» Articles » PMID: 25602514

Combined Sub-optimal Doses of Rosuvastatin and Bexarotene Impair Angiotensin II-induced Arterial Mononuclear Cell Adhesion Through Inhibition of Nox5 Signaling Pathways and Increased RXR/PPARα and RXR/PPARγ Interactions

Overview
Specialty Endocrinology
Date 2015 Jan 21
PMID 25602514
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

Aim: Mononuclear cell (MC) infiltration into the arterial subendothelium is a key event in atherogenesis. Rosuvastatin (Rosu) and bexarotene (Bex) exert anti-inflammatory activity, but serious dose-related adverse effects have emerged. The need for safer and effective strategies to prevent and treat atherosclerosis led us to test the effect of combined use of both drugs on angiotensin II (Ang-II)-induced arterial MC recruitment.

Results: Vehicle, Rosu (10-30 nM), Bex (0.3-1 μM), or a combination of both were administered to human umbilical arterial endothelial cells (HUAECs) 20 h before stimulation with 1 μM Ang-II (4 h). Surprisingly, a combination of Rosu (10 nM)+Bex (0.3 μM), which did not influence Ang-II-induced MC recruitment when either stimulus was studied alone, significantly reduced this response. This effect was accompanied by diminished Ang-II-induced ICAM-1, VCAM-1, and CX3CL1 endothelial expression and CXCL1, CXCL8, CCL2, and CCL5 production. Preincubation of HUAECs with Rosu+Bex inhibited Nox5 expression and Nox5-induced RhoA activation stimulated by Ang-II through increased RXRα, PPARα, and PPARγ expression in addition to RXRα/PPARα and RXRα/PPARγ interactions. In vivo, combined but not single administration of Rosu (1.25 mg/kg/day) and Bex (10 mg/kg/day) significantly diminished Ang-II-induced arteriolar leukocyte adhesion in the cremasteric microcirculation of C57BL/6 mice and atherosclerotic lesion formation in apoE(-/-) mice subjected to an atherogenic diet.

Innovation And Conclusion: Combined administration of Bex+Rosu at suboptimal doses may constitute a new alternative and effective therapy in the control of the vascular inflammation associated to cardiometabolic disorders, since they synergize in their anti-inflammatory actions and may counteract their associated adverse effects.

Citing Articles

NADPH Oxidase 5 (NOX5) Upregulates MMP-10 Production and Cell Migration in Human Endothelial Cells.

Marques J, Ainzua E, Orbe J, Martinez-Azcona M, Martinez-Gonzalez J, Zalba G Antioxidants (Basel). 2024; 13(10).

PMID: 39456453 PMC: 11504164. DOI: 10.3390/antiox13101199.


Inhibition of the RXRA-PPARα-FABP4 signaling pathway alleviates vascular cellular aging by an SGLT2 inhibitor in an atherosclerotic mice model.

Zhang W, Wang L, Wang Y, Fang Y, Cao R, Fang Z Sci China Life Sci. 2024; 67(12):2678-2691.

PMID: 39225895 DOI: 10.1007/s11427-024-2602-7.


Circadian rhythms of risk factors and management in atherosclerotic and hypertensive vascular disease: Modern chronobiological perspectives of an ancient disease.

Geng Y, Smolensky M, Sum-Ping O, Hermida R, Castriotta R Chronobiol Int. 2022; 40(1):33-62.

PMID: 35758140 PMC: 10355310. DOI: 10.1080/07420528.2022.2080557.


iTRAQ-derived quantitative proteomics uncovers the neuroprotective property of bexarotene in a mice model of cerebral ischemia-reperfusion injury.

Liu H, Wang H, Chen S, Liu S, Tian X, Dong Z Saudi Pharm J. 2022; 30(5):585-594.

PMID: 35693438 PMC: 9177454. DOI: 10.1016/j.jsps.2022.02.012.


Activation of the Constitutive Androstane Receptor Inhibits Leukocyte Adhesiveness to Dysfunctional Endothelium.

Lopez-Riera M, Ortega R, Hueso L, Montesinos M, Gomez-Cabrera M, Sanz M Int J Mol Sci. 2021; 22(17).

PMID: 34502180 PMC: 8431649. DOI: 10.3390/ijms22179267.


References
1.
Dzau V . Theodore Cooper Lecture: Tissue angiotensin and pathobiology of vascular disease: a unifying hypothesis. Hypertension. 2001; 37(4):1047-52. DOI: 10.1161/01.hyp.37.4.1047. View

2.
Fan L, Douglas G, Bendall J, McNeill E, Crabtree M, Hale A . Endothelial cell-specific reactive oxygen species production increases susceptibility to aortic dissection. Circulation. 2014; 129(25):2661-72. PMC: 5357047. DOI: 10.1161/CIRCULATIONAHA.113.005062. View

3.
Libby P . Inflammation in atherosclerosis. Nature. 2002; 420(6917):868-74. DOI: 10.1038/nature01323. View

4.
Kleemann R, Princen H, Emeis J, Jukema J, Fontijn R, Horrevoets A . Rosuvastatin reduces atherosclerosis development beyond and independent of its plasma cholesterol-lowering effect in APOE*3-Leiden transgenic mice: evidence for antiinflammatory effects of rosuvastatin. Circulation. 2003; 108(11):1368-74. DOI: 10.1161/01.CIR.0000086460.55494.AF. View

5.
Farol L, Hymes K . Bexarotene: a clinical review. Expert Rev Anticancer Ther. 2004; 4(2):180-8. DOI: 10.1586/14737140.4.2.180. View