Abstract

Background. The epidemiology of pulmonary hypertension (PH) is characterized by a female preponderance, whereas males share higher severity of the disease. Objective. To compare the severity of experimental PH between male and female athymic rats. Methods. PH was induced in 11 male and 11 female athymic rats (resp., SU_M and SU_F groups) using an inhibitor of VEGF-receptors I and II, semaxanib (40 mg/kg). After 28 days, right ventricular (RV) remodeling, systolic function, and hemodynamics were measured using echocardiography and a pressure-volume admittance catheter. Morphometric analyses of lung vasculature and RV myocardium were performed. Results. Four weeks after semaxanib injection, RV end-systolic pressure was higher in SU_M than in SU_F. Males developed marked RV enlargement and systolic dysfunction compared to females. Impairment of RV-PA coupling efficiency was observed only in SU_M. The smooth muscle cells of the pulmonary arteries switched from a contractile state to a dedifferentiated state only in males. Conclusions. Female athymic rats were protected against the development of severe PH. RV-PA coupling was preserved in females through limitation of pulmonary artery muscularization. Control of smooth muscle cells plasticity may be a promising therapeutic approach to reverse established vascular remodeling in PH patients.

Highlights

  • Pulmonary hypertension (PH) is a disabling disease characterized by higher prevalence in females [1]

  • Induction of experimental pulmonary hypertension (PH) resulted in a significant enlargement of the right ventricle after 3 weeks in males compared to females (RVEDD: 5.6 ± 0.7 versus 2.5 ± 0.4 mm, P < 0.01)

  • Increased Ea combined to altered end-systolic elastance (Ees) in male rats resulted in impairment of right ventricular (RV)-PA coupling efficiency, while ventricular-arterial coupling was preserved

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Summary

Introduction

Pulmonary hypertension (PH) is a disabling disease characterized by higher prevalence in females [1]. Estrogens exhibit protective effects on the pulmonary vasculature in classical models of PH in rodents including the chronic hypoxia and monocrotaline models [3, 4]. We induced PH in male and female rats to investigate the influence of gender difference on the development and severity of PH. The epidemiology of pulmonary hypertension (PH) is characterized by a female preponderance, whereas males share higher severity of the disease. To compare the severity of experimental PH between male and female athymic rats. PH was induced in 11 male and 11 female athymic rats (resp., SU M and SU F groups) using an inhibitor of VEGFreceptors I and II, semaxanib (40 mg/kg). Female athymic rats were protected against the development of severe PH. Control of smooth muscle cells plasticity may be a promising therapeutic approach to reverse established vascular remodeling in PH patients

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