Ameliorative effect of metformin on cyclophosphamide-induced memory impairment in mice

被引:35
作者
Alhowail, A. H. [1 ]
Chigurupati, S. [2 ]
Sajid, S. [1 ]
Mani, V. [1 ]
机构
[1] Qassim Univ, Coll Pharm, Dept Pharmacol & Toxicol, Al Qassim, Saudi Arabia
[2] Qassim Univ, Dept Med Chem & Pharmacognosy, Coll Pharm, Buraydah, Saudi Arabia
关键词
Metformin; Chemobrain; Cyclophosphamide; Cognitive impairment; COGNITIVE IMPAIRMENT; CHEMOTHERAPY; PATHWAYS;
D O I
10.26355/eurrev_201911_19460
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
-OBJECTIVE: Cyclophosphamide (CYP) is a chemotherapeutic agent that is widely used as an adjuvant cancer treatment. Unfortunately, this drug is associated with secondary side effects, including cognitive impairment up to 70% of cancer survivors. The mechanism of this memory impairment is unclear. Thus, to understand the cognitive impairments caused by this chemotherapeutic agent, a clinically relevant dose to cancer treatment was used in mice to establish the chemobrain models, and the spatial memory of these mice was assessed using multiple behavior tests. In addition, metformin (MET) is widely used as an anti-diabetic drug and protects against oxidative stress and hepatotoxicity. Thus, this study tested the protective effects of MET in the chemobrain models. MATERIALS AND METHODS: Four groups of mice, which weighed about 18-30 g, were collected and divided into 4 groups: control, CYP, MET, and CYP+MET groups. A 100 mg/kg dose of CYP was administered intraperitoneal (on alternate days) for a total of 4 doses. MET was dissolved in the mice's drinking water bottles at a 5 mg/ml concentration from day zero to the end of the treatment period. The mice's memory was tested using hippocampal-dependent tests, including the Y-maze, novel object recognition, and elevated plus maze tests. These tests were performed for three consecutive days after 24 h of the last dose of CYP. RESULTS: The mice treated with CYP exhibited a decline in memory function in all the behavioral test studies, and this decline was significant in the Y-maze test. However, this decline was rescued by MET administration. CONCLUSIONS: The clinically relevant model suggests that CYP treatment causes a decline in mice models spatial memory that might be improved by MET administration.
引用
收藏
页码:9660 / 9666
页数:7
相关论文
共 27 条
  • [1] Metformin Eased Cognitive Impairment Induced by Chronic L-methionine Administration: Potential Role of Oxidative Stress
    Alzoubi, Karem. H.
    Khabour, Omar. F.
    Al-Azzam, Sayer I.
    Tashtoush, Murad H.
    Mhaidat, Nizar M.
    [J]. CURRENT NEUROPHARMACOLOGY, 2014, 12 (02) : 186 - 192
  • [2] The novel object recognition memory: neurobiology, test procedure, and its modifications
    Antunes, M.
    Biala, G.
    [J]. COGNITIVE PROCESSING, 2012, 13 (02) : 93 - 110
  • [3] The Rodent Hippocampus Is Essential for Nonspatial Object Memory
    Cohen, Sarah J.
    Munchow, Alcira H.
    Rios, Lisa M.
    Zhang, Gongliang
    Asgeirsdottir, Herborg N.
    Stackman, Robert W., Jr.
    [J]. CURRENT BIOLOGY, 2013, 23 (17) : 1685 - 1690
  • [4] Colvin OM, 1999, CURR PHARM DESIGN, V5, P555
  • [5] Elazzazy Shereen, 2014, Onco Targets Ther, V7, P1641, DOI 10.2147/OTT.S66350
  • [6] Metformin Improves Learning and Memory in the SAMP8 Mouse Model of Alzheimer's Disease
    Farr, Susan A.
    Roesler, Elizabeth
    Niehoff, Michael L.
    Roby, Deborah A.
    McKee, Alexis
    Morley, John E.
    [J]. JOURNAL OF ALZHEIMERS DISEASE, 2019, 68 (04) : 1699 - 1710
  • [7] Metformin protects the brain against ischemia/reperfusion injury through PI3K/Akt1/JNK3 signaling pathways in rats
    Ge, Xu-Hua
    Zhu, Guo-Ji
    Geng, De-Qin
    Zhang, Han-Zhi
    He, Juan-Mei
    Guo, Ai-Zhen
    Ma, Lin-Lin
    Yu, De-Hua
    [J]. PHYSIOLOGY & BEHAVIOR, 2017, 170 : 115 - 123
  • [8] Chemotherapy improves survival and quality of life in advanced pancreatic and biliary cancer
    Glimelius, B
    Hoffman, K
    Sjoden, PO
    Jacobsson, G
    Sellstrom, H
    Enander, LK
    Linne, T
    Svensson, C
    [J]. ANNALS OF ONCOLOGY, 1996, 7 (06) : 593 - 600
  • [9] Janjua A, 2014, PAK J PHARM SCI, V27, P1863
  • [10] Komada Munekazu, 2008, J Vis Exp, DOI 10.3791/1088