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酚酸可预防性激素缺乏诱导的小鼠骨丢失和骨髓脂肪生成。

Phenolic acids prevent sex-steroid deficiency-induced bone loss and bone marrow adipogenesis in mice.

机构信息

Arkansas Children's Nutrition Center, Little Rock, Arkansas 72205, USA; Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.

Undergraduate Pre-Medical Program, University of Arkansas at Fayetteville, Fayetteville, Arkansas 72701, USA.

出版信息

J Nutr Biochem. 2024 May;127:109601. doi: 10.1016/j.jnutbio.2024.109601. Epub 2024 Feb 15.

Abstract

Phenolic acids, such as hippuric acid (HA) and 3-(3-hydroxyphenyl) propionic acid (3-3-PPA), can be produced from microbiome digestion of polyphenols. Previously it was found that HA and 3-3-PPA facilitate bone formation and suppress bone resorption. However, the mechanism of action by which HA and 3-3-PPA protect bone from degeneration is currently unknown. In this report, we present that HA and 3-3-PPA suppression of bone resorption is able to ameliorate bone loss in an ovariectomy (OVX) osteopenic mouse model though not to the extent of Zoledronic acid (ZA). HA and 3-3-PPA treatments were shown to significantly decrease bone marrow adipocyte-like cell formation and inhibited gene expression of key adipogenesis regulator peroxisome proliferator activated receptor gamma (PPARγ) and lipoprotein lipase (Lpl) in bone from OVX mice. In addition, ChIP experiments showed that the association between PPARγ and Lpl promoter region in preadipocyte-like cells was significantly suppressed following HA or 3-3-PPA treatment. Contrasting HA and 3-3-PPA, ZA significantly increased TRAP activity in the area close to growth plate and significantly suppressed bone cell proliferation. These data suggest that phenolics acids such as HA or 3-3-PPA may prevent bone degeneration after OVX through suppression of inflammatory milieu in the bone.

摘要

酚酸,如马尿酸(HA)和 3-(3-羟基苯基)丙酸(3-3-PPA),可以通过微生物组对多酚的消化产生。以前发现 HA 和 3-3-PPA 有助于骨形成并抑制骨吸收。然而,HA 和 3-3-PPA 保护骨骼免受退化的作用机制目前尚不清楚。在本报告中,我们提出 HA 和 3-3-PPA 抑制骨吸收能够通过改善去卵巢(OVX)骨质疏松小鼠模型中的骨丢失,但不如唑来膦酸(ZA)。HA 和 3-3-PPA 处理可显著减少骨髓脂肪细胞样细胞的形成,并抑制 OVX 小鼠骨中关键脂肪生成调节剂过氧化物酶体增殖物激活受体γ(PPARγ)和脂蛋白脂肪酶(Lpl)的基因表达。此外,ChIP 实验表明,在脂肪细胞样前体细胞中,PPARγ 与 Lpl 启动子区域之间的结合在 HA 或 3-3-PPA 处理后显著受到抑制。与 HA 和 3-3-PPA 相反,ZA 显著增加了生长板附近区域的 TRAP 活性,并显著抑制了骨细胞增殖。这些数据表明,HA 或 3-3-PPA 等酚酸可能通过抑制骨内炎症环境来预防 OVX 后的骨退化。

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