全系统AMPK激活剂MK-8722改善葡萄糖平衡,但诱导心脏缩
Robert W Myers1, Hong-Ping Guan2, Juliann Ehrhart3
1In Vitro Pharmacology, Merck Research Laboratories, Kenilworth, NJ 07033, USA. robertwmyersphd@gmail.com iyassu@kallyope.com.
概括
一种新的药物MK-8722激活了5'- 氨酸单酸激活蛋白激酶 (AMPK),以改善葡萄糖的吸收和合成. 这显示了新陈代谢调节的前景,而不会导致低血糖.
科学领域:
- 生物化学
- 代谢调节
- 药理学
背景情况:
- 5 - 氨酸单酸激活蛋白激酶 (AMPK) 对于能量稳定至关重要.
- 由于缺乏有效的药理工具,人们对AMPK的作用和治疗潜力存在限制.
研究的目的:
- 开发和描述所有12种哺乳动物AMPK复合物的新型激活剂.
- 在体内研究AMPK激活的生理效应.
主要方法:
- 开发MK-8722,一个直接的,全ostericAMPK激活剂.
- 给动物和 rhesus 子 (包括糖尿病模型) 用MK- 8722
- 评估葡萄糖吸收,糖原合成,血糖和心脏参数.
主要成果:
- 在骨肌肉中强烈激活AMPK,导致胰岛素独立的葡萄糖吸收和糖原合成.
- 在没有低血糖的情况下观察到血糖的显著改善.
- 观察到心脏缩和心脏糖原增加,但没有明显的功能问题.
结论:
- MK-8722是一种强大的AMPK激活剂,具有治疗代谢障碍的潜力.
- 激活AMPK可以有效降低血糖,而不依赖于胰岛素.
- 需要进一步的研究才能充分了解长期MK-8722治疗对心脏的影响.
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