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高脂肪饮食改变哺乳结局:可能涉及炎症和 5-羟色胺能途径。

High fat diet alters lactation outcomes: possible involvement of inflammatory and serotonergic pathways.

机构信息

Department of Molecular and Cellular Physiology, College of Medicine, University of Cincinnati, Cincinnati, Ohio, United States of America.

出版信息

PLoS One. 2012;7(3):e32598. doi: 10.1371/journal.pone.0032598. Epub 2012 Mar 5.

Abstract

Delay in the onset of lactogenesis has been shown to occur in women who are obese, however the mechanism altered within the mammary gland causing the delay remains unknown. Consumption of high fat diets (HFD) has been previously determined to result decreased litters and litter numbers in rodent models due to a decrease in fertility. We examined the effects of feeding a HFD (60% kcal from fat) diet versus a low-fat diet (LFD; 10% kcal from fat) to female Wistar rats on lactation outcomes. Feeding of HFD diet resulted in increased pup weights compared to pups from LFD fed animals for 4 d post-partum. Lactation was delayed in mothers on HFD but they began to produce copious milk volumes beginning 2 d post-partum, and milk yield was similar to LFD by day 3. Mammary glands collected from lactating animals on HFD diet, displayed a disrupted morphologies, with very few and small alveoli. Consistently, there was a significant decrease in the mRNA expression of milk protein genes, glucose transporter 1 (GLUT1) and keratin 5 (K5), a luminobasal cell marker in the mammary glands of HFD lactating animals. Expression of tryptophan hydroxylase 1 (TPH1), the rate-limiting enzyme in serotonin (5-HT) biosynthesis, and the 5-HT(7) receptor (HTR7), which regulates mammary gland involution, were significantly increased in mammary glands of HFD animals. Additionally, we saw elevation of the inflammatory markers interleukin-6 (IL-6) and tumor necrosis factor-α (TNF- α). These results indicate that consumption of HFD impairs mammary parenchymal tissue and impedes its ability to synthesize and secrete milk, possibly through an increase in 5-HT production within the mammary gland leading to an inflammatory process.

摘要

已经证明,肥胖女性的泌乳起始会延迟,然而,导致这种延迟的乳腺内机制尚不清楚。先前的研究表明,高脂肪饮食(HFD)会导致啮齿动物模型的产仔数和仔鼠数量减少,这是由于生育能力下降所致。我们研究了给雌性 Wistar 大鼠喂食 HFD(脂肪供能比 60%)和低脂饮食(LFD;脂肪供能比 10%)对泌乳的影响。产后 4 天,与 LFD 喂养的仔鼠相比,HFD 喂养的仔鼠体重增加。HFD 喂养的母鼠泌乳延迟,但产后 2 天开始产生大量乳汁,第 3 天的产奶量与 LFD 相似。从 HFD 喂养的泌乳动物的乳腺组织中可以看出,其形态紊乱,只有很少的小腺泡。一致的是,HFD 泌乳动物乳腺中乳蛋白基因、葡萄糖转运蛋白 1(GLUT1)和角蛋白 5(K5)的 mRNA 表达显著减少,K5 是乳腺的亮细胞标志物。色氨酸羟化酶 1(TPH1),5-羟色胺(5-HT)生物合成的限速酶,和 5-HT7 受体(HTR7)的表达显著增加,HTR7 调节乳腺退化。此外,我们还观察到炎症标志物白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的升高。这些结果表明,HFD 的摄入会损害乳腺实质组织,并阻碍其合成和分泌乳汁的能力,这可能是通过增加乳腺内 5-HT 的产生,导致炎症过程。

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