THE FETAL EXPRESSION OF PROENKEPHALIN MESSENGER-RNAS AND MET-ENKEPHALIN IMMUNOREACTIVITY IN THE HYPOTHALAMOSEPTAL TRACT AND ADJACENT HYPOTHALAMIC AREAS OF THE GUINEA-PIG BRAIN
V. Mitchell et al., THE FETAL EXPRESSION OF PROENKEPHALIN MESSENGER-RNAS AND MET-ENKEPHALIN IMMUNOREACTIVITY IN THE HYPOTHALAMOSEPTAL TRACT AND ADJACENT HYPOTHALAMIC AREAS OF THE GUINEA-PIG BRAIN, Developmental brain research, 86(1-2), 1995, pp. 67-80
The development of the enkephalinergic hypothalamoseptal tract in the
guinea pig brain was studied from embryonic day 30 until birth. Proenk
ephalin (PE) mRNAs were detected in the hypothalamic magnocellular dor
sal nucleus (MDN) by in situ hybridization with a synthetic S-35-label
ed oligonucleotide. The Met-enkephalin-like immunoreactivity (Met-enk-
LI) in the MDN and the lateral septum (LS) was detected with antibodie
s against Met-enkephalin, on adjacent cryostat sections. At the same t
ime, an immunohistochemical study of the arrangement of enkephalinergi
c axon terminals in the LS at birth was performed at the electron micr
oscopic level. PE mRNAs were first found to be expressed in the MDN at
embryonic day 32 (E32) and increased to reach a maximal level at E48.
Met-enk-LI was consistently detectable from E38 in numerous perikarya
of the MDN as well as in nerve terminals of the LS. The number of Met
-enk-LI cells of the MDN decreased after this stage until birth, where
as positive nerve endings in the LS increased. At the electron microsc
opic level, numerous cell bodies of the LS at birth were consistently
surrounded by Met-enk immunoreactive nerve terminals. Cells expressing
the PE gene and Met-enk-LI were also observed from E38 to E44 in the
periventricular area. Some of these cells were found double-labeled wi
th Met-enkephalin and Somatostatin antisera. The enkephalinergic syste
m of the hypothalamoseptal tract appears at early embryonic stages and
may be essential in regulating septal neuronal functions early in ges
tation. Differing ontogenic onsets of the enkephalinergic hypothalamos
eptal and periventricular-median eminence tracts suggest possible deve
lopmental and functional differences.