Choi Esther, Baek Seoyoung, Baek Kuanglim, Kim Hye-Kyeong
Department of Food Science and Nutrition, The Catholic University of Korea, Bucheon 14662, Korea.
Nutr Res Pract. 2021 Oct;15(5):568-578. doi: 10.4162/nrp.2021.15.5.568. Epub 2021 Apr 8.
BACKGROUND/OBJECTIVES: L. (guava) leaves have been shown to exhibit hypoglycemic and antidiabetic effects in rodents. This study investigated the effects of guava leaf extract on adipogenesis, glucose uptake, and lipolysis of adipocytes to examine whether the antidiabetic properties are mediated through direct effects on adipocytes.
MATERIALS/METHODS: 3T3-L1 cells were treated with 25, 50, 100 µg/mL of methanol extract from guava leaf extract (GLE) or 0.1% dimethyl sulfoxide as a control. Lipid accumulation was evaluated with Oil Red O Staining and AdipoRed assay. Immunoblotting was performed to measure the expression of adipogenic transcription factors, fatty acid synthase (FAS), and AMP-activated protein kinase (AMPK). Glucose uptake under basal or insulin-stimulated condition was measured using a glucose analog 2-[-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-D-glucose. Lipolysis from fully differentiated adipocytes was measured by free fatty acids release into the culture medium in the presence or absence of epinephrine.
Oil Red O staining and AdipoRed assay have shown that GLE treatment reduced lipid accumulation during adipocyte differentiation. Mitotic clonal expansion, an early essential event for adipocyte differentiation, was inhibited by GLE treatment. GLE inhibited the expression of transcription factors involved in adipocyte differentiation, such as peroxisome proliferator-activated receptor γ (PPARγ), CCAAT/enhancer-binding protein α (C/EBPα), and sterol regulatory element-binding protein-1c (SREBP-1c). FAS expression was also decreased while the phosphorylation of AMPK was increased by GLE treatment. In addition, GLE increased insulin-induced glucose uptake into adipocytes. In lipid-filled mature adipocytes, GLE enhanced epinephrine-induced lipolysis but reduced basal lipolysis dose-dependently.
The results show that GLE inhibits adipogenesis and improves adipocyte function by reducing basal lipolysis and increasing insulin-stimulated glucose uptake in adipocytes, which can be partly associated with antidiabetic effects of guava leaves.
背景/目的:番石榴叶已被证明在啮齿动物中具有降血糖和抗糖尿病作用。本研究调查了番石榴叶提取物对脂肪生成、葡萄糖摄取和脂肪细胞脂解的影响,以检验其抗糖尿病特性是否通过对脂肪细胞的直接作用介导。
材料/方法:用25、50、100μg/mL的番石榴叶提取物甲醇提取物(GLE)或0.1%二甲亚砜作为对照处理3T3-L1细胞。用油红O染色和AdipoRed测定法评估脂质积累。进行免疫印迹以测量脂肪生成转录因子、脂肪酸合酶(FAS)和AMP活化蛋白激酶(AMPK)的表达。在基础或胰岛素刺激条件下,使用葡萄糖类似物2-[-(7-硝基苯并-2-恶唑-1,3-二氮杂环丁烷-4-基)氨基]-2-脱氧-D-葡萄糖测量葡萄糖摄取。通过在有无肾上腺素的情况下向培养基中释放游离脂肪酸来测量完全分化的脂肪细胞的脂解。
油红O染色和AdipoRed测定法表明,GLE处理减少了脂肪细胞分化过程中的脂质积累。有丝分裂克隆扩增是脂肪细胞分化早期的一个重要事件,GLE处理抑制了该过程。GLE抑制参与脂肪细胞分化的转录因子的表达,如过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT/增强子结合蛋白α(C/EBPα)和固醇调节元件结合蛋白-1c(SREBP-1c)。GLE处理还降低了FAS的表达,同时增加了AMPK的磷酸化。此外,GLE增加了胰岛素诱导的脂肪细胞对葡萄糖的摄取。在充满脂质的成熟脂肪细胞中,GLE增强了肾上腺素诱导的脂解,但剂量依赖性地降低了基础脂解。
结果表明,GLE通过减少基础脂解和增加胰岛素刺激的脂肪细胞葡萄糖摄取来抑制脂肪生成并改善脂肪细胞功能,这可能部分与番石榴叶的抗糖尿病作用相关。