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Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice

BACKGROUND: Stroke is the second most common cause of death and may result in various disabilities; thus, identification of neuroprotective therapeutic agents is important. Peucedani Radix (PR), the root of Angelica decursiva, is a well-known remedy for damp and phlegm in Korean medicine and has als...

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Autores principales: Jung, So-Youn, Kim, Kyoung-Min, Cho, Suin, Lim, Sehyun, Lim, Chiyeon, Kim, Young Kyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655947/
https://www.ncbi.nlm.nih.gov/pubmed/29090015
http://dx.doi.org/10.1186/s13020-017-0151-z
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author Jung, So-Youn
Kim, Kyoung-Min
Cho, Suin
Lim, Sehyun
Lim, Chiyeon
Kim, Young Kyun
author_facet Jung, So-Youn
Kim, Kyoung-Min
Cho, Suin
Lim, Sehyun
Lim, Chiyeon
Kim, Young Kyun
author_sort Jung, So-Youn
collection PubMed
description BACKGROUND: Stroke is the second most common cause of death and may result in various disabilities; thus, identification of neuroprotective therapeutic agents is important. Peucedani Radix (PR), the root of Angelica decursiva, is a well-known remedy for damp and phlegm in Korean medicine and has also been shown to exert antioxidant and anti-inflammatory activities. This study was performed to investigate the mechanism underlying the anti-inflammatory effect of methanol extract of PR (PRex) on cerebral ischemic injury. METHODS: C57BL/6 male mice were orally administered PRex (20, 60, or 200 mg/kg) at 2 days, 1 day, and 1 h prior to middle cerebral artery occlusion (MCAO). Twenty-four hours after MCAO, the infarct volume was measured and the neurological deficit score was assessed. The inflammatory-related substances in the ipsilateral hemisphere were determined by western blotting, DCFH-DA assay, TBARS assay, and ELISA. RESULTS: PRex pretreatment significantly decreased the infarct volume at 24 h after MCAO. Moreover, PRex effectively suppressed the expression of iNOS, ROS, MDA, and pro-inflammatory cytokines, such as IL-1β and TNF-α, in brain tissue of mice with MCAO-induced brain injury. CONCLUSIONS: PRex protected neurons from ischemic brain injury in mice through its antioxidant and anti-inflammatory activities. Our results suggested that PR could be a promising candidate in the therapy of ischemia-induced brain damage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13020-017-0151-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-56559472017-10-31 Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice Jung, So-Youn Kim, Kyoung-Min Cho, Suin Lim, Sehyun Lim, Chiyeon Kim, Young Kyun Chin Med Research BACKGROUND: Stroke is the second most common cause of death and may result in various disabilities; thus, identification of neuroprotective therapeutic agents is important. Peucedani Radix (PR), the root of Angelica decursiva, is a well-known remedy for damp and phlegm in Korean medicine and has also been shown to exert antioxidant and anti-inflammatory activities. This study was performed to investigate the mechanism underlying the anti-inflammatory effect of methanol extract of PR (PRex) on cerebral ischemic injury. METHODS: C57BL/6 male mice were orally administered PRex (20, 60, or 200 mg/kg) at 2 days, 1 day, and 1 h prior to middle cerebral artery occlusion (MCAO). Twenty-four hours after MCAO, the infarct volume was measured and the neurological deficit score was assessed. The inflammatory-related substances in the ipsilateral hemisphere were determined by western blotting, DCFH-DA assay, TBARS assay, and ELISA. RESULTS: PRex pretreatment significantly decreased the infarct volume at 24 h after MCAO. Moreover, PRex effectively suppressed the expression of iNOS, ROS, MDA, and pro-inflammatory cytokines, such as IL-1β and TNF-α, in brain tissue of mice with MCAO-induced brain injury. CONCLUSIONS: PRex protected neurons from ischemic brain injury in mice through its antioxidant and anti-inflammatory activities. Our results suggested that PR could be a promising candidate in the therapy of ischemia-induced brain damage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13020-017-0151-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-24 /pmc/articles/PMC5655947/ /pubmed/29090015 http://dx.doi.org/10.1186/s13020-017-0151-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Jung, So-Youn
Kim, Kyoung-Min
Cho, Suin
Lim, Sehyun
Lim, Chiyeon
Kim, Young Kyun
Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice
title Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice
title_full Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice
title_fullStr Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice
title_full_unstemmed Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice
title_short Effects of pretreatment with methanol extract of Peucedani Radix on transient ischemic brain injury in mice
title_sort effects of pretreatment with methanol extract of peucedani radix on transient ischemic brain injury in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655947/
https://www.ncbi.nlm.nih.gov/pubmed/29090015
http://dx.doi.org/10.1186/s13020-017-0151-z
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