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AKR-501(YM477)是一种新型口服活性血小板生成素受体激动剂。

AKR-501 (YM477) a novel orally-active thrombopoietin receptor agonist.

作者信息

Fukushima-Shintani Mari, Suzuki Ken-ichi, Iwatsuki Yoshiyuki, Abe Masaki, Sugasawa Keizo, Hirayama Fukushi, Kawasaki Tomihisa, Nakahata Tatsutoshi

机构信息

QA, RA and Pharmacovigilance, Astellas Pharma Inc, Tokyo, Japan.

出版信息

Eur J Haematol. 2009 Apr;82(4):247-54. doi: 10.1111/j.1600-0609.2008.01198.x. Epub 2009 Jan 16.

Abstract

Thrombopoietin (TPO) is the principal physiologic regulator of platelet production. We have searched for small molecule compounds that mimic the action of TPO by using human TPO receptor-expressed in Ba/F3 cells, resulting in the discovery of AKR-501 (YM477). AKR-501 specifically targeted the TPO receptor and stimulated megakaryocytopoiesis throughout the development and maturation of megakaryocytes just as rhTPO did. AKR-501, however, was shown to be effective only in humans and chimpanzees with high species specificity. Therefore, we examined the in vivo platelet-increasing effect of AKR-501 in human platelet producing non-obese diabetic/severe combined immunodeficiency (NOD/SCID) mice transplanted with human fetal liver CD34(+) cells. Daily oral administration of AKR-501 dose-dependently increased the number of human platelets in these mice, with significance achieved at doses of 1 mg/kg and above. The peak unbound plasma concentrations of AKR-501 after administration at 1 mg/kg in NOD/SCID mice were similar to those observed following administration of an active oral dose in human subjects. These results suggest that AKR-501 is an orally-active TPO receptor agonist that may be useful in the treatment of patients with thrombocytopenia.

摘要

血小板生成素(TPO)是血小板生成的主要生理调节因子。我们通过利用在Ba/F3细胞中表达的人TPO受体,寻找模拟TPO作用的小分子化合物,从而发现了AKR - 501(YM477)。AKR - 501特异性靶向TPO受体,并在巨核细胞的整个发育和成熟过程中刺激巨核细胞生成,就像重组人血小板生成素(rhTPO)一样。然而,AKR - 501仅在人类和黑猩猩中显示出有效性,具有高度的物种特异性。因此,我们检测了AKR - 501在移植了人胎肝CD34(+)细胞的人血小板生成非肥胖糖尿病/严重联合免疫缺陷(NOD/SCID)小鼠体内的血小板增加效应。每天口服AKR - 501可使这些小鼠体内的人血小板数量呈剂量依赖性增加,在1mg/kg及以上剂量时具有显著性。在NOD/SCID小鼠中以1mg/kg给药后,AKR - 501的非结合血浆峰值浓度与在人类受试者中给予活性口服剂量后观察到的浓度相似。这些结果表明,AKR - 501是一种口服活性TPO受体激动剂,可能对治疗血小板减少症患者有用。

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