EFFECT OF NERVE GROWTH-FACTOR ON THE LESIONED SEPTOHIPPOCAMPAL CHOLINERGIC SYSTEM OF AGED RATS

被引:16
作者
HE, YS
YAO, ZB
CHEN, YC
机构
[1] Department of Anatomy, Sun Yat-sen University of Medical Sciences, Guangzhou
基金
中国国家自然科学基金;
关键词
NERVE GROWTH FACTOR; CHOLINE ACETYLTRANSFERASE; HIPPOCAMPUS; SEPTUM; BRAIN AGING; SPROUTING;
D O I
10.1016/0006-8993(91)90674-K
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nerve growth factor (NGF) was injected intraventricularly into aged (24 months) rats with unilateral lesions of the lateral fimbria. The activity of choline acetyltransferase (ChAT) was determined in the septum and hippocampus from the normal unlesioned rats, lesioned and cytochrome c-treated rats (controls), and lesioned and NGF-treated rats at different times after the lesion. NGF-injection for 15 days after the lesion resulted in an increase of the ChAT activity in both the contralateral hippocampus and the entire septum, to about 130% of that in the normal animals, but resulted in a slight increase in the ipsilateral lesioned hippocampus, when compared to the activity in the ipsilateral side of the cytochrome c-treated controls. NGF-injection for 30 days after the lesion resulted in a 48% increase of the ChAT activity in the ipsilateral hippocampus as compared to cytochrome c-treated controls, but failed to result in a significant increase in the contralateral hippocampus. These findings indicate that atrophic cholinergic neurons in aged animals are similarly responsive to NGF treatment, like these in the young animals. Moreover, these findings suggest that the responses of basal forebrain cholinergic neurons to NGF treatment varies with time after the lesion and imply that the NGF administration can promote the collateral sprouting from spared cholinergic fibers after the lesion in the aged forebrain.
引用
收藏
页码:159 / 163
页数:5
相关论文
共 28 条
[1]  
BAO Z-Q, 1982, Acta Pharmacologica Sinica, V3, P166
[2]   NGF AMPLIFIES EXPRESSION OF NGF RECEPTOR MESSENGER-RNA IN FOREBRAIN CHOLINERGIC NEURONS OF RATS [J].
CAVICCHIOLI, L ;
FLANIGAN, TP ;
VANTINI, G ;
FUSCO, M ;
POLATO, P ;
TOFFANO, G ;
WALSH, FS ;
LEON, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1989, 1 (03) :258-262
[3]   RECOVERY OF CHOLINE-ACETYLTRANSFERASE AND ACETYLCHOLINESTERASE ACTIVITIES IN THE IPSILATERAL HIPPOCAMPUS FOLLOWING UNILATERAL, PARTIAL TRANSECTION OF THE FIMBRIA IN RATS [J].
DRAVID, AR ;
VANDEUSEN, EB .
BRAIN RESEARCH, 1983, 277 (01) :169-174
[4]   RECOVERY OF ENZYME MARKERS FOR CHOLINERGIC TERMINALS IN SEPTO-TEMPORAL REGIONS OF THE HIPPOCAMPUS FOLLOWING SELECTIVE FIMBRIAL LESIONS IN ADULT-RATS [J].
DRAVID, AR ;
VANDEUSEN, EB .
BRAIN RESEARCH, 1984, 324 (01) :119-128
[5]   NERVE GROWTH-FACTOR AFFECTS UNINJURED, ADULT-RAT SEPTOHIPPOCAMPAL CHOLINERGIC NEURONS [J].
FUSCO, M ;
ODERFELDNOWAK, B ;
VANTINI, G ;
SCHIAVO, N ;
GRADKOWSKA, M ;
ZAREMBA, M ;
LEON, A .
NEUROSCIENCE, 1989, 33 (01) :47-52
[6]   CELLS OF ORIGIN OF THE VENTRAL CHOLINERGIC SEPTOHIPPOCAMPAL PATHWAY UNDERGOING COMPENSATORY COLLATERAL SPROUTING FOLLOWING FIMBRIA-FORNIX TRANSECTION [J].
GAGE, FH ;
BJORKLUND, A ;
STENEVI, U .
NEUROSCIENCE LETTERS, 1984, 44 (02) :211-216
[7]   FUNCTIONAL CORRELATES OF COMPENSATORY COLLATERAL SPROUTING BY AMINERGIC AND CHOLINERGIC AFFERENTS IN THE HIPPOCAMPAL-FORMATION [J].
GAGE, FH ;
BJORKLUND, A ;
STENEVI, U ;
DUNNETT, SB .
BRAIN RESEARCH, 1983, 268 (01) :39-47
[8]   RETROGRADE CELL CHANGES IN MEDIAL SEPTUM AND DIAGONAL BAND FOLLOWING FIMBRIA-FORNIX TRANSECTION - QUANTITATIVE TEMPORAL ANALYSIS [J].
GAGE, FH ;
WICTORIN, K ;
FISCHER, W ;
WILLIAMS, LR ;
VARON, S ;
BJORKLUND, A .
NEUROSCIENCE, 1986, 19 (01) :241-255
[9]   REINNERVATION OF THE PARTIALLY DEAFFERENTED HIPPOCAMPUS BY COMPENSATORY COLLATERAL SPROUTING FROM SPARED CHOLINERGIC AND NORADRENERGIC AFFERENTS [J].
GAGE, FH ;
BJORKLUND, A ;
STENEVI, U .
BRAIN RESEARCH, 1983, 268 (01) :27-37
[10]   TIME COURSE OF THE ELEVATION OF NERVE GROWTH-FACTOR (NGF) CONTENT IN THE HIPPOCAMPUS AND SEPTUM FOLLOWING LESIONS OF THE SEPTOHIPPOCAMPAL PATHWAY IN RATS [J].
GASSER, UE ;
WESKAMP, G ;
OTTEN, U ;
DRAVID, AR .
BRAIN RESEARCH, 1986, 376 (02) :351-356