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机构地区:[1]空军总医院呼吸内科,北京100036 [2]华中科技大学同济医学院附属同济医院呼吸内科,湖北武汉430030
出 处:《中国病理生理杂志》2008年第9期1784-1788,共5页Chinese Journal of Pathophysiology
摘 要:目的:探讨内皮素-1受体(ETA)拮抗剂BQ123对慢性缺氧大鼠肺动脉平滑肌细胞(PASMCs)电压门控钾通道(KV)活性的影响。方法:将12只Wistar大鼠随机分为对照组和慢性缺氧组,每组6只。用急性酶分离法(胶原酶+木瓜酶)获得单个PASMCs,用全细胞膜片钳记录方法,观察BQ123对2组大鼠PASMCs电压门控钾电流(IKV)的影响。结果:(1)在2组大鼠,ET-1(10-8mol·L-1)对PASMCs IKV都可产生抑制作用,+50 mV时的抑制率分别是(60.21±5.32)%和(71.04±6.58)%。(2)对照组大鼠,单独使用BQ123对PASMCs IKV无影响(P>0.05,n=5),在此基础上使用ET-1,ET-1对IKV的抑制作用依然存在。(3)慢性缺氧组大鼠,单独使用BQ123可增加PASMCs IKV,+50mV从(98.36±12.04)pA/pF至(105.76±12.13)pA/pF,但差异无显著(P>0.05,n=6),同时使用ET-1后发现BQ123可部分抵消ET-1对IKV的抑制作用,+50 mV从(28.49±6.69)pA/pF升至(74.19±9.74)pA/pF(P<0.01,n=6)。结论:常氧时,ET-1对IKV的抑制作用不是通过ETA介导的。但在缺氧条件下,ETA拮抗剂BQ123可部分拮抗ET-1对IKV的抑制作用,说明缺氧时ETA受体介导了ET-1对IKV抑制作用。AIM: To study the effect of BQ123 on voltage - gated K^+ current in pulmonary artery smooth muscle cells (PASMCs) from chronic hypoxic rats. METHODS: Twelve age and body weight matched Wistar rats were randomly divided into control and chronic hypoxic group. Single PASMCs were obtained with acute enzyme (collagnase I plus papain) dispersing method. Using the whole cell patch - clamp technique in freshly isolated PASMCs from normorxic and hypoxic rats, the effects of ET - 1 and BQ123, a selective ETA receptor antagonist, on voltage - gated K^+ current were recorded. RESULTS: (1) ET - 1 (10^-8 mol · L^-1 ) caused inhibition of K^+ current in PASMCs from normoxic and hypoxic rats. The effect of ET - 1 on K^+ current in PASMCs from hypoxic rats was greater than that from normoxic rats [ + 50 mV, percent inhibition were (71.04 ± 6. 58) % and (60. 21 ± 5.32) %, respectively, P 〈 0. 01, n = 6 ]. (2) In normoxic PASMCs, neither BQ123 alone produced influence on the IKv (P 〉 0. 05, n = 5 ) , nor ETA receptor blockade had change of ET- 1 mediated IKv inhibition. (3) In chronic hypoxic PASMCs, BQ123 significantly reduced the effect of ET - 1 mediated IKv inhibition, from (28. 49 ± 6. 69 ) pA/pF to (74. 19 ± 9. 74 ) pA/pF at + 50 mV ( P 〈 0. 01, n = 6 ). CONCLUSION: In normoxic condition, the effect of ET - 1 on IKv of PASMCs is not mediated by BQ123, a selective ETA receptor antagonist. During exposure to chronic hypoxia, the inhibition of ET - 1 on IKv of PASMCs is partly mediated by BQ123, namely, ETA receptor mediates the effect of ET - 1 on IKv of chronic hypoxic PASMCs.
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