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内源性一氧化碳在低氧性肺动脉高压血管重塑中的作用

[The role of endogenous carbon monoxide in vascular remodeling in hypoxic pulmonary hypertension].

作者信息

Zhen Guo-hua, Zhang Zhen-xiang, Xu Yong-jian

机构信息

Institue of Respiratory Disease, Tongji Hospital, Tongji Medical University, Wuban Hubei 430030, China.

出版信息

Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2002 Nov;18(4):374-7.

Abstract

AIM

To investigate the expression of heme oxygenase-1 gene and production of endogenous carbon monoxide in the rat lung tissue at different time points of chronic hypoxic pulmonary hypertension and the effect of hemin, an inducer of heme oxygenase, on the expression of HO-1 gene and production of endogenous carbon monoxide and pulmonary hypertension.

METHODS

We recreated a rat model of hypoxic pulmonary hypertension by intermittent normal pressure hypoxia (10% O2). The following assays were carried out: Reverse transcriptase polymerase chain reaction (RT-PCR) were performed to determine the level of HO-1 mRNA in rat lung tissue, double wave length spectrophotometry was used to evaluate the quantity of COHb in arterial blood, cardiac catheterization was used to measure the right ventricular systolic pressure (RVSP) and HE staining was performed in dissected lung tissue to observe the pathologic changes of the intra-acinar pulmonary arteries(IAPA).

RESULTS

(DT here was low level of HO-1 mRNA in normal rat lung tissue, but the level of HO-1 mRNA increased by 2-4 times in the lung tissue of hypoxic rats (P < 0.01). The quantity of COHb was 2-3 times as those of control group (P < 0.01 or P < 0.05). These were accompanied by the increase of RVSP and the thickness of IAPA. (2) Hemin could maintain the HO-1 mRNA and COHb in the hypoxic rat lung tissue at a high level, and partially suppressed the increase of rat RVSP, ameliorated the pathologic changes of IAPA.

CONCLUSION

The upregulation of the expression of HO-1 gene and production of CO in the rat lung of hypoxic pulmonary hypertension plays a role of inhibition in the development of hypoxic pulmonary hypertension. Hemin has a therapeutic effect on hypoxic pulmonary hypertension.

摘要

目的

探讨慢性低氧性肺动脉高压大鼠肺组织中血红素加氧酶-1基因的表达及内源性一氧化碳的生成,以及血红素加氧酶诱导剂血红素对血红素加氧酶-1基因表达、内源性一氧化碳生成及肺动脉高压的影响。

方法

采用间歇性常压低氧(10%氧气)建立大鼠低氧性肺动脉高压模型。进行以下检测:采用逆转录聚合酶链反应(RT-PCR)检测大鼠肺组织中血红素加氧酶-1 mRNA水平,采用双波长分光光度法评估动脉血中碳氧血红蛋白含量,采用心脏导管插入术测量右心室收缩压(RVSP),对分离的肺组织进行苏木精-伊红(HE)染色观察腺泡内肺动脉(IAPA)的病理变化。

结果

(1)正常大鼠肺组织中血红素加氧酶-1 mRNA水平较低,但低氧大鼠肺组织中血红素加氧酶-1 mRNA水平升高2-4倍(P<0.01)。碳氧血红蛋白含量是对照组的2-3倍(P<0.01或P<0.05)。同时伴有右心室收缩压升高和腺泡内肺动脉厚度增加。(2)血红素可使低氧大鼠肺组织中的血红素加氧酶-1 mRNA和碳氧血红蛋白维持在高水平,并部分抑制大鼠右心室收缩压升高,改善腺泡内肺动脉的病理变化。

结论

低氧性肺动脉高压大鼠肺组织中血红素加氧酶-1基因表达上调及一氧化碳生成增加对低氧性肺动脉高压的发展起抑制作用。血红素对低氧性肺动脉高压有治疗作用。

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