Literature DB >> 19406619

Anticonvulsant and acute neurotoxic effects of imperatorin, osthole and valproate in the maximal electroshock seizure and chimney tests in mice: a comparative study.

Jarogniew J Luszczki1, Ewa Wojda, Marta Andres-Mach, Wojciech Cisowski, Michal Glensk, Kazimierz Glowniak, Stanislaw J Czuczwar.   

Abstract

The aim of this study was to determine and compare the anticonvulsant and acute adverse (neurotoxic) effects of imperatorin and osthole (two natural coumarin derivatives) with valproate (a classical antiepileptic drug) in the maximal electroshock seizure and chimney tests in mice. The anticonvulsant and acute adverse effects of imperatorin, osthole and valproate were determined at 15, 30, 60 and 120 min after their systemic (i.p.) administration. The evaluation of time-course and dose-response relationships for imperatorin, osthole and valproate in the maximal electroshock seizure test revealed that the compounds produced a clear-cut antielectroshock action in mice and the experimentally derived ED(50) values for imperatorin ranged between 167 and 290 mg/kg, those for osthole ranged from 253 to 639 mg/kg, whereas the ED(50) values for valproate ranged from 189 to 255 mg/kg. The evaluation of acute neurotoxic effects in the chimney test revealed that the TD(50) values for imperatorin ranged between 329 and 443 mg/kg, the TD(50) values for osthole ranged from 531 to 648 mg/kg, while the TD(50) values for valproate ranged from 363 to 512 mg/kg. The protective index (as a ratio of TD(50) and ED(50) values) for imperatorin ranged between 1.13 and 2.60, for osthole ranged from 0.83 to 2.44, and for valproate ranged between 1.72 and 2.00. In conclusion, both natural coumarin derivatives deserve more attention from a preclinical point of view as compounds possessing some potentially favorable activities in terms of suppression of seizures, quite similar to those reported for valproate.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19406619     DOI: 10.1016/j.eplepsyres.2009.03.027

Source DB:  PubMed          Journal:  Epilepsy Res        ISSN: 0920-1211            Impact factor:   3.045


  24 in total

1.  Furanocoumarins are a novel class of modulators for the transient receptor potential vanilloid type 1 (TRPV1) channel.

Authors:  Xingjuan Chen; Weiyang Sun; Nicholas G Gianaris; Ashley M Riley; Theodore R Cummins; Jill C Fehrenbacher; Alexander G Obukhov
Journal:  J Biol Chem       Date:  2014-02-25       Impact factor: 5.157

Review 2.  Awareness and current knowledge of epilepsy.

Authors:  Asmat Ullah Khan; Muhammad Akram; Muhammad Daniyal; Naheed Akhter; Muhammad Riaz; Naheed Akhtar; Mohammad Ali Shariati; Fozia Anjum; Samreen Gul Khan; Abida Parveen; Saeed Ahmad
Journal:  Metab Brain Dis       Date:  2019-10-11       Impact factor: 3.584

3.  Development of a high throughput screen for allosteric modulators of melanocortin-4 receptor signaling using a real time cAMP assay.

Authors:  Jacques Pantel; Savannah Y Williams; Dehui Mi; Julien Sebag; Jackie D Corbin; C David Weaver; Roger D Cone
Journal:  Eur J Pharmacol       Date:  2011-02-04       Impact factor: 4.432

4.  Stereodefined alkenes with a fluoro-chloro terminus as a uniquely enabling compound class.

Authors:  Qinghe Liu; Yucheng Mu; Tobias Koengeter; Richard R Schrock; Amir H Hoveyda
Journal:  Nat Chem       Date:  2022-02-17       Impact factor: 24.274

5.  Imperatorin Relieved Ulcerative Colitis by Regulating the Nrf-2/ARE/HO-1 Pathway in Rats.

Authors:  Min Luo; Yin Luo
Journal:  Inflammation       Date:  2020-10-23       Impact factor: 4.092

6.  Possible involvement of PPAR-γ in the anticonvulsant effect of Aegle marmelos (L.) Correa.

Authors:  Rajbir Bhatti; Jatinder Singh; Kunal Nepali; M P S Ishar
Journal:  Neurochem Res       Date:  2013-05-05       Impact factor: 3.996

7.  Insights into structure-activity relationship of GABAA receptor modulating coumarins and furanocoumarins.

Authors:  Judith Singhuber; Igor Baburin; Gerhard F Ecker; Brigitte Kopp; Steffen Hering
Journal:  Eur J Pharmacol       Date:  2011-07-05       Impact factor: 4.432

8.  Osthole, a herbal compound, alleviates nucleus pulposus-evoked nociceptive responses through the suppression of overexpression of acid-sensing ion channel 3 (ASIC3) in rat dorsal root ganglion.

Authors:  Qiu-Lan He; Yuling Chen; Jian Qin; Sui-Lin Mo; Ming Wei; Jin-Jun Zhang; Mei-Na Li; Xue-Nong Zou; Shu-Feng Zhou; Xiao-Wu Chen; Lai-Bao Sun
Journal:  Med Sci Monit       Date:  2012-06

Review 9.  Review on natural coumarin lead compounds for their pharmacological activity.

Authors:  K N Venugopala; V Rashmi; B Odhav
Journal:  Biomed Res Int       Date:  2013-03-24       Impact factor: 3.411

Review 10.  Osthole: A Review on Its Bioactivities, Pharmacological Properties, and Potential as Alternative Medicine.

Authors:  Zhong-Rong Zhang; Wing Nang Leung; Ho Yee Cheung; Chun Wai Chan
Journal:  Evid Based Complement Alternat Med       Date:  2015-07-13       Impact factor: 2.629

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.