Journal article

Effects of Dimethylarginine Dimethylaminohydrolase-1 Overexpression on the Response of the Pulmonary Vasculature to Hypoxia


Authors listBakr, Adel; Pak, Oleg; Taye, Ashraf; Hamada, Farid; Hemeida, Ramadan; Janssen, Wiebke; Gierhardt, Mareike; Ghofrani, Hossein A.; Seeger, Werner; Grimminger, Friedrich; Schermuly, Ralph T.; Witzenrath, Martin; Brandes, Ralf P.; Huang, Ngan; Cooke, John P.; Weissmann, Norbert; Sommer, Natascha

Publication year2013

Pages491-500

JournalAmerican Journal of Respiratory Cell and Molecular Biology

Volume number49

Issue number3

ISSN1044-1549

Open access statusGreen

DOI Linkhttps://doi.org/10.1165/rcmb.2012-0330OC

PublisherAmerican Thoracic Society


Abstract
Acute and sustained hypoxic pulmonary vasoconstriction (HPV), as well as chronic pulmonary hypertension (PH), is modulated by nitric oxide (NO). NO synthesis can be decreased by asymmetric dimethylarginine (ADMA), which is degraded by dimethylarginine dimethylaminohydrolase-1 (DDAH1). Weinvestigated the effects of DDAH1 overexpression (DDAH1(tg)) on HPV and chronic hypoxia-induced PH. HPV was measured during acute (10 min) and sustained (3 h) hypoxia in isolated mouse lungs. Chronic PH was induced by the exposure of mice to 4 weeks of hypoxia. ADMA and cyclic 3',5'-guanosine monophosphate (cGMP) were determined by ELISA, and NO generation was determined by chemiluminescence. DDAH1 overexpression exerted no effects on acute HPV. However, DDAH1(tg) mice showed decreased sustained HPV compared with wild-type (WT) mice. Concomitantly, ADMA was decreased, and concentrations of NO and cGMP were significantly increased in DDAH1(tg). The administration of either N-omega-nitro-L-arginine or 1H-[1,2,4] oxadiazolo [4,3-a] quinoxalin-1-one potentiated sustained HPV and partly abolished the differences in sustained HPV between WT and DDAH1(tg) mice. The overexpression of DDAH1 exerted no effect on the development of chronic hypoxia-induced PH. DDAH1 overexpression selectively decreased the sustained phase of HPV, partly via activation of the NO-cGMP pathway. Thus, increased ADMA concentrations modulate sustained HPV, but not acute HPV or chronic hypoxia-induced PH.



Citation Styles

Harvard Citation styleBakr, A., Pak, O., Taye, A., Hamada, F., Hemeida, R., Janssen, W., et al. (2013) Effects of Dimethylarginine Dimethylaminohydrolase-1 Overexpression on the Response of the Pulmonary Vasculature to Hypoxia, American Journal of Respiratory Cell and Molecular Biology, 49(3), pp. 491-500. https://doi.org/10.1165/rcmb.2012-0330OC

APA Citation styleBakr, A., Pak, O., Taye, A., Hamada, F., Hemeida, R., Janssen, W., Gierhardt, M., Ghofrani, H., Seeger, W., Grimminger, F., Schermuly, R., Witzenrath, M., Brandes, R., Huang, N., Cooke, J., Weissmann, N., & Sommer, N. (2013). Effects of Dimethylarginine Dimethylaminohydrolase-1 Overexpression on the Response of the Pulmonary Vasculature to Hypoxia. American Journal of Respiratory Cell and Molecular Biology. 49(3), 491-500. https://doi.org/10.1165/rcmb.2012-0330OC



Keywords


ARTERIESasymmetric dimethylarginineASYMMETRIC DIMETHYLARGININEcyclic guanosine monophosphateHYPERCAPNIAhypoxia-induced pulmonary hypertensionHYPOXIC PULMONARY VASOCONSTRICTIONMETHYLARGININE METABOLISMNITRIC-OXIDE PRODUCTIONVASOCONSTRICTION

Last updated on 2025-10-06 at 10:14