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Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice
The study aims to investigate the effects of (-)-Linarinic acid (LA) and one of its derivatives (LA(d)) on brain injury induced by ischemia. Malonaldehyde (MDA) is determined as an index for lipid peroxidation both in vitro and vivo. Mice were pre-treated with LA and LA(d) for 3 d. Thereafter, they...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shenyang Pharmaceutical University
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032232/ https://www.ncbi.nlm.nih.gov/pubmed/32104326 http://dx.doi.org/10.1016/j.ajps.2016.07.008 |
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author | Wang, Yihan Zhao, Chao Wang, Qiujv Wen, Huimin Gu, Yaru Fan, Linlin Ma, Chao Cheng, Maosheng Zhang, Yuyang |
author_facet | Wang, Yihan Zhao, Chao Wang, Qiujv Wen, Huimin Gu, Yaru Fan, Linlin Ma, Chao Cheng, Maosheng Zhang, Yuyang |
author_sort | Wang, Yihan |
collection | PubMed |
description | The study aims to investigate the effects of (-)-Linarinic acid (LA) and one of its derivatives (LA(d)) on brain injury induced by ischemia. Malonaldehyde (MDA) is determined as an index for lipid peroxidation both in vitro and vivo. Mice were pre-treated with LA and LA(d) for 3 d. Thereafter, they were induced to have incomplete cerebral ischemia with both bilateral carotid artery occlusion and hypotension (BCAOH). In the first part of the in vivo experiment, mice were divided into four groups: sham (control), ischemia, ischemia + LA (200 mg/kg, i.g.) and ischemia + LA(d) (200 mg/kg, i.g.). In the second part, the dose-response of LA(d) was investigated at 100, 200 and 400 mg/kg i.g., respectively. A modified neurological severity score was developed for evaluating behavioral deficits of the mice with ischemia. Brains of the mice were excised in order to determinate MDA after ischemia for 6 h. Survival time, survival rate, neurological injury score and MDA level in brains were observed. Results were: 1) The data in vitro showed that both LA and LA(d) could inhibit the generation of MDA. IC(50) values obtained by Probit analysis were 2.9 mM for LA(d) and 4.88 mM for LA; 2) BCAOH could significantly shorten the survival span, reduce the survival rate and cause neurological deficits, which were associated with high level of lipid hydroperoxide production in cerebral tissues; 3) LA(d) decreased lipid peroxidation and improved the neurological outcome more than LA. It is concluded that LA(d) offers a better neuroprotection than LA against brain damage caused by cerebral ischemia. |
format | Online Article Text |
id | pubmed-7032232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Shenyang Pharmaceutical University |
record_format | MEDLINE/PubMed |
spelling | pubmed-70322322020-02-26 Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice Wang, Yihan Zhao, Chao Wang, Qiujv Wen, Huimin Gu, Yaru Fan, Linlin Ma, Chao Cheng, Maosheng Zhang, Yuyang Asian J Pharm Sci Original Research Article The study aims to investigate the effects of (-)-Linarinic acid (LA) and one of its derivatives (LA(d)) on brain injury induced by ischemia. Malonaldehyde (MDA) is determined as an index for lipid peroxidation both in vitro and vivo. Mice were pre-treated with LA and LA(d) for 3 d. Thereafter, they were induced to have incomplete cerebral ischemia with both bilateral carotid artery occlusion and hypotension (BCAOH). In the first part of the in vivo experiment, mice were divided into four groups: sham (control), ischemia, ischemia + LA (200 mg/kg, i.g.) and ischemia + LA(d) (200 mg/kg, i.g.). In the second part, the dose-response of LA(d) was investigated at 100, 200 and 400 mg/kg i.g., respectively. A modified neurological severity score was developed for evaluating behavioral deficits of the mice with ischemia. Brains of the mice were excised in order to determinate MDA after ischemia for 6 h. Survival time, survival rate, neurological injury score and MDA level in brains were observed. Results were: 1) The data in vitro showed that both LA and LA(d) could inhibit the generation of MDA. IC(50) values obtained by Probit analysis were 2.9 mM for LA(d) and 4.88 mM for LA; 2) BCAOH could significantly shorten the survival span, reduce the survival rate and cause neurological deficits, which were associated with high level of lipid hydroperoxide production in cerebral tissues; 3) LA(d) decreased lipid peroxidation and improved the neurological outcome more than LA. It is concluded that LA(d) offers a better neuroprotection than LA against brain damage caused by cerebral ischemia. Shenyang Pharmaceutical University 2017-03 2016-08-04 /pmc/articles/PMC7032232/ /pubmed/32104326 http://dx.doi.org/10.1016/j.ajps.2016.07.008 Text en © 2017 Shenyang Pharmaceutical University. Production and hosting by Elsevier B.V. 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 Research Article Wang, Yihan Zhao, Chao Wang, Qiujv Wen, Huimin Gu, Yaru Fan, Linlin Ma, Chao Cheng, Maosheng Zhang, Yuyang Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice |
title | Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice |
title_full | Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice |
title_fullStr | Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice |
title_full_unstemmed | Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice |
title_short | Investigation of Linarinic acid and one of its derivatives against cerebral ischemia in mice |
title_sort | investigation of linarinic acid and one of its derivatives against cerebral ischemia in mice |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7032232/ https://www.ncbi.nlm.nih.gov/pubmed/32104326 http://dx.doi.org/10.1016/j.ajps.2016.07.008 |
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