Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity

Recent advances in astaxanthin encapsulation have been reported, but hepatotoxic effect remains unclear. The present investigation therefore aimed to examine the effects of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on liver toxicity. Wistar rats were divided into 6 gro...

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Main Authors: Niracha Yanyium, Wanida Sukketsiri, Pennapa Chonpathompikunlert, Wanwimol Klaypradit, Jirawat Saetan, Marais, Sebastien, Supita Tanasawet
Format: Article
Language:English
Published: Penerbit Universiti Kebangsaan Malaysia 2024
Online Access:http://journalarticle.ukm.my/23636/
http://journalarticle.ukm.my/23636/1/SDD%201.pdf
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author Niracha Yanyium,
Wanida Sukketsiri,
Pennapa Chonpathompikunlert,
Wanwimol Klaypradit,
Jirawat Saetan,
Marais, Sebastien
Supita Tanasawet,
author_facet Niracha Yanyium,
Wanida Sukketsiri,
Pennapa Chonpathompikunlert,
Wanwimol Klaypradit,
Jirawat Saetan,
Marais, Sebastien
Supita Tanasawet,
author_sort Niracha Yanyium,
building UKM Institutional Repository
collection Online Access
description Recent advances in astaxanthin encapsulation have been reported, but hepatotoxic effect remains unclear. The present investigation therefore aimed to examine the effects of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on liver toxicity. Wistar rats were divided into 6 groups as control (C), and receiving vitamin E (VE), astaxanthin commercial (AC), astaxanthin extracted from white shrimp shells (AE), astaxanthin encapsulation into powder form (AP), and blank powder (BP). The evaluation of liver in response to astaxanthin administration was then assessed in terms of biochemical parameters and histopathological features. Liver enzymes, aspartate aminotransferase (AST) and alanine aminotransferase (ALT), showed no significant differences among all groups of treatment. Histopathological study showed no abnormal changes on liver tissue including hepatic inflammation. Our data demonstrated that astaxanthin encapsulation did not increase the expression of NF-ҡB nuclear translocation and CYP2E1 in comparison with the control group. Additionally, in this study, the consumption of astaxanthin and vitamin E resulted in a reduction in the oxidative stress index (OSI), while the levels of antioxidant enzymes, including glutathione peroxidase (GPx) and superoxide dismutase (SOD), were significantly increased compared to the control group. Our data suggested that astaxanthin encapsulation does not cause hepatic toxicity, contributing useful information in the applications of astaxanthin encapsulation technology.
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spelling oai:generic.eprints.org:236362024-06-06T08:03:37Z http://journalarticle.ukm.my/23636/ Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity Niracha Yanyium, Wanida Sukketsiri, Pennapa Chonpathompikunlert, Wanwimol Klaypradit, Jirawat Saetan, Marais, Sebastien Supita Tanasawet, Recent advances in astaxanthin encapsulation have been reported, but hepatotoxic effect remains unclear. The present investigation therefore aimed to examine the effects of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on liver toxicity. Wistar rats were divided into 6 groups as control (C), and receiving vitamin E (VE), astaxanthin commercial (AC), astaxanthin extracted from white shrimp shells (AE), astaxanthin encapsulation into powder form (AP), and blank powder (BP). The evaluation of liver in response to astaxanthin administration was then assessed in terms of biochemical parameters and histopathological features. Liver enzymes, aspartate aminotransferase (AST) and alanine aminotransferase (ALT), showed no significant differences among all groups of treatment. Histopathological study showed no abnormal changes on liver tissue including hepatic inflammation. Our data demonstrated that astaxanthin encapsulation did not increase the expression of NF-ҡB nuclear translocation and CYP2E1 in comparison with the control group. Additionally, in this study, the consumption of astaxanthin and vitamin E resulted in a reduction in the oxidative stress index (OSI), while the levels of antioxidant enzymes, including glutathione peroxidase (GPx) and superoxide dismutase (SOD), were significantly increased compared to the control group. Our data suggested that astaxanthin encapsulation does not cause hepatic toxicity, contributing useful information in the applications of astaxanthin encapsulation technology. Penerbit Universiti Kebangsaan Malaysia 2024 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/23636/1/SDD%201.pdf Niracha Yanyium, and Wanida Sukketsiri, and Pennapa Chonpathompikunlert, and Wanwimol Klaypradit, and Jirawat Saetan, and Marais, Sebastien and Supita Tanasawet, (2024) Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity. Sains Malaysiana, 53 (2). pp. 239-248. ISSN 0126-6039 https://www.ukm.my/jsm/english_journals/vol53num2_2024/contentsVol53num2_2024.html
spellingShingle Niracha Yanyium,
Wanida Sukketsiri,
Pennapa Chonpathompikunlert,
Wanwimol Klaypradit,
Jirawat Saetan,
Marais, Sebastien
Supita Tanasawet,
Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity
title Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity
title_full Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity
title_fullStr Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity
title_full_unstemmed Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity
title_short Evaluation of encapsulated astaxanthin from white shrimp shells (Litopenaeus vannamei) on hepatotoxicity
title_sort evaluation of encapsulated astaxanthin from white shrimp shells (litopenaeus vannamei) on hepatotoxicity
url http://journalarticle.ukm.my/23636/
http://journalarticle.ukm.my/23636/
http://journalarticle.ukm.my/23636/1/SDD%201.pdf