Yasuda Nobuyuki, Nagakura Tadashi, Inoue Takashi, Yamazaki Kazuto, Katsutani Naruo, Takenaka Osamu, Clark Richard, Matsuura Fumiyoshi, Emori Eita, Yoshikawa Seiji, Kira Kazunobu, Ikuta Hironori, Okada Toshimi, Saeki Takao, Asano Osamu, Tanaka Isao
Tsukuba Research laboratories, Eisai Co., Ltd., 5-1-3, Tokodai, Tsukuba, Ibaraki, 300-2635, Japan.
Eur J Pharmacol. 2006 Oct 24;548(1-3):181-7. doi: 10.1016/j.ejphar.2006.08.011. Epub 2006 Aug 16.
Dipeptidyl peptidase IV (DPP-IV) inhibitors are expected to become a useful new class of anti-diabetic agent. The aim of the present study is to characterize the in vitro and in vivo profile of E3024, 3-but-2-ynyl-5-methyl-2-piperazin-1-yl-3,5-dihydro-4H-imidazo[4,5-d]pyridazin-4-one tosylate, which is a novel imidazopyridazinone-derived DPP-IV inhibitor. E3024 inhibited recombinant human and mouse DPP-IV with IC50 values of approximately 100 nM. E3024 inhibited DPP-IV in human, mouse, rat and canine plasma with IC50 values of 140 to 400 nM. In contrast, E3024 did not inhibit DPP-8 or DPP-9 activity. Kinetic analysis indicated that E3024 is a competitive DPP-IV inhibitor. In Zucker fa/fa rats, E3024 (1 mg/kg) reduced glucose excursion after glucose load, with increases in plasma insulin and active glucagon-like peptide-1 levels. In fasted rats, this compound did not cause hypoglycemia. In a rat 4-week toxicological study, no notable changes were found at doses up to 750 mg/kg. The present preclinical studies indicate that E3024 is a novel selective DPP-IV inhibitor with anti-diabetic effects and a good safety profile.
二肽基肽酶IV(DPP-IV)抑制剂有望成为一类新型的有效抗糖尿病药物。本研究的目的是对新型咪唑并哒嗪酮衍生的DPP-IV抑制剂E3024(3-丁-2-炔基-5-甲基-2-哌嗪-1-基-3,5-二氢-4H-咪唑并[4,5-d]哒嗪-4-酮甲苯磺酸盐)的体外和体内特性进行表征。E3024抑制重组人及小鼠DPP-IV的IC50值约为100 nM。E3024抑制人、小鼠、大鼠和犬血浆中的DPP-IV,IC50值为140至400 nM。相比之下,E3024不抑制DPP-8或DPP-9的活性。动力学分析表明E3024是一种竞争性DPP-IV抑制剂。在Zucker fa/fa大鼠中,E3024(1 mg/kg)可降低葡萄糖负荷后的血糖波动,同时使血浆胰岛素和活性胰高血糖素样肽-1水平升高。在禁食大鼠中,该化合物不会导致低血糖。在一项大鼠4周毒理学研究中,剂量高达750 mg/kg时未发现明显变化。目前的临床前研究表明,E3024是一种新型选择性DPP-IV抑制剂,具有抗糖尿病作用且安全性良好。