Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.

Since Marine sponge Dysidea avara is regarded as a source of anti-inflammatory compounds, we decided to evaluate its potential anti-psoriatic activity in a psoriasis Imiquimod-induced in the mouse model. Psoriatic mice were treated with three different methanolic extracts of Dysidea avara compared w...

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Main Authors: Mostafa Khaledi, Behzad Sharif Makhmal Zadeh, Annahita Rezaie, Melika Nazemi, Mehdi Safdarian, Mohammad Bagher Nabavi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0241582
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spelling doaj-b660d13c608048f8963725ffc3c308982021-03-04T12:24:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-011511e024158210.1371/journal.pone.0241582Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.Mostafa KhalediBehzad Sharif Makhmal ZadehAnnahita RezaieMelika NazemiMehdi SafdarianMohammad Bagher NabaviSince Marine sponge Dysidea avara is regarded as a source of anti-inflammatory compounds, we decided to evaluate its potential anti-psoriatic activity in a psoriasis Imiquimod-induced in the mouse model. Psoriatic mice were treated with three different methanolic extracts of Dysidea avara compared with betamethasone-treated mice in in- vivo studies. Clinical skin severity was assessed with the psoriasis area index (PASI), whilst ELISA detected the expression of TNF-α, IL-17A, and IL-22. Dysidea avara activity was studied by employing GC-MS (to distinguish compounds), HPTLC (for skin permeation and accumulation), and SEA DOCK to predict single compound potential anti-inflammatory activity. After 7 days of treatment, mice treated with Dysidea avara displayed a dose-dependent, statistically significant improvement compared to controls (p< 0.001). In line with the clinical results, ELISA revealed a statistically significant decrease in IL-22, IL-17A, and TNF-α after treatment; the same SEA DOCK analysis suggests a possible anti-psoriatic activity of the extracts.https://doi.org/10.1371/journal.pone.0241582
collection DOAJ
language English
format Article
sources DOAJ
author Mostafa Khaledi
Behzad Sharif Makhmal Zadeh
Annahita Rezaie
Melika Nazemi
Mehdi Safdarian
Mohammad Bagher Nabavi
spellingShingle Mostafa Khaledi
Behzad Sharif Makhmal Zadeh
Annahita Rezaie
Melika Nazemi
Mehdi Safdarian
Mohammad Bagher Nabavi
Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.
PLoS ONE
author_facet Mostafa Khaledi
Behzad Sharif Makhmal Zadeh
Annahita Rezaie
Melika Nazemi
Mehdi Safdarian
Mohammad Bagher Nabavi
author_sort Mostafa Khaledi
title Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.
title_short Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.
title_full Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.
title_fullStr Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.
title_full_unstemmed Chemical profiling and anti-psoriatic activity of marine sponge (Dysidea avara) in induced imiquimod-psoriasis-skin model.
title_sort chemical profiling and anti-psoriatic activity of marine sponge (dysidea avara) in induced imiquimod-psoriasis-skin model.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description Since Marine sponge Dysidea avara is regarded as a source of anti-inflammatory compounds, we decided to evaluate its potential anti-psoriatic activity in a psoriasis Imiquimod-induced in the mouse model. Psoriatic mice were treated with three different methanolic extracts of Dysidea avara compared with betamethasone-treated mice in in- vivo studies. Clinical skin severity was assessed with the psoriasis area index (PASI), whilst ELISA detected the expression of TNF-α, IL-17A, and IL-22. Dysidea avara activity was studied by employing GC-MS (to distinguish compounds), HPTLC (for skin permeation and accumulation), and SEA DOCK to predict single compound potential anti-inflammatory activity. After 7 days of treatment, mice treated with Dysidea avara displayed a dose-dependent, statistically significant improvement compared to controls (p< 0.001). In line with the clinical results, ELISA revealed a statistically significant decrease in IL-22, IL-17A, and TNF-α after treatment; the same SEA DOCK analysis suggests a possible anti-psoriatic activity of the extracts.
url https://doi.org/10.1371/journal.pone.0241582
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