Emai:marketing@kangtya.com
业务咨询专线:400-780-8018
Tel: +1(626)986-9880(U.S. - West Coast)
0044 7790 816 954 (Europe)
Email: marketing@medicilon.com
地址:上海市浦东新区川大路585号
邮编:201299
电话:+86 (21) 5859-1500(总机)
传真:+86 (21) 5859-6369
© 2023 上海z6尊龙生物医药股份有限公司 保留所有权利 沪ICP备87831543号-3
业务咨询
中国:
Email: marketing@kangtya.com
业务咨询专线:400-780-8018
(仅限服务咨询,其他事宜请拨打川沙总部电话)
川沙总部电话: +86 (21) 5859-1500
海外:
+1(626)986-9880(U.S. - West Coast)
0044 7790 816 954 (Europe)
Email:marketing@medicilon.com
z6尊龙请回答为您讲解GLP-1 作用机制。
GLP-1结合GLP-1R(1)后,GLP-1R在胰岛β细胞中偶联Gas蛋白,激活腺苷环化酶(AC),促使cAMP在细胞内含量升高,可激活蛋白激酶A(PKA)和cAMP调节的鸟嘌呤核苷酸交换因子2(Epac-2)。
After activation by full agonists such as GLP-1,GLP-1R(1) couples with Gas activates adenolate cyclase(AC),and causes the accumulation of cAMP.With increasing cAMP levels, protein kinase A(PKA) and the exchange protein directly activated by cAMP-2(Epac-2) are also activated.
PKA 和 Epac-2 可以关闭ATP依赖的钾离子通道,使细胞膜去极化;还可以激活电压依赖的钙离子通道(VDCC)使钙离子内流并产生动作电位,这些途径最终都会刺激血糖依赖性胰岛素的分泌。
PKA and Epac-2 trigger the closure of KATP and KV channels,which depolarizes the cell membrane opens voltage-dependent Calcium channels(VDCC) and causes Calcium influx and the promotion of insulin secretion by the islet beta cells