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1 Department of Physiology, Charles University Second Medical School, Prague, Czech Republic; Department of Pathological Physiology, Charles University Second Medical School and Centre for Experimental Cardiovascular Research, Prague, Czech Republic
2 Deprtment of Medical Chemistry and Biochemistry, Charles University Second Medical School, Prague, Czech Republic; Department of Pathological Physiology, Charles University Second Medical School and Centre for Experimental Cardiovascular Research, Prague, Czech Republic
3 Department of Pathology, Charles University Second Medical School, Prague, Czech Republic
4 Department of Pathological Physiology, Charles University Second Medical School and Centre for Experimental Cardiovascular Research, Prague, Czech Republic
* To whom correspondence should be addressed. E-mail: Jan.Herget{at}lfmotol.cuni.cz.
Chronic hypoxia induces lung vascular remodeling, which results in pulmonary hypertension. We hypothesized that a previously found increase in collagenolytic activity of matrix metalloproteinases during hypoxia promotes pulmonary vascular remodeling and hypertension. To test this hypothesis, rats were exposed to hypoxia (FIO2=0.1; 3 weeks) and treated with a metalloproteinase inhibitor, Batimastat (30 mg/kg body weight, daily IP injection). Hypoxia-induced increases in concentration of collagen breakdown products and in collagenolytic activity in pulmonary vessels were inhibited by Batimastat, attesting to the effectiveness of Batimastat administration. Batimastat markedly reduced hypoxic pulmonary hypertension: pulmonary arterial blood pressure was 32 ± 3 mmHg in hypoxic controls, 24 ± 1 mmHg in Batimastat-treated hypoxic rats, and 16 ± 1 mmHg in normoxic controls. Right ventricular hypertrophy and muscularization of peripheral lung vessels were also diminished. Batimastat had no influence on systemic arterial pressure or cardiac output and was without any effect in rats kept in normoxia. We conclude that stimulation of collagenolytic activity in chronic hypoxia is a substantial causative factor in the pathogenesis of pulmonary vascular remodeling and hypertension.
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