Miasiro N, Karaki H, Paiva A C
Department of Biophysics, Escola Paulista de Medicina, São Paulo, Brazil.
Eur J Pharmacol. 1995 Oct 24;285(3):247-54. doi: 10.1016/0014-2999(95)00409-e.
IRL1620, a specific endothelin ETB receptor agonist, induced relaxation followed by contraction in the guinea-pig ileum, as did endothelin-1. Both components of the response were concentration-dependent in the range studied. Repeated administration of IRL1620 induced tachyphylaxis only of the contractile component, whereas endothelin-1 desensitized both components. BQ-123 (cyclo[D-Trp-D-Asp-Pro-D-Val-Leu]), a specific endothelin ETA receptor antagonist, did not inhibit the relaxation induced by either agonist, although it did inhibit the contraction induced by endothelin-1, but not by IRL1620. PD145065 (Ac-(D-Bhg-Leu-Asp-Ile-Ile-Trp) (D-Bhg = 5H-dibenzyl[a,d]cycloheptene-10,11-dihydroglycine)), a combined endothelin ETA/endothelin ETB receptor antagonist, inhibited the contractile effects of both endothelin-1 and IRL1620 and also inhibited the relaxation induced by IRL1620. Apamin, a Ca(2+)-activated K+ channel blocker, inhibited only the endothelin-1-induced relaxation. Our studies suggest that two endothelin ETB receptor subtypes mediate relaxation in the guinea-pig ileum: one is less sensitive to PD145065 but apamin-inhibitable, and the other is more sensitive to PD145065 but not apamin-inhibitable. Our results also suggest that both endothelin ETA and endothelin ETB receptor subtypes mediate contraction in the ileum.
IRL1620是一种特异性内皮素ETB受体激动剂,与内皮素-1一样,可使豚鼠回肠先舒张后收缩。在所研究的浓度范围内,反应的两个组成部分均呈浓度依赖性。重复给予IRL1620仅使收缩成分产生快速耐受性,而内皮素-1使两个成分均脱敏。BQ-123(环[D-色氨酸-D-天冬氨酸-脯氨酸-D-缬氨酸-亮氨酸])是一种特异性内皮素ETA受体拮抗剂,虽然它能抑制内皮素-1诱导的收缩,但不能抑制两种激动剂诱导的舒张,对IRL1620诱导的收缩也无抑制作用。PD145065(Ac-(D-Bhg-亮氨酸-天冬氨酸-异亮氨酸-异亮氨酸-色氨酸),D-Bhg = 5H-二苄基[a,d]环庚烯-10,11-二氢甘氨酸)是一种内皮素ETA/内皮素ETB受体联合拮抗剂,可抑制内皮素-1和IRL1620的收缩作用,也能抑制IRL1620诱导的舒张。蜂毒明肽是一种钙激活钾通道阻滞剂,仅抑制内皮素-1诱导的舒张。我们的研究表明,两种内皮素ETB受体亚型介导豚鼠回肠的舒张:一种对PD145065不太敏感但可被蜂毒明肽抑制,另一种对PD145065更敏感但不能被蜂毒明肽抑制。我们的结果还表明,内皮素ETA和内皮素ETB受体亚型均介导回肠的收缩。