Arginase inhibition restores NOS coupling and reverses endothelial dysfunction and vascular stiffness in old rats

Author:

Kim Jae Hyung1,Bugaj Lukasz J.2,Oh Young Jun13,Bivalacqua Trinity J.4,Ryoo Sungwoo5,Soucy Kevin G.2,Santhanam Lakshmi1,Webb Alanah2,Camara Andre1,Sikka Gautam1,Nyhan Daniel1,Shoukas Artin A.2,Ilies Monica6,Christianson David W.6,Champion Hunter C.7,Berkowitz Dan E.12

Affiliation:

1. Department of 1Anesthesiology and Critical Care Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland;

2. Department of 2Biomedical Engineering, Johns Hopkins Medical Institutions, Baltimore, Maryland;

3. Department of Anesthesiology and Pain Medicine, Yonsei University, Seoul, Korea; and

4. Department of 3Urology, Johns Hopkins Medical Institutions, Baltimore, Maryland;

5. Biology Program, Division of Life Sciences, Kangwon National University, Chuncheon, Korea

6. Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania;

7. Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania;

Abstract

There is increasing evidence that upregulation of arginase contributes to impaired endothelial function in aging. In this study, we demonstrate that arginase upregulation leads to endothelial nitric oxide synthase (eNOS) uncoupling and that in vivo chronic inhibition of arginase restores nitroso-redox balance, improves endothelial function, and increases vascular compliance in old rats. Arginase activity in old rats was significantly increased compared with that shown in young rats. Old rats had significantly lower nitric oxide (NO) and higher superoxide (O2) production than young. Acute inhibition of both NOS, with NG-nitro-l-arginine methyl ester, and arginase, with 2( S)-amino- 6-boronohexanoic acid (ABH), significantly reduced O2 production in old rats but not in young. In addition, the ratio of eNOS dimer to monomer in old rats was significantly decreased compared with that shown in young rats. These results suggest that eNOS was uncoupled in old rats. Although the expression of arginase 1 and eNOS was similar in young and old rats, inducible NOS (iNOS) was significantly upregulated. Furthermore, S-nitrosylation of arginase 1 was significantly elevated in old rats. These findings support our previously published finding that iNOS nitrosylates and activates arginase 1 (Santhanam et al., Circ Res 101: 692–702, 2007). Chronic arginase inhibition in old rats preserved eNOS dimer-to-monomer ratio and significantly reduced O2 production and enhanced endothelial-dependent vasorelaxation to ACh. In addition, ABH significantly reduced vascular stiffness in old rats. These data indicate that iNOS-dependent S-nitrosylation of arginase 1 and the increase in arginase activity lead to eNOS uncoupling, contributing to the nitroso-redox imbalance, endothelial dysfunction, and vascular stiffness observed in vascular aging. We suggest that arginase is a viable target for therapy in age-dependent vascular stiffness.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology

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