PMID- 8366347 OWN - NLM STAT- MEDLINE DCOM- 19931005 LR - 20191101 IS - 0270-6474 (Print) IS - 1529-2401 (Electronic) IS - 0270-6474 (Linking) VI - 13 IP - 9 DP - 1993 Sep TI - Cholinergic regulation of brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) but not neurotrophin-3 (NT-3) mRNA levels in the developing rat hippocampus. PG - 3818-26 AB - In previous experiments it has been demonstrated that the synthesis of BDNF (brain-derived neurotrophic factor) and NGF in neurons of the hippocampus is regulated by neuronal activity. The glutamate system is predominantly responsible for upregulation and the GABAergic system for downregulation both in vitro and in vivo (Zafra et al., 1990, 1991). The aim of the present study is to examine the extent to which the cholinergic system is also involved in the regulation of NGF and BDNF mRNA and whether the regulatory contribution of the cholinergic system changes during development. Partial transection of the fimbria fornix bundle in the second postnatal week resulted in a reduction of BDNF and NGF mRNA levels in the hippocampus, suggesting that septal cholinergic input is involved in the regulation of hippocampal BDNF and NGF mRNA levels. Because the fimbria fornix bundle also contains fibers other than cholinergic ones, we further evaluated the importance of the cholinergic influence by injecting pilocarpine, a muscarinic agonist. Pilocarpine markedly increased hippocampal BDNF and NGF mRNA levels in both early postnatal and adult rats. In situ hybridization experiments demonstrated that pilocarpine led to an increase in BDNF expression in the CA1-CA4 regions of the hippocampus and in the dentate gyrus. However, pilocarpine increased NGF mRNA only in those neurons of the dentate gyrus and CA1-CA4 regions that also expressed NGF mRNA in the controls.(ABSTRACT TRUNCATED AT 250 WORDS) FAU - da Penha Berzaghi, M AU - da Penha Berzaghi M AD - Department of Neurochemistry, Max Planck Institute for Psychiatry, Planegg Martinsried, Germany. FAU - Cooper, J AU - Cooper J FAU - Castren, E AU - Castren E FAU - Zafra, F AU - Zafra F FAU - Sofroniew, M AU - Sofroniew M FAU - Thoenen, H AU - Thoenen H FAU - Lindholm, D AU - Lindholm D LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Neurosci JT - The Journal of neuroscience : the official journal of the Society for Neuroscience JID - 8102140 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Nerve Growth Factors) RN - 0 (Nerve Tissue Proteins) RN - 0 (Neurotrophin 3) RN - 0 (RNA Probes) RN - 0 (RNA, Messenger) RN - 01MI4Q9DI3 (Pilocarpine) RN - 6384-92-5 (N-Methylaspartate) RN - 6LR8C1B66Q (Dizocilpine Maleate) RN - DL48G20X8X (Scopolamine) RN - SIV03811UC (Kainic Acid) SB - IM MH - Aging/*metabolism MH - Animals MH - Animals, Newborn MH - Brain-Derived Neurotrophic Factor MH - Cerebral Ventricles/drug effects/*physiology MH - Dizocilpine Maleate/pharmacology MH - Gene Expression/*drug effects MH - Hippocampus/drug effects/growth & development/*metabolism MH - In Situ Hybridization MH - Injections, Intraventricular MH - Kainic Acid/*pharmacology MH - Male MH - N-Methylaspartate/administration & dosage/pharmacology MH - Nerve Growth Factors/*biosynthesis MH - Nerve Tissue Proteins/*biosynthesis MH - Neurons/drug effects/*metabolism/physiology MH - Neurotrophin 3 MH - Pilocarpine/*pharmacology MH - Pyramidal Tracts/drug effects/growth & development/metabolism MH - RNA Probes MH - RNA, Messenger/*metabolism MH - Rats MH - Rats, Wistar MH - Scopolamine/pharmacology MH - Transcription, Genetic/drug effects PMC - PMC6576436 EDAT- 1993/09/01 00:00 MHDA- 1993/09/01 00:01 PMCR- 1994/03/01 CRDT- 1993/09/01 00:00 PHST- 1993/09/01 00:00 [pubmed] PHST- 1993/09/01 00:01 [medline] PHST- 1993/09/01 00:00 [entrez] PHST- 1994/03/01 00:00 [pmc-release] AID - 10.1523/JNEUROSCI.13-09-03818.1993 [doi] PST - ppublish SO - J Neurosci. 1993 Sep;13(9):3818-26. doi: 10.1523/JNEUROSCI.13-09-03818.1993.