Sulforaphane Repairs Oxidative Stress Damage Induced by Oxidized Fish Oil by Activating <i>Nrf2</i> in <i>Litopenaeus vannamei</i>

Nuclear factor erythroid 2-related factor 2 (Nrf2) is an essential component in regulating oxidative stress. Sulforaphane (SFN) is a natural antioxidant and gene <i>Nrf2</i> agonist that can increase the antioxidant capacity of the organism and reduce oxidative stress. However, research on the repair of oxidative stress damage by SFN in aquatic animals remains extremely scarce. In order to further explore the function and role of SFN in the repair of oxidative stress injury in aquatic animals, this study took <i>Litopenaeus vannamei</i> as the research object. We established an oxidative stress model of <i>L. vannamei</i> through 6% oxidized fish oil (OFO) feeding. Methods, such as RNA interference (RNAi), qPCR, histopathological analysis, and TUNEL assay, were used to detect the changes in the oxidative stress status of <i>L. vannamei</i>. The results showed that the expression of <i>Nrf2</i> in the hepatopancreas of <i>L. vannamei</i> in the double-stranded RNA (dsRNA)-<i>Nrf2</i> + SFN group was significantly higher than that in the dsRNA-<i>Nrf2</i> group and control group at 24 h (<i>p</i> < 0.05). The transcription levels of antioxidant and autophagy genes in the SFN group were significantly higher than those in the control group (<i>p</i> < 0.05), and the expression of related genes in the dsRNA-<i>Nrf2</i> + SFN group was also higher than that in the dsRNA-<i>Nrf2</i> group. Histopathology showed that <i>Nrf2</i> knockdown would aggravate hepatopancreatic apoptosis and vacuolation, while SFN treatment after <i>Nrf2</i> knockdown could alleviate hepatopancreatic injury and apoptosis caused by OFO. The results indicated that SFN could repair the oxidative stress injury of <i>L. vannamei</i> induced by OFO by activating <i>Nrf2</i>. This study investigated the role of SFN in alleviating and repairing the oxidative stress damage in <i>L. vannamei</i> caused by OFO, aiming to provide a theoretical basis for the research on the antioxidant effect of SFN and the regulation of the antioxidant capacity of shrimp.

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Journal
Aquaculture Nutrition
Published
2025-01-01
DOI
https://doi.org/10.1155/anu/6665220
Primary Topic
Genomics, phytochemicals, and oxidative stress
Type
article
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article

Sulforaphane Repairs Oxidative Stress Damage Induced by Oxidized Fish Oil by Activating Nrf2 in Litopenaeus vannamei

Huiling Liu, Jichang Jian, Shiping Yang, Junliang Luo et al.
Aquaculture Nutrition
Genomics, phytochemicals, and oxidative stress
article

Sulforaphane Repairs Oxidative Stress Damage Induced by Oxidized Fish Oil by Activating Nrf2 in Litopenaeus vannamei

Huiling Liu, Jichang Jian, Shiping Yang, Junliang Luo, Shuanghu Cai, Lin Feng
article en

Abstract

Nuclear factor erythroid 2-related factor 2 (Nrf2) is an essential component in regulating oxidative stress. Sulforaphane (SFN) is a natural antioxidant and gene <i>Nrf2</i> agonist that can increase the antioxidant capacity of the organism and reduce oxidative stress. However, research on the repair of oxidative stress damage by SFN in aquatic animals remains extremely scarce. In order to further explore the function and role of SFN in the repair of oxidative stress injury in aquatic animals, this study took <i>Litopenaeus vannamei</i> as the research object. We established an oxidative stress model of <i>L. vannamei</i> through 6% oxidized fish oil (OFO) feeding. Methods, such as RNA interference (RNAi), qPCR, histopathological analysis, and TUNEL assay, were used to detect the changes in the oxidative stress status of <i>L. vannamei</i>. The results showed that the expression of <i>Nrf2</i> in the hepatopancreas of <i>L. vannamei</i> in the double-stranded RNA (dsRNA)-<i>Nrf2</i> + SFN group was significantly higher than that in the dsRNA-<i>Nrf2</i> group and control group at 24 h (<i>p</i> < 0.05). The transcription levels of antioxidant and autophagy genes in the SFN group were significantly higher than those in the control group (<i>p</i> < 0.05), and the expression of related genes in the dsRNA-<i>Nrf2</i> + SFN group was also higher than that in the dsRNA-<i>Nrf2</i> group. Histopathology showed that <i>Nrf2</i> knockdown would aggravate hepatopancreatic apoptosis and vacuolation, while SFN treatment after <i>Nrf2</i> knockdown could alleviate hepatopancreatic injury and apoptosis caused by OFO. The results indicated that SFN could repair the oxidative stress injury of <i>L. vannamei</i> induced by OFO by activating <i>Nrf2</i>. This study investigated the role of SFN in alleviating and repairing the oxidative stress damage in <i>L. vannamei</i> caused by OFO, aiming to provide a theoretical basis for the research on the antioxidant effect of SFN and the regulation of the antioxidant capacity of shrimp.

Aquaculture NutritionVol. 2025(1)
Guangdong Ocean University (CN)
Openalex Percentile: Top 80%
Genomics, phytochemicals, and oxidative stress
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