Tolerance Assessment of Atractylodes macrocephala Polysaccharide in the Diet of Largemouth Bass ( Micropterus salmoides ).
Bo DongLiyun WuQiaozhen ChenWenjie XuDinggang LiDong HanXiaoming ZhuHaokun LiuYunxia YangShouqi XieJunyan JinPublished in: Antioxidants (Basel, Switzerland) (2022)
Atractylodes macrocephala polysaccharide (AMP) can enhance antioxidant defense and anti-inflammation, as the tolerance levels of AMP in aquaculture is important for additive utilization. However, the tolerance dose of AMP is unknown. We assess the tolerance levels of AMP in juvenile largemouth bass (3.38 ± 0.11 g) by feeding them a 0, 400, 4000, or 8000 mg/kg AMP supplemented diet for 10 weeks. The 400 mg/kg AMP dose increased growth performance. The Nrf2/Keap1 signaling pathway was activated, as indicated by Keap1 and Nrf2 protein levels in the liver. Enhanced activity of antioxidant enzymes (SOD, GPx), together with increased mRNA levels of antioxidant genes ( sod , gpx ) and decreased accumulation of reactive oxygen species (ROS) and MDA, was found in the liver, implying the antioxidant effect of AMP. Nutrient absorption was enhanced by AMP, as reflected by the increased length of intestinal villi and microvilli. However, 4000 and 8000 mg/kg AMP induced oxidant stress, as indicated by increased plasma ALT and AST content and decreased mRNA levels of antioxidant genes ( sod , gpx ) in the liver and intestinal tissues. Inflammatory reactions were also induced by high doses of AMP, as reflected by enhanced levels of pro-inflammatory cytokines ( tnfα , nfκb ) in the liver, intestinal, and kidney tissues and inhibited levels of anti-inflammatory cytokines ( tgfβ , iκb ). Histological analysis reveals inflammatory cell infiltration and tissue damage. Thus, the safe tolerance margin of AMP supplement for largemouth bass was 400-4000 mg/kg.
Keyphrases
- protein kinase
- oxidative stress
- signaling pathway
- anti inflammatory
- reactive oxygen species
- gene expression
- diabetic rats
- dna damage
- induced apoptosis
- stem cells
- cell death
- mesenchymal stem cells
- cell therapy
- single cell
- binding protein
- bone marrow
- transcription factor
- inflammatory response
- lps induced
- dna methylation