Abolfazl Rad; Seyyed Mehdi Beheshti nasr; Hasan Ramshini
Volume 21, Issue 5 , September and October 2014, , Pages 711-718
Abstract
Background and purpose: Minocycline has got the anti-inflammatory and neuroprotective effects. Considering the interaction between cell death and seizure, and on the other hand, Kindling which increases expression NMDA receptors in brain, the aim of this study is to investigate the effect of minocycline ...
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Background and purpose: Minocycline has got the anti-inflammatory and neuroprotective effects. Considering the interaction between cell death and seizure, and on the other hand, Kindling which increases expression NMDA receptors in brain, the aim of this study is to investigate the effect of minocycline on gene expression of NMDA receptor in hippocampus and piriform brain areas on amygdale kindling acquisition in rats.
Materials and Methods: In this experimental study, three animal groups of 24 Wistar rats received kindling stimulations (twice daily within 6 hours intervals) after being stereotaxic operated and taking one week recovery period. In first Group (n=8) animals did not received daily kindling stimulations. Animals of the second and the third Groups (n=8) respectively had been injected by saline (1ml/kg) and minocycline (25 mg/kg), 60 minutes before receiving kindling stimulations. Two hours after last stimulation animal’s brains were removed and the changes of NR2A gene subunit of NMDA receptor in the hippocampus and piriform cortex were measured and compared relative to the control group. Datawere analyzed using ANOVA and Tukey post hoc tests at significant level of P
Seyed Mehdi Beheshti Nasr; Mohammad Mohammadzadeh; Hasan Ramshini
Volume 21, Issue 2 , May and June 2014, , Pages 352-361
Abstract
Introduction: Minocycline has anticonvulsant effects. Since some antiepileptic drugs increase the neurotransmitter GABA in the brain, the aim of this study is the effect of minocycline on gene expression of GABAA receptor in hippocampus and piriform brain areas on amygdale kindling acquisition in rat.
Methods: ...
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Introduction: Minocycline has anticonvulsant effects. Since some antiepileptic drugs increase the neurotransmitter GABA in the brain, the aim of this study is the effect of minocycline on gene expression of GABAA receptor in hippocampus and piriform brain areas on amygdale kindling acquisition in rat.
Methods: In this experimental study, three group (24 Wistar rats), after stereotaxic surgery and 1 week recovery period, received kindling stimulations(twice daily at 6 hours interval). Group 1(n=8) did not receive daily kindling stimulations. Group 2 (n=8) received intraperitoneal saline (1ml/kg) and Group 3 (n=8) received intraperitoeneal minocycline (25 mg/kg) 60 min before kindling stimulation and respectively. Two hours after the last stimulation, animals’ brains were removed and the changes of gene expression by γ2 subunit of GABAAreceptor in the hippocampus and piriform cortex were measured and compared with the control group. Data was analyzed using one-way ANOVA and Tukey post hoc tests (P
Ali Moghimi; Mohammad Mohammad-Zadeh; Seyyed Mehdi Beheshti Nasr
Volume 19, Issue 1 , March and April 2012, , Pages 14-25
Abstract
Background: Minocycline is an antibiotic and anti-inflammatory drug. In addition, its neuroprotective effects have been shown. Since there is interaction between cell death and seizure, the aim of this study is examination of the role of minocycline on amygdala-kindled seizures in rat.
Materials and ...
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Background: Minocycline is an antibiotic and anti-inflammatory drug. In addition, its neuroprotective effects have been shown. Since there is interaction between cell death and seizure, the aim of this study is examination of the role of minocycline on amygdala-kindled seizures in rat.
Materials and Methods: In this experimental study, three groups of animals (18 rats), after stereotaxic surgery and 1-week recovery period, received twice daily kindling stimulations. In fully kindled animals of groups 1-3, minocycline was injected intraperitoneally in doses 12.5 (n = 7), 25 (n = 5) and 50 (n = 6) mg/kg, respectively, 60 minutes before stimulation. Afterdischarge duration (ADD), stage 4 latency (S4L), Stage 5 Duration (S5D) and Seizure Duration (SD) were recorded and compared with related control groups (the same animals that had received saline 1 day before). A p-value of less than 0.05 was considered to represent a significant difference.
Results: In fully kindled animals who had received minocycline (50 and 25 mg/kg), ADD decreased significantly. When minocycline was delivered, S5D decreased 38.3% (p < 0.001), 34% (p