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Antidiabetic Effect of Oral Borapetol B Compound Isolated from the Plant Tinospora crispa by Stimulating Insulin Release

机译:通过刺激胰岛素的释放从植物脆皮草中分离得到的口服硼砂甲酚B化合物具有抗糖尿病作用

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摘要

Aims. To evaluate the antidiabetic properties of borapetol B known as compound 1 (C1) isolated from Tinospora crispa in normoglycemic control Wistar (W) and spontaneously type 2 diabetic Goto-Kakizaki (GK) rats. Methods. The effect of C1 on blood glucose and plasma insulin was assessed by an oral glucose tolerance test. The effect of C1 on insulin secretion was assessed by batch incubation and perifusion experiments using isolated pancreatic islets. Results. An acute oral administration of C1 improved blood glucose levels in treated versus placebo groups with areas under glucose curves 0–120 min being 72 ± 17 versus 344 ± 10 mmol/L (P < 0.001) and 492 ± 63 versus 862 ± 55 mmol/L (P < 0.01) in W and GK rats, respectively. Plasma insulin levels were increased by 2-fold in treated W and GK rats versus placebo group at 30 min (P < 0.05). C1 dose-dependently increased insulin secretion from W and GK isolated islets at 3.3 mM and 16.7 mM glucose. The perifusions of isolated islets indicated that C1 did not cause leakage of insulin by damaging islet beta cells (P < 0.001). Conclusion. This study provides evidence that borapetol B (C1) has antidiabetic properties mainly due to its stimulation of insulin release.
机译:目的为了评估在正常血糖控制Wistar(W)和自发2型糖尿病Goto-Kakizaki(GK)大鼠中从香叶Tinospora crispa分离出的被称为化合物1(C1)的甲硼替洛B的抗糖尿病特性。方法。通过口服葡萄糖耐量试验评估C1对血糖和血浆胰岛素的作用。通过使用分离的胰岛的分批孵育和灌注试验评估了C1对胰岛素分泌的作用。结果。急性口服C1可改善治疗组和安慰剂组的血糖水平,葡萄糖曲线下0–120 min的面积分别为72±17 vs 344±10 mmol / L(P <0.001)和492±63 vs 862±55 mmol / L在W和GK大鼠中分别为L(P <0.01)。与安慰剂组相比,经治疗的W和GK大鼠血浆胰岛素水平在30min时增加了2倍(P <0.05)。 C1剂量依赖性地增加了W和GK分离的胰岛在3.3 mM和16.7 mM葡萄糖下的胰岛素分泌。分离的胰岛的灌注表明,C1不会通过破坏胰岛β细胞而引起胰岛素泄漏(P <0.001)。结论。这项研究提供的证据表明,波普拉托B(C1)具有抗糖尿病特性,主要是因为它刺激了胰岛素的释放。

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