Mammary Protein Synthesis upon Long-Term Nutritional Restriction Was Attenuated by Oxidative-Stress-Induced Inhibition of Vacuolar H+-Adenosine Triphosphatase/Mechanistic Target of Rapamycin Complex 1 Signaling

被引:2
|
作者
Zhong, Heju [1 ]
Song, Yumo [1 ]
Wang, Peng [1 ]
Feng, Bin [1 ]
Zhang, Xiaoling [1 ]
Che, Lianqiang [1 ]
Lin, Yan [1 ]
Xu, Shengyu [1 ]
Li, Jian [1 ]
Wu, De [1 ]
Fang, Zhengfeng [1 ]
机构
[1] Sichuan Agr Univ, Anim Nutr Inst, Minist Educ, Key Lab Anim Dis Resistance Nutr, Chengdu 611130, Sichuan, Peoples R China
关键词
mTORC1; v-ATPase; oxidative stress; lysosome; beta-casein synthesis; METHIONINE; GROWTH; SOWS; METABOLOMICS; INFLAMMATION; CONSUMPTION; APOPTOSIS; OBESITY; ATPASE;
D O I
10.1021/acs.jafc.9b02170
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
To determine how nutritional restriction compromised milk synthesis, sows were fed 100% (control) or 76% (restricted) of the recommended feed allowance from postpartum day (PD)-1 to PD-28. In comparison to the control, more body reserves loss, increased plasma triglyceride and high-density lipoprotein cholesterol levels, and decreased plasma methionine concentrations were observed in the restricted group at PD-21. The increased plasma malondialdehyde level, decreased plasma histidine and taurine concentrations, and decreased glutathione peroxidase activity were observed at PD-28 when backfat loss further increased in the restricted group. In mammary glands, vacuolar H+-adenosine triphosphatase (v-ATPase), as the upstream of the mechanistic target of rapamycin (mTOR) signaling, showed decreased activity, while phosphorylation of mTOR, S6 kinase, and eukaryotic translation initiation factor 4E-binding protein 1 and beta-casein abundance all decreased following feed restriction. Altogether, long-term nutrition restriction could induce progressively aggravated oxidative stress and compromise mammary protein synthesis through repression of v-ATPase/mTORC1 signaling.
引用
收藏
页码:8950 / 8957
页数:8
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  • [1] Nutritional restriction induced oxidative stress might compromise mammary protein synthesis through inhibition of v-ATPase/mTORC1 signaling
    Zhong, H.
    Song, Y.
    Fang, Z.
    Feng, B.
    Zhang, X.
    Che, L.
    Lin, Y.
    Xu, S.
    Li, J.
    Wu, D.
    Fang, Z.
    JOURNAL OF ANIMAL SCIENCE, 2018, 96 : 264 - 265