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内源性环磷酸腺苷(cAMP)对出生后绵羊原位灌注肺中肺液吸收的调节作用。

The regulation of lung liquid absorption by endogenous cAMP in postnatal sheep lungs perfused in situ.

作者信息

Stephens R H, Benjamin A R, Walters D V

机构信息

Department of Child Health, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK.

出版信息

J Physiol. 1998 Sep 1;511 ( Pt 2)(Pt 2):587-97. doi: 10.1111/j.1469-7793.1998.587bh.x.

Abstract
  1. The lungs of two groups of lambs aged 0-2 weeks and 6-12 weeks were artificially perfused in situ with warmed and oxygenated sheep blood. The airspaces of the lungs were filled with liquid containing an impermeant tracer to allow estimation of net liquid movement across the pulmonary epithelium at rest and after administration of certain drugs. 2. Dibutyryl cAMP (dB-cAMP, 10-4 M) stimulated the rate of lung liquid (LL) absorption in the lungs of four neonatal sheep aged 9-12 days, from -1.43 +/- 0.2 to -2.75 +/- 0.3 ml h-1 (kg body wt)-1 (P < 0.05, comparison of regression lines by Student's t test), but had no effect in four juvenile sheep aged 6-12 weeks (P > 0.10). 3. Theophylline, a non-selective phosphodiesterase (PDE) inhibitor (5 x 10-4 M), increased LL absorption from a resting rate of -1.55 +/- 0.3 to -3.62 +/- 0.5 ml h-1 kg-1 in the lungs of four sheep aged 1-12 days and from -1.47 +/- 0.3 to -3.73 +/- 0.4 ml h-1 kg-1 in four sheep aged 6-12 weeks (P < 0.05, Student's paired t test). 4. The beta-adrenergic antagonist sotalol (10-4 M) reduced LL absorption rate from -1.47 +/- 0.1 to -1.22 +/- 0.1 ml h-1 kg-1 (P < 0.01) in the lungs of four sheep aged 4-13 days, while theophylline given after sotalol had no effect. In four sheep aged 6-12 weeks, sotalol had no effect on LL absorption rate, whereas theophylline given after sotalol increased LL absorption rate from -1.06 +/- 0.1 to -1.92 +/- 0.2 ml h-1 kg-1 (P < 0.05). 5. The A1/A2 purinergic receptor blocker 7-(beta-chloroethyl) theophylline (CET; given at 5 x 10-6 M and 10-4 M) had no effect on LL absorption rate in the lungs of four sheep aged 6-12 weeks, confirming that theophylline produced its effect of increasing LL absorption by inhibiting PDE hydrolytic activity. 6. The selective PDE IV (cAMP-specific) PDE inhibitor rolipram was given in the perfused lungs of seven sheep aged 6-12 weeks at doses between 10-8 and 10-4 M, increasing LL absorption rate at concentrations of 10-6 M and above; the half-maximal effective concentration was estimated to be 5.9 x 10-7 M. 7. Rolipram (10-5 M) increased LL absorption rate from -1.99 +/- 0.2 to -3.18 +/- 0.5 ml h-1 kg-1 in the perfused lungs of four sheep aged 6-11 days, and from -1.21 +/- 0.4 to -3.45 +/- 0.3 ml h-1 kg-1 in the perfused lungs of four sheep aged 6-12 weeks (P < 0.05). Sotalol (10-4 M) reduced LL absorption rate from -3.39 +/- 0.8 to -2. 18 +/- 0.4 ml h-1 kg-1 (P < 0.05) in four sheep aged 10-14 days, while rolipram given after sotalol had no effect. In four sheep aged 6-12 weeks, sotalol had no effect on resting LL absorption rate, whereas rolipram given after sotalol increased absorption rate from -1.27 +/- 0.1 to -2.02 +/- 0.6 ml h-1 kg-1 (P < 0.05). 8. We conclude that cAMP mediates a component of LL absorption postnatally, and that while beta-adrenergic stimulation was the sole source of endogenous cAMP in neonates, this was not the case in juveniles, in whom cAMP originated, at least in part, from other sources.
摘要
  1. 两组羔羊(0 - 2周龄和6 - 12周龄)的肺在原位用温热且充氧的绵羊血液进行人工灌注。肺的气腔充满含有不透性示踪剂的液体,以估计静息状态下以及给予某些药物后跨肺上皮的液体净移动情况。2. 二丁酰环磷腺苷(dB - cAMP,10⁻⁴ M)刺激了4只9 - 12日龄新生绵羊肺中肺液(LL)的吸收速率,从 - 1.43 ± 0.2 增加至 - 2.75 ± 0.3 ml·h⁻¹·(kg体重)⁻¹(P < 0.05,通过学生t检验比较回归线),但对4只6 - 12周龄的幼年绵羊没有影响(P > 0.10)。3. 茶碱,一种非选择性磷酸二酯酶(PDE)抑制剂(5×10⁻⁴ M),使4只1 - 12日龄绵羊肺中LL的吸收从静息速率 - 1.55 ± 0.3 增加至 - 3.62 ± 0.5 ml·h⁻¹·kg⁻¹,使4只6 - 12周龄绵羊肺中LL的吸收从 - 1.47 ± 0.3 增加至 - 3.73 ± 0.4 ml·h⁻¹·kg⁻¹(P < 0.05,学生配对t检验)。4. β - 肾上腺素能拮抗剂索他洛尔(10⁻⁴ M)使4只4 - 13日龄绵羊肺中LL的吸收速率从 - 1.47 ± 0.1 降低至 - 1.22 ± 0.1 ml·h⁻¹·kg⁻¹(P < 0.01),而在索他洛尔之后给予茶碱则没有效果。在4只6 - 12周龄的绵羊中,索他洛尔对LL吸收速率没有影响,而在索他洛尔之后给予茶碱使LL吸收速率从 - 1.06 ± 0.1 增加至 - 1.92 ± 0.2 ml·h⁻¹·kg⁻¹(P < 0.05)。5. A1/A2嘌呤能受体阻滞剂7 - (β - 氯乙基)茶碱(CET;以5×10⁻⁶ M和10⁻⁴ M给予)对4只6 - 12周龄绵羊肺中LL的吸收速率没有影响,证实茶碱通过抑制PDE水解活性产生增加LL吸收的作用。6. 选择性PDE IV(cAMP特异性)PDE抑制剂咯利普兰以10⁻⁸至10⁻⁴ M的剂量给予7只6 - 12周龄绵羊的灌注肺中,在浓度为10⁻⁶ M及以上时增加LL吸收速率;估计半数有效浓度为5.9×10⁻⁷ M。7. 咯利普兰(10⁻⁵ M)使4只6 - 11日龄绵羊灌注肺中LL的吸收速率从 - 1.99 ± 0.2 增加至 - 3.18 ± 0.5 ml·h⁻¹·kg⁻¹,使4只6 - 12周龄绵羊灌注肺中LL的吸收速率从 - 1.21 ± 0.4 增加至 - 3.45 ± 0.3 ml·h⁻¹·kg⁻¹(P < 0.05)。索他洛尔(10⁻⁴ M)使4只10 - 14日龄绵羊肺中LL的吸收速率从 - 3.39 ± 0.8 降低至 - 2.18 ± 0.4 ml·h⁻¹·kg⁻¹(P < 0.05),而在索他洛尔之后给予咯利普兰则没有效果。在4只6 - 12周龄的绵羊中,索他洛尔对静息LL吸收速率没有影响,而在索他洛尔之后给予咯利普兰使吸收速率从 - 1.27 ± 0.1 增加至 - 2.02 ± 0.6 ml·h⁻¹·kg⁻¹(P < 0.05)。8. 我们得出结论,cAMP介导出生后LL吸收的一部分,并且虽然β - 肾上腺素能刺激是新生儿内源性cAMP的唯一来源,但在幼年绵羊中并非如此,幼年绵羊中的cAMP至少部分来自其他来源。

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