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烷基黄嘌呤衍生物的研究。II. 新型支气管扩张剂1-甲基-3-丙基黄嘌呤(MPX)的药代动力学和药效学研究。

Studies on alkyl-xanthine derivatives. II. Pharmacokinetic and pharmacodynamic studies of a new bronchodilator, 1-methyl-3-propylxanthine (MPX).

作者信息

Ruttikorn A, Takagi K, Nadai M, Kuzuya T, Ogawa K, Miyamoto K, Hasegawa T

机构信息

Department of Hospital Pharmacy, Nagoya University School of Medicine, Japan.

出版信息

Jpn J Pharmacol. 1988 Nov;48(3):341-7. doi: 10.1254/jjp.48.341.

Abstract

A new xanthine derivative bronchodilator, 1-methyl-3-propylxanthine (MPX), and 1-methyl-3-butylxanthine (MBX) were synthesized. We evaluated their relaxant effects on tracheal smooth muscle isolated from guinea pigs and pharmacokinetic characteristics in rats using 1,3-dimethylxanthine (theophylline, TPH) as the reference drug. Dose-dependent relaxant effects were observed in the concentration range of 1 x 10(-6) to 1 x 10(-4) M, and both MPX and MBX exert very much stronger relaxant effects than TPH with nearly equal potency. There were significant differences in the pharmacokinetic and physico-chemical properties among these drugs, both MPX and MBX having shorter half-lives, higher plasma protein binding in vivo and stronger hydrophobicity compared to TPH. The present study suggested that the N3-alkyl chain length is significant for increasing the relaxant effect and affecting the pharmacokinetic and physico-chemical properties of these drugs.

摘要

合成了一种新型黄嘌呤衍生物支气管扩张剂1-甲基-3-丙基黄嘌呤(MPX)和1-甲基-3-丁基黄嘌呤(MBX)。我们以1,3-二甲基黄嘌呤(茶碱,TPH)作为参比药物,评估了它们对豚鼠离体气管平滑肌的舒张作用以及在大鼠体内的药代动力学特征。在1×10⁻⁶至1×10⁻⁴ M的浓度范围内观察到剂量依赖性舒张作用,MPX和MBX的舒张作用均比TPH强得多,且效力几乎相等。这些药物在药代动力学和物理化学性质方面存在显著差异,与TPH相比,MPX和MBX的半衰期均较短,体内血浆蛋白结合率较高,疏水性更强。本研究表明,N3-烷基链长度对于增强这些药物的舒张作用以及影响其药代动力学和物理化学性质具有重要意义。

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