Mishra Awanish, Punia Jasmine Kaur, Bladen Chris, Zamponi Gerald W, Goel Rajesh Kumar
a Department of Pharmaceutical Sciences and Drug Research ; Punjabi University ; Patiala , Punjab , India.
b Department of Physiology & Pharmacology ; Hotchkiss Brain Institute and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary ; Calgary , Alberta , Canada.
Channels (Austin). 2015;9(5):317-23. doi: 10.1080/19336950.2015.1092836.
Piperine, a natural compound isolated from the fruits of Piper, is known to modulate several neurotransmitter systems such as serotonin, norepinephrine, and GABA, all of which have been linked to the development of convulsions. Fruits of Piper species have been suggested as means for managing seizure disorders. The present study was designed to elucidate the anticonvulsant effect of piperine and its mechanisms of action using in-silico, in-vivo and in-vitro techniques.PASS software was used to determine its possible activity and mechanisms. Furthermore the latency for development of convulsions and mortality rate was recorded in different experimental mouse models of epilepsy (pentylenetetrazole, maximal electroshock, NMDA, picrotoxin, bicuculline, BAYK-8644, strychnine-induced convulsions) after administration of various doses of piperine (5, 10 and 20 mg/kg, i.p.). Finally, the effect of piperine on Na(+) and Ca(2+) channels were evaluated using the whole cell patch clamp techniqueOur results revealed that piperine decreased mortality in the MES-induced seizure model. Moreover, piperine (10 mg/kg) delayed the onset of tonic clonic convulsions in the pentylenetetrazole test and reduced associated mortality. Furthermore, an anticonvulsant dose of piperine also delayed the onset of tonic clonic seizures in strychnine, picrotoxin and BAY K-8644. Complete protection against mortality was observed in BAYK-8644 induced convulsions. Finally, whole cell patch clamp analysis suggested an inhibitory effect of piperine on Na(+) channels. Together, our data suggest Na(+) channel antagonist activity as a contributor to the complex anticonvulsant mechanisms of piperine.
胡椒碱是从胡椒果实中分离出的一种天然化合物,已知它可调节多种神经递质系统,如血清素、去甲肾上腺素和γ-氨基丁酸,所有这些都与惊厥的发生有关。有人提出胡椒属植物的果实可作为治疗癫痫疾病的手段。本研究旨在利用计算机模拟、体内和体外技术阐明胡椒碱的抗惊厥作用及其作用机制。使用PASS软件确定其可能的活性和机制。此外,在给予不同剂量的胡椒碱(5、10和20毫克/千克,腹腔注射)后,记录癫痫不同实验小鼠模型(戊四氮、最大电休克、N-甲基-D-天冬氨酸、印防己毒素、荷包牡丹碱、BAYK-8644、士的宁诱发惊厥)中惊厥发作的潜伏期和死亡率。最后,使用全细胞膜片钳技术评估胡椒碱对钠(Na⁺)和钙(Ca²⁺)通道的影响。我们的结果显示,胡椒碱可降低最大电休克诱发癫痫模型中的死亡率。此外,胡椒碱(10毫克/千克)可延迟戊四氮试验中强直性阵挛性惊厥的发作并降低相关死亡率。此外,抗惊厥剂量的胡椒碱还可延迟士的宁、印防己毒素和BAY K-8644诱发的强直性阵挛性癫痫发作的发作时间。在BAYK-8644诱发的惊厥中观察到对死亡率的完全保护作用。最后,全细胞膜片钳分析表明胡椒碱对钠(Na⁺)通道有抑制作用。总之,我们的数据表明钠(Na⁺)通道拮抗剂活性是胡椒碱复杂抗惊厥机制的一个促成因素。