E. Tahmasebi , H. Monsef-Esfahani , M. Vazirian , P. Sharafi-Badr , M. Sharifzadeh , S.N. Sadati Lamardi
{"title":"大叶芍药根提取物对戊四唑诱导的小鼠癫痫模型的抗惊厥作用","authors":"E. Tahmasebi , H. Monsef-Esfahani , M. Vazirian , P. Sharafi-Badr , M. Sharifzadeh , S.N. Sadati Lamardi","doi":"10.1016/j.nrleng.2021.08.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>In the present study, anticonvulsant effects of aqueous extract (AE), hydro-alcoholic crude extract (HE), and its fractions (F-CHCl<sub>3</sub>, F-EtOAc, F-MeOH) of <em>Paeonia daurica</em> subsp. <em>macrophylla</em> (<em>P. daurica</em> ssp. <em>macrophylla</em>) root examined by using a pentylenetetrazol-induced model (PTZ) on mice.</p></div><div><h3>Methods</h3><p>HE and its fractions as well as AE, in concentrations of (100, 200 and 400<!--> <!-->mg/kg), valproate (Val) (100 and 200<!--> <!-->mg/kg), and saline (negative control) (10<!--> <!-->mg/kg) were injected intraperitoneally (i.p.) 30<!--> <!-->min before PTZ (80<!--> <!-->mg/kg, i.p.). The time taken before the onset of myoclonic convulsions (MC), MC duration, time taken before the onset of generalized tonic-clonic seizures (GTCS), the duration of GTCS, and the percentage of GTCS and mortality protection recorded. The plant's anticonvulsant mechanisms were assessed using flumazenil (5<!--> <!-->mg/kg, i.p.) before AE (100, 200, and 400<!--> <!-->mg/kg, i.p.) injection. GraphPad Prism software was used to compare the differences between various treatment groups with one-way analysis of variance (ANOVA) followed by Tukey–Krammer multiple comparison tests.</p></div><div><h3>Results</h3><p>All the plant samples except F-EtOAc significantly delayed the onset and decreased the duration of PTZ-induced MCS and GTCS, and significantly reduced the GTCS and mortality rate. Pretreatment with flumazenil diminished the significant anticonvulsant effects of AE against PTZ-induced seizures.</p></div><div><h3>Conclusions</h3><p>It can report that extract of <em>P</em>. <em>daurica</em> ssp. <em>macrophylla</em> might be a helpful guide for future studies in the treatment of epilepsy.</p></div>","PeriodicalId":94155,"journal":{"name":"Neurologia","volume":"39 4","pages":"Pages 329-339"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S217358082400035X/pdfft?md5=3ba45cb7f228c23924ab5ab3a9963386&pid=1-s2.0-S217358082400035X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Anticonvulsant effects of Paeonia daurica subsp. macrophylla root extracts in pentylenetetrazol-induced seizure models in mice\",\"authors\":\"E. Tahmasebi , H. Monsef-Esfahani , M. Vazirian , P. Sharafi-Badr , M. Sharifzadeh , S.N. Sadati Lamardi\",\"doi\":\"10.1016/j.nrleng.2021.08.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>In the present study, anticonvulsant effects of aqueous extract (AE), hydro-alcoholic crude extract (HE), and its fractions (F-CHCl<sub>3</sub>, F-EtOAc, F-MeOH) of <em>Paeonia daurica</em> subsp. <em>macrophylla</em> (<em>P. daurica</em> ssp. <em>macrophylla</em>) root examined by using a pentylenetetrazol-induced model (PTZ) on mice.</p></div><div><h3>Methods</h3><p>HE and its fractions as well as AE, in concentrations of (100, 200 and 400<!--> <!-->mg/kg), valproate (Val) (100 and 200<!--> <!-->mg/kg), and saline (negative control) (10<!--> <!-->mg/kg) were injected intraperitoneally (i.p.) 30<!--> <!-->min before PTZ (80<!--> <!-->mg/kg, i.p.). The time taken before the onset of myoclonic convulsions (MC), MC duration, time taken before the onset of generalized tonic-clonic seizures (GTCS), the duration of GTCS, and the percentage of GTCS and mortality protection recorded. The plant's anticonvulsant mechanisms were assessed using flumazenil (5<!--> <!-->mg/kg, i.p.) before AE (100, 200, and 400<!--> <!-->mg/kg, i.p.) injection. GraphPad Prism software was used to compare the differences between various treatment groups with one-way analysis of variance (ANOVA) followed by Tukey–Krammer multiple comparison tests.</p></div><div><h3>Results</h3><p>All the plant samples except F-EtOAc significantly delayed the onset and decreased the duration of PTZ-induced MCS and GTCS, and significantly reduced the GTCS and mortality rate. Pretreatment with flumazenil diminished the significant anticonvulsant effects of AE against PTZ-induced seizures.</p></div><div><h3>Conclusions</h3><p>It can report that extract of <em>P</em>. <em>daurica</em> ssp. <em>macrophylla</em> might be a helpful guide for future studies in the treatment of epilepsy.</p></div>\",\"PeriodicalId\":94155,\"journal\":{\"name\":\"Neurologia\",\"volume\":\"39 4\",\"pages\":\"Pages 329-339\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S217358082400035X/pdfft?md5=3ba45cb7f228c23924ab5ab3a9963386&pid=1-s2.0-S217358082400035X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurologia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S217358082400035X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurologia","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S217358082400035X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Anticonvulsant effects of Paeonia daurica subsp. macrophylla root extracts in pentylenetetrazol-induced seizure models in mice
Introduction
In the present study, anticonvulsant effects of aqueous extract (AE), hydro-alcoholic crude extract (HE), and its fractions (F-CHCl3, F-EtOAc, F-MeOH) of Paeonia daurica subsp. macrophylla (P. daurica ssp. macrophylla) root examined by using a pentylenetetrazol-induced model (PTZ) on mice.
Methods
HE and its fractions as well as AE, in concentrations of (100, 200 and 400 mg/kg), valproate (Val) (100 and 200 mg/kg), and saline (negative control) (10 mg/kg) were injected intraperitoneally (i.p.) 30 min before PTZ (80 mg/kg, i.p.). The time taken before the onset of myoclonic convulsions (MC), MC duration, time taken before the onset of generalized tonic-clonic seizures (GTCS), the duration of GTCS, and the percentage of GTCS and mortality protection recorded. The plant's anticonvulsant mechanisms were assessed using flumazenil (5 mg/kg, i.p.) before AE (100, 200, and 400 mg/kg, i.p.) injection. GraphPad Prism software was used to compare the differences between various treatment groups with one-way analysis of variance (ANOVA) followed by Tukey–Krammer multiple comparison tests.
Results
All the plant samples except F-EtOAc significantly delayed the onset and decreased the duration of PTZ-induced MCS and GTCS, and significantly reduced the GTCS and mortality rate. Pretreatment with flumazenil diminished the significant anticonvulsant effects of AE against PTZ-induced seizures.
Conclusions
It can report that extract of P. daurica ssp. macrophylla might be a helpful guide for future studies in the treatment of epilepsy.