Buchan K W, Magnusson H, Rabe K F, Sumner M J, Watts I S
Biology Division, Glaxo Research and Development Ltd., Herts, UK.
Eur J Pharmacol. 1994 Aug 1;260(2-3):221-6. doi: 10.1016/0014-2999(94)90340-9.
We have characterised the endothelin receptor mediating contraction of human isolated pulmonary artery. Endothelin-1 induced a concentration-dependent contraction of human endothelium-denuded pulmonary artery (EC50 5.6 nM). In contrast, endothelin-3 produced only a small contraction (approximately 12% of maximum endothelin-1 response) at the highest concentration tested (1 microM). The ETB receptor-selective agonist, sarafotoxin S6c (0.1 nM to 1 microM) did not cause contraction of human pulmonary artery. Pretreatment of human pulmonary artery with BQ123 (1-10 microM), an ETA receptor-selective blocking drug, resulted in a concentration-dependent, surmountable antagonism of endothelin-1-induced contractions (apparent pKB 6.6-7.0). Schild analyses yielded a shallow slope (0.58), which was significantly less than unity and, consequently, the calculated pA2 (8.1) was greater than the individual pKB values. Pretreatment of human pulmonary artery with Ro 46-2005 (30 microM), a non-peptide. non-selective endothelin receptor-blocking drug, resulted in a surmountable antagonism of endothelin-1-induced contractions (apparent pKB 5.5). In conclusion, endothelin-1-induced contraction of human pulmonary artery appears to be mediated predominantly via ETA receptors, although the shallow Schild slope observed with BQ123 indicates possible receptor heterogeneity.
我们已对介导人离体肺动脉收缩的内皮素受体进行了特性描述。内皮素 -1 可引起人去内皮肺动脉的浓度依赖性收缩(半数有效浓度 [EC50] 为 5.6 nM)。相比之下,内皮素 -3 在最高测试浓度(1 μM)时仅产生微小收缩(约为内皮素 -1 最大反应的 12%)。ETB 受体选择性激动剂沙拉毒素 S6c(0.1 nM 至 1 μM)不会引起人肺动脉收缩。用 ETA 受体选择性阻断药物 BQ123(1 - 10 μM)预处理人肺动脉,会导致内皮素 -1 诱导的收缩出现浓度依赖性、可克服的拮抗作用(表观 pKB 为 6.6 - 7.0)。希尔德分析得出的斜率较浅(0.58),显著小于 1,因此,计算得出的 pA2(8.1)大于各个 pKB 值。用非肽类、非选择性内皮素受体阻断药物 Ro 46 - 2005(30 μM)预处理人肺动脉,会导致内皮素 -1 诱导的收缩出现可克服的拮抗作用(表观 pKB 为 5.5)。总之,内皮素 -1 诱导的人肺动脉收缩似乎主要通过 ETA 受体介导,尽管用 BQ123 观察到的希尔德斜率较浅表明可能存在受体异质性。