Gupta Mrinal, Rumman Mohammad, Singh Babita, Mahdi Abbas Ali, Pandey Shivani
Department of Biochemistry, King George's Medical University, Lucknow, Uttar Pradesh, India.
Department of Biosciences, Integral University, Lucknow, Uttar Pradesh, India.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Mar;397(3):1647-1658. doi: 10.1007/s00210-023-02703-2. Epub 2023 Sep 14.
Berberine (BBR), a bioactive compound isolated from Coptidis Rhizoma, possesses diverse pharmacological activities including anti-bacterial, anti-inflammatory, antitumor, hypolipidemic, and anti-diabetic. However, its role as an anti-diabetic agent in animal models of dexamethasone (Dex)-induced diabetes remains unknown. Studies have shown that natural compounds including aloe, caper, cinnamon, cocoa, green and black tea, and turmeric can be used for treating Type 2 diabetes mellitus (DM). Compared to conventional drugs, natural compounds have less side effects and are easily available. Herein, we studied the anti-diabetic effects of BBR in a mice model of Dex-induced diabetes. HepG2 cell line was used for glucose release and glycogen synthesis studies. Cell proliferation was measured by methylthiotetrazole (MTT) assay. For animal studies, mice were treated with Dex (2 mg/kg, i.m.) for 30 days and effect of BBR at the doses 100, 200, and 500 mg/kg (p.o.) was analyzed. Glucose, insulin, and pyruvate tests were performed for evaluating the development of the diabetic model. Echo MRI was performed to assess the fat mass. Further, to elucidate the mechanism of action of BBR, mRNA expression of genes regulating gluconeogenesis, glucose uptake, and glycolysis was analyzed. In vitro BBR had no impact on cell viability up to a concentration of 50 μM. Moreover, BBR suppressed the hepatic glucose release and improved glucose tolerance in HepG2 cells. In vivo, BBR improved glucose homeostasis in diabetic mice as evidenced by enhanced glucose clearance, increased glycolysis, elevated glucose uptake, and decreased gluconeogenesis. Further, Dex treatment increased the total fat mass in mice, which was ameliorated by BBR treatment. BBR improves glucose tolerance by increasing glucose clearance, inhibiting hepatic glucose release, and decreasing obesity. Thus, BBR may become a potential therapeutic agent for treating glucocorticoid-induced diabetes and obesity in the future.
黄连素(BBR)是从黄连根茎中分离出的一种生物活性化合物,具有多种药理活性,包括抗菌、抗炎、抗肿瘤、降血脂和抗糖尿病作用。然而,其在 dexamethasone(Dex)诱导的糖尿病动物模型中作为抗糖尿病药物的作用尚不清楚。研究表明,包括芦荟、刺山柑、肉桂、可可、绿茶和红茶以及姜黄在内的天然化合物可用于治疗 2 型糖尿病(DM)。与传统药物相比,天然化合物副作用较小且易于获得。在此,我们研究了 BBR 在 Dex 诱导的糖尿病小鼠模型中的抗糖尿病作用。使用 HepG2 细胞系进行葡萄糖释放和糖原合成研究。通过甲基噻唑四唑(MTT)法测量细胞增殖。对于动物研究,小鼠用 Dex(2 mg/kg,腹腔注射)处理 30 天,并分析 BBR 在 100、200 和 500 mg/kg(口服)剂量下的作用。进行葡萄糖、胰岛素和丙酮酸测试以评估糖尿病模型的发展。进行 Echo MRI 以评估脂肪量。此外,为了阐明 BBR 的作用机制,分析了调节糖异生、葡萄糖摄取和糖酵解的基因的 mRNA 表达。在体外,BBR 在浓度高达 50 μM 时对细胞活力没有影响。此外,BBR 抑制 HepG2 细胞中的肝葡萄糖释放并改善葡萄糖耐量。在体内,BBR 改善了糖尿病小鼠的葡萄糖稳态,表现为葡萄糖清除增强、糖酵解增加、葡萄糖摄取升高和糖异生减少。此外,Dex 处理增加了小鼠的总脂肪量,而 BBR 处理改善了这一情况。BBR 通过增加葡萄糖清除、抑制肝葡萄糖释放和减轻肥胖来改善葡萄糖耐量。因此,BBR 未来可能成为治疗糖皮质激素诱导的糖尿病和肥胖的潜在治疗药物。