Yin Jun, Xing Huili, Ye Jianping
Department of Endocrinology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai 200092, China.
Metabolism. 2008 May;57(5):712-7. doi: 10.1016/j.metabol.2008.01.013.
Berberine has been shown to regulate glucose and lipid metabolism in vitro and in vivo. This pilot study was to determine the efficacy and safety of berberine in the treatment of type 2 diabetes mellitus patients. In study A, 36 adults with newly diagnosed type 2 diabetes mellitus were randomly assigned to treatment with berberine or metformin (0.5 g 3 times a day) in a 3-month trial. The hypoglycemic effect of berberine was similar to that of metformin. Significant decreases in hemoglobin A1c (from 9.5%+/-0.5% to 7.5%+/-0.4%, P<.01), fasting blood glucose (from 10.6+/-0.9 mmol/L to 6.9+/-0.5 mmol/L, P<.01), postprandial blood glucose (from 19.8+/-1.7 to 11.1+/-0.9 mmol/L, P<.01), and plasma triglycerides (from 1.13+/-0.13 to 0.89+/-0.03 mmol/L, P<.05) were observed in the berberine group. In study B, 48 adults with poorly controlled type 2 diabetes mellitus were treated supplemented with berberine in a 3-month trial. Berberine acted by lowering fasting blood glucose and postprandial blood glucose from 1 week to the end of the trial. Hemoglobin A1c decreased from 8.1%+/-0.2% to 7.3%+/-0.3% (P<.001). Fasting plasma insulin and homeostasis model assessment of insulin resistance index were reduced by 28.1% and 44.7% (P<.001), respectively. Total cholesterol and low-density lipoprotein cholesterol were decreased significantly as well. During the trial, 20 (34.5%) patients experienced transient gastrointestinal adverse effects. Functional liver or kidney damages were not observed for all patients. In conclusion, this pilot study indicates that berberine is a potent oral hypoglycemic agent with beneficial effects on lipid metabolism.
黄连素已被证明在体外和体内均可调节糖脂代谢。这项初步研究旨在确定黄连素治疗2型糖尿病患者的疗效和安全性。在研究A中,36名新诊断的2型糖尿病成年患者被随机分配接受黄连素或二甲双胍治疗(0.5克,每日3次),为期3个月。黄连素的降糖效果与二甲双胍相似。黄连素组患者的糖化血红蛋白显著降低(从9.5%±0.5%降至7.5%±0.4%,P<0.01),空腹血糖(从10.6±0.9毫摩尔/升降至6.9±0.5毫摩尔/升,P<0.01),餐后血糖(从19.8±1.7降至11.1±0.9毫摩尔/升,P<0.01),以及血浆甘油三酯(从1.13±0.13降至0.89±0.03毫摩尔/升,P<0.05)。在研究B中,48名血糖控制不佳的2型糖尿病成年患者在为期3个月的试验中接受了黄连素补充治疗。从试验第1周直至结束,黄连素通过降低空腹血糖和餐后血糖发挥作用。糖化血红蛋白从8.1%±0.2%降至7.3%±0.3%(P<0.001)。空腹血浆胰岛素和胰岛素抵抗指数的稳态模型评估分别降低了28.1%和44.7%(P<0.001)。总胆固醇和低密度脂蛋白胆固醇也显著降低。在试验期间,20名(34.5%)患者出现短暂的胃肠道不良反应。所有患者均未观察到肝肾功能损害。总之,这项初步研究表明黄连素是一种有效的口服降糖药物,对脂质代谢具有有益作用。