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
[51]   Abnormal reaction to central nervous system injury in mice lacking glial fibrillary acidic protein and vimentin [J].
Pekny, M ;
Johansson, CB ;
Eliasson, C ;
Stakeberg, J ;
Wallén, Å ;
Perlmann, T ;
Lendahl, U ;
Betsholtz, C ;
Berthold, CH ;
Frisén, J .
JOURNAL OF CELL BIOLOGY, 1999, 145 (03) :503-514
[52]   Presynaptic homeostasis at CNS nerve terminals compensates for lack of a key Ca2+ entry pathway [J].
Piedras-Rentería, ES ;
Pyle, JL ;
Diehn, M ;
Glickfeld, LL ;
Harata, NC ;
Cao, YQ ;
Kavalali, ET ;
Brown, PO ;
Tsien, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (10) :3609-3614
[53]   Glial-neuronal signaling mechanisms underlying the neuroinflammatory effects of manganese [J].
Popichak, Katriana A. ;
Afzali, Maryam F. ;
Kirkley, Kelly S. ;
Tjalkens, Ronald B. .
JOURNAL OF NEUROINFLAMMATION, 2018, 15
[54]  
Prasad C. S., 2005, Indian Journal of Dairy Science, V58, P109
[55]  
Reimer R.J., 2014, KEY MOL VESICULAR NE, DOI 10.1016/B978-0-12-801238-3.04801-7
[56]  
Reimer R.J., 2009, ENCY NEUROSCIENCE
[57]   Vesicular neurotransmitter transport and the presynaptic regulation of quantal size [J].
Reimer, RJ ;
Fon, EA ;
Edwards, RH .
CURRENT OPINION IN NEUROBIOLOGY, 1998, 8 (03) :405-412
[58]  
Rossi D., 2004, EXCITOTOXICITY NEURO
[59]   Specific coupling of NMDA receptor activation to nitric oxide neurotoxicity by PSD-95 protein [J].
Sattler, R ;
Xiang, ZG ;
Lu, WY ;
Hafner, M ;
MacDonald, JF ;
Tymianski, M .
SCIENCE, 1999, 284 (5421) :1845-1848
[60]   ANXIOGENIC-LIKE EFFECT OF GLYCINE AND D-SERINE MICROINJECTED INTO DORSAL PERIAQUEDUCTAL GRAY-MATTER OF RATS [J].
SCHMITT, ML ;
COELHO, W ;
LOPESDESOUZA, AS ;
GUIMARAES, FS ;
CAROBREZ, AP .
NEUROSCIENCE LETTERS, 1995, 189 (02) :93-96