DEVELOPMENTAL EXPRESSION OF SOMATOSTATIN IN MOUSE-BRAIN .1. IMMUNOCYTOCHEMICAL STUDIES

被引:50
作者
FORLONI, G
HOHMANN, C
COYLE, JT
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT PSYCHIAT,MEYER 4-163,600 N WOLFE ST,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT PHARMACOL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROSCI,BALTIMORE,MD 21205
[4] MARIO NEGRI INST PHARMACOL RES,I-20157 MILAN,ITALY
来源
DEVELOPMENTAL BRAIN RESEARCH | 1990年 / 53卷 / 01期
关键词
Basal forebrain; Cerebral cortex; Cholinergic afferent; Somatostatin;
D O I
10.1016/0165-3806(90)90120-N
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The postnatal development of the distribution of somatostatin immunoreactive (SOMLI) neurons and fibers in the forebrain of the Balb/C mouse and their relationship to cholinergic afferents have been examined. SOMLI was first discernable in the hypothalamus on postnatal day (PND) 3 and increased gradually to reach adult levels by PND 30. In the limbic system, SOMLI is detectable at birth. In all other structures of the forebrain, SOMLI could be observed by PND 3 but the distribution, density and morphology of the immunoreactive neurons evolved over the following 2-3 weeks. In general, SOMLI cells and fibers increased for 1-3 weeks after their initial appearance and subsequently declined to achieve adult levels. The distribution pattern of SOMLI elements in adult mouse brain was similar to previous reports in rat with a few notable differences in thalamus, olfactory structures and, to a lesser degree, cortex and hippocampus. The temporal pattern of SOMLI expression in extrahypothalamus forebrain regions, during development, suggests a role of this peptide in differentiation and synapse formation. Such an hypothesis receives further support from neonatal lesions of the basal forebrain which resulted in transient cortical cholinergic deafferentation, a delay of cortical differentiation and a transient increase in the number of SOMLI cells in cortex. © 1990.
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页码:6 / 25
页数:20
相关论文
共 91 条
[61]  
NAUS CCG, 1988, J COMP NEUROL, V269, P446
[62]  
NOBAU F, 1985, DEV BRAIN RES, V20, P296
[63]   BRAIN-DEVELOPMENT IN DWARF MICE [J].
NOGUCHI, T .
PROGRESS IN NEUROBIOLOGY, 1988, 31 (02) :149-170
[64]  
OERTEL WH, 1983, J NEUROSCI, V3, P1322
[65]   GENETIC-MAPPING AND ANALYSIS OF SOMATOSTATIN EXPRESSION IN SNELL DWARF MICE [J].
OHARA, BF ;
BENDOTTI, C ;
REEVES, RH ;
OSTERGRANITE, ML ;
COYLE, JT ;
GEARHART, JD .
MOLECULAR BRAIN RESEARCH, 1988, 4 (04) :283-292
[66]   NEUROCHEMICAL CHANGES IN MURINE TRISOMY 16 - DELAY IN CHOLINERGIC AND CATECHOLAMINERGIC SYSTEMS [J].
OZAND, PT ;
HAWKINS, RL ;
COLLINS, RM ;
REED, WD ;
BAAB, PJ ;
OSTERGRANITE, ML .
JOURNAL OF NEUROCHEMISTRY, 1984, 43 (02) :401-408
[67]  
Palkovits M., 1985, HDB CHEM NEUROANAT 1, V4, P1
[68]  
PATEL YC, 1978, CLIN RES, V26, pA845
[69]  
PIEROTTI AR, 1983, NEUROSCI LETT, V63, P243
[70]   N-TERMINALLY EXTENDED SOMATOSTATIN - PRIMARY STRUCTURE OF SOMATOSTATIN-28 [J].
PRADAYROL, L ;
JORNVALL, H ;
MUTT, V ;
RIBET, A .
FEBS LETTERS, 1980, 109 (01) :55-58