饮食磷限制诱导黄斑蝶磷脂缺乏、内质网应激、炎症反应和肠道微生物群紊乱。

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Frontiers in Immunology Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI:10.3389/fimmu.2025.1592806
Zixiang Wu, Jiarong Guo, Kangle Lu, Kai Song, Ling Wang, Ruijuan Ma, Chunxiao Zhang, Xueshan Li
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引用次数: 0

摘要

本研究从磷脂含量和功能、内质网应激、炎症反应和肠道菌群等方面评价了低磷对斑鲈(Lateolabrax maculatus)的影响。配制有效磷水平分别为0.37%(低磷,LP)和0.75%(正常磷,NP)的饲料,每天2次喂鱼(3.53±0.34 g)至饱腹,连续10周。与NP组相比,LP组鱼体增重较低,腹脂率较高。进一步研究表明,低脂饲料降低了血清、肝脏和腹部脂肪组织中的磷脂含量,诱导内质网应激,破坏肝脏和腹部脂肪组织的脂质代谢,并引起腹部脂肪组织的炎症反应。此外,与饲喂NP饲料的鱼相比,LP饲料降低了肠道微生物多样性。与饲喂NP饲料的鱼相比,饲喂LP饲料的鱼表现出肠道中潜在代谢促进益生菌(如乳酸乳球菌)丰度的减少和潜在致病菌(如Plesiomonas)丰度的增加。PICRUSt2功能预测的结果也证实了饲喂LP饲料的鱼发生代谢紊乱以及代谢能力降低。上述结果表明,低脂饲料降低了斑鲈的磷脂含量,诱导内质网应激和炎症反应,进而干扰了斑鲈的脂质代谢和肠道微生物群。这些负面影响导致低脂饲料喂养的斑鲈比NP饲料喂养的斑鲈生长更差,腹部脂肪率更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dietary phosphorus restriction induced phospholipid deficiency, endoplasmic reticulum stress, inflammatory response and gut microbiota disorders in Lateolabrax maculatus.

This study evaluated the effects of low phosphorus on spotted seabass (Lateolabrax maculatus) from the perspective of phospholipid content and function, endoplasmic reticulum (ER) stress, inflammatory response and gut microbiota. Two diets were prepared to contain available phosphorus levels of 0.37% (low-phosphorus, LP) and 0.75% (normal-phosphorus, NP) and feed fish (3.53 ± 0.34 g) to satiety twice daily for 10 weeks. Compared with fish fed the NP diet, fish fed the LP diet showed lower body weight gain and higher abdominal fat percentage. Further studies showed that the LP diet decreased the content of phospholipid in the serum, liver, and abdominal fat tissue and induced ER stress and disruption of lipid metabolism in both of the liver and abdominal fat tissue and inflammatory responses in abdominal fat tissue. Furthermore, compared with fish fed the NP diet, the LP diet reduced microbial diversity in the gut. In contrast to fish fed the NP diet, fish fed the LP diet exhibited a decrease in the abundance of potential metabolically promoted probiotics (e.g., Lactococcus lactis) and an increase in the abundance of potential pathogenic bacteria (e.g., Plesiomonas) in the gut. The results of PICRUSt2 functional prediction also validated the metabolic disorders occurring in fish fed the LP diet as well as the reduced metabolic capacity. These results suggested that the LP diet decreased phospholipid content, induced ER stress and inflammatory responses then disturbed lipid metabolism and gut microbiota in spotted seabass. These negative effects contributed to poorer growth and higher percentage of abdominal fat in spotted seabass fed the LP diet than those of spotted seabass fed the NP diet.

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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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