Ja. Carr et al., ALTERATIONS IN BRAIN AND PITUITARY BETA-ENDORPHIN CONTENT IN GENETICALLY EPILEPSY-PRONE RATS, Epilepsy research, 31(2), 1998, pp. 113-122
We measured beta-endorphin concentrations in the anterior and neuroint
ermediate lobes of the pituitary gland and in microdissected brain reg
ions of moderate-seizure genetically epilepsy-prone rats (GEPR-3), sev
ere-seizure GEPR-9s and Sprague-Dawley non-epileptic control rats. Pla
sma concentrations of beta-endorphin and alpha-melanocyte-stimulating
hormone (alpha-MSH) were also measured as indicators of pituitary POMC
-peptide secretion. Concentrations of beta-endorphin in the anterior l
obe of GEPR-3s were 53% higher compared to controls and 57% higher com
pared to GEPR-9s. There were no differences in neurointermediate lobe
beta-endorphin concentrations between control and either GEPR strain.
Plasma beta-endorphin concentrations were significantly lower in GEPR-
9s than controls. Plasma levels of alpha-MSH did not differ between co
ntrol and GEPRs. In the hypothalamus of GEPR-9s beta-endorphin concent
rations in the arcuate nucleus were significantly greater than in GEPR
-3s. Concentrations of beta-endorphin in the central amygdala of GEPR-
9s were two- to threefold greater than in control or GEPR-3s. beta-End
orphin concentrations in the central gray of GEPR-3s were 58% lower th
an control or GEPR-9s. These data suggest that anterior lobe beta-endo
rphin secretion is reduced in GEPR-9s. Furthermore, brain endorphinerg
ic pathways appear to be differentially altered in GEPR-3s and GEPR-9s
. Alterations in pituitary beta-endorphin secretion and brain endorphi
nergic systems may contribute to seizure susceptibility in GEPRs and t
o differences in seizure severity between GEPR-3s and GEPR-9s. (C) 199
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