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Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice

BACKGROUND: Biosynthesis of leukotriene (LT) by arachidonic acid involves 5-lipoxygenase (5-LO) as an important precursor. Here, we evaluated the role of pseudohypericin (PHP) for its postulated 5-LO inhibitory activity along with a Cys-LT receptor antagonist zafirlukast (ZFL) against inflammatory r...

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Autores principales: Chen, Xiao-Gang, Hua, Fu, Wang, Shou-Guo, Xu, Yong-Yi, Yue, Hai-Tao, Sun, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078184/
https://www.ncbi.nlm.nih.gov/pubmed/30122897
http://dx.doi.org/10.2147/DDDT.S154814
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author Chen, Xiao-Gang
Hua, Fu
Wang, Shou-Guo
Xu, Yong-Yi
Yue, Hai-Tao
Sun, Jin
author_facet Chen, Xiao-Gang
Hua, Fu
Wang, Shou-Guo
Xu, Yong-Yi
Yue, Hai-Tao
Sun, Jin
author_sort Chen, Xiao-Gang
collection PubMed
description BACKGROUND: Biosynthesis of leukotriene (LT) by arachidonic acid involves 5-lipoxygenase (5-LO) as an important precursor. Here, we evaluated the role of pseudohypericin (PHP) for its postulated 5-LO inhibitory activity along with a Cys-LT receptor antagonist zafirlukast (ZFL) against inflammatory response and tissue injury in mice. MATERIALS AND METHODS: The spinal injury was induced by two-level laminectomy of T6 and T7 vertebrae. The inflammation was assessed by histology, inflammatory mediators by enzyme-linked immunosorbent assay, apoptosis by Annexin-V, FAS staining, terminal deoxynucleoti-dyltransferase-mediated UTP end labeling (TUNEL) assay and expression of Bax and Bcl-2 by Western blot. Effect on motor recovery of hind limbs was evaluated for 10 days postinjury. RESULTS: The spinal injury resulted in tissue damage, apoptosis, edema, infiltration of neutrophils with increased expression of tumor necrosis factor-α (TNF-α) and cyclooxygenase-2 (COX-2). The spinal tissue showed elevated levels of prostaglandin E(2) (PGE2), and LTB(4) and increased phosphorylation of injured extracellular signal-regulated kinase-1/2 (ERK1/2). The PHP, ZFL and combination decreased inflammation, tissue injury and infiltration of neutrophils. Treatment also decreased the levels of PGE(2), phosphorylation of extracellular signal-regulated kinase-1/2 (pERK 1/2), LT, TNF-α and COX-2 with a marked reduction in apoptosis and improved the motor function. CONCLUSION: The present study confirmed 5-LO antagonist activity of PHP and established its neuroprotective role along with ZFL.
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spelling pubmed-60781842018-08-17 Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice Chen, Xiao-Gang Hua, Fu Wang, Shou-Guo Xu, Yong-Yi Yue, Hai-Tao Sun, Jin Drug Des Devel Ther Original Research BACKGROUND: Biosynthesis of leukotriene (LT) by arachidonic acid involves 5-lipoxygenase (5-LO) as an important precursor. Here, we evaluated the role of pseudohypericin (PHP) for its postulated 5-LO inhibitory activity along with a Cys-LT receptor antagonist zafirlukast (ZFL) against inflammatory response and tissue injury in mice. MATERIALS AND METHODS: The spinal injury was induced by two-level laminectomy of T6 and T7 vertebrae. The inflammation was assessed by histology, inflammatory mediators by enzyme-linked immunosorbent assay, apoptosis by Annexin-V, FAS staining, terminal deoxynucleoti-dyltransferase-mediated UTP end labeling (TUNEL) assay and expression of Bax and Bcl-2 by Western blot. Effect on motor recovery of hind limbs was evaluated for 10 days postinjury. RESULTS: The spinal injury resulted in tissue damage, apoptosis, edema, infiltration of neutrophils with increased expression of tumor necrosis factor-α (TNF-α) and cyclooxygenase-2 (COX-2). The spinal tissue showed elevated levels of prostaglandin E(2) (PGE2), and LTB(4) and increased phosphorylation of injured extracellular signal-regulated kinase-1/2 (ERK1/2). The PHP, ZFL and combination decreased inflammation, tissue injury and infiltration of neutrophils. Treatment also decreased the levels of PGE(2), phosphorylation of extracellular signal-regulated kinase-1/2 (pERK 1/2), LT, TNF-α and COX-2 with a marked reduction in apoptosis and improved the motor function. CONCLUSION: The present study confirmed 5-LO antagonist activity of PHP and established its neuroprotective role along with ZFL. Dove Medical Press 2018-08-01 /pmc/articles/PMC6078184/ /pubmed/30122897 http://dx.doi.org/10.2147/DDDT.S154814 Text en © 2018 Chen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Chen, Xiao-Gang
Hua, Fu
Wang, Shou-Guo
Xu, Yong-Yi
Yue, Hai-Tao
Sun, Jin
Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice
title Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice
title_full Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice
title_fullStr Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice
title_full_unstemmed Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice
title_short Zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice
title_sort zafirlukast in combination with pseudohypericin attenuates spinal cord injury and motor function in experimental mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078184/
https://www.ncbi.nlm.nih.gov/pubmed/30122897
http://dx.doi.org/10.2147/DDDT.S154814
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