Moderate lesion of the rat cholinergic septohippocampal pathway increases hippocampal nerve growth factor synthesis: Evidence for long-term compensatory changes?

被引:27
作者
Hellweg, R
Humpel, C
Lowe, A
Hortnagl, H
机构
[1] HUMBOLDT UNIV BERLIN, FAC MED CHARITE, INST PHARMACOL & TOXICOL, D-10098 BERLIN, GERMANY
[2] FREE UNIV BERLIN, DEPT PSYCHIAT, BERLIN, GERMANY
[3] UNIV INNSBRUCK, DEPT PSYCHIAT, A-6020 INNSBRUCK, AUSTRIA
[4] UNIV VIENNA, INST BIOCHEM PHARMACOL, VIENNA, AUSTRIA
来源
MOLECULAR BRAIN RESEARCH | 1997年 / 45卷 / 01期
关键词
ethylcholine aziridinium (AF64A); brain-derived neurotrophic factor (BDNF); cholinergic basal forebrain; neurotrophin-3 (NT-3); nerve growth factor (NGF); septohippocampal pathway; choline acetyltransferase (ChAT);
D O I
10.1016/S0169-328X(96)00310-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Moderate lesions of the septohippocampal pathway by intraventricular infusions of ethylcholine aziridinium (AF64A) induced a dose-dependent decrease of hippocampal choline acetyltransferase (ChAT) activity, which partially recovered between 1 and 5 weeks after treatment. The cholinergic deficit was associated with an increase in nerve growth factor (NGF) mRNA only within the hippocampal dentate gyms and hilus by maximally 51% and 111% 3 and 7 weeks after AF64A treatment, respectively, whereas no changes in brain-derived neurotrophic factor- and neurotrophin-3 mRNA were observed. The content of NGF protein transiently increased in the ventral part of the hippocampus 3 weeks after AF64A infusion but returned to control levels at 5 weeks. At that time, however, NGF content as well as ChAT activity were significantly increased in the septum, suggesting an increased utilization of NGF by the remaining cholinergic neurons. Thus, the present data provide correlative evidence for a critical role of endogenous NGF in neuroregeneration and plasticity of the cholinergic basal forebrain in case of incipient damage.
引用
收藏
页码:177 / 181
页数:5
相关论文
共 25 条
[1]   DEGENERATION OF RAT CHOLINERGIC BASAL FOREBRAIN NEURONS AND REACTIVE CHANGES IN NERVE GROWTH-FACTOR EXPRESSION AFTER CHRONIC NEUROTOXIC INJURY .2. REACTIVE EXPRESSION OF THE NERVE GROWTH-FACTOR GENE IN ASTROCYTES [J].
ARENDT, T ;
BRUCKNER, MK ;
KRELL, T ;
PAGLIUSI, S ;
KRUSKA, L ;
HEUMANN, R .
NEUROSCIENCE, 1995, 65 (03) :647-659
[2]   DEGENERATION OF RAT CHOLINERGIC BASAL FOREBRAIN NEURONS AND REACTIVE CHANGES IN NERVE GROWTH-FACTOR EXPRESSION AFTER CHRONIC NEUROTOXIC INJURY .1. DEGENERATION AND PLASTIC RESPONSE OF BASAL FOREBRAIN NEURONS [J].
ARENDT, T ;
BRUCKNER, MK ;
PAGLIUSI, S ;
KRELL, T .
NEUROSCIENCE, 1995, 65 (03) :633-645
[3]   DEVELOPMENTAL-CHANGES OF NERVE GROWTH-FACTOR AND ITS MESSENGER-RNA IN THE RAT HIPPOCAMPUS - COMPARISON WITH CHOLINE-ACETYLTRANSFERASE [J].
AUBURGER, G ;
HEUMANN, R ;
HELLWEG, R ;
KORSCHING, S ;
THOENEN, H .
DEVELOPMENTAL BIOLOGY, 1987, 120 (02) :322-328
[4]   REGULATION OF NEUROTROPHIN AND TRKA, TRKB AND TRKC TYROSINE KINASE RECEPTOR MESSENGER-RNA EXPRESSION IN KINDLING [J].
BENGZON, J ;
KOKAIA, Z ;
ERNFORS, P ;
KOKAIA, M ;
LEANZA, G ;
NILSSON, OG ;
PERSSON, H ;
LINDVALL, O .
NEUROSCIENCE, 1993, 53 (02) :433-446
[5]   FUNCTION AND EVOLUTION IN THE NGF FAMILY AND ITS RECEPTORS [J].
EBENDAL, T .
JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 32 (04) :461-470
[6]  
ELTAMER A, 1992, NEUROPHARMACOLOGY, V31, P397
[7]   NERVE GROWTH-FACTOR MESSENGER-RNA IN PERIPHERAL AND CENTRAL RAT-TISSUES AND IN THE HUMAN CENTRAL-NERVOUS-SYSTEM - LESION EFFECTS IN THE RAT-BRAIN AND LEVELS IN ALZHEIMERS-DISEASE [J].
GOEDERT, M ;
FINE, A ;
HUNT, SP ;
ULLRICH, A .
MOLECULAR BRAIN RESEARCH, 1986, 1 (01) :85-92
[8]   NGF level in the rat sciatic nerve is decreased after long-term consumption of ethanol [J].
Hellweg, R ;
Baethge, C ;
Hartung, HD ;
Bruckner, MK ;
Arendt, T .
NEUROREPORT, 1996, 7 (03) :777-780
[9]  
HORTNAGL H, 1993, J NEUROSCI, V13, P2939
[10]  
HORTNAGL H, IN RPESS BRAIN RES B