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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.
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页码:8950 / 8957
页数:8
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