Thirstrup S, Nielsen-Kudsk F, Dahl R
Institute of Pharmacology, University of Aarhus, Denmark.
Eur J Pharmacol. 1998 Mar 26;345(3):289-97. doi: 10.1016/s0014-2999(98)00027-2.
Pharmacodynamic effects produced by terbutaline (10 nM), theophylline (10 microM), sodium nitroprusside (30 nM), levcromakalim (0.3 microM) or isradipine (1 nM) on frequency-dependent relaxations induced by electric field stimulation of either proximal or distal parts of isolated guinea-pig trachea were studied in vitro. Preparations were depleted for tachykinins by capsaicin, pretreated with atropine (0.1 microM) and contracted by histamine (2 microM). Drug effects were studied in preparations with combined adrenergic and inhibitory non-adrenergic non-cholinergic (NANC) innervation and in preparations with inhibitory NANC innervation either with or without additional treatment with N(G)-nitro-L-arginine methyl ester (L-NAME) (100 microM). In preparations with combined adrenergic and inhibitory NANC innervation terbutaline, sodium nitroprusside, levcromakalim and isradipine significantly reduced relaxant responses to electric field stimulation in proximal preparations, whereas distal preparations were only affected by terbutaline. In preparations with inhibitory NANC innervation without L-NAME pretreatment, terbutaline significantly enhanced relaxant responses to electric field stimulation only in distal preparations, whereas theophylline, sodium nitroprusside and levcromakalim significantly augmented responses to electric field stimulation in both proximal and distal preparations. In preparations with inhibitory NANC innervation pretreated with L-NAME, theophylline significantly inhibited relaxant responses in distal preparations, whereas sodium nitroprusside, levcromakalim and isradipine significantly augmented relaxant responses to electric field stimulation in proximal preparations. It was concluded that drugs used in the present study can modulate the effects of inhibitory autonomic and NANC neurotransmission in isolated guinea-pig trachea. Furthermore, it was shown that some variation in drug effects exists in relation to proximal and distal parts of guinea-pig trachea.
在体外研究了特布他林(10 nM)、茶碱(10 μM)、硝普钠(30 nM)、左卡尼汀(0.3 μM)或伊拉地平(1 nM)对豚鼠离体气管近端或远端电场刺激诱导的频率依赖性舒张的药效学作用。用辣椒素使制剂中的速激肽耗竭,用阿托品(0.1 μM)预处理,并用组胺(2 μM)使其收缩。在具有肾上腺素能和抑制性非肾上腺素能非胆碱能(NANC)联合神经支配的制剂以及具有抑制性NANC神经支配的制剂中,研究了药物作用,这些制剂分别经过或未经过N(G)-硝基-L-精氨酸甲酯(L-NAME)(100 μM)的额外处理。在具有肾上腺素能和抑制性NANC联合神经支配的制剂中,特布他林、硝普钠、左卡尼汀和伊拉地平显著降低了近端制剂对电场刺激的舒张反应,而远端制剂仅受特布他林影响。在未用L-NAME预处理的具有抑制性NANC神经支配的制剂中,特布他林仅在远端制剂中显著增强了对电场刺激的舒张反应,而茶碱、硝普钠和左卡尼汀在近端和远端制剂中均显著增强了对电场刺激的反应。在用L-NAME预处理的具有抑制性NANC神经支配的制剂中,茶碱显著抑制了远端制剂的舒张反应,而硝普钠、左卡尼汀和伊拉地平显著增强了近端制剂对电场刺激的舒张反应。得出的结论是,本研究中使用的药物可以调节豚鼠离体气管中抑制性自主神经和NANC神经传递的作用。此外,还表明药物作用在豚鼠气管的近端和远端部分存在一些差异。