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靛玉红通过激活过氧化物酶体增殖物激活受体 γ 促进 3T3-L1 细胞脂肪分化和减少脂质堆积。

Indirubin promotes adipocyte differentiation and reduces lipid accumulation in 3T3‑L1 cells via peroxisome proliferator‑activated receptor γ activation.

机构信息

Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Tohoku Medical and Pharmaceutical University, Sendai, Miyagi 981‑8558, Japan.

出版信息

Mol Med Rep. 2020 Mar;21(3):1552-1560. doi: 10.3892/mmr.2020.10946. Epub 2020 Jan 16.

Abstract

The peroxisome proliferator‑activated receptor γ (PPARγ) plays an important role in insulin sensitivity and adipocyte differentiation. It is known as ligand‑receptor that improves insulin sensitivity in type 2 diabetes mellitus. Several kinds of indigo plant have been already used to treat diabetes in oriental traditional medicine, but its mechanism has not been clarified yet. To investigate the effect of indirubin, which is a component of Polygonum tinctorium on the cell differentiation and adipprocess in 3T3‑L1 cells, 3T3‑L1 cells were cultured to determine the effect of cell differentiation and glucose uptake with indirubin. As a result, Indirubin compound enhanced adipocyte differentiation in 3T3‑L1 cells similar to rosiglitazone. This effect was terminated by cotreatment with GW9662, a PPARγ antagonist. In mature 3T3‑L1 adipocytes, the lipid droplet size and accumulation were reduced by this compound. The basal and insulin‑stimulated glucose uptakes were also significantly increased. In addition, indirubin treatment significantly enhanced estrogen level by 1.64‑fold with mature adipocytes which can be attributed to its aromatase activity. Conclutionaly, this finding suggested that indirubin is a potential anti‑diabetic compound for type 2 diabetes mellitus by promoting adipocyte differentiation and glucose uptake via PPARγ.

摘要

过氧化物酶体增殖物激活受体γ(PPARγ)在胰岛素敏感性和脂肪细胞分化中发挥重要作用。它作为配体-受体,可改善 2 型糖尿病的胰岛素敏感性。几种靛蓝植物已被用于东方传统医学治疗糖尿病,但尚未阐明其机制。为了研究靛玉红(Polygonum tinctorium 的一种成分)对 3T3-L1 细胞中细胞分化和脂肪形成的影响,培养 3T3-L1 细胞以确定靛玉红对细胞分化和葡萄糖摄取的影响。结果表明,靛玉红化合物可增强 3T3-L1 细胞中的脂肪细胞分化,类似于罗格列酮。这种作用通过与 PPARγ 拮抗剂 GW9662 共同处理而终止。在成熟的 3T3-L1 脂肪细胞中,该化合物可减小和减少脂滴的大小和积累。基础和胰岛素刺激的葡萄糖摄取也显著增加。此外,靛玉红处理可使成熟脂肪细胞中的雌激素水平显著提高 1.64 倍,这归因于其芳香酶活性。综上所述,该发现表明,靛玉红通过促进脂肪细胞分化和葡萄糖摄取,通过 PPARγ 成为 2 型糖尿病的潜在抗糖尿病化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfea/7003043/5ca0fde6d531/MMR-21-03-1552-g00.jpg

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