Dinh Xuan A T, Higenbottam T W, Clelland C, Pepke-Zaba J, Cremona G, Wallwork J
Department of Respiratory Physiology, Papworth Hospital, Cambridge.
Br J Pharmacol. 1990 Jan;99(1):9-10. doi: 10.1111/j.1476-5381.1990.tb14643.x.
A comparison has been made between the endothelium-dependent relaxation of pulmonary arteries (PA) obtained at heart-lung transplantation from 4 patients with Eisenmenger's syndrome and secondary pulmonary hypertension, and PA obtained at lobectomy from 4 patients with lung carcinoma, the controls. All vascular rings were studied immediately after lung excision. PA rings from control patients dose-dependently relaxed to cumulative doses of acetylcholine (ACh, 10(-10) to 10(-5) M), achieving a maximal relaxation of 80 +/- 5% (mean +/- s.e. mean) from precontraction with phenylephrine. By contrast, PA rings from Eisenmenger's syndrome patients achieved a maximal relaxation of only 34 +/- 12% (P less than 0.05, unpaired t test), with even paradoxical contraction at high doses of ACh (10(-6) to 10(-5) M). Sodium nitroprusside (10(-4) M) relaxed all PA rings, with and without endothelium (carefully removed before study), obtained from both control and Eisenmenger's syndrome patients. These results provide the first evidence that endothelium-dependent relaxation of PA mediated by endothelium-derived relaxing factors is impaired in Eisenmenger's syndrome patients with secondary pulmonary hypertension.
对4例艾森曼格综合征合并继发性肺动脉高压患者在心肺移植时获取的肺动脉(PA)以及4例肺癌患者在肺叶切除时获取的PA(作为对照)的内皮依赖性舒张进行了比较。所有血管环均在肺切除后立即进行研究。对照患者的PA环对乙酰胆碱(ACh,10⁻¹⁰至10⁻⁵M)的累积剂量呈剂量依赖性舒张,与用去氧肾上腺素预收缩相比,最大舒张率达到80±5%(平均值±标准误平均值)。相比之下,艾森曼格综合征患者的PA环最大舒张率仅为34±12%(P<0.05,未配对t检验),在高剂量ACh(10⁻⁶至10⁻⁵M)时甚至出现反常收缩。硝普钠(10⁻⁴M)使从对照患者和艾森曼格综合征患者获取的所有PA环(无论有无内皮,研究前已小心去除)舒张。这些结果首次证明,在合并继发性肺动脉高压的艾森曼格综合征患者中,由内皮衍生舒张因子介导的PA内皮依赖性舒张受损。