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Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation

In the present study, effects of salbutamol on the inflammatory parameters, angiogenesis, interleukin-1 beta (IL-1β) and vascular endothelial growth factor (VEGF) levels were investigated in an air pouch model of inflammation. Inflammation was induced by intrapouch administration of 1% solution of s...

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Autores principales: Eteraf-Oskouei, Tahereh, Akbarzadeh-Atashkhosrow, Arezu, Maghsudi, Milad, Najafi, Moslem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615866/
https://www.ncbi.nlm.nih.gov/pubmed/28974974
http://dx.doi.org/10.4103/1735-5362.213981
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author Eteraf-Oskouei, Tahereh
Akbarzadeh-Atashkhosrow, Arezu
Maghsudi, Milad
Najafi, Moslem
author_facet Eteraf-Oskouei, Tahereh
Akbarzadeh-Atashkhosrow, Arezu
Maghsudi, Milad
Najafi, Moslem
author_sort Eteraf-Oskouei, Tahereh
collection PubMed
description In the present study, effects of salbutamol on the inflammatory parameters, angiogenesis, interleukin-1 beta (IL-1β) and vascular endothelial growth factor (VEGF) levels were investigated in an air pouch model of inflammation. Inflammation was induced by intrapouch administration of 1% solution of sterile carrageenan in male Wistar rats. Salbutamol (125, 250 and 500 µg/rat) and salbutamol (500 µg/rat) plus propranolol (100 μg/rat) were injected intrapouch. After 6 and 72 h, fluid inside the pouches was collected to measure volume of exudates, leukocytes number and IL-1β levels. To determine angiogenesis, the granulation tissues were dissected out and weighed 3 days after carrageenan injection, then hemoglobin concentration was assessed using a hemoglobin assay kit. In addition, amount of VEGF in the exudates was measured 72 h after induction of inflammation. Leukocyte accumulation and the volume of exudates were significantly inhibited by salbutamol administration. In addition, salbutamol decreased the production of VEGF and IL-1β. Moreover, all used doses of salbutamol significantly inhibited angiogenesis. Interestingly, effects of salbutamol on the attenuation of angiogenesis and inflammatory parameters was similar to diclofenac sodium. Co-administration of propranolol with salbutamol clearly reversed anti-inflammatory effects of salbutamol. Salbutamol can decrease acute and chronic inflammation by β(2)-adrenergic receptors activation. The observed IL-1β and VEGF inhibitory properties of salbutamol may be responsible for anti-inflammatory and anti-angiogenic effect of the agent.
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spelling pubmed-56158662017-10-04 Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation Eteraf-Oskouei, Tahereh Akbarzadeh-Atashkhosrow, Arezu Maghsudi, Milad Najafi, Moslem Res Pharm Sci Original Article In the present study, effects of salbutamol on the inflammatory parameters, angiogenesis, interleukin-1 beta (IL-1β) and vascular endothelial growth factor (VEGF) levels were investigated in an air pouch model of inflammation. Inflammation was induced by intrapouch administration of 1% solution of sterile carrageenan in male Wistar rats. Salbutamol (125, 250 and 500 µg/rat) and salbutamol (500 µg/rat) plus propranolol (100 μg/rat) were injected intrapouch. After 6 and 72 h, fluid inside the pouches was collected to measure volume of exudates, leukocytes number and IL-1β levels. To determine angiogenesis, the granulation tissues were dissected out and weighed 3 days after carrageenan injection, then hemoglobin concentration was assessed using a hemoglobin assay kit. In addition, amount of VEGF in the exudates was measured 72 h after induction of inflammation. Leukocyte accumulation and the volume of exudates were significantly inhibited by salbutamol administration. In addition, salbutamol decreased the production of VEGF and IL-1β. Moreover, all used doses of salbutamol significantly inhibited angiogenesis. Interestingly, effects of salbutamol on the attenuation of angiogenesis and inflammatory parameters was similar to diclofenac sodium. Co-administration of propranolol with salbutamol clearly reversed anti-inflammatory effects of salbutamol. Salbutamol can decrease acute and chronic inflammation by β(2)-adrenergic receptors activation. The observed IL-1β and VEGF inhibitory properties of salbutamol may be responsible for anti-inflammatory and anti-angiogenic effect of the agent. Medknow Publications & Media Pvt Ltd 2017-10 /pmc/articles/PMC5615866/ /pubmed/28974974 http://dx.doi.org/10.4103/1735-5362.213981 Text en Copyright: © 2017 Research in Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Eteraf-Oskouei, Tahereh
Akbarzadeh-Atashkhosrow, Arezu
Maghsudi, Milad
Najafi, Moslem
Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation
title Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation
title_full Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation
title_fullStr Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation
title_full_unstemmed Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation
title_short Effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation
title_sort effects of salbutamol on the inflammatory parameters and angiogenesis in the rat air pouch model of inflammation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615866/
https://www.ncbi.nlm.nih.gov/pubmed/28974974
http://dx.doi.org/10.4103/1735-5362.213981
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