Kalsner S
Br J Pharmacol. 1976 Oct;58(2):261-6. doi: 10.1111/j.1476-5381.1976.tb10404.x.
The effects of oxytetracycline, an inhibitor of amine binding in connective tissue, on the responses of perfused rabbit ear arteries to sympathetic nerve stimulation and to intraluminally administered noradrenaline were examined. The contractions of aortic strips to catecholamines in the presence of oxytetracycline were also examined. Oxytetracycline (0.1 mM) had no discernable effect on the magnitude of constrictions, measured as reductions in flow, produced by either nerve stimulation (0.5-10 Hz) or noradrenaline (0.5-50 ng) in the ear artery. In addition, the time taken for vessels to recover towards control flow values after endogenously released or exogenously applied noradrenaline had acted was not increased by oxytetracycline. Oxytetracycline (0.1 mM) did not alter the position or shape of the concentration-response curve to noradrenaline nor did it enhance the amplitude of individual responses to catecholamines in aortic strips. It is concluded, contrary to the observations of Powis (1973), that oxytetracycline does not increase the magnitude or duration of responses to sympathetic nerve activation or to catecholamines and that binding to connective tissue is of no material consequence in terminating their action in vascular tissue.
考察了土霉素(一种结缔组织中胺结合抑制剂)对灌注兔耳动脉对交感神经刺激及腔内给予去甲肾上腺素反应的影响。还考察了土霉素存在时主动脉条对儿茶酚胺的收缩反应。土霉素(0.1 mM)对神经刺激(0.5 - 10 Hz)或去甲肾上腺素(0.5 - 50 ng)在耳动脉中引起的以流量减少衡量的收缩幅度无明显影响。此外,土霉素并未增加内源性释放或外源性给予的去甲肾上腺素作用后血管恢复至对照流量值所需的时间。土霉素(0.1 mM)既未改变主动脉条对去甲肾上腺素浓度 - 反应曲线的位置或形状,也未增强对儿茶酚胺的单个反应幅度。与Powis(1973年)的观察结果相反,得出的结论是,土霉素不会增加对交感神经激活或儿茶酚胺反应的幅度或持续时间,并且与结缔组织的结合在终止其在血管组织中的作用方面并无实质影响。