Datumetine exposure alters hippocampal neurotransmitters system in C57BL/6 mice

被引:1
作者
Ishola, Azeez Olakunle [1 ,2 ]
Imam, Aminu [1 ]
Ajao, Moyosore Salihu [1 ]
机构
[1] Univ Ilorin, Dept Anat, Ilorin, Nigeria
[2] Afe Babalola Univ, Dept Anat, Ado Ekiti, Nigeria
关键词
Datumetine; NMDARl excitotoxicity; NMDA RECEPTOR ACTIVATION; CENTRAL-NERVOUS-SYSTEM; HUNTINGTONS-DISEASE; SYNAPTIC VESICLES; PYRAMIDAL NEURONS; DOPAMINE; SEROTONIN; TRANSMISSION; INVOLVEMENT; MODULATION;
D O I
10.1080/01480545.2020.1776315
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Our previous study showed that datumetine modulates NMDAR activity with long term exposure leading to memory deficit and altered NMDAR signaling. We aim to explore the neurotransmitters perturbations of acute datumetine-NMDAR interaction. Fifteen C57/BL6 mice were used for the study, they are divided into three groups of 5 animals each. Animals were administered DMSO (DMSO/Control), 0.25 mg/kg body weight of datumetine (0.25 Datumetine) and 1 mg/kg bodyweight of datumetine (1.0 Datumetine) intraperitoneally for 14 days. At the end of treatment, animals were euthanized in isofluorane chamber, perfused transcardially with 1XPBS followed by PFA. Immunofluorescence procedure was done to check the distribution of neurons, astrocytes, microglia and major neuronal subtypes in the hippocampus. Expansion and electron microscopy techniques were used to assess the condition of the synapses. Quantitative data were expressed as mean +/- SEM and analyzed using ANOVA with Tukey post hoc usingp < 0.05 as significant. Datumetine increased the expression of CD11b, GFAP, vGlut1, GABA, CHRNA7 and TH while expression of TrPH and NeuN were reduced in the hippocampus compared to control animals. Synaptic loss was evident in datumetine exposed animals with reduced synaptic vesicles accompanied by a thickness of postsynaptic density than that of control animals. This study concludes that acute datumetine exposure alters hippocampal neurotransmitter systems.
引用
收藏
页码:785 / 798
页数:14
相关论文
共 86 条
[1]   Postsynaptic Complexin Controls AMPA Receptor Exocytosis during LTP [J].
Ahmad, Mohiuddin ;
Polepalli, Jai S. ;
Goswami, Debanjan ;
Yang, Xiaofei ;
Kaeser-Woo, Yea Jin ;
Suedhof, Thomas C. ;
Malenka, Robert C. .
NEURON, 2012, 73 (02) :260-267
[2]   FUNCTIONAL INTERACTIONS BETWEEN GLUTAMATE AND DOPAMINE IN THE RAT STRIATUM [J].
AMALRIC, M ;
OUAGAZZAL, A ;
BAUNEZ, C ;
NIEOULLON, A .
NEUROCHEMISTRY INTERNATIONAL, 1994, 25 (02) :123-131
[3]  
[Anonymous], 2017, Drugs Monitoring Platform
[4]  
[Anonymous], 2018, World. Drug Report -Executive Summary-Conclusions and Policy Implications
[5]   Removing Brakes on Adult Brain Plasticity: From Molecular to Behavioral Interventions [J].
Bavelier, Daphne ;
Levi, Dennis M. ;
Li, Roger W. ;
Dan, Yang ;
Hensch, Takao K. .
JOURNAL OF NEUROSCIENCE, 2010, 30 (45) :14964-14971
[6]   Modulation of defensive behavior by periaqueductal gray NMDA/glycine-B receptor [J].
Carobrez, AP ;
Teixeira, KV ;
Graeff, FG .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2001, 25 (7-8) :697-709
[7]   Astrocytes: Key Regulators of Neuroinflammation [J].
Colombo, Emanuela ;
Farina, Cinthia .
TRENDS IN IMMUNOLOGY, 2016, 37 (09) :608-620
[8]  
D'Souza Manoranjan S, 2011, Addict Sci Clin Pract, V6, P4
[9]   Homeostatic Control of Presynaptic Neurotransmitter Release [J].
Davis, Graeme W. ;
Mueller, Martin .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 77, 2015, 77 :251-270
[10]   NMDA-coupled periaqueductal gray glycine receptors modulate anxioselective drug effects on plus-maze performance [J].
De Souza, MM ;
Schenberg, LC ;
Carobrez, ADP .
BEHAVIOURAL BRAIN RESEARCH, 1998, 90 (02) :157-165