Srilatha B R, Ananda S
Department of Studies in Chemistry, University of Mysore , Manasagangothri, Mysore, Karnataka , India.
Pharm Biol. 2014 May;52(5):597-602. doi: 10.3109/13880209.2013.858268. Epub 2013 Nov 20.
Traditional medicine is used by over 60% of the world's population for health care. Mukia maderaspatana (L.) M. Roem. (Cucurbitaceae) (Mukia) is extensively used in folklore medicine as an antidiabetic plant. It is rich in phenolics that contribute to its medicinal properties.
Mukia extract and phenolics such as quercetin and phloroglucinol are investigated for their in vitro antidiabetic activity.
Quercetin, phloroglucinol, and methanol extract of the dried whole plant (0.25 and 0.5 mg/ml) were studied for the inhibition of gluconeogenesis in rat liver slices and glucose uptake in isolated rat hemi-diaphragm (50 and 100 µg/ml). Phenolics of Mukia were analyzed by HPLC.
Glucose (1.2 mg/g/h) was synthesized from pyruvate and the synthesis was completely inhibited by insulin (1 U/ml). Quercetin at 0.25 and 0.5 mg/ml caused 65% and 89% inhibition (0.42 mg/g/h and 0.13 mg/g/h glucose). Addition of insulin did not increase inhibition. Phloroglucinol inhibited 100% glucose production with or without insulin. Mukia (0.25 mg/ml) inhibited gluconeogenesis (0.65 mg/g/h) by 45%, and with insulin, inhibition increased to 50% (0.59 mg/g/h). At 0.5 mg/ml, glucose production was stimulated by1.2-fold, but with insulin it was inhibited by 89% (0.13 mg/g/h glucose). Mukia had no effect on glucose uptake, but potentiated the action of insulin mediated glucose uptake (152.82 ± 13.30 mg/dl/g/30 min) compared with insulin control (112.41 ± 9.14 mg/dl/g/30 min) (p < 0.05). HPLC analysis revealed the presence of phenolics.
Results provide scientific rationale for the use of Mukia in folk medicine as an antidiabetic nutraceutical.
世界上超过60%的人口使用传统医学进行医疗保健。马㼎儿(Mukia maderaspatana (L.) M. Roem.)(葫芦科)在民间医学中被广泛用作抗糖尿病植物。它富含酚类物质,这些酚类物质赋予了其药用特性。
研究马㼎儿提取物以及槲皮素和间苯三酚等酚类物质的体外抗糖尿病活性。
研究了槲皮素、间苯三酚以及干燥全株的甲醇提取物(0.25和0.5毫克/毫升)对大鼠肝切片糖异生的抑制作用以及对分离的大鼠半膈肌葡萄糖摄取的影响(50和100微克/毫升)。采用高效液相色谱法分析马㼎儿的酚类物质。
丙酮酸可合成葡萄糖(1.2毫克/克/小时),胰岛素(1单位/毫升)可完全抑制该合成过程。0.25和0.5毫克/毫升的槲皮素分别导致65%和89%的抑制率(葡萄糖生成量分别为0.42毫克/克/小时和0.13毫克/克/小时)。添加胰岛素并未增强抑制作用。无论有无胰岛素存在,间苯三酚均能100%抑制葡萄糖生成。马㼎儿(0.25毫克/毫升)使糖异生(0.65毫克/克/小时)降低45%,加入胰岛素后,抑制率增至50%(0.59毫克/克/小时)。在0.5毫克/毫升时,可以使葡萄糖生成量增加1.2倍,但加入胰岛素后,抑制率达89%(葡萄糖生成量为0.13毫克/克/小时)。马㼎儿对葡萄糖摄取无影响,但与胰岛素对照组(112.41±9.14毫克/分升/克/30分钟)相比,可增强胰岛素介导的葡萄糖摄取作用(152.82±13.30毫克/分升/克/30分钟)(p<0.05)。高效液相色谱分析显示存在酚类物质。
研究结果为马㼎儿在民间医学中作为抗糖尿病营养保健品的应用提供了科学依据。