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The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin

BACKGROUND: No dose of aspirin is free of bleeding risk. Even at a dose as low as 75 mg/day, the risk of upper gastrointestinal bleeding is twice as high as among nonusers. Nanoemulsions (NEs) are emulsion systems with droplet size in nanometer scale in which oil or water droplets are finely dispers...

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Autores principales: Mahmoud, Fatma Abd Elhalim, Hashem, Khalid S, Hussein Elkelawy, Asmaa Mohammed M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554396/
https://www.ncbi.nlm.nih.gov/pubmed/26345150
http://dx.doi.org/10.2147/IJN.S86947
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author Mahmoud, Fatma Abd Elhalim
Hashem, Khalid S
Hussein Elkelawy, Asmaa Mohammed M
author_facet Mahmoud, Fatma Abd Elhalim
Hashem, Khalid S
Hussein Elkelawy, Asmaa Mohammed M
author_sort Mahmoud, Fatma Abd Elhalim
collection PubMed
description BACKGROUND: No dose of aspirin is free of bleeding risk. Even at a dose as low as 75 mg/day, the risk of upper gastrointestinal bleeding is twice as high as among nonusers. Nanoemulsions (NEs) are emulsion systems with droplet size in nanometer scale in which oil or water droplets are finely dispersed in the opposite phase with the help of a suitable surfactant to stabilize the system. OBJECTIVES: The objective of this study was to determine the effect of aspirin NE in comparison to conventional aspirin. MATERIALS AND METHODS: A total of 24 male rats were used in the study and arbitrarily assigned to four groups. Group 1 was the control group, and was given saline. Group 2 was given blank NE 1.5 mL/kg orally. Group 3 was given aspirin 30 mg/kg body weight orally. Group 4 was given aspirin NE 30 mg/kg body weight orally. Rats were killed, and gastric tissue was quickly excised after dissection of the animals. The tissues were divided into three pieces. The first one was kept in formalin 10% for pathological investigation. The second piece was kept in liquid nitrogen for molecular investigation. The third piece was homogenized in ten volumes of ice-cold phosphate-buffered saline (pH 7) using a Teflon homogenizer until a uniform suspension was obtained. The homogenate was centrifuged at 4,000 rpm for 30 minutes at 4°C to separate the supernatant from cellular debris. The supernatant was then used for the estimation of biochemical assays. RESULTS: The present study shows that aspirin has a toxic effect on the stomach as a result of inducing marked oxidative damage and the release of reactive oxygen species. This was shown by the significant increase in TNFα, iNOS, prostaglandin E(2), and malondialdehyde levels, and also a significant decrease in glutathione, glutathione reductase, glutathione peroxidase, catalase, and superoxide dismutase. In the aspirin-treated group compared to the control group, the NE had a protective effect on the stomach and caused less injury than aspirin, indicated by significant decreases in TNFα, iNOS, prostaglandin E(2), and malondialdehyde levels, and also significant increases in glutathione, glutathione reductase, glutathione peroxidase, catalase, and superoxide dismutase. The biochemical results were confirmed by histopathological studies. CONCLUSION: Aspirin nanoemulsion has less toxic effect on the gastric mucosa compared to ordinary aspirin. This can be indicated by the increase of the antioxidant activity and the decrease of the inflammatory mediators in the gastric tissue.
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spelling pubmed-45543962015-09-04 The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin Mahmoud, Fatma Abd Elhalim Hashem, Khalid S Hussein Elkelawy, Asmaa Mohammed M Int J Nanomedicine Original Research BACKGROUND: No dose of aspirin is free of bleeding risk. Even at a dose as low as 75 mg/day, the risk of upper gastrointestinal bleeding is twice as high as among nonusers. Nanoemulsions (NEs) are emulsion systems with droplet size in nanometer scale in which oil or water droplets are finely dispersed in the opposite phase with the help of a suitable surfactant to stabilize the system. OBJECTIVES: The objective of this study was to determine the effect of aspirin NE in comparison to conventional aspirin. MATERIALS AND METHODS: A total of 24 male rats were used in the study and arbitrarily assigned to four groups. Group 1 was the control group, and was given saline. Group 2 was given blank NE 1.5 mL/kg orally. Group 3 was given aspirin 30 mg/kg body weight orally. Group 4 was given aspirin NE 30 mg/kg body weight orally. Rats were killed, and gastric tissue was quickly excised after dissection of the animals. The tissues were divided into three pieces. The first one was kept in formalin 10% for pathological investigation. The second piece was kept in liquid nitrogen for molecular investigation. The third piece was homogenized in ten volumes of ice-cold phosphate-buffered saline (pH 7) using a Teflon homogenizer until a uniform suspension was obtained. The homogenate was centrifuged at 4,000 rpm for 30 minutes at 4°C to separate the supernatant from cellular debris. The supernatant was then used for the estimation of biochemical assays. RESULTS: The present study shows that aspirin has a toxic effect on the stomach as a result of inducing marked oxidative damage and the release of reactive oxygen species. This was shown by the significant increase in TNFα, iNOS, prostaglandin E(2), and malondialdehyde levels, and also a significant decrease in glutathione, glutathione reductase, glutathione peroxidase, catalase, and superoxide dismutase. In the aspirin-treated group compared to the control group, the NE had a protective effect on the stomach and caused less injury than aspirin, indicated by significant decreases in TNFα, iNOS, prostaglandin E(2), and malondialdehyde levels, and also significant increases in glutathione, glutathione reductase, glutathione peroxidase, catalase, and superoxide dismutase. The biochemical results were confirmed by histopathological studies. CONCLUSION: Aspirin nanoemulsion has less toxic effect on the gastric mucosa compared to ordinary aspirin. This can be indicated by the increase of the antioxidant activity and the decrease of the inflammatory mediators in the gastric tissue. Dove Medical Press 2015-08-24 /pmc/articles/PMC4554396/ /pubmed/26345150 http://dx.doi.org/10.2147/IJN.S86947 Text en © 2015 Mahmoud et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. 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
Mahmoud, Fatma Abd Elhalim
Hashem, Khalid S
Hussein Elkelawy, Asmaa Mohammed M
The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin
title The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin
title_full The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin
title_fullStr The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin
title_full_unstemmed The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin
title_short The effect of aspirin nanoemulsion on TNFα and iNOS in gastric tissue in comparison with conventional aspirin
title_sort effect of aspirin nanoemulsion on tnfα and inos in gastric tissue in comparison with conventional aspirin
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554396/
https://www.ncbi.nlm.nih.gov/pubmed/26345150
http://dx.doi.org/10.2147/IJN.S86947
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