<abstract xmlns="http://www.w3.org/1999/xhtml">
<sec id="j_jvetres-2021-0051_s_005">
<h3>Introduction</h3>
<p>Ozone is not harmful itself; however, it directly oxidises biomolecules and produces radical-dependent cytotoxicity. Exposure to ozone is by inhalation and therefore the lungs develop the main anti-inflammatory response, while ozone has an indirect impact on the other organs. This study investigated the local and systemic effects of the ozone-associated inflammatory response.</p>
</sec>
<sec id="j_jvetres-2021-0051_s_006">
<h3>Material and Methods</h3>
<p>Three groups each of 5 Wistar Han rats aged 6 months were exposed for 2h to airborne ozone at 0.5 ppm and a fourth identical group were unexposed controls. Sacrifice was at 3h after exposure for control rats and one experimental group and at 24 h and 48 h for the others. Lung and liver samples were evaluated for changes in expression of transforming growth factor beta 1, anti-inflammatory interleukin 10, pro-inflammatory tumour necrosis factor alpha and interleukin 1 beta and two nuclear factor kappa-light-chain-enhancer of B cells subunit genes. Total RNA was isolated from the samples in spin columns and cDNA was synthesised in an RT-PCR. Expression levels were compared to those of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and analysed statistically.</p></sec>
<sec id="j_jvetres-2021-0051_s_007">
<h3>Results</h3>
<p>All variables changed non-linearly over time comparing experimental groups to the control. Conspicuous expression changes in the subunit genes and cytokines were observed in both evaluated organs.</p></sec>
<sec id="j_jvetres-2021-0051_s_008">
<h3>Conclusion</h3>
<p>Locally and systemically, inflammation responses to ozone inhalation include regulation of certain genes’ expression. The mechanisms are unalike in lungs and liver but ozone exerts a similar effect in both organs. A broader range of variables influential on ozone response should be studied in the future.</p></sec>
</abstract>

Introduction
Ozone is not harmful itself; however, it directly oxidises biomolecules and produces radical-dependent cytotoxicity. Exposure to ozone is by inhalation and therefore the lungs develop the main anti-inflammatory response, while ozone has an indirect impact on the other organs. This study investigated the local and systemic effects of the ozone-associated inflammatory response.


Material and Methods
Three groups each of 5 Wistar Han rats aged 6 months were exposed for 2h to airborne ozone at 0.5 ppm and a fourth identical group were unexposed controls. Sacrifice was at 3h after exposure for control rats and one experimental group and at 24 h and 48 h for the others. Lung and liver samples were evaluated for changes in expression of transforming growth factor beta 1, anti-inflammatory interleukin 10, pro-inflammatory tumour necrosis factor alpha and interleukin 1 beta and two nuclear factor kappa-light-chain-enhancer of B cells subunit genes. Total RNA was isolated from the samples in spin columns and cDNA was synthesised in an RT-PCR. Expression levels were compared to those of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and analysed statistically.

Results
All variables changed non-linearly over time comparing experimental groups to the control. Conspicuous expression changes in the subunit genes and cytokines were observed in both evaluated organs.

Conclusion
Locally and systemically, inflammation responses to ozone inhalation include regulation of certain genes’ expression. The mechanisms are unalike in lungs and liver but ozone exerts a similar effect in both organs. A broader range of variables influential on ozone response should be studied in the future.

Local and systemic influence of toxic levels of airborne ozone on the inflammatory response in rats

Journal of Veterinary Research

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Introduction
Ozone is not harmful itself; however, it directly oxidises biomolecules and produces radical-dependent cytotoxicity. Exposure to ozone is by...

Local and systemic influence of toxic levels of airborne ozone on the inflammatory response in rats

Article Category: Review article

Online veröffentlicht: 06. Okt. 2021

Seitenbereich: 513 - 517

Eingereicht: 27. Apr. 2020

Akzeptiert: 09. Sept. 2021

DOI: https://doi.org/10.2478/jvetres-2021-0051

Schlüsselwörter
ozone, free radicals, inflammatory response, respiratory tract inflammation, rat

© 2021 M. Chmielewska-Krzesińska, K. Wąsowicz, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Local and systemic influence of toxic levels of airborne ozone on the inflammatory response in rats

Article Category: Review article

Online veröffentlicht: 06. Okt. 2021

Seitenbereich: 513 - 517

Eingereicht: 27. Apr. 2020

Akzeptiert: 09. Sept. 2021

DOI: https://doi.org/10.2478/jvetres-2021-0051

Schlüsselwörterozone, free radicals, inflammatory response, respiratory tract inflammation, rat

© 2021 M. Chmielewska-Krzesińska, K. Wąsowicz, published by Sciendo

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Schlüsselwörter
ozone, free radicals, inflammatory response, respiratory tract inflammation, rat