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Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats

The current study evaluated the anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats. Rats were assigned to the following groups: group I, sham (normal rats); group II, control (asthmatic rats); group III, E. hirta extract (100 µg/100 µl) and group IV, E....

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Autores principales: Xia, Mingyue, Liu, Ling, Qiu, Ruiqin, Li, Mingli, Huang, Wei, Ren, Gaowei, Zhang, Jinghui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211143/
https://www.ncbi.nlm.nih.gov/pubmed/30382409
http://dx.doi.org/10.1186/s13568-018-0707-z
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author Xia, Mingyue
Liu, Ling
Qiu, Ruiqin
Li, Mingli
Huang, Wei
Ren, Gaowei
Zhang, Jinghui
author_facet Xia, Mingyue
Liu, Ling
Qiu, Ruiqin
Li, Mingli
Huang, Wei
Ren, Gaowei
Zhang, Jinghui
author_sort Xia, Mingyue
collection PubMed
description The current study evaluated the anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats. Rats were assigned to the following groups: group I, sham (normal rats); group II, control (asthmatic rats); group III, E. hirta extract (100 µg/100 µl) and group IV, E. hirta extract (200 µg/100 µl). We performed a phytoscreening analysis of E. hirta extract. Inflammatory cell counts in the bronchoalveolar lavage fluid, levels of anti-inflammatory and antioxidant markers, apoptosis, and a histopathological analysis were carried out. An open field test determined anxiolytic activity, an elevated plus maze, a hole board test, and a cross test. The presence of 9,12,15-octadecatrien-1-ol, pentadecylic acid, ethyl linoleate, 1,2,3-trihydroxy benzene, gamma-tocopherol, 5-hydroxymethyl-2-furancarboxaldehyde, myristic acid, 7,10-octadecadienoic acid methyl ester, phytol, ethyl palmitate, and squalene in E. hirta extract was noted. Following treatment with E. hirta extract, total leukocytes, eosinophils, tumor necrosis factor-α (TNF-α), interleukin (IL-6), and lipid peroxidation were reduced, whereas antioxidant levels were increased. The mRNA expression levels of TNF-α, inducible nitric oxide synthase, IL-6, cyclooxygenase-2, caspase-3, p53, nerve growth factor precursor, and Bax were reduced, whereas that of Bcl-2 was increased. Apoptosis and caspase-3 protein expression were significantly reduced. Treatment of rats with E. hirta extract significantly reduced inflammation and eosinophil infiltration in the lungs. Taken together, these results led us to conclude that E. hirta extract has anti-inflammatory and anxiolytic effects on neonatal asthmatic rats with inflammation.
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spelling pubmed-62111432018-11-13 Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats Xia, Mingyue Liu, Ling Qiu, Ruiqin Li, Mingli Huang, Wei Ren, Gaowei Zhang, Jinghui AMB Express Original Article The current study evaluated the anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats. Rats were assigned to the following groups: group I, sham (normal rats); group II, control (asthmatic rats); group III, E. hirta extract (100 µg/100 µl) and group IV, E. hirta extract (200 µg/100 µl). We performed a phytoscreening analysis of E. hirta extract. Inflammatory cell counts in the bronchoalveolar lavage fluid, levels of anti-inflammatory and antioxidant markers, apoptosis, and a histopathological analysis were carried out. An open field test determined anxiolytic activity, an elevated plus maze, a hole board test, and a cross test. The presence of 9,12,15-octadecatrien-1-ol, pentadecylic acid, ethyl linoleate, 1,2,3-trihydroxy benzene, gamma-tocopherol, 5-hydroxymethyl-2-furancarboxaldehyde, myristic acid, 7,10-octadecadienoic acid methyl ester, phytol, ethyl palmitate, and squalene in E. hirta extract was noted. Following treatment with E. hirta extract, total leukocytes, eosinophils, tumor necrosis factor-α (TNF-α), interleukin (IL-6), and lipid peroxidation were reduced, whereas antioxidant levels were increased. The mRNA expression levels of TNF-α, inducible nitric oxide synthase, IL-6, cyclooxygenase-2, caspase-3, p53, nerve growth factor precursor, and Bax were reduced, whereas that of Bcl-2 was increased. Apoptosis and caspase-3 protein expression were significantly reduced. Treatment of rats with E. hirta extract significantly reduced inflammation and eosinophil infiltration in the lungs. Taken together, these results led us to conclude that E. hirta extract has anti-inflammatory and anxiolytic effects on neonatal asthmatic rats with inflammation. Springer Berlin Heidelberg 2018-11-01 /pmc/articles/PMC6211143/ /pubmed/30382409 http://dx.doi.org/10.1186/s13568-018-0707-z Text en © The Author(s) 2018 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.
spellingShingle Original Article
Xia, Mingyue
Liu, Ling
Qiu, Ruiqin
Li, Mingli
Huang, Wei
Ren, Gaowei
Zhang, Jinghui
Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats
title Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats
title_full Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats
title_fullStr Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats
title_full_unstemmed Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats
title_short Anti-inflammatory and anxiolytic activities of Euphorbia hirta extract in neonatal asthmatic rats
title_sort anti-inflammatory and anxiolytic activities of euphorbia hirta extract in neonatal asthmatic rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211143/
https://www.ncbi.nlm.nih.gov/pubmed/30382409
http://dx.doi.org/10.1186/s13568-018-0707-z
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