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Immune enhancement activities of silk lutein extract from Bombyx mori cocoons
BACKGROUND: Declining immune function poses an important clinical challenge worldwide and supplementation with natural products that possessing immune enhancing properties is a promising approach for preventing or delaying immune function decline. Cocoons from yellow silkworms are a significant sour...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101717/ https://www.ncbi.nlm.nih.gov/pubmed/25027489 http://dx.doi.org/10.1186/0717-6287-47-15 |
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author | Promphet, Porkaew Bunarsa, Sirirat Sutheerawattananonda, Manote Kunthalert, Duangkamol |
author_facet | Promphet, Porkaew Bunarsa, Sirirat Sutheerawattananonda, Manote Kunthalert, Duangkamol |
author_sort | Promphet, Porkaew |
collection | PubMed |
description | BACKGROUND: Declining immune function poses an important clinical challenge worldwide and supplementation with natural products that possessing immune enhancing properties is a promising approach for preventing or delaying immune function decline. Cocoons from yellow silkworms are a significant source of lutein, and this unexplored silk extract could be a viable alternative source for dietary lutein. This study assessed immunomodulatory activities of the silk lutein extract. Female BALB/c mice orally received lutein, either as silk or marigold extracts (10 or 20 mg/kg daily), or vehicle only (1% tween 80 in PBS pH 7.4) for 4 weeks. Natural killer (NK) cell activity, specific antibody production, lymphocyte subpopulations, mitogen-induced lymphocyte proliferation, and cytokine production were examined. RESULTS: Silk lutein extract increased NK cell activity, and the effect was dose-related whereas marigold lutein extract was ineffective. Silk lutein extract dose-dependently enhanced antibody production in pre-immunized mice but marigold lutein extract had no effect. Feeding with silk lutein extract increased the populations of CD3+ and CD4 + CD3 + cells. Silk lutein extract also stimulated concanavalin A- and lipopolysaccharide-induced proliferations of T and B lymphocytes, respectively. Moreover, silk lutein extract increased IL-2 and IFN-γ production while the effect of marigold lutein extract was undetectable. CONCLUSIONS: Together, silk lutein extract enhanced both innate and adaptive immune functions. This preparation may prove to be an effective supplement for strengthened immunity. |
format | Online Article Text |
id | pubmed-4101717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41017172014-07-18 Immune enhancement activities of silk lutein extract from Bombyx mori cocoons Promphet, Porkaew Bunarsa, Sirirat Sutheerawattananonda, Manote Kunthalert, Duangkamol Biol Res Research Article BACKGROUND: Declining immune function poses an important clinical challenge worldwide and supplementation with natural products that possessing immune enhancing properties is a promising approach for preventing or delaying immune function decline. Cocoons from yellow silkworms are a significant source of lutein, and this unexplored silk extract could be a viable alternative source for dietary lutein. This study assessed immunomodulatory activities of the silk lutein extract. Female BALB/c mice orally received lutein, either as silk or marigold extracts (10 or 20 mg/kg daily), or vehicle only (1% tween 80 in PBS pH 7.4) for 4 weeks. Natural killer (NK) cell activity, specific antibody production, lymphocyte subpopulations, mitogen-induced lymphocyte proliferation, and cytokine production were examined. RESULTS: Silk lutein extract increased NK cell activity, and the effect was dose-related whereas marigold lutein extract was ineffective. Silk lutein extract dose-dependently enhanced antibody production in pre-immunized mice but marigold lutein extract had no effect. Feeding with silk lutein extract increased the populations of CD3+ and CD4 + CD3 + cells. Silk lutein extract also stimulated concanavalin A- and lipopolysaccharide-induced proliferations of T and B lymphocytes, respectively. Moreover, silk lutein extract increased IL-2 and IFN-γ production while the effect of marigold lutein extract was undetectable. CONCLUSIONS: Together, silk lutein extract enhanced both innate and adaptive immune functions. This preparation may prove to be an effective supplement for strengthened immunity. BioMed Central 2014-04-28 /pmc/articles/PMC4101717/ /pubmed/25027489 http://dx.doi.org/10.1186/0717-6287-47-15 Text en © Promphet et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Promphet, Porkaew Bunarsa, Sirirat Sutheerawattananonda, Manote Kunthalert, Duangkamol Immune enhancement activities of silk lutein extract from Bombyx mori cocoons |
title | Immune enhancement activities of silk lutein extract from Bombyx mori cocoons |
title_full | Immune enhancement activities of silk lutein extract from Bombyx mori cocoons |
title_fullStr | Immune enhancement activities of silk lutein extract from Bombyx mori cocoons |
title_full_unstemmed | Immune enhancement activities of silk lutein extract from Bombyx mori cocoons |
title_short | Immune enhancement activities of silk lutein extract from Bombyx mori cocoons |
title_sort | immune enhancement activities of silk lutein extract from bombyx mori cocoons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101717/ https://www.ncbi.nlm.nih.gov/pubmed/25027489 http://dx.doi.org/10.1186/0717-6287-47-15 |
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