Williams J H, Meara J R, Azmitia E C
Department of Anatomy, University of Cambridge, U.K.
Behav Brain Res. 1990 Oct 30;40(1):37-44. doi: 10.1016/0166-4328(90)90040-l.
Microinjections of 5,7-dihydroxytryptamine (5,7-DHT) into the fornix-fimbria (FF) reduced dorsal hippocampal [3]5-HT uptake to 40% of control levels. The FF 5,7-DHT lesions increased nocturnal activity in photocell cages, but reduced central ambulation in diurnal open field tests. The lesions also disrupted both habituation of rearing across days in the open field and alternation in a Y-maze. Hence FF-derived hippocampal 5-HT terminals participate in controlling activity, but their role depends on the test apparatus and procedures.
向穹窿-海马伞(FF)微量注射5,7-二羟基色胺(5,7-DHT)可使背侧海马[3]5-羟色胺摄取减少至对照水平的40%。FF 5,7-DHT损伤增加了光电管笼中的夜间活动,但在白天旷场试验中减少了中央走动。这些损伤还破坏了旷场中数天内竖毛习惯化以及Y迷宫中的交替行为。因此,源自FF的海马5-羟色胺终末参与活动控制,但其作用取决于测试装置和程序。