Cargando…
Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway
Asthma is a persistent inflammatory disease of the bronchi characterized by oxidative stress, airway remodeling, and inflammation. Echinochrome (Ech) is a dark-red pigment with antioxidant and anti-inflammatory activities. In this research, we aimed to investigate the effects of Ech against asthma-i...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455754/ https://www.ncbi.nlm.nih.gov/pubmed/37623736 http://dx.doi.org/10.3390/md21080455 |
_version_ | 1785096528856088576 |
---|---|
author | Abdelmawgood, Islam Ahmed Mahana, Noha Ahmed Badr, Abeer Mahmoud Mohamed, Ayman Saber Al Shawoush, Abdeljalil Mohamed Atia, Tarek Abdelrazak, Amir Elhadi Sakr, Hader I. |
author_facet | Abdelmawgood, Islam Ahmed Mahana, Noha Ahmed Badr, Abeer Mahmoud Mohamed, Ayman Saber Al Shawoush, Abdeljalil Mohamed Atia, Tarek Abdelrazak, Amir Elhadi Sakr, Hader I. |
author_sort | Abdelmawgood, Islam Ahmed |
collection | PubMed |
description | Asthma is a persistent inflammatory disease of the bronchi characterized by oxidative stress, airway remodeling, and inflammation. Echinochrome (Ech) is a dark-red pigment with antioxidant and anti-inflammatory activities. In this research, we aimed to investigate the effects of Ech against asthma-induced inflammation, oxidative stress, and histopathological alterations in the spleen, liver, and kidney in mice. Mice were divided into four groups (n = 8 for each): control, asthmatic, and asthmatic mice treated intraperitoneally with 0.1 and 1 mg/kg of Ech. In vitro, findings confirmed the antioxidant and anti-inflammatory activities of Ech. Ech showed antiasthmatic effects by lowering the serum levels of immunoglobulin E (IgE), interleukin 4 (IL-4), and interleukin 1β (IL-1β). It attenuated oxidative stress by lowering malondialdehyde (MDA) and nitric oxide (NO) contents and increasing reduced glutathione (GSH), superoxide dismutase (SOD), glutathione-s-transferase (GST), and catalase (CAT) in the liver, spleen, and kidney. Moreover, it protected asthma-induced kidney and liver functions by increasing total protein and albumin and decreasing aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatinine, urea, and uric acid levels. Additionally, it ameliorated histopathological abnormalities in the lung, liver, spleen, and kidney. Additionally, molecular docking studies were used to examine the interactions between Ech and Kelch-like ECH-associated protein 1 (Keap1). PCR and Western blot analyses confirmed the association of Ech with Keap1 and, consequently, the regulatory role of Ech in the Keap1-(nuclear factor erythroid 2-related factor 2) Nrf2 signaling pathway in the liver, spleen, and kidney. According to our findings, Ech prevented asthma and its complications in the spleen, liver, and kidney. Inhibition of inflammation and oxidative stress are two of echinochrome’s therapeutic actions in managing asthma by modulating the Keap1/Nrf2 signaling pathway. |
format | Online Article Text |
id | pubmed-10455754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104557542023-08-26 Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway Abdelmawgood, Islam Ahmed Mahana, Noha Ahmed Badr, Abeer Mahmoud Mohamed, Ayman Saber Al Shawoush, Abdeljalil Mohamed Atia, Tarek Abdelrazak, Amir Elhadi Sakr, Hader I. Mar Drugs Article Asthma is a persistent inflammatory disease of the bronchi characterized by oxidative stress, airway remodeling, and inflammation. Echinochrome (Ech) is a dark-red pigment with antioxidant and anti-inflammatory activities. In this research, we aimed to investigate the effects of Ech against asthma-induced inflammation, oxidative stress, and histopathological alterations in the spleen, liver, and kidney in mice. Mice were divided into four groups (n = 8 for each): control, asthmatic, and asthmatic mice treated intraperitoneally with 0.1 and 1 mg/kg of Ech. In vitro, findings confirmed the antioxidant and anti-inflammatory activities of Ech. Ech showed antiasthmatic effects by lowering the serum levels of immunoglobulin E (IgE), interleukin 4 (IL-4), and interleukin 1β (IL-1β). It attenuated oxidative stress by lowering malondialdehyde (MDA) and nitric oxide (NO) contents and increasing reduced glutathione (GSH), superoxide dismutase (SOD), glutathione-s-transferase (GST), and catalase (CAT) in the liver, spleen, and kidney. Moreover, it protected asthma-induced kidney and liver functions by increasing total protein and albumin and decreasing aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatinine, urea, and uric acid levels. Additionally, it ameliorated histopathological abnormalities in the lung, liver, spleen, and kidney. Additionally, molecular docking studies were used to examine the interactions between Ech and Kelch-like ECH-associated protein 1 (Keap1). PCR and Western blot analyses confirmed the association of Ech with Keap1 and, consequently, the regulatory role of Ech in the Keap1-(nuclear factor erythroid 2-related factor 2) Nrf2 signaling pathway in the liver, spleen, and kidney. According to our findings, Ech prevented asthma and its complications in the spleen, liver, and kidney. Inhibition of inflammation and oxidative stress are two of echinochrome’s therapeutic actions in managing asthma by modulating the Keap1/Nrf2 signaling pathway. MDPI 2023-08-18 /pmc/articles/PMC10455754/ /pubmed/37623736 http://dx.doi.org/10.3390/md21080455 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Abdelmawgood, Islam Ahmed Mahana, Noha Ahmed Badr, Abeer Mahmoud Mohamed, Ayman Saber Al Shawoush, Abdeljalil Mohamed Atia, Tarek Abdelrazak, Amir Elhadi Sakr, Hader I. Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway |
title | Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway |
title_full | Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway |
title_fullStr | Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway |
title_full_unstemmed | Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway |
title_short | Echinochrome Ameliorates Physiological, Immunological, and Histopathological Alterations Induced by Ovalbumin in Asthmatic Mice by Modulating the Keap1/Nrf2 Signaling Pathway |
title_sort | echinochrome ameliorates physiological, immunological, and histopathological alterations induced by ovalbumin in asthmatic mice by modulating the keap1/nrf2 signaling pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10455754/ https://www.ncbi.nlm.nih.gov/pubmed/37623736 http://dx.doi.org/10.3390/md21080455 |
work_keys_str_mv | AT abdelmawgoodislamahmed echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway AT mahananohaahmed echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway AT badrabeermahmoud echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway AT mohamedaymansaber echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway AT alshawoushabdeljalilmohamed echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway AT atiatarek echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway AT abdelrazakamirelhadi echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway AT sakrhaderi echinochromeamelioratesphysiologicalimmunologicalandhistopathologicalalterationsinducedbyovalbumininasthmaticmicebymodulatingthekeap1nrf2signalingpathway |