Upregulation of BDNF mRNA and trkB mRNA in the Nigrostriatal System and in the Lesion Site Following Unilateral Transection of the Medial Forebrain Bundle

• Published in: Experimental neurology 2000-01, Vol.161 (1), p.38-48
• Main Authors: Venero, J.L., Vizuete, M.L., Revuelta, M., Vargas, C., Cano, J., Machado, A.
• Format: Article
• Language: English
• Subjects: Animals; Axons - chemistry; Axons - metabolism; Axotomy; Biological and medical sciences; brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - genetics; Brain-Derived Neurotrophic Factor - metabolism; Corpus Striatum - chemistry; Corpus Striatum - metabolism; Dopamine - metabolism; Gene Expression - physiology; Image Processing, Computer-Assisted; In Situ Hybridization; Injuries of the orbit. Foreign bodies of the eye. Diseases due to physical agents; injury; medial forebrain bundle; Medial Forebrain Bundle - physiology; Medial Forebrain Bundle - surgery; Medical sciences; MFB; neurotrophins; rat; Rats; Rats, Wistar; Receptor, trkB - genetics; Receptor, trkB - metabolism; RNA, Messenger - metabolism; striatum; substantia nigra; Substantia Nigra - chemistry; Substantia Nigra - metabolism; Traumas. Diseases due to physical agents; trkB; Up-Regulation - physiology
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1006/exnr.1999.7243

We have performed unilateral transection of the medial forebrain bundle (MFB) and studied BDNF mRNA and trkB mRNA levels at different postlesion times in the nigrostriatal system by means of in situ hybridization. BDNF mRNA levels were transiently induced in the substantia nigra pars compacta at 1 day postaxotomy. The disposition of BDNF mRNA expressing cells at this postlesion time in substantia nigra mimicked that of the dopaminergic neurons expressing the mRNA for the dopamine transporter. TrkB mRNA levels remained unaltered in the ventral mesencephalon at the different postlesion times examined—1 to 14 days. In contrast, trkB mRNA levels were significantly induced in the striatum at the longer postlesion time examined—14 days—when all neurodegenerative events are completed. It is becoming apparent that nigral BDNF mRNA levels are anterogradely transported to its target tissue in striatum. However, following axotomy, the lesion site represents a second potential target for BDNF action. Consequently, we also analyzed the pattern of mRNA expression for BDNF and trkB at the lesion site where dopaminergic axons are disconnected. There, we found notable inductions of both BDNF mRNA and trkB mRNA levels at 4 days postaxotomy. BDNF mRNA expressing cells were confined at the site of axotomy, which coincided precisely to that showing induction of trkB mRNA. Altogether, our results anticipate promising trophic roles of BNDF in the injured nigrostriatal system.