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Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis

Ginkgo biloba extract (GBE) is a plant extract obtained from the leaves of G biloba tree. The aim of this study was to evaluate the clinicopathologic characteristics and therapeutic effects of GBE on ischemic colitis (IC). Forty-seven patients with IC were divided as GBE group (n = 30) and routine g...

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Autores principales: Fang, Haiming, Zhang, Chenhong, Wang, Jiajia, Xu, Zhen, Qian, Cheng, Zhang, Lijiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393153/
https://www.ncbi.nlm.nih.gov/pubmed/30170462
http://dx.doi.org/10.1097/MD.0000000000012166
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author Fang, Haiming
Zhang, Chenhong
Wang, Jiajia
Xu, Zhen
Qian, Cheng
Zhang, Lijiu
author_facet Fang, Haiming
Zhang, Chenhong
Wang, Jiajia
Xu, Zhen
Qian, Cheng
Zhang, Lijiu
author_sort Fang, Haiming
collection PubMed
description Ginkgo biloba extract (GBE) is a plant extract obtained from the leaves of G biloba tree. The aim of this study was to evaluate the clinicopathologic characteristics and therapeutic effects of GBE on ischemic colitis (IC). Forty-seven patients with IC were divided as GBE group (n = 30) and routine group (n = 17). The routine group was given routine therapy, and the GBE group was given routine therapies plus GBE intravenous injection. Clinicopathologic characteristics, endoscopy findings, serum antioxidant enzymes, and inflammatory mediators were evaluated. About 89.3% initial symptom was acute-onset abdominal cramping and abdominal pain followed with hematochezia. The lesions were mainly located in sigmoid colon (80.8%). Serum level of superoxide dismutase (SOD) in patients with IC was significantly decreased (P < .05), while methane dicarboxylic aldehyde (MDA), tumor necrosis factor alpha (TNF-α), and interleukin-6 (IL-6) levels were significantly increased (P < .05). However, serum procalcitonin (PCT) level showed no significant change. Treatment of GBE resulted in quick remittance of abdominal pain and hematochezia, and significant attenuation of colon macroscopic and histologic damage in all patients. Furthermore, the treatment also significantly increased SOD levels, decreased MDA, TNF-α, and IL-6 levels (P < .05). Acute-onset abdominal cramping or abdominal pain followed with hematochezia was the mainly initial symptom of IC, and sigmoid and descending colons were the common vulnerable sites. GBE exerted a beneficial effect on IC with faster symptom relief and better mucosal healing, possibly through scavenging oxidative-free radicals and downregulating inflammatory mediators. GBE may be a promising candidate for protection against IC.
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spelling pubmed-63931532019-03-15 Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis Fang, Haiming Zhang, Chenhong Wang, Jiajia Xu, Zhen Qian, Cheng Zhang, Lijiu Medicine (Baltimore) Research Article Ginkgo biloba extract (GBE) is a plant extract obtained from the leaves of G biloba tree. The aim of this study was to evaluate the clinicopathologic characteristics and therapeutic effects of GBE on ischemic colitis (IC). Forty-seven patients with IC were divided as GBE group (n = 30) and routine group (n = 17). The routine group was given routine therapy, and the GBE group was given routine therapies plus GBE intravenous injection. Clinicopathologic characteristics, endoscopy findings, serum antioxidant enzymes, and inflammatory mediators were evaluated. About 89.3% initial symptom was acute-onset abdominal cramping and abdominal pain followed with hematochezia. The lesions were mainly located in sigmoid colon (80.8%). Serum level of superoxide dismutase (SOD) in patients with IC was significantly decreased (P < .05), while methane dicarboxylic aldehyde (MDA), tumor necrosis factor alpha (TNF-α), and interleukin-6 (IL-6) levels were significantly increased (P < .05). However, serum procalcitonin (PCT) level showed no significant change. Treatment of GBE resulted in quick remittance of abdominal pain and hematochezia, and significant attenuation of colon macroscopic and histologic damage in all patients. Furthermore, the treatment also significantly increased SOD levels, decreased MDA, TNF-α, and IL-6 levels (P < .05). Acute-onset abdominal cramping or abdominal pain followed with hematochezia was the mainly initial symptom of IC, and sigmoid and descending colons were the common vulnerable sites. GBE exerted a beneficial effect on IC with faster symptom relief and better mucosal healing, possibly through scavenging oxidative-free radicals and downregulating inflammatory mediators. GBE may be a promising candidate for protection against IC. Wolters Kluwer Health 2018-08-21 /pmc/articles/PMC6393153/ /pubmed/30170462 http://dx.doi.org/10.1097/MD.0000000000012166 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Research Article
Fang, Haiming
Zhang, Chenhong
Wang, Jiajia
Xu, Zhen
Qian, Cheng
Zhang, Lijiu
Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis
title Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis
title_full Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis
title_fullStr Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis
title_full_unstemmed Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis
title_short Therapeutic effects of Ginkgo biloba extract against acute ischemic colitis
title_sort therapeutic effects of ginkgo biloba extract against acute ischemic colitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393153/
https://www.ncbi.nlm.nih.gov/pubmed/30170462
http://dx.doi.org/10.1097/MD.0000000000012166
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