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肝素对缺氧性肺动脉高压的部分逆转作用。

Partial reversal of hypoxic pulmonary hypertension by heparin.

作者信息

Hassoun P M, Thompson B T, Hales C A

机构信息

Department of Medicine, Massachusetts General Hospital, Boston 02114.

出版信息

Am Rev Respir Dis. 1992 Jan;145(1):193-6. doi: 10.1164/ajrccm/145.1.193.

DOI:10.1164/ajrccm/145.1.193
PMID:1731584
Abstract

Chronic hypoxia produces pulmonary hypertension and an increase in medial thickness of pulmonary arteries that reach maximal values after 10 days of hypoxia. We previously showed that heparin given during the first 10 days of hypoxia reduced the development of both pulmonary hypertension and vascular remodeling in the guinea pig. To determine if heparin could reverse established hypoxic pulmonary hypertension and vascular remodeling, we administered heparin by continuous subcutaneous infusion (20 U/kg/h) for the last 7 days of a 21-day exposure to hypoxia (10% O2, balance N2) and compared these animals with normal saline-infused hypoxic control and room air-exposed animals. Hypoxia increased pulmonary artery pressure from 11 +/- 1 mm Hg (mean +/- SEM) in room air animals to 20 +/- 2 mm Hg (p less than 0.05) in saline-treated hypoxic control animals. Heparin reduced pulmonary artery pressure to 16 +/- 1 mm Hg (p less than 0.05 versus hypoxic control and room air control animals). Total pulmonary resistance (TPR) increased with hypoxia from 0.043 +/- 0.003 mm Hg x min x kg-1 x ml-1 in room air to 0.090 +/- 0.004 in hypoxia (p less than 0.05), and in the rise in TPR was also partially reversed by heparin to 0.068 +/- 0.0003 (p less than 0.05). The percentage of medial thickness of alveolar duct arteries increased from 5.8 +/- 0.6% in room air to 9.5 +/- 0.1% (p less than 0.05) after 3 wk of hypoxia, and heparin therapy partially reversed the increase in medial thickness to 7.2 +/- 0.7% (p less than 0.05 versus both hypoxia control and room air).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

慢性低氧可导致肺动脉高压,并使肺动脉中层厚度增加,在低氧10天后达到最大值。我们之前发现,在低氧的前10天给予肝素可减少豚鼠肺动脉高压和血管重塑的发生。为了确定肝素是否能逆转已形成的低氧性肺动脉高压和血管重塑,我们在21天低氧暴露(10%氧气,其余为氮气)的最后7天通过持续皮下输注给予肝素(20 U/kg/h),并将这些动物与输注生理盐水的低氧对照动物和暴露于室内空气的动物进行比较。低氧使室内空气环境动物的肺动脉压从11±1 mmHg(均值±标准误)升高至生理盐水处理的低氧对照动物的20±2 mmHg(p<0.05)。肝素使肺动脉压降至16±1 mmHg(与低氧对照动物和室内空气对照动物相比,p<0.05)。总肺阻力(TPR)随低氧从室内空气环境的0.043±0.003 mmHg·min·kg⁻¹·ml⁻¹升高至低氧环境的0.090±0.004(p<0.05),肝素也使TPR的升高部分逆转至0.068±0.0003(p<0.05)。低氧3周后,肺泡导管动脉中层厚度百分比从室内空气环境的5.8±0.6%增加至9.5±0.1%(p<0.05),肝素治疗使中层厚度增加部分逆转至7.2±0.7%(与低氧对照动物和室内空气对照动物相比,p<0.05)。(摘要截断于250字)

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