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Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice

BACKGROUND: Uncaria sinensis (US) has long been used in traditional Korean medicine to relieve various nervous-related symptoms and cardiovascular disease. We recently showed the neuroprotective and cerebrovascular protective effects of US on cerebral ischemia; however, its effects on the blood–brai...

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Autores principales: Seo, Hyung Bum, Kang, Bo Kyung, Kim, Ji Hyun, Choi, Young Whan, Hong, Jin Woo, Choi, Byung Tae, Shin, Hwa Kyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443505/
https://www.ncbi.nlm.nih.gov/pubmed/26012470
http://dx.doi.org/10.1186/s12906-015-0678-4
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author Seo, Hyung Bum
Kang, Bo Kyung
Kim, Ji Hyun
Choi, Young Whan
Hong, Jin Woo
Choi, Byung Tae
Shin, Hwa Kyoung
author_facet Seo, Hyung Bum
Kang, Bo Kyung
Kim, Ji Hyun
Choi, Young Whan
Hong, Jin Woo
Choi, Byung Tae
Shin, Hwa Kyoung
author_sort Seo, Hyung Bum
collection PubMed
description BACKGROUND: Uncaria sinensis (US) has long been used in traditional Korean medicine to relieve various nervous-related symptoms and cardiovascular disease. We recently showed the neuroprotective and cerebrovascular protective effects of US on cerebral ischemia; however, its effects on the blood–brain barrier (BBB) are poorly understood. In this study, the effects of partially purified components of US (PPUS) on BBB disruption were investigated in mice subjected to ischemic brain injury. METHODS: Focal cerebral ischemia was induced in C57BL/6J mice by photothrombotic cortical ischemia. PPUS was injected intraperitoneally 30 min before ischemic insults. Infarct volume, neurological score, wire-grip test, Evans blue leakage and brain water content were then examined 24 h after ischemic brain injury. RESULTS: Infarct volume was significantly reduced and neurological deficit and motor deficit were greatly improved in PPUS-pretreated mice relative to those treated with vehicle following photothrombotic cortical ischemia. Brain edema-induced change of Evans blue extravasation and water content in the ipsilateral hemisphere were alleviated by treatment with PPUS. In addition, PPUS significantly reduced ischemic brain injury-induced degradation of tight junction proteins and elevation of matrix metalloproteinase-9 (MMP-9). CONCLUSIONS: PPUS prevents cerebral ischemic damage by BBB protection, and these effects were associated with inhibition of tight junction degradation and MMP-9 induction.
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spelling pubmed-44435052015-05-27 Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice Seo, Hyung Bum Kang, Bo Kyung Kim, Ji Hyun Choi, Young Whan Hong, Jin Woo Choi, Byung Tae Shin, Hwa Kyoung BMC Complement Altern Med Research Article BACKGROUND: Uncaria sinensis (US) has long been used in traditional Korean medicine to relieve various nervous-related symptoms and cardiovascular disease. We recently showed the neuroprotective and cerebrovascular protective effects of US on cerebral ischemia; however, its effects on the blood–brain barrier (BBB) are poorly understood. In this study, the effects of partially purified components of US (PPUS) on BBB disruption were investigated in mice subjected to ischemic brain injury. METHODS: Focal cerebral ischemia was induced in C57BL/6J mice by photothrombotic cortical ischemia. PPUS was injected intraperitoneally 30 min before ischemic insults. Infarct volume, neurological score, wire-grip test, Evans blue leakage and brain water content were then examined 24 h after ischemic brain injury. RESULTS: Infarct volume was significantly reduced and neurological deficit and motor deficit were greatly improved in PPUS-pretreated mice relative to those treated with vehicle following photothrombotic cortical ischemia. Brain edema-induced change of Evans blue extravasation and water content in the ipsilateral hemisphere were alleviated by treatment with PPUS. In addition, PPUS significantly reduced ischemic brain injury-induced degradation of tight junction proteins and elevation of matrix metalloproteinase-9 (MMP-9). CONCLUSIONS: PPUS prevents cerebral ischemic damage by BBB protection, and these effects were associated with inhibition of tight junction degradation and MMP-9 induction. BioMed Central 2015-05-27 /pmc/articles/PMC4443505/ /pubmed/26012470 http://dx.doi.org/10.1186/s12906-015-0678-4 Text en © Seo et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Seo, Hyung Bum
Kang, Bo Kyung
Kim, Ji Hyun
Choi, Young Whan
Hong, Jin Woo
Choi, Byung Tae
Shin, Hwa Kyoung
Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice
title Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice
title_full Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice
title_fullStr Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice
title_full_unstemmed Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice
title_short Partially purified components of Uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice
title_sort partially purified components of uncaria sinensis attenuate blood brain barrier disruption after ischemic brain injury in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443505/
https://www.ncbi.nlm.nih.gov/pubmed/26012470
http://dx.doi.org/10.1186/s12906-015-0678-4
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