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Comparative Analysis of Apigenin-3 Acetate versus Apigenin and Methyl-Prednisolone in Inhibiting Proliferation and Gene Expression of Th1 Cells in Multiple Sclerosis
OBJECTIVE: In spite of the advances in therapeutic modalities, morbidity, due to multiple sclerosis (MS), still remains high. Therefore, a large body of research is endeavouring to discover or develop novel therapies with improved efficacy for treating MS patients. In the present study, we examined...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royan Institute
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257058/ https://www.ncbi.nlm.nih.gov/pubmed/37300292 http://dx.doi.org/10.22074/CELLJ.2023.1971743.1154 |
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author | Kasiri, Neda Ghannadian, Seyed Mostafa Hosseini, Reza Ahmadi, Leila Rahmati, Mahshid Ashtari, Fereshteh Pourazar, Abbasali Eskandari, Nahid |
author_facet | Kasiri, Neda Ghannadian, Seyed Mostafa Hosseini, Reza Ahmadi, Leila Rahmati, Mahshid Ashtari, Fereshteh Pourazar, Abbasali Eskandari, Nahid |
author_sort | Kasiri, Neda |
collection | PubMed |
description | OBJECTIVE: In spite of the advances in therapeutic modalities, morbidity, due to multiple sclerosis (MS), still remains high. Therefore, a large body of research is endeavouring to discover or develop novel therapies with improved efficacy for treating MS patients. In the present study, we examined the immunomodulatory effects of apigenin (Api) on peripheral blood mononuclear cells (PBMCs) isolated from MS patients. We also developed an acetylated form of Api (apigenin- 3-acetate) to improve In its blood-brain barrier (BBB) permeability. Additionally, we compared its anti-inflammatory properties to original Api and methyl-prednisolone-acetate (a standard therapy), as a potential option in treating MS patients. MATERIALS AND METHODS: The current study was an experimental-interventional research. The half maximal inhibitory concentration (IC(50)) values for apigenin-3-acetate, apigenin, and methyl-prednisolone-acetate were determined in healthy volunteers’ PBMCs (n=3). Gene expressions of T-box transcription factor (TBX21 or T-bet) and IFN-γ, as well as proliferation of T cells isolated from MS patients’ PBMCs (n=5), were examined in co-cultures of apigenin-3-acetate, Api and methyl-prednisolone-acetate after 48 hours of treatment, using quantitative reverse transcription polymerase chain reaction (qRT-PCR). RESULTS: Our findings showed that apigenin-3-acetate, apigenin, and methyl-prednisolone-acetate at concentrations of 80, 80, and 2.5 M could inhibit Th1 cell proliferation after 48 hours (P=0.001, P=0.036, and P=0.047, respectively); they also inhibited T-bet (P=0.015, P=0.019, and P=0.022) and interferon-γ (IFN-γ) gene expressions (P=0.0001). CONCLUSION: Our findings suggested that Api may have anti-inflammatory properties, possibly by inhibiting proliferation of IFN-producing Th1 cells. Moreover, comparative immunomodulatory effects were found for the acetylated version of apigenin-3-acetate versus Api and methyl-prednisolone-acetate. |
format | Online Article Text |
id | pubmed-10257058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-102570582023-06-11 Comparative Analysis of Apigenin-3 Acetate versus Apigenin and Methyl-Prednisolone in Inhibiting Proliferation and Gene Expression of Th1 Cells in Multiple Sclerosis Kasiri, Neda Ghannadian, Seyed Mostafa Hosseini, Reza Ahmadi, Leila Rahmati, Mahshid Ashtari, Fereshteh Pourazar, Abbasali Eskandari, Nahid Cell J Original Article OBJECTIVE: In spite of the advances in therapeutic modalities, morbidity, due to multiple sclerosis (MS), still remains high. Therefore, a large body of research is endeavouring to discover or develop novel therapies with improved efficacy for treating MS patients. In the present study, we examined the immunomodulatory effects of apigenin (Api) on peripheral blood mononuclear cells (PBMCs) isolated from MS patients. We also developed an acetylated form of Api (apigenin- 3-acetate) to improve In its blood-brain barrier (BBB) permeability. Additionally, we compared its anti-inflammatory properties to original Api and methyl-prednisolone-acetate (a standard therapy), as a potential option in treating MS patients. MATERIALS AND METHODS: The current study was an experimental-interventional research. The half maximal inhibitory concentration (IC(50)) values for apigenin-3-acetate, apigenin, and methyl-prednisolone-acetate were determined in healthy volunteers’ PBMCs (n=3). Gene expressions of T-box transcription factor (TBX21 or T-bet) and IFN-γ, as well as proliferation of T cells isolated from MS patients’ PBMCs (n=5), were examined in co-cultures of apigenin-3-acetate, Api and methyl-prednisolone-acetate after 48 hours of treatment, using quantitative reverse transcription polymerase chain reaction (qRT-PCR). RESULTS: Our findings showed that apigenin-3-acetate, apigenin, and methyl-prednisolone-acetate at concentrations of 80, 80, and 2.5 M could inhibit Th1 cell proliferation after 48 hours (P=0.001, P=0.036, and P=0.047, respectively); they also inhibited T-bet (P=0.015, P=0.019, and P=0.022) and interferon-γ (IFN-γ) gene expressions (P=0.0001). CONCLUSION: Our findings suggested that Api may have anti-inflammatory properties, possibly by inhibiting proliferation of IFN-producing Th1 cells. Moreover, comparative immunomodulatory effects were found for the acetylated version of apigenin-3-acetate versus Api and methyl-prednisolone-acetate. Royan Institute 2023-05 2023-05-28 /pmc/articles/PMC10257058/ /pubmed/37300292 http://dx.doi.org/10.22074/CELLJ.2023.1971743.1154 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited. https://creativecommons.org/licenses/by-nc/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial 3.0 (CC BY-NC 3.0) License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kasiri, Neda Ghannadian, Seyed Mostafa Hosseini, Reza Ahmadi, Leila Rahmati, Mahshid Ashtari, Fereshteh Pourazar, Abbasali Eskandari, Nahid Comparative Analysis of Apigenin-3 Acetate versus Apigenin and Methyl-Prednisolone in Inhibiting Proliferation and Gene Expression of Th1 Cells in Multiple Sclerosis |
title | Comparative Analysis of Apigenin-3 Acetate versus Apigenin and
Methyl-Prednisolone in Inhibiting Proliferation and Gene
Expression of Th1 Cells in Multiple Sclerosis |
title_full | Comparative Analysis of Apigenin-3 Acetate versus Apigenin and
Methyl-Prednisolone in Inhibiting Proliferation and Gene
Expression of Th1 Cells in Multiple Sclerosis |
title_fullStr | Comparative Analysis of Apigenin-3 Acetate versus Apigenin and
Methyl-Prednisolone in Inhibiting Proliferation and Gene
Expression of Th1 Cells in Multiple Sclerosis |
title_full_unstemmed | Comparative Analysis of Apigenin-3 Acetate versus Apigenin and
Methyl-Prednisolone in Inhibiting Proliferation and Gene
Expression of Th1 Cells in Multiple Sclerosis |
title_short | Comparative Analysis of Apigenin-3 Acetate versus Apigenin and
Methyl-Prednisolone in Inhibiting Proliferation and Gene
Expression of Th1 Cells in Multiple Sclerosis |
title_sort | comparative analysis of apigenin-3 acetate versus apigenin and
methyl-prednisolone in inhibiting proliferation and gene
expression of th1 cells in multiple sclerosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257058/ https://www.ncbi.nlm.nih.gov/pubmed/37300292 http://dx.doi.org/10.22074/CELLJ.2023.1971743.1154 |
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