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围产期兔肺阻力动脉中内皮素受体的发育

Development of endothelin receptors in perinatal rabbit pulmonary resistance arteries.

作者信息

Docherty C, MacLean M R

机构信息

Division of Neuroscience and Biomedical Systems, Institute of Biomedical and Life Sciences, University of Glasgow.

出版信息

Br J Pharmacol. 1998 Jul;124(6):1165-74. doi: 10.1038/sj.bjp.0701950.

Abstract
  1. Contractile responses to endothelin-1 (ET-1) and sarafotoxin S6c (S6c) were studied in pulmonary resistance arteries (approximately 320 microm i.d.) from fetal, 0-24 h, 4 day and 7 day rabbits. The effects of the ET(A)-selective antagonist FR139317, the selective ET(B) receptor antagonist BQ-788 and the non-selective ET(A)/ ET(B) receptor antagonist SB 209670, on these responses, were determined. Acetylcholine-induced vasodilation and noradrenaline-evoked contractions were also examined. 2. ET-1 potency was in the following order (pEC50 values): fetal (8.7) = 0-24 h (8.8) = 4 day (8.6) > 7 day (8.0). The order of potency for S6c was 7 days (11.1) = 4 days (10.8) > 0-24 h (9.7) > fetal (8.6). Hence, S6c and ET-1 were equipotent in the fetus but S6c was increasingly more potent than ET-1 with increasing age, being some 1000 times more potent by 7 days. By 7 days, responses to ET-1 were also resistant to both FR139317 and BQ-788. FR139317 inhibited responses to ET-1 in vessels from 0-24 h and 4 day, but not fetal, rabbits (pKb: 6.4 in 4 day rabbits). BQ-788 inhibited responses to ET-1 at all age points except for 7 days (pKb: 6.7 at 0-24 h; 6.2 at 4 days). BQ-788 inhibited responses to S6c at all age points (pKb: 8.5 at 4 days). SB 209670 inhibited responses to ET-1 and S6c at 0-24 h and 4 days (pKb for ET-1: 8.3 and 8.0 respectively; pKb for S6c: 9.2 and 10.2 respectively). 3. Acetylcholine (1 microM) induced vasodilation at all age points (inhibited by 100 microM L-N(omega)-nitroarginine methylester) although the degree of vasodilation was significantly reduced (approximately 75%) at 0-24 h. Noradrenaline induced contraction at all age points except 7 days and its response was significantly enhanced at 0-24 h. 4. Over the first week of life, the potency of S6c increases whilst that to ET-1 decreases suggesting differential development of responses to ET-1 and S6c and heterogeneity of ET(A)- or 'ET(B)-like' receptor-mediated responses. There is no synergism between ET(A) and ET(B) receptors at birth but this is established by 7 days. Immediately after birth rabbit Pulmonary Resistance Arteries are hyperresponsive to ET-1 and noradrenaline but exhibit impaired nitric-oxide dependent vasodilation.
摘要
  1. 研究了内皮素 -1(ET -1)和沙罗毒素 S6c(S6c)对胎兔、出生 0 - 24 小时、4 日龄和 7 日龄兔的肺阻力动脉(内径约 320 微米)的收缩反应。测定了 ET(A) 选择性拮抗剂 FR139317、选择性 ET(B) 受体拮抗剂 BQ - 788 和非选择性 ET(A)/ET(B) 受体拮抗剂 SB 209670 对这些反应的影响。还检测了乙酰胆碱诱导的血管舒张和去甲肾上腺素引起的收缩。2. ET -1 的效价顺序如下(pEC50 值):胎兔(8.7)=出生 0 - 24 小时(8.8)= 4 日龄(8.6)>7 日龄(8.0)。S6c 的效价顺序为 7 日龄(11.1)= 4 日龄(10.8)>出生 0 - 24 小时(9.7)>胎兔(8.6)。因此,S6c 和 ET -1 在胎兔中效力相当,但随着年龄增长,S6c 比 ET -1 的效力越来越强,到 7 日龄时约强 1000 倍。到 7 日龄时,对 ET -1 的反应对 FR139317 和 BQ - 788 均有抗性。FR139317 抑制出生 0 - 24 小时和 4 日龄兔血管对 ET -1 的反应,但对胎兔无抑制作用(4 日龄兔的 pKb:6.4)。BQ - 788 抑制除 7 日龄外所有年龄段对 ET -1 的反应(出生 0 - 24 小时的 pKb:6.7;第 4 天的 pKb:6.2)。BQ - 788 抑制所有年龄段对 S6c 的反应(4 日龄时的 pKb:8.5)。SB 209670 抑制出生 0 - 24 小时和 4 日龄时对 ET -1 和 S6c 的反应(ET -1 的 pKb 分别为 8.3 和 8.0;S6c 的 pKb 分别为 9.2 和 10.2)。3. 乙酰胆碱(1 微摩尔)在所有年龄段均诱导血管舒张(被 100 微摩尔 L - N(ω)-硝基精氨酸甲酯抑制),尽管在出生 0 - 24 小时时血管舒张程度显著降低(约 75%)。去甲肾上腺素在除 7 日龄外的所有年龄段均诱导收缩,且在出生 0 - 24 小时时其反应显著增强。4. 在出生后的第一周内,S6c 的效力增加而对 ET -1 的效力降低,这表明对 ET -1 和 S6c 的反应发育存在差异,以及 ET(A) 或“ET(B) 样”受体介导的反应存在异质性。出生时 ET(A) 和 ET(B) 受体之间没有协同作用,但在 7 日龄时建立了协同作用。出生后即刻兔肺阻力动脉对 ET -1 和去甲肾上腺素反应过度,但一氧化氮依赖性血管舒张受损。

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