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Chrysophanol, Physcion, Hesperidin and Curcumin Modulate the Gene Expression of Pro-Inflammatory Mediators Induced by LPS in HepG2: In Silico and Molecular Studies

Identifieur interne : 000597 ( Main/Exploration ); précédent : 000596; suivant : 000598

Chrysophanol, Physcion, Hesperidin and Curcumin Modulate the Gene Expression of Pro-Inflammatory Mediators Induced by LPS in HepG2: In Silico and Molecular Studies

Auteurs : Nabil Mohamed Selim [Égypte] ; Abdullah Abdurrahman Elgazar [Égypte] ; Nabil Mohie Abdel-Hamid [Égypte] ; Mohammed Rizk Abu El-Magd [Égypte] ; Aziz Yasri [Maroc] ; Hala Mohamed El Hefnawy [Égypte] ; Mansour Sobeh [Maroc, Allemagne]

Source :

RBID : PMC:6770650

Abstract

Hepatitis is an inflammatory condition that can develop hepatocellular carcinoma. Traditional medicine has always been the pillar of medical practice. However, it became less compatible with the current understanding of the diseases and the possible treatment. Therefore, in silico tools could be utilized for building the bridge between the legacy of the past and the current medical approaches allowing access to new therapeutic discoveries. In this work, a Chinese traditional medicine database was screened using structure-based virtual screening to identify molecules that could inhibit p38 alpha mitogen-activated protein kinase (MAPK). Out of the identified compounds, four selected compounds: chrysophanol, physcion, curcumin and hesperidin were isolated from their respective sources and their structures were confirmed by spectroscopic methods. These compounds decreased the gene expression of tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6) and interleukin-1beta (IL-1β) in lipopolysaccharide (LPS) induced inflammation in a hepatocellular carcinoma cell line (HepG2) in a dose-dependent manner. The molecular docking study revealed the specificity of these compounds towards p38 MAPK rather than other MAPKs. In conclusion, the molecular and in silico studies suggest that the isolated compounds could be a potential treatment for hepatitis by resolving inflammation controlled by MAPKs, thus limiting the development of further complications and lower side effects.


Url:
DOI: 10.3390/antiox8090371
PubMed: 31484451
PubMed Central: 6770650


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>Hepatitis is an inflammatory condition that can develop hepatocellular carcinoma. Traditional medicine has always been the pillar of medical practice. However, it became less compatible with the current understanding of the diseases and the possible treatment. Therefore, in silico tools could be utilized for building the bridge between the legacy of the past and the current medical approaches allowing access to new therapeutic discoveries. In this work, a Chinese traditional medicine database was screened using structure-based virtual screening to identify molecules that could inhibit p38 alpha mitogen-activated protein kinase (MAPK). Out of the identified compounds, four selected compounds: chrysophanol, physcion, curcumin and hesperidin were isolated from their respective sources and their structures were confirmed by spectroscopic methods. These compounds decreased the gene expression of tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6) and interleukin-1beta (IL-1β) in lipopolysaccharide (LPS) induced inflammation in a hepatocellular carcinoma cell line (HepG2) in a dose-dependent manner. The molecular docking study revealed the specificity of these compounds towards p38 MAPK rather than other MAPKs. In conclusion, the molecular and in silico studies suggest that the isolated compounds could be a potential treatment for hepatitis by resolving inflammation controlled by MAPKs, thus limiting the development of further complications and lower side effects.</p>
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<name sortKey="Shi, X" uniqKey="Shi X">X. Shi</name>
</author>
<author>
<name sortKey="Wen, S" uniqKey="Wen S">S. Wen</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Moon, P D" uniqKey="Moon P">P.-D. Moon</name>
</author>
<author>
<name sortKey="Han, N R" uniqKey="Han N">N.-R. Han</name>
</author>
<author>
<name sortKey="Lee, J S" uniqKey="Lee J">J.S. Lee</name>
</author>
<author>
<name sortKey="Hong, S" uniqKey="Hong S">S. Hong</name>
</author>
<author>
<name sortKey="Yoo, M S" uniqKey="Yoo M">M.-S. Yoo</name>
</author>
<author>
<name sortKey="Kim, H J" uniqKey="Kim H">H.-J. Kim</name>
</author>
<author>
<name sortKey="Kim, J H" uniqKey="Kim J">J.-H. Kim</name>
</author>
<author>
<name sortKey="Kang, S" uniqKey="Kang S">S. Kang</name>
</author>
<author>
<name sortKey="Jee, H W" uniqKey="Jee H">H.-W. Jee</name>
</author>
<author>
<name sortKey="Kim, H M" uniqKey="Kim H">H.-M. Kim</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Jeong, H J" uniqKey="Jeong H">H.-J. Jeong</name>
</author>
<author>
<name sortKey="Kim, H Y" uniqKey="Kim H">H.-Y. Kim</name>
</author>
<author>
<name sortKey="Kim, H M" uniqKey="Kim H">H.-M. Kim</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Kim, H P" uniqKey="Kim H">H.P. Kim</name>
</author>
<author>
<name sortKey="Son, K H" uniqKey="Son K">K.H. Son</name>
</author>
<author>
<name sortKey="Chang, H W" uniqKey="Chang H">H.W. Chang</name>
</author>
<author>
<name sortKey="Kang, S S" uniqKey="Kang S">S.S. Kang</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<affiliations>
<list>
<country>
<li>Allemagne</li>
<li>Maroc</li>
<li>Égypte</li>
</country>
</list>
<tree>
<country name="Égypte">
<noRegion>
<name sortKey="Selim, Nabil Mohamed" sort="Selim, Nabil Mohamed" uniqKey="Selim N" first="Nabil Mohamed" last="Selim">Nabil Mohamed Selim</name>
</noRegion>
<name sortKey="Abdel Hamid, Nabil Mohie" sort="Abdel Hamid, Nabil Mohie" uniqKey="Abdel Hamid N" first="Nabil Mohie" last="Abdel-Hamid">Nabil Mohie Abdel-Hamid</name>
<name sortKey="Abu El Magd, Mohammed Rizk" sort="Abu El Magd, Mohammed Rizk" uniqKey="Abu El Magd M" first="Mohammed Rizk" last="Abu El-Magd">Mohammed Rizk Abu El-Magd</name>
<name sortKey="El Hefnawy, Hala Mohamed" sort="El Hefnawy, Hala Mohamed" uniqKey="El Hefnawy H" first="Hala Mohamed" last="El Hefnawy">Hala Mohamed El Hefnawy</name>
<name sortKey="Elgazar, Abdullah Abdurrahman" sort="Elgazar, Abdullah Abdurrahman" uniqKey="Elgazar A" first="Abdullah Abdurrahman" last="Elgazar">Abdullah Abdurrahman Elgazar</name>
</country>
<country name="Maroc">
<noRegion>
<name sortKey="Yasri, Aziz" sort="Yasri, Aziz" uniqKey="Yasri A" first="Aziz" last="Yasri">Aziz Yasri</name>
</noRegion>
<name sortKey="Sobeh, Mansour" sort="Sobeh, Mansour" uniqKey="Sobeh M" first="Mansour" last="Sobeh">Mansour Sobeh</name>
</country>
<country name="Allemagne">
<noRegion>
<name sortKey="Sobeh, Mansour" sort="Sobeh, Mansour" uniqKey="Sobeh M" first="Mansour" last="Sobeh">Mansour Sobeh</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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