Inhaled iloprost reverses vascular remodeling in chronic experimental pulmonary hypertension
- PMID: 15879421
- DOI: 10.1164/rccm.200502-296OC
Inhaled iloprost reverses vascular remodeling in chronic experimental pulmonary hypertension
Abstract
Rationale: Inhaled iloprost is an effective therapy for pulmonary arterial hypertension (PAH). However, no study to date has addressed the effects of inhaled iloprost on changes to pulmonary vascular structure that occur in PAH.
Objectives: The present study was designed to investigate chronic antiremodeling effects of inhaled iloprost in monocrotaline (MCT)-induced PAH in rats.
Methods: Four weeks after a single injection of MCT, after full establishment of PAH, rats were nebulized with iloprost at a dose of 6 microg . kg(-1) . day(-1), or underwent sham nebulization with saline.
Results: After 2 weeks of inhalation therapy, right ventricular pressure and pulmonary vascular resistance were reversed in rats treated with iloprost, but not in sham-treated control animals. Systemic arterial pressure was unaffected. In addition, right heart hypertrophy, the degree of pulmonary artery muscularization, and the medial wall thickness of intraacinar pulmonary arteries regressed in response to iloprost. Furthermore, the MCT-induced increase in matrix metalloproteinase-2 and -9 activities and tenascin-C expression was suppressed.
Conclusions: We conclude that the inhalation of iloprost reverses PAH and vascular structural remodeling in MCT-treated rats. This regimen suggests the possibility of an antiremodeling therapy in PAH.
Similar articles
-
Antiremodeling effects of iloprost and the dual-selective phosphodiesterase 3/4 inhibitor tolafentrine in chronic experimental pulmonary hypertension.Circ Res. 2004 Apr 30;94(8):1101-8. doi: 10.1161/01.RES.0000126050.41296.8E. Epub 2004 Mar 18. Circ Res. 2004. PMID: 15031263
-
Urantide alleviates monocrotaline induced pulmonary arterial hypertension in Wistar rats.Pulm Pharmacol Ther. 2011 Aug;24(4):386-93. doi: 10.1016/j.pupt.2011.03.003. Epub 2011 Mar 15. Pulm Pharmacol Ther. 2011. PMID: 21396478
-
Assessment of the endothelial functions in monocrotaline-induced pulmonary hypertension.Clin Exp Hypertens. 2013;35(3):220-7. doi: 10.3109/10641963.2012.721838. Epub 2012 Sep 11. Clin Exp Hypertens. 2013. PMID: 22967272
-
Inhaled iloprost in pulmonary arterial hypertension.Ann Pharmacother. 2005 Jul-Aug;39(7-8):1265-74. doi: 10.1345/aph.1E575. Ann Pharmacother. 2005. PMID: 15976392 Review.
-
Clinical pharmacology and efficacy of inhaled iloprost for the treatment of pulmonary arterial hypertension.Expert Rev Clin Pharmacol. 2011 Mar;4(2):197-205. doi: 10.1586/ecp.10.136. Expert Rev Clin Pharmacol. 2011. PMID: 22115402 Review.
Cited by
-
Factors Associated with Ineffectiveness of Sildenafil Treatment in Patients with End-Stage Heart Failure and Elevated Pulmonary Vascular Resistance.J Clin Med. 2020 Nov 2;9(11):3539. doi: 10.3390/jcm9113539. J Clin Med. 2020. PMID: 33147835 Free PMC article.
-
Galectin-3 Promotes ROS, Inflammation, and Vascular Fibrosis in Pulmonary Arterial Hypertension.Adv Exp Med Biol. 2021;1303:13-32. doi: 10.1007/978-3-030-63046-1_2. Adv Exp Med Biol. 2021. PMID: 33788185
-
TGF-β and BMPR2 Signaling in PAH: Two Black Sheep in One Family.Int J Mol Sci. 2018 Aug 31;19(9):2585. doi: 10.3390/ijms19092585. Int J Mol Sci. 2018. PMID: 30200294 Free PMC article. Review.
-
Novel approaches to treat experimental pulmonary arterial hypertension: a review.J Biomed Biotechnol. 2010;2010:702836. doi: 10.1155/2010/702836. Epub 2010 Mar 22. J Biomed Biotechnol. 2010. PMID: 20339474 Free PMC article. Review.
-
PDGF and TGF-β promote tenascin-C expression in subepithelial myofibroblasts and contribute to intestinal mucosal protection in mice.Br J Pharmacol. 2014 Jan;171(2):375-88. doi: 10.1111/bph.12452. Br J Pharmacol. 2014. PMID: 24116743 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical