[Effect of elastase inhibitor on pulmonary hypertension induced by monocrotaline].

Abstract

OBJECTIVE:

Pulmonary hypertension is a proliferative vascular disease characterized by pulmonary vascular structural remodeling. Until now, the pathogenesis of pulmonary hypertension is still not fully understood. Although considerable progress has been made, there is, to date, no cure for advanced pulmonary vascular disease. Recently, a number of studies suggest that endogenous vascular elastase (EVE) play a role in the vascular changes associated with pulmonary hypertension. The purpose of the study was to determine whether an elastase inhibitor might reverse advanced pulmonary vascular disease produced in rats by injection of monocrotaline.

METHODS:

One hundred and twenty male Sprague-Dawley rats were used in this study. The rats were divided into three groups: control, model and ZD-0892 groups. In the model and ZD-0892 groups, the rats were subjected to a single subcutaneous injection of monocrotaline (60 mg/kg) in the hind flank, while the rats in control group received an equivalent volume of 0.9% saline. From day 21, the rats in the ZD-0892 and model groups received twice-daily gavage tube feedings of either ZD-0892 at a dose of 240 mg/kg per day or its administration vehicle, while the rats in control group were subjected to an equivalent volume of 0.9% saline. On days 21, 28 and 35 post-injection, the elastolytic activity was measured with a fluorescence microplate reader and pulmonary artery pressure was detected via catheterization. Meanwhile, the lungs were evaluated morphologically, using the barium-gelatin perfusion technique.

RESULTS:

The injection of monocrotaline led to severe pulmonary hypertension in rats 21 days later and pulmonary artery elastolytic activity increased remarkably. A 1-week treatment with ZD-0892 resulted in declines in elastase activity. This was associated with significant declines in pulmonary artery pressure, decreases in muscularization of peripheral arteries and reductions in medial hypertrophy. After 2 weeks, elastase activity returned to normal level. Pulmonary artery pressure and structure were normalized.

CONCLUSION:

Increased elastase activity is important in the development of vascular changes and progressive pulmonary hypertension. ZD-0892 can suppress the elastase activity and completely reverse the fatal pulmonary hypertension induced by monocrotaline in rats.

• Authors: Li-jun Fu, Ai-qing Zhou, Jie Shen, Wu Zhao, Fen Li
• Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics (Zhonghua Er Ke Za Zhi) Vol. 42 Issue 5 Pg. 375-8 (May 2004) ISSN: 0578-1310 [Print] China
• PMID: 15189699 (Publication Type: Comparative Study, English Abstract, Journal Article)

Chemical References

• Pyrroles
• Sulfonamides
• ZD 0892
• Monocrotaline
• Pancreatic Elastase

Topics

• Animals
• Hypertension, Pulmonary (chemically induced, drug therapy)
• Male
• Monocrotaline (toxicity)
• Pancreatic Elastase (antagonists & inhibitors)
• Pulmonary Artery (drug effects, pathology, physiopathology)
• Pyrroles (pharmacology)
• Rats
• Rats, Sprague-Dawley
• Sulfonamides (pharmacology)