Antiepileptic effects of quinine in the pentylenetetrazole model of seizure

被引:32
作者
Nassiri-Asl, Marjan [1 ]
Zamansoltani, Farzaneh [2 ]
Torabinejad, Behnam
机构
[1] Qazvin Univ Med Sci, Sch Med, Dept Pharmacol, Qazvin, Iran
[2] Qazvin Univ Med Sci, Sch Med, Dept Anat, Qazvin, Iran
来源
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2009年 / 18卷 / 02期
关键词
Quinine; Gap junction channels; Seizure; Pentylenetetrazole; GAP-JUNCTION BLOCKERS; EPILEPTIFORM ACTIVITY; IN-VITRO; SYNCHRONIZATION; EPILEPSY; OSCILLATIONS; HIPPOCAMPUS; FIELD; EPILEPTOGENESIS; INTERNEURONS;
D O I
10.1016/j.seizure.2008.08.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Quinine, is an anti-malarial drug that specifically blocks connexin 36 (Cx36) at gap junction channels. Quinine has suppressed ictal epileptiform activity in vitro without decreasing neuronal excitability. Thus, we considered the possible anticonvulsant effects of quinine in the pentylenetetrazole (FFZ) model of seizure. Moreover, we studied the hypnotic effect and locomotor activity of quinine in mice. In the PTZ model, quinine at the dose of 60 mg/kg increased the latency of seizure. However, quinine at 40-60 mg/kg decreased the duration of seizure, dose dependently. In the potentiation of pentobarbitone sleep test, quinine significantly increased sleeping time and decreased latency to fall asleep at doses of 50 and 60 mg/kg in mice. Also, quinine decreased total locomotion in the present study. It can be concluded that quinine possesses anticonvulsant and hypnotic effects, which could contribute to the control of seizure. (c) 2008 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:129 / 132
页数:4
相关论文
共 37 条
  • [1] The role of synchrony and oscillations in the motor output
    Baker, SN
    Kilner, JM
    Pinches, EM
    Lemon, RN
    [J]. EXPERIMENTAL BRAIN RESEARCH, 1999, 128 (1-2) : 109 - 117
  • [2] Expression of connexin36 in the adult and developing rat brain
    Belluardo, N
    Mudò, G
    Trovato-Salinaro, A
    Le Gurun, S
    Charollais, A
    Serre-Beinier, V
    Amato, G
    Haefliger, JA
    Meda, P
    Condorelli, DF
    [J]. BRAIN RESEARCH, 2000, 865 (01) : 121 - 138
  • [3] Quinine suppresses extracellular potassium transients and ictal epileptiform activity without decreasing neuronal excitability in vitro
    Bikson, M
    Bihi, RI
    Vreugdenhil, M
    Köhling, R
    Fox, JE
    Jefferys, JGR
    [J]. NEUROSCIENCE, 2002, 115 (01) : 251 - 261
  • [4] Anticonvulsive effects of quinine on penicillin-induced epileptiform activity:: An in vivo study
    Bostanci, M. Oemer
    Bagirici, Faruk
    [J]. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2007, 16 (02): : 166 - 172
  • [5] Gap junctions and inhibitory synapses modulate inspiratory motoneuron synchronization
    Bou-Flores, C
    Berger, AJ
    [J]. JOURNAL OF NEUROPHYSIOLOGY, 2001, 85 (04) : 1543 - 1551
  • [6] The role of gap junctions in seizures
    Carlen, PL
    Skinner, F
    Zhang, L
    Naus, C
    Kushnir, M
    Velazquez, JLP
    [J]. BRAIN RESEARCH REVIEWS, 2000, 32 (01) : 235 - 241
  • [7] A detailed ethological analysis of the mouse open field test: effects of diazepam, chlordiazepoxide and an extremely low frequency pulsed magnetic field
    Choleris, E
    Thomas, AW
    Kavaliers, M
    Prato, FS
    [J]. NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2001, 25 (03) : 235 - 260
  • [8] Dendritic shrinkage and dye-coupling between rat hippocampal CA1 pyramidal cells in the tetanus toxin model of epilepsy
    Colling, SB
    Man, WDC
    Draguhn, A
    Jefferys, JGR
    [J]. BRAIN RESEARCH, 1996, 741 (1-2) : 38 - 43
  • [9] DANDIYA PC, 1959, J PHARMACOL EXP THER, V125, P353
  • [10] de Curtis M, 1998, J NEUROSCI, V18, P7543