Cargando…
Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells
BACKGROUND: Ligusticum porteri roots have been traditionally used in folk medicine, but the scientific basis is unclear. OBJECTIVE: To investigate the cytotoxicity, antioxidant, and immunomodulatory effects of L. porteri root extract on human promyelocytic leukemia (HL-60) cells and H(2)O(2)-induced...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5424556/ https://www.ncbi.nlm.nih.gov/pubmed/28539739 http://dx.doi.org/10.4103/0974-8490.204641 |
_version_ | 1783235153260183552 |
---|---|
author | Nguyen, Khanh Sparks, Jean Omoruyi, Felix |
author_facet | Nguyen, Khanh Sparks, Jean Omoruyi, Felix |
author_sort | Nguyen, Khanh |
collection | PubMed |
description | BACKGROUND: Ligusticum porteri roots have been traditionally used in folk medicine, but the scientific basis is unclear. OBJECTIVE: To investigate the cytotoxicity, antioxidant, and immunomodulatory effects of L. porteri root extract on human promyelocytic leukemia (HL-60) cells and H(2)O(2)-induced oxidative damaged HL-60 cells. MATERIALS AND METHODS: HL-60 cells were incubated with different concentrations of root extract, and cells were harvested for viability assays on day 3 and 7. Cytokine levels (interferon-gamma [IFN-γ], interleukin-2 [IL-2], and interleukin-10 [IL-10]) and antioxidant indexes (malondialdehyde [MDA], reduced glutathione [GSH], superoxide dismutase [SOD], and catalase [CAT]) in H(2)O(2)-induced-stressed HL-60 were measured after 2 days. RESULTS: The viability of HL-60 challenged with H(2)O(2) declined by 42% compared to unstressed cells. After 7 days of incubation with 200 or 400 μg/mL L. porteri, the viability of HL-60 cells was two-fold higher than the control. Stressed HL-60 cells treated with 100, 200, and 400 μg/mL L. porteri reduced the lipid peroxidation by 12%–13%. We noted an increase in GSH levels, SOD and CAT activities in stressed HL-60 supplemented with 400 μg/mL root extract. Treatment with 400 μg/mL L. porteri significantly (P < 0.05) increased IFN-γ and IL-2 in H(2)O(2)-challenged cells. CONCLUSION: Our data do not support the use of the extract as an antiproliferation and differentiation therapy for acute promyelocytic leukemia. The protective function of L. porteri root extract against oxidative stress could occur through increasing GSH and higher expression of antioxidant enzymes. SUMMARY: Findings from this study may not support the use of Ligusticum porteri root extract as an antiproliferation and differentiation therapy for acute promyelocytic leukemia. Our data suggest that L. porteri root extract may be a potential antioxidant with protective effect against the oxidation of reduced glutathione (GSH). Treatment with L. porteri root extract may be effective in preventing oxidative damage through increasing the activities of antioxidant enzymes (superoxide dismutase [SOD] and catalase [CAT]) in acute promyelocytic leukemia cells. [Image: see text] |
format | Online Article Text |
id | pubmed-5424556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54245562017-05-24 Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells Nguyen, Khanh Sparks, Jean Omoruyi, Felix Pharmacognosy Res Original Article BACKGROUND: Ligusticum porteri roots have been traditionally used in folk medicine, but the scientific basis is unclear. OBJECTIVE: To investigate the cytotoxicity, antioxidant, and immunomodulatory effects of L. porteri root extract on human promyelocytic leukemia (HL-60) cells and H(2)O(2)-induced oxidative damaged HL-60 cells. MATERIALS AND METHODS: HL-60 cells were incubated with different concentrations of root extract, and cells were harvested for viability assays on day 3 and 7. Cytokine levels (interferon-gamma [IFN-γ], interleukin-2 [IL-2], and interleukin-10 [IL-10]) and antioxidant indexes (malondialdehyde [MDA], reduced glutathione [GSH], superoxide dismutase [SOD], and catalase [CAT]) in H(2)O(2)-induced-stressed HL-60 were measured after 2 days. RESULTS: The viability of HL-60 challenged with H(2)O(2) declined by 42% compared to unstressed cells. After 7 days of incubation with 200 or 400 μg/mL L. porteri, the viability of HL-60 cells was two-fold higher than the control. Stressed HL-60 cells treated with 100, 200, and 400 μg/mL L. porteri reduced the lipid peroxidation by 12%–13%. We noted an increase in GSH levels, SOD and CAT activities in stressed HL-60 supplemented with 400 μg/mL root extract. Treatment with 400 μg/mL L. porteri significantly (P < 0.05) increased IFN-γ and IL-2 in H(2)O(2)-challenged cells. CONCLUSION: Our data do not support the use of the extract as an antiproliferation and differentiation therapy for acute promyelocytic leukemia. The protective function of L. porteri root extract against oxidative stress could occur through increasing GSH and higher expression of antioxidant enzymes. SUMMARY: Findings from this study may not support the use of Ligusticum porteri root extract as an antiproliferation and differentiation therapy for acute promyelocytic leukemia. Our data suggest that L. porteri root extract may be a potential antioxidant with protective effect against the oxidation of reduced glutathione (GSH). Treatment with L. porteri root extract may be effective in preventing oxidative damage through increasing the activities of antioxidant enzymes (superoxide dismutase [SOD] and catalase [CAT]) in acute promyelocytic leukemia cells. [Image: see text] Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5424556/ /pubmed/28539739 http://dx.doi.org/10.4103/0974-8490.204641 Text en Copyright: © 2017 Pharmacognosy Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Nguyen, Khanh Sparks, Jean Omoruyi, Felix Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells |
title | Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells |
title_full | Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells |
title_fullStr | Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells |
title_full_unstemmed | Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells |
title_short | Effects of Ligusticum porteri (Osha) Root Extract on Human Promyelocytic Leukemia Cells |
title_sort | effects of ligusticum porteri (osha) root extract on human promyelocytic leukemia cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5424556/ https://www.ncbi.nlm.nih.gov/pubmed/28539739 http://dx.doi.org/10.4103/0974-8490.204641 |
work_keys_str_mv | AT nguyenkhanh effectsofligusticumporteriosharootextractonhumanpromyelocyticleukemiacells AT sparksjean effectsofligusticumporteriosharootextractonhumanpromyelocyticleukemiacells AT omoruyifelix effectsofligusticumporteriosharootextractonhumanpromyelocyticleukemiacells |