Document Type
Article
Language
eng
Format of Original
9 p.
Publication Date
10-2016
Publisher
Wiley
Source Publication
Microcirculation
Source ISSN
1073-9688
Abstract
Objective
The potential contribution of CYP4A enzymes to endothelial dysfunction in Dahl salt-sensitive rats was determined by comparison to SS-5BN consomic rats having chromosome 5 carrying CYP4A alleles from the BN rat introgressed into the SS genetic background.
Methods
The following experiments were performed in cerebral arteries from HS-fed SS and SS-5BN rats ± the SOD inhibitor DETC and/or the superoxide scavenger Tempol: (i) endothelial function was determined via video microscopy ± acute addition of the CYP4A inhibitor DDMS or Tempol; (ii) vascular oxidative stress was assessed with DHE fluorescence ± acute addition of DDMS, l-NAME, or PEG-SOD; and (iii) CYP4A protein levels were compared by western blotting.
Results
In DETC-treated SS-5BN and HS-fed SS rats, (i) DDMS or Tempol ameliorated vascular dysfunction, (ii) DDMS reduced vascular oxidative stress to control levels, (iii) chronic Tempol treatment reduced vascular CYP4A protein expression, and (iv) combined treatment with Tempol and l-NAME prevented the reduction in CYP4A protein expression in MCA of HS-fed SS rats.
Conclusion
The CYP4A pathway plays a role in vascular dysfunction in SS rats and there appears to be a direct role of reduced NO availability due to salt-induced oxidant stress in upregulating CYP4A enzyme expression.
Recommended Citation
Lukaszewicz, Kathleen M.; Paudyal, Mahesh P.; Falck, John R.; and Lombard, Julian H., "Role of Vascular Reactive Oxygen Species in Regulating Cytochrome P450-4A Enzyme Expression in Dahl Salt-Sensitive Rats" (2016). Physical Therapy Faculty Research and Publications. 134.
https://epublications.marquette.edu/phys_therapy_fac/134
Comments
Accepted version. Microcirculation, Vol. 23, No. 7 (October 2016): 540-548. DOI. © 2016 Wiley-Blackwell. Used with permission.
Kathleen M. Lukaszewicz was affiliated with the Medical College of Wisconsin at the time of publication.