Concealed role of red blood cells in pathogenesis of pulmonary arterial hypertension: Decreased red blood cell nitric oxide generation and effect of Rho-Kinase inhibitor fasudil

Article type: Research Article

Authors: Basarici, Ibrahim^a | Özen, Nur^b | Kilavuz, Ece^b | Kısak, Fatih^b | Basrali, Filiz^b | Yaras, Nazmi^c | Koksoy, Sadi^d | Celik, Mukadder Levent^{b; e} | Ulker, Pinar^{b; *}

Affiliations: [a] Department of Cardiology, Medical Faculty, Akdeniz University, Antalya, Turkey | [b] Department of Physiology, Medical Faculty, Akdeniz University, Antalya, Turkey | [c] Department of Biophysics, Medical Faculty, AkdenizUniversity, Antalya, Turkey | [d] Department of Medical Microbiology, Medical Faculty, AkdenizUniversity, Antalya, Turkey | [e] Department of Internal Medicine, University of Health Sciences Antalya Training and Research Hospital, Antalya, Turkey

Correspondence: [*] Corresponding author: Assoc. Prof.Dr. Pinar Ulker, PhD, Department of Physiology, Akdeniz University Medical Faculty, Antalya, Turkey. Tel.: +90(242)2496960; E-mail: ulkerpinar@akdeniz.edu.tr.

Abstract: BACKGROUND:Pulmonary arterial hypertension (PAH) is a devastating disease characterized with alterations in pulmonary vasculature yielding increased pulmonary arterial resistance. Emerging evidences suggest important regulatory roles of red blood cells (RBCs) on nitric oxide (NO) bioavailability, mainly by modulating their endothelial nitric oxide synthase (eNOS) enzyme activity. OBJECTIVE:The aim of this pilot study was to evaluate the alterations in RBC eNOS activity and intracellular NO generation in PAH patients and the modulatory effects of Rho-Kinase (ROCK) inhibitors. METHODS:RBCs were isolated from patients with PAH and age-matched healthy subjects and were analyzed for their eNOS activity and NO generation capacity under the conditions of the presence or absence of ROCK inhibitor, fasudil. Phosphotidylserine (PS) exposure was also defined. RESULTS:eNOS activity and intracellular NO generation were lower in RBC from PAH patients. ROCK inhibitor increased basal eNOS activity and improved NO generation capacity of RBC of PAH patients to healthy control levels. PS exposure levels were also higher in RBC of PAH patients. CONCLUSIONS:This study provides first evidences for decreased RBC eNOS activity due to its ROCK mediated negative regulation in PAH patients. Considering increased ROCK activity contribution to progression of PAH, ROCK inhibition influences NO bioavailability through RBC eNOS, in addition to endothelial eNOS.

Keywords: Pulmonary hypertension, eNOS, red blood cell, Rho-Kinase, fasudil

DOI: 10.3233/CH-200892

Journal: Clinical Hemorheology and Microcirculation, vol. 76, no. 4, pp. 535-548, 2020