycogenolytic
neuromodulatory input are discussed. (C) 2001 Elsevier Science B.V. All rig
hts reserved.