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Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits

BACKGROUND: Hydroxysafflor Yellow A (HSYA), which is one of the most important active ingredients of the Chinese herb Carthamus tinctorius L, is widely used in the treatment of cerebrovascular and cardiovascular diseases. However, the potential protective effect of HSYA in spinal cord ischemia/reper...

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Autores principales: Shan, Le-qun, Ma, Sai, Qiu, Xiu-chun, Zhou, Yong, Zhang, Yong, Zheng, Lian-he, Ren, Peng-cheng, Wang, Yu-cai, Fan, Qing-yu, Ma, Bao-an
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928239/
https://www.ncbi.nlm.nih.gov/pubmed/20707889
http://dx.doi.org/10.1186/1471-2202-11-98
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author Shan, Le-qun
Ma, Sai
Qiu, Xiu-chun
Zhou, Yong
Zhang, Yong
Zheng, Lian-he
Ren, Peng-cheng
Wang, Yu-cai
Fan, Qing-yu
Ma, Bao-an
author_facet Shan, Le-qun
Ma, Sai
Qiu, Xiu-chun
Zhou, Yong
Zhang, Yong
Zheng, Lian-he
Ren, Peng-cheng
Wang, Yu-cai
Fan, Qing-yu
Ma, Bao-an
author_sort Shan, Le-qun
collection PubMed
description BACKGROUND: Hydroxysafflor Yellow A (HSYA), which is one of the most important active ingredients of the Chinese herb Carthamus tinctorius L, is widely used in the treatment of cerebrovascular and cardiovascular diseases. However, the potential protective effect of HSYA in spinal cord ischemia/reperfusion (I/R) injury is still unknown. METHODS: Thirty-nine rabbits were randomly divided into three groups: sham group, I/R group and HSYA group. All animals were sacrificed after neurological evaluation with modified Tarlov criteria at the 48th hour after reperfusion, and the spinal cord segments (L4-6) were harvested for histopathological examination, biochemical analysis and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) staining. RESULTS: Neurological outcomes in HSYA group were slightly improved compared with those in I/R group. Histopathological analysis revealed that HSYA treatment attenuated I/R induced necrosis in spinal cords. Similarly, alleviated oxidative stress was indicated by decreased malondialdehyde (MDA) level and increased superoxide dismutase (SOD) activity after HSYA treatment. Moreover, as seen from TUNEL results, HSYA also protected neurons from I/R-induced apoptosis in rabbits. CONCLUSIONS: These findings suggest that HSYA may protect spinal cords from I/R injury by alleviating oxidative stress and reducing neuronal apoptosis in rabbits.
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spelling pubmed-29282392010-08-26 Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits Shan, Le-qun Ma, Sai Qiu, Xiu-chun Zhou, Yong Zhang, Yong Zheng, Lian-he Ren, Peng-cheng Wang, Yu-cai Fan, Qing-yu Ma, Bao-an BMC Neurosci Research Article BACKGROUND: Hydroxysafflor Yellow A (HSYA), which is one of the most important active ingredients of the Chinese herb Carthamus tinctorius L, is widely used in the treatment of cerebrovascular and cardiovascular diseases. However, the potential protective effect of HSYA in spinal cord ischemia/reperfusion (I/R) injury is still unknown. METHODS: Thirty-nine rabbits were randomly divided into three groups: sham group, I/R group and HSYA group. All animals were sacrificed after neurological evaluation with modified Tarlov criteria at the 48th hour after reperfusion, and the spinal cord segments (L4-6) were harvested for histopathological examination, biochemical analysis and terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling (TUNEL) staining. RESULTS: Neurological outcomes in HSYA group were slightly improved compared with those in I/R group. Histopathological analysis revealed that HSYA treatment attenuated I/R induced necrosis in spinal cords. Similarly, alleviated oxidative stress was indicated by decreased malondialdehyde (MDA) level and increased superoxide dismutase (SOD) activity after HSYA treatment. Moreover, as seen from TUNEL results, HSYA also protected neurons from I/R-induced apoptosis in rabbits. CONCLUSIONS: These findings suggest that HSYA may protect spinal cords from I/R injury by alleviating oxidative stress and reducing neuronal apoptosis in rabbits. BioMed Central 2010-08-13 /pmc/articles/PMC2928239/ /pubmed/20707889 http://dx.doi.org/10.1186/1471-2202-11-98 Text en Copyright ©2010 Shan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shan, Le-qun
Ma, Sai
Qiu, Xiu-chun
Zhou, Yong
Zhang, Yong
Zheng, Lian-he
Ren, Peng-cheng
Wang, Yu-cai
Fan, Qing-yu
Ma, Bao-an
Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits
title Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits
title_full Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits
title_fullStr Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits
title_full_unstemmed Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits
title_short Hydroxysafflor Yellow A protects spinal cords from ischemia/reperfusion injury in rabbits
title_sort hydroxysafflor yellow a protects spinal cords from ischemia/reperfusion injury in rabbits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2928239/
https://www.ncbi.nlm.nih.gov/pubmed/20707889
http://dx.doi.org/10.1186/1471-2202-11-98
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