Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.
Eur Respir J. 2011 Oct;38(4):851-60. doi: 10.1183/09031936.00167010. Epub 2011 Mar 15.
Endothelin receptor antagonists are used to treat idiopathic pulmonary arterial hypertension (IPAH), but human pulmonary arterial endothelin receptor expression is not well defined. We hypothesised that disease and treatment would modify normal receptor distribution in pulmonary resistance arteries of children. Using immunohistochemistry and semiquantitative analysis, we investigated endothelin receptor subtypes A and B (ET(A) and ET(B), respectively), and endothelial nitric oxide synthase (eNOS) expression in peripheral pulmonary arteries of tissue from untreated children with IPAH (n=7), following extended combined bosentan and epoprostenol therapy (n=5) and from normal subjects (n=5). Clinical, haemodynamic and pathological abnormalities were severe and advanced in all IPAH cases. ET(A) was detected in pulmonary arterial endothelial cells of all normal and diseased tissue and cultured cells. Endothelial ET(A), ET(B) and eNOS expression was reduced in patent, plexiform and dilatation lesions of untreated cases, but in treated cases, ET(A) and ET(B) were normal and eNOS increased. In smooth muscle, ET(A) expression was reduced in treated cases but ET(B) expression increased in all arteries of both treated and untreated cases. In summary, ET(A) is expressed on human pulmonary arterial endothelium. In IPAH, combination treatment with bosentan and epoprostenol had a more marked influence on endothelin receptor expression of endothelial than smooth muscle cells.
内皮素受体拮抗剂用于治疗特发性肺动脉高压(IPAH),但人类肺血管内皮素受体的表达尚未完全明确。我们假设疾病和治疗会改变儿童肺阻力血管中正常受体的分布。我们采用免疫组织化学和半定量分析方法,研究了未接受治疗的 IPAH 患儿(n=7)、接受延长联合波生坦和依前列醇治疗的患儿(n=5)和正常对照者(n=5)的组织外周肺小动脉中内皮素受体 A 和 B(分别为 ET(A)和 ET(B))和内皮型一氧化氮合酶(eNOS)的表达。所有 IPAH 病例的临床、血液动力学和病理异常均严重且进展。ET(A)在所有正常和病变组织及培养细胞的肺血管内皮细胞中均可检测到。在未治疗的病例中,有管腔通畅、丛状和扩张病变的肺动脉内皮 ET(A)、ET(B)和 eNOS 表达减少,但在治疗病例中,ET(A)和 ET(B)正常,而 eNOS 增加。在平滑肌中,ET(A)在治疗病例中减少,而在所有治疗和未治疗病例的所有动脉中,ET(B)表达增加。总之,ET(A)在人肺血管内皮中表达。在 IPAH 中,波生坦和依前列醇联合治疗对内皮细胞内皮素受体表达的影响比对平滑肌细胞更为显著。