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从三叶崖爬藤植物中提取的Borapetol B 化合物通过刺激胰岛素释放发挥降血糖作用。

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

机构信息

Department of Molecular Medicine and Surgery, Karolinska Institutet, Karolinska University Hospital, 171 76 Stockholm, Sweden ; Department of Diabetes, Cardiovascular, Diabetes and Nutrition Research Centre, Institute for Medical Research, 50588 Jalan Pahang, Kuala Lumpur, Malaysia.

出版信息

Evid Based Complement Alternat Med. 2013;2013:727602. doi: 10.1155/2013/727602. Epub 2013 Nov 10.

Abstract

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.

摘要

目的。评估从三叶崖爬藤中分离得到的化合物 1(C1)的抗糖尿病特性,该化合物在正常血糖控制的 Wistar(W)和自发性 2 型糖尿病 Goto-Kakizaki(GK)大鼠中具有降血糖作用。

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影响。通过分批孵育和胰岛灌注实验评估 C1 对胰岛素分泌的影响。

结果。急性口服 C1 可改善治疗组与安慰剂组的血糖水平,W 和 GK 大鼠的 0-120 分钟血糖曲线下面积分别为 72±17mmol/L 与 344±10mmol/L(P<0.001)和 492±63mmol/L 与 862±55mmol/L(P<0.01)。与安慰剂组相比,治疗组的 W 和 GK 大鼠在 30 分钟时血浆胰岛素水平增加了 2 倍(P<0.05)。C1 可剂量依赖性地增加 W 和 GK 分离胰岛在 3.3mM 和 16.7mM 葡萄糖时的胰岛素分泌。胰岛灌注实验表明,C1 不会通过破坏胰岛β细胞导致胰岛素漏出(P<0.001)。

结论。本研究提供了证据表明,三叶崖爬藤素 B(C1)具有抗糖尿病特性,主要是由于其刺激胰岛素释放。

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