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Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity

The anticonvulsant potential of Ficus carica methanol-extract (Fc) has been studied. It was found that Fc most active fraction is rich in oligosaccharides (OFG). (1)H, (13)C NMR and Nano-ESI, MALDI MS, and LC-MS techniques proved that OFG contains alpha-glucopyranoside oligomer in high amounts. Both...

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Detalles Bibliográficos
Autores principales: Raafat, K., Wurglics, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701940/
https://www.ncbi.nlm.nih.gov/pubmed/31453121
http://dx.doi.org/10.1016/j.jtcme.2018.01.007
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author Raafat, K.
Wurglics, M.
author_facet Raafat, K.
Wurglics, M.
author_sort Raafat, K.
collection PubMed
description The anticonvulsant potential of Ficus carica methanol-extract (Fc) has been studied. It was found that Fc most active fraction is rich in oligosaccharides (OFG). (1)H, (13)C NMR and Nano-ESI, MALDI MS, and LC-MS techniques proved that OFG contains alpha-glucopyranoside oligomer in high amounts. Both Fc and OFG reduced strychnine (STR) convulsion-action. Fc and OFG fully protected the experimental-animals from STR-lethality. The intracerebroventricular-administration (ICV) of Fc or OFG in combination with glycine in ethanol-treated mice caused a dose-dependent returning to a 2nd-loss of righting-reflex (LORR), and was antagonized by STR. FC and OFG ICV injection counteracted STR-inhibition, confirming that Fc/OFG anticonvulsant mechanism of action was mediated by potentiation of glycine receptor. These results support Fc and OFG potential anticonvulsant-activity with good safety-profile.
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spelling pubmed-67019402019-08-26 Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity Raafat, K. Wurglics, M. J Tradit Complement Med Original article The anticonvulsant potential of Ficus carica methanol-extract (Fc) has been studied. It was found that Fc most active fraction is rich in oligosaccharides (OFG). (1)H, (13)C NMR and Nano-ESI, MALDI MS, and LC-MS techniques proved that OFG contains alpha-glucopyranoside oligomer in high amounts. Both Fc and OFG reduced strychnine (STR) convulsion-action. Fc and OFG fully protected the experimental-animals from STR-lethality. The intracerebroventricular-administration (ICV) of Fc or OFG in combination with glycine in ethanol-treated mice caused a dose-dependent returning to a 2nd-loss of righting-reflex (LORR), and was antagonized by STR. FC and OFG ICV injection counteracted STR-inhibition, confirming that Fc/OFG anticonvulsant mechanism of action was mediated by potentiation of glycine receptor. These results support Fc and OFG potential anticonvulsant-activity with good safety-profile. Elsevier 2018-09-28 /pmc/articles/PMC6701940/ /pubmed/31453121 http://dx.doi.org/10.1016/j.jtcme.2018.01.007 Text en © 2018 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Raafat, K.
Wurglics, M.
Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity
title Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity
title_full Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity
title_fullStr Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity
title_full_unstemmed Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity
title_short Phytochemical analysis of Ficus carica L. active compounds possessing anticonvulsant activity
title_sort phytochemical analysis of ficus carica l. active compounds possessing anticonvulsant activity
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6701940/
https://www.ncbi.nlm.nih.gov/pubmed/31453121
http://dx.doi.org/10.1016/j.jtcme.2018.01.007
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