PMID- 25475686 OWN - NLM STAT- MEDLINE DCOM- 20150514 LR - 20191210 IS - 1872-7972 (Electronic) IS - 0304-3940 (Linking) VI - 586 DP - 2015 Jan 23 TI - Memantine exerts functional recovery by improving BDNF and GDNF expression in 3-nitropropionic acid intoxicated mice. PG - 1-7 LID - S0304-3940(14)00914-8 [pii] LID - 10.1016/j.neulet.2014.11.036 [doi] AB - Memantine (MN), a NMDA blocker is well known for its protective effect against various neurodegenerative diseases. However, its role in improving motor function and regulation of neurotrophic factors in Huntington's disease (HD) has not been studied yet. In the present study, we have investigated the effect of MN against 3-nitropropionic acid (3NP), induced motor impairment, and alterations in the expression of brain-derived neurotrophic factor (BDNF) and glial cell-derived neurotrophic factor (GDNF) in mice brain. Further, its role in mitochondrial function was assessed by measuring succinate dehydrogenase (SDH) activity. Glial fibrillary acidic protein (GFAP) and neuronal nuclei (NeuN) immunoreactivity were studied to evaluate the role of MN on glial and neuronal function. Its effect on apoptosis was adjudged by studying the expression of apoptotic markers. MN restored motor functions with an associated up-regulation in neurotrophin expression. MN also enhanced brain SDH activity and decreased glutamate content. MN ameliorated striatal neuronal loss, reduced GFAP immunoreactivity, and exhibited protective effect against neuronal apoptosis. Data from the current study demonstrated that MN exerted neuroprotective effect against 3NP induced neuropathology. Restoration of motor function by MN might be through regulation of neurotrophin expression. MN can therefore be a useful therapeutic choice in the symptomatic management of HD. CI - Copyright (c) 2014 Elsevier Ireland Ltd. All rights reserved. FAU - Ranju, Vijayan AU - Ranju V AD - Centre for Toxicology and Developmental Research, Sri Ramachandra University, Chennai 600116, India; Department of Biotechnology, Dr. M.G.R. Educational and Research Institute, Maduravoyal, Chennai 600095, India. FAU - Sathiya, Sekar AU - Sathiya S AD - Centre for Toxicology and Developmental Research, Sri Ramachandra University, Chennai 600116, India; Department of Biotechnology, Dr. M.G.R. Educational and Research Institute, Maduravoyal, Chennai 600095, India. FAU - Kalaivani, Periyathambi AU - Kalaivani P AD - Centre for Toxicology and Developmental Research, Sri Ramachandra University, Chennai 600116, India. FAU - Priya, Raju Jyothi AU - Priya RJ AD - Centre for Toxicology and Developmental Research, Sri Ramachandra University, Chennai 600116, India. FAU - Saravana Babu, Chidambaram AU - Saravana Babu C AD - Centre for Toxicology and Developmental Research, Sri Ramachandra University, Chennai 600116, India. Electronic address: ceftpublications@gmail.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20141202 PL - Ireland TA - Neurosci Lett JT - Neuroscience letters JID - 7600130 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (DNA-Binding Proteins) RN - 0 (Glial Cell Line-Derived Neurotrophic Factor) RN - 0 (Nerve Tissue Proteins) RN - 0 (NeuN protein, mouse) RN - 0 (Nitro Compounds) RN - 0 (Nuclear Proteins) RN - 0 (Propionates) RN - 0 (Receptors, N-Methyl-D-Aspartate) RN - EC 1.3.99.1 (Succinate Dehydrogenase) RN - QY4L0FOX0D (3-nitropropionic acid) RN - W8O17SJF3T (Memantine) SB - IM MH - Animals MH - Apoptosis/drug effects MH - Brain/cytology/*drug effects/metabolism MH - Brain-Derived Neurotrophic Factor/*metabolism MH - DNA-Binding Proteins MH - Glial Cell Line-Derived Neurotrophic Factor/*metabolism MH - Male MH - Memantine/*pharmacology MH - Mice, Inbred C57BL MH - Motor Activity/*drug effects MH - Nerve Tissue Proteins/metabolism MH - Nitro Compounds/*toxicity MH - Nuclear Proteins/metabolism MH - Propionates/*toxicity MH - Receptors, N-Methyl-D-Aspartate/*antagonists & inhibitors MH - Succinate Dehydrogenase/metabolism OTO - NOTNLM OT - 3NP OT - BDNF OT - GDNF OT - GFAP OT - Memantine OT - NeuN EDAT- 2014/12/06 06:00 MHDA- 2015/05/15 06:00 CRDT- 2014/12/06 06:00 PHST- 2014/09/04 00:00 [received] PHST- 2014/11/18 00:00 [revised] PHST- 2014/11/25 00:00 [accepted] PHST- 2014/12/06 06:00 [entrez] PHST- 2014/12/06 06:00 [pubmed] PHST- 2015/05/15 06:00 [medline] AID - S0304-3940(14)00914-8 [pii] AID - 10.1016/j.neulet.2014.11.036 [doi] PST - ppublish SO - Neurosci Lett. 2015 Jan 23;586:1-7. doi: 10.1016/j.neulet.2014.11.036. Epub 2014 Dec 2.