Barroso Wermerson Assunção, Serra Mariana Barreto, Abreu Iracelle Carvalho, Barbeiro Hermes Vieira, Fiamoncini Jarlei, de Alvarenga José Fernando Rinaldi, de Souza Heraldo Possolo, de Lima Thais Martins
Emergency Medicine Department, Medical School, University of São Paulo, São Paulo-SP, Brazil.
Physiological Sciences Department, Laboratory of Research and Post-graduation in Pharmacology (LPPF), Federal University of Maranhão, São Luís, Brazil.
Phytother Res. 2022 Feb;36(2):951-962. doi: 10.1002/ptr.7366. Epub 2022 Jan 11.
We investigate the effect of the banana green peels extract (BPE) as a preventive treatment against NAFLD in high-fat diet fed mice. Mice received daily doses of 100 or 250 mg/kg of BPE for 12 weeks along with the high-fat diet. BPE reduced weight gain (p < .0001), adipose tissue hypertrophy (p < .0001), and improved glucose homeostasis (p < .0001). Plasma levels of glucose-dependent insulinotropic polypeptide, triglycerides, total cholesterol, LDL-cholesterol, non-esterified fatty acids, aspartate and alanine transaminase, leptin, and resistin were decreased in BPE treated mice (p < .05). BPE effects on lipid metabolism were associated with decreased gene expression of lipogenic enzymes and increased expression of enzymes related to fatty acid and cholesterol degradation (p < .05). Plasma and liver bile acid (BA) profiles were modulated by BPE, with positive correlations between specific BA and UCP-1, CPT-1 and PGC-1β expression in brown adipose tissue (p < .05). BPE reduced hepatic steatosis and inflammation, possibly due to reduced p65 NF-κB nuclear translocation (p < .05) and modulation of oxidative stress (p < .05). These data indicate that BPE is a source of phytochemical compounds with promising effects toward the prevention of metabolic disorders associated with obesity.
我们研究了香蕉青皮提取物(BPE)对高脂饮食喂养小鼠非酒精性脂肪性肝病(NAFLD)的预防作用。小鼠在高脂饮食的同时,每天接受100或250mg/kg的BPE剂量,持续12周。BPE减轻了体重增加(p < 0.0001)、脂肪组织肥大(p < 0.0001),并改善了葡萄糖稳态(p < 0.0001)。在接受BPE治疗的小鼠中,葡萄糖依赖性促胰岛素多肽、甘油三酯、总胆固醇、低密度脂蛋白胆固醇、非酯化脂肪酸、天冬氨酸和丙氨酸转氨酶、瘦素和抵抗素的血浆水平均降低(p < 0.05)。BPE对脂质代谢的影响与脂肪生成酶的基因表达降低以及与脂肪酸和胆固醇降解相关酶的表达增加有关(p < 0.05)。BPE调节了血浆和肝脏胆汁酸(BA)谱,特定BA与棕色脂肪组织中UCP-1、CPT-1和PGC-1β表达之间呈正相关(p < 0.05)。BPE减轻了肝脏脂肪变性和炎症,可能是由于p65 NF-κB核转位减少(p < 0.05)和氧化应激调节(p < 0.05)。这些数据表明,BPE是一种植物化学化合物来源,对预防与肥胖相关的代谢紊乱具有有前景的作用。