Mechanism of low temperature-induced intestinal damage in Danio rerio and the mitigating effect of alanylglutamine

IF 4.4 Q1 ENVIRONMENTAL SCIENCES
Peng Chu , Yanfang Li , Xiaomen Han , Xiaojun Li , Yuxi Liu , Zhongxing Tang , Shaowu Yin , Tao Wang
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引用次数: 0

Abstract

Recent cold waves and abrupt seasonal temperature drops have significantly impacted aquaculture, slowing fish growth and causing mass mortality. The intestine plays a crucial role in digestion, nutrient absorption, metabolism, and physiological regulation. However, studies on the molecular mechanisms of fish intestinal response to low-temperature stress and methods to mitigate damage are limited. This study investigated the intestinal response of Danio rerio to low temperatures with three groups: a control group at 28 ​°C (CT28), a cryogenic group at 18 ​°C (ST18), and an extreme cryogenic group at 10 ​°C (LT10), with time points of 0, 12, 24, and 48 ​h. Results showed significant structural changes in the 18 ​°C group, with inflammatory infiltration starting at 24 ​h. Damage worsened in the 10 ​°C group, showing severe inflammation. Tunel staining revealed increased cell apoptosis with lower temperatures and longer exposure, peaking at 10 ​°C and 48 ​h following exposure (p ​< ​0.05). Alcian blue periodic acid-schiff stain revealed that lower temperatures promote an increase in the number of goblet cells. Metabolomics analysis compared intestinal metabolites between CT28 vs. ST18 and CT28 vs. LT10. Fifty-three metabolites were shared between the CT28_ST18 and CT28_LT10 groups in positive ion mode, and 16 in negative mode, with 22 and 9 metabolites showing linear changes. These 31 metabolites could serve as potential indicators for low-temperature stress in D. rerio. Specifically, eight metabolites from the lysophosphatidylcholine (LPC) group increased significantly, while antioxidant alanylglutamine (AGD) decreased. Supplementing the diet with 0.5% AGD reduced intestinal damage, and 1.0% AGD improved low-temperature tolerance. This study provides new insights into the molecular mechanisms of fish response to cold stress and lays the foundation for future research.
低温诱导小鼠肠道损伤的机制及丙氨酰谷氨酰胺的缓解作用
最近的寒潮和季节性气温骤降严重影响了水产养殖,减缓了鱼类生长并造成大量死亡。肠道在消化、营养吸收、代谢和生理调节中起着至关重要的作用。然而,鱼类肠道对低温胁迫反应的分子机制和减轻低温胁迫损伤的方法研究有限。本研究采用28°C对照组(CT28)、18°C低温组(ST18)和10°C极低温组(LT10)三组,时间点分别为0、12、24和48 h,研究了斑马鱼肠道对低温的反应。结果显示,18°C组组织结构发生明显变化,炎症浸润开始于24 h。10℃组损伤加重,出现严重炎症。隧道染色显示,温度越低,暴露时间越长,细胞凋亡增加,在暴露后10°C和48 h达到峰值(p < 0.05)。阿利新蓝周期性酸希夫染色显示,较低的温度促进杯状细胞数量的增加。代谢组学分析比较了CT28与ST18、CT28与LT10的肠道代谢物。CT28_ST18组和CT28_LT10组在正离子模式下共有53种代谢物,在负离子模式下共有16种代谢物,其中22种和9种代谢物呈线性变化。这31种代谢物可作为D. rerio低温胁迫的潜在指标。其中,溶血磷脂酰胆碱(LPC)组8种代谢物显著升高,抗氧化剂丙氨酰谷氨酰胺(AGD)降低。饲粮中添加0.5% AGD可减少肠道损伤,添加1.0% AGD可提高低温耐受性。本研究为鱼类冷应激反应的分子机制提供了新的认识,并为今后的研究奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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