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豚鼠中速激肽的支气管收缩和降压作用与药代动力学的关系——神经肽K在外神经裂解为神经激肽A的证据

Bronchoconstrictor and hypotensive effects in relation to pharmacokinetics of tachykinins in the guinea-pig--evidence for extraneuronal cleavage of neuropeptide K to neurokinin A.

作者信息

Martling C R, Theodorsson-Norheim E, Norheim I, Lundberg J M

机构信息

Department of Anaesthesia, Karolinska Hospital, Stockholm, Sweden.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1987 Aug;336(2):183-9. doi: 10.1007/BF00165803.

Abstract
  1. The biological effects of the tachykinins substance P (SP), neurokinin A (NKA) and neuropeptide K (NPK) were studied in relation to their pharmacokinetic properties in the guinea-pig in vivo. 2. NKA and NPK exerted a considerably larger bronchoconstrictor effect than SP. The effect of NPK was slow in onset and had a long duration. The three tachykinins showed similar hypotensive effects although NPK had a longer duration of action than SP and NKA. 3. The disappearance of NPK-like immunoreactivity (-LI) from plasma after i.v. infusion of synthetic NPK was biphasic with apparent half-lives of 0.9 min and 6 min. The plasma half-life of NKA-LI was less than 2 min, while plasma SP-LI was degraded before biochemical analysis could be performed. 4. In guinea-pig plasma at 37 degrees C in vitro, NKA- and NPK-LI were stable for 10 min, while SP-LI disappeared with a half-life of 10 s. 5. Reversed phase HPLC analysis of plasma collected after an i.v. infusion of NPK for 25 min, indicated a partial cleavage of NPK into NKA. 6. It is concluded that potency of the biological effects of SP, NKA and NPK in the guinea-pig in vivo, may not only be attributed to activation of multiple tachykinin receptors but must also be related to the marked differences in pharmacokinetical properties between the tachykinins. Furthermore, whereas SP is rapidly degraded in plasma, NKA and NPK seem to be metabolized in other compartments.
摘要
  1. 研究了速激肽P物质(SP)、神经激肽A(NKA)和神经肽K(NPK)在豚鼠体内的生物学效应及其药代动力学特性。2. NKA和NPK的支气管收缩效应比SP大得多。NPK的效应起效缓慢且持续时间长。三种速激肽显示出相似的降压效应,尽管NPK的作用持续时间比SP和NKA长。3. 静脉注射合成NPK后,血浆中NPK样免疫反应性(-LI)的消失呈双相,表观半衰期分别为0.9分钟和6分钟。NKA-LI的血浆半衰期小于2分钟,而血浆SP-LI在进行生化分析之前就已降解。4. 在37℃的豚鼠血浆中,体外NKA-LI和NPK-LI稳定10分钟,而SP-LI以10秒的半衰期消失。5. 静脉注射NPK 25分钟后收集的血浆进行反相高效液相色谱分析,表明NPK部分裂解为NKA。6. 得出结论,SP、NKA和NPK在豚鼠体内的生物学效应强度,可能不仅归因于多种速激肽受体的激活,还必须与速激肽之间药代动力学特性的显著差异有关。此外,SP在血浆中迅速降解,而NKA和NPK似乎在其他部位代谢。

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