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母体低脂和高脂饮食会降低新生败血症小鼠的存活率并改变细胞因子信号传导。

Maternal low-fat and high-fat diet decreases survival and alters cytokine signaling in neonatal mice with sepsis.

作者信息

Bodilly Lauren, Weiner Sarah, Bermick Jennifer

出版信息

bioRxiv. 2025 Aug 1:2025.07.30.667518. doi: 10.1101/2025.07.30.667518.

Abstract

OBJECTIVE

Maternal malnutrition increases susceptibility to sepsis and mortality in neonates. The reason for this increased susceptibility remains unknown. We aimed to evaluate bacterial burden and serum cytokine levels in septic neonatal mice born to dams with malnutrition.

METHODS

6-week-old C57BL/6 dams were placed on a low-fat (LFD) (10% kcal from fat), control (CD) (18% kcal from fat), or high-fat (HFD) (60% kcal from fat) diet for 3 weeks prior to breeding. Sepsis was induced in P4-P6 offspring via intraperitoneal injection. Mice were monitored for survival. At 12h after sepsis, serum and peritoneal wash fluid were collected for bacterial count and serum cytokine levels. In the absence of infection, P4-P6 offspring had untargeted serum metabolomics performed.

RESULTS

Septic offspring of dams fed LFD and HFD had significantly higher mortality than offspring of dams fed CD. There was no difference in serum or peritoneal wash bacterial loads. Maternal diet and sepsis caused changes in basal serum cytokine levels, with HFD causing decreased cytokine elevation during sepsis. Maternal LFD and HFD altered similar metabolomic pathways in offspring.

CONCLUSION

Maternal LFD and HFD decrease survival during neonatal sepsis and alter serum cytokines and the metabolome, supporting a role for maternal nutrition in neonatal immune function and infection susceptibility.

摘要

目的

母体营养不良会增加新生儿患败血症的易感性和死亡率。这种易感性增加的原因尚不清楚。我们旨在评估营养不良母鼠所生败血症新生小鼠的细菌负荷和血清细胞因子水平。

方法

6周龄的C57BL/6母鼠在繁殖前3周分别给予低脂(LFD)(10%千卡来自脂肪)、对照(CD)(18%千卡来自脂肪)或高脂(HFD)(60%千卡来自脂肪)饮食。通过腹腔注射在P4 - P6代后代中诱导败血症。监测小鼠的存活率。败血症发生后12小时,收集血清和腹腔冲洗液用于细菌计数和血清细胞因子水平检测。在无感染情况下,对P4 - P6代后代进行非靶向血清代谢组学检测。

结果

喂食LFD和HFD的母鼠所生败血症后代的死亡率显著高于喂食CD的母鼠所生后代。血清或腹腔冲洗液中的细菌载量没有差异。母体饮食和败血症导致基础血清细胞因子水平发生变化,HFD导致败血症期间细胞因子升高幅度降低。母体LFD和HFD改变了后代相似的代谢途径。

结论

母体LFD和HFD会降低新生儿败血症期间的存活率,并改变血清细胞因子和代谢组,支持母体营养在新生儿免疫功能和感染易感性中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98f5/12324520/462ca94ef162/nihpp-2025.07.30.667518v1-f0001.jpg

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