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The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β
OBJECTIVE: To investigate the modulated effects of HRF on cyclooxygenase isoform expression and its activity, using the human umbilical vein endothelial cell (HUVEC) model induced by interleukin-1 beta (IL-1β). METHODS: Cells were treated with indomethacin (positive control), HRF, and its components...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682063/ https://www.ncbi.nlm.nih.gov/pubmed/29234444 http://dx.doi.org/10.1155/2017/9383272 |
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author | Palo, Titchaporn Thaworn, Athiwat Charoenkij, Phornnapa Thamsermsang, Onusa Chotewuttakorn, Sirikul Tripatara, Pinpat Laohapand, Tawee Akarasereenont, Pravit |
author_facet | Palo, Titchaporn Thaworn, Athiwat Charoenkij, Phornnapa Thamsermsang, Onusa Chotewuttakorn, Sirikul Tripatara, Pinpat Laohapand, Tawee Akarasereenont, Pravit |
author_sort | Palo, Titchaporn |
collection | PubMed |
description | OBJECTIVE: To investigate the modulated effects of HRF on cyclooxygenase isoform expression and its activity, using the human umbilical vein endothelial cell (HUVEC) model induced by interleukin-1 beta (IL-1β). METHODS: Cells were treated with indomethacin (positive control), HRF, and its components at various concentrations prior to treatment with IL-1β at 24 h. Cell viability was determined by MTT assay. Moreover, the anti-inflammatory effects of HRF and its components through mRNA and protein expression were established using real-time quantitative PCR and Western blot, respectively. COX activity was identified via exogenous and endogenous PGE(2) productions using the EIA. RESULT: There was no cytotoxicity in HUVECs treated with HRF. None of the experimental conditions used in the study affected the expression of COX-1, but COX-2 protein expression was inhibited at concentrations under 10 µg/mL. Despite the significantly increased levels of exogenous PGE(2), HRF had no effect on COX-2 mRNA expression. However, the production of PGE(2) was lower at a concentration of 100 µg/mL HRF than at a concentration below 10 µg/mL. Interestingly, each component of HRF revealed different effects of the Ha-Rak formula. CONCLUSION: Our preliminary findings suggest that HRF and its components provide diverse modulation of COX-2 and PGE(2) at the in vitro level. |
format | Online Article Text |
id | pubmed-5682063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56820632017-12-11 The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β Palo, Titchaporn Thaworn, Athiwat Charoenkij, Phornnapa Thamsermsang, Onusa Chotewuttakorn, Sirikul Tripatara, Pinpat Laohapand, Tawee Akarasereenont, Pravit Evid Based Complement Alternat Med Research Article OBJECTIVE: To investigate the modulated effects of HRF on cyclooxygenase isoform expression and its activity, using the human umbilical vein endothelial cell (HUVEC) model induced by interleukin-1 beta (IL-1β). METHODS: Cells were treated with indomethacin (positive control), HRF, and its components at various concentrations prior to treatment with IL-1β at 24 h. Cell viability was determined by MTT assay. Moreover, the anti-inflammatory effects of HRF and its components through mRNA and protein expression were established using real-time quantitative PCR and Western blot, respectively. COX activity was identified via exogenous and endogenous PGE(2) productions using the EIA. RESULT: There was no cytotoxicity in HUVECs treated with HRF. None of the experimental conditions used in the study affected the expression of COX-1, but COX-2 protein expression was inhibited at concentrations under 10 µg/mL. Despite the significantly increased levels of exogenous PGE(2), HRF had no effect on COX-2 mRNA expression. However, the production of PGE(2) was lower at a concentration of 100 µg/mL HRF than at a concentration below 10 µg/mL. Interestingly, each component of HRF revealed different effects of the Ha-Rak formula. CONCLUSION: Our preliminary findings suggest that HRF and its components provide diverse modulation of COX-2 and PGE(2) at the in vitro level. Hindawi 2017 2017-10-29 /pmc/articles/PMC5682063/ /pubmed/29234444 http://dx.doi.org/10.1155/2017/9383272 Text en Copyright © 2017 Titchaporn Palo et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Palo, Titchaporn Thaworn, Athiwat Charoenkij, Phornnapa Thamsermsang, Onusa Chotewuttakorn, Sirikul Tripatara, Pinpat Laohapand, Tawee Akarasereenont, Pravit The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β |
title | The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β |
title_full | The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β |
title_fullStr | The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β |
title_full_unstemmed | The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β |
title_short | The Effects of Thai Herbal Ha-Rak Formula on COX Isoform Expression in Human Umbilical Vein Endothelial Cells Induced by IL-1β |
title_sort | effects of thai herbal ha-rak formula on cox isoform expression in human umbilical vein endothelial cells induced by il-1β |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682063/ https://www.ncbi.nlm.nih.gov/pubmed/29234444 http://dx.doi.org/10.1155/2017/9383272 |
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