Valli P, Zucca G, Seghezzi R, Botta L
Boll Soc Ital Biol Sper. 1984 Jun 30;60(6):1191-7.
The effects of the following vasoactive drugs: Bencyclan fumarate, Cetiedil citrate, Cinepazide maleate, Dihydroergocristine methane sulphonate, Nafthydrofuril acid oxalate, Papaverine hydrochloride, Piribedil monomethane sulphonate, Raubasine, Thymoxamine hydrochloride and Xanthinol nicotinate, in concentrations ranging between 0.001 - 2 mM, were tested on the compound action potentials led off from human isolated sympathetic ganglions. The experiments, carried out on 50 isolated lumbar ganglion preparations removed from 23 subjects with arteriopathy of the limbs, indicated that all the drugs are able to impair the synaptic transmission, although at different concentrations. These findings are in favour of the hypothesis that the vasodilatatory effects observed after therapeutic treatment of patients with vasoactive drugs are partially produced by the vasodilatation following the depression of the sympathetic nervous transmission.
对从人体分离出的交感神经节引出的复合动作电位,测试了以下血管活性药物在浓度范围为0.001 - 2 mM时的作用:富马酸苄环烷、枸橼酸西替地尔、马来酸桂哌齐特、甲磺酸二氢麦角隐亭、草酸萘呋胺酯、盐酸罂粟碱、甲磺酸匹立哌唑、萝巴新、盐酸百里胺和烟酸占替诺。对从23例肢体动脉病患者身上取下的50个分离的腰神经节标本进行的实验表明,所有药物均能损害突触传递,尽管所需浓度不同。这些发现支持了这样一种假说,即血管活性药物治疗患者后观察到的血管舒张作用部分是由交感神经传递受抑制后的血管舒张所产生的。