PMID- 30572228 OWN - NLM STAT- MEDLINE DCOM- 20190403 LR - 20200106 IS - 2299-5684 (Electronic) IS - 1734-1140 (Linking) VI - 71 IP - 1 DP - 2019 Feb TI - Ascorbic acid attenuates cognitive impairment and brain oxidative stress in ovariectomized mice. PG - 133-138 LID - S1734-1140(18)30204-4 [pii] LID - 10.1016/j.pharep.2018.10.001 [doi] AB - BACKGROUND: Menopause is associated with increased oxidative stress and memory impairment. Based on the antioxidant property of ascorbic acid (AA), It's effect on cognitive function, the serum level of the brain-derived neurotrophic factor (BDNF) and the activity of antioxidant enzymes within the brain in ovariectomized (OVX) mice was investigated. METHODS: AA (100, 300 and 500 mg/kg), was orally administrated per day in OVX mice for 30 days. Tactile learning and working memory were evaluated by the novel object recognition task and T-maze continuous alternation task, respectively. The levels of serum BDNF were measured and animals' brains were analyzed for the superoxide dismutase (SOD) and glutathione peroxidase (GPx) activity. RESULTS: AA prevented from the deleterious effects of ovariectomy on learning memory (300 and 500 mg/kg) and working memory (100 and 500 mg/kg). The serum BDNF level was also increased in OVX animals treated with AA (100 and 500 mg/kg). Furthermore, AA (500 mg/kg) increased the SOD and GPx activity in the brain of OVX animals. CONCLUSIONS: Collectively, the results of the present study suggest that AA might be an appropriate choice in loss or reduction of estradiol for the amelioration of cognitive impairment. CI - Copyright (c) 2018 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier B.V. All rights reserved. FAU - Delrobaei, Fatemeh AU - Delrobaei F AD - Student Research Committee, Rafsanjan University of Medical Sciences, Rafsanjan, Iran. FAU - Fatemi, Iman AU - Fatemi I AD - Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran; Department of Physiology and Pharmacology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran. FAU - Shamsizadeh, Ali AU - Shamsizadeh A AD - Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran; Department of Physiology and Pharmacology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran. FAU - Allahtavakoli, Mohammad AU - Allahtavakoli M AD - Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran; Department of Physiology and Pharmacology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran. Electronic address: m_alahtavakoli@rums.ac.ir. LA - eng PT - Journal Article DEP - 20181003 PL - Switzerland TA - Pharmacol Rep JT - Pharmacological reports : PR JID - 101234999 RN - 0 (Antioxidants) RN - 0 (Bdnf protein, mouse) RN - 0 (Brain-Derived Neurotrophic Factor) RN - EC 1.11.1.9 (Glutathione Peroxidase) RN - EC 1.15.1.1 (Superoxide Dismutase) RN - PQ6CK8PD0R (Ascorbic Acid) SB - IM MH - Animals MH - Antioxidants/*pharmacology MH - Ascorbic Acid/*pharmacology MH - Behavior, Animal/*drug effects MH - Brain/*drug effects/metabolism/physiopathology MH - Brain-Derived Neurotrophic Factor/blood MH - Cognition/*drug effects MH - Cognition Disorders/metabolism/physiopathology/*prevention & control/psychology MH - Disease Models, Animal MH - Female MH - Glutathione Peroxidase/metabolism MH - Maze Learning/drug effects MH - Memory, Short-Term/drug effects MH - *Menopause MH - Mice MH - *Ovariectomy MH - Oxidative Stress/*drug effects MH - Recognition, Psychology/drug effects MH - Superoxide Dismutase/metabolism OTO - NOTNLM OT - Ascorbic acid OT - Learning and memory OT - Ovariectomy OT - Oxidative stress EDAT- 2018/12/21 06:00 MHDA- 2019/04/04 06:00 CRDT- 2018/12/21 06:00 PHST- 2018/04/16 00:00 [received] PHST- 2018/09/15 00:00 [revised] PHST- 2018/10/02 00:00 [accepted] PHST- 2018/12/21 06:00 [pubmed] PHST- 2019/04/04 06:00 [medline] PHST- 2018/12/21 06:00 [entrez] AID - S1734-1140(18)30204-4 [pii] AID - 10.1016/j.pharep.2018.10.001 [doi] PST - ppublish SO - Pharmacol Rep. 2019 Feb;71(1):133-138. doi: 10.1016/j.pharep.2018.10.001. Epub 2018 Oct 3.