Martin-Iverson M T, Todd K G, Altar C A
Department of Psychiatry, Walter Mackenzie Health Sciences Centre, University of Alberta, Edmonton, Canada.
J Neurosci. 1994 Mar;14(3 Pt 1):1262-70. doi: 10.1523/JNEUROSCI.14-03-01262.1994.
To investigate behavioral and neurochemical effects of neurotrophic factors in vivo, rats received continuous 14 d infusions of either brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), or vehicle unilaterally into the substantia nigra. BDNF and NT-3 decreased body weights, an effect that was sustained over the infusion period. BDNF elevated daytime and nocturnal locomotion compared with infusions of vehicle or NT-3. At 2 weeks, a systemic injection of amphetamine (1.5 mg/kg, s.c.) increased the frequencies and durations of rotations contraversive to the side of BDNF and NT-3 infusions. Both factors attenuated amphetamine-induced locomotion without affecting amphetamine-induced stereotyped behaviors such as sniffing, head movements, and snout contact with cage surfaces. Only BDNF induced backward walking, and this response was augmented by amphetamine. BDNF, but not NT-3, increased dopamine turnover in the striatum ipsilateral to the infusion relative to the contralateral striatum. Both trophic factors decreased dopamine turnover in the infused substantia nigra relative to the contralateral hemisphere and increased 5-HT turnover in the striatum of both sides. Contraversive rotations were positively correlated with dopamine content decreases and 5-HT turnover increases in the striatum ipsilateral to the infused substantia nigra. Backward walking was positively correlated with increased dopamine and 5-HT turnover in the striatum of the infused hemisphere. Supranigral infusions of BDNF and NT-3 alter circadian rhythms, spontaneous motor activity, body weights, and amphetamine-induced behaviors including locomotion and contraversive rotations. These behavioral effects of the neurotrophins are consistent with a concomitant activation of dopamine and 5-HT systems in vivo.
为了研究神经营养因子在体内的行为和神经化学作用,大鼠连续14天单侧向黑质内注射脑源性神经营养因子(BDNF)、神经营养素-3(NT-3)或溶剂。BDNF和NT-3使体重下降,这种作用在注射期间持续存在。与注射溶剂或NT-3相比,BDNF提高了白天和夜间的运动能力。在2周时,皮下注射苯丙胺(1.5mg/kg)增加了与BDNF和NT-3注射侧相反方向的旋转频率和持续时间。两种因子都减弱了苯丙胺诱导的运动,而不影响苯丙胺诱导的刻板行为,如嗅探、头部运动和口鼻与笼壁的接触。只有BDNF诱导向后行走,并且这种反应被苯丙胺增强。与对侧纹状体相比,BDNF而非NT-3增加了注射侧纹状体中的多巴胺周转率。相对于对侧半球,两种营养因子都降低了注射侧黑质中的多巴胺周转率,并增加了两侧纹状体中的5-羟色胺周转率。与注射侧黑质同侧纹状体中的多巴胺含量降低和5-羟色胺周转率增加呈正相关。向后行走与注射半球纹状体中多巴胺和5-羟色胺周转率增加呈正相关。黑质上注射BDNF和NT-3会改变昼夜节律、自发运动活动、体重以及苯丙胺诱导的行为,包括运动和反向旋转。神经营养因子的这些行为效应与体内多巴胺和5-羟色胺系统的同时激活是一致的。