The Expression of Genes CYP1A1, CYP1B1, and CYP2J3 in Distinct Regions of the Heart and Its Possible Contribution to the Development of Hypertension
- PMID: 39457686
- PMCID: PMC11505345
- DOI: 10.3390/biomedicines12102374
The Expression of Genes CYP1A1, CYP1B1, and CYP2J3 in Distinct Regions of the Heart and Its Possible Contribution to the Development of Hypertension
Abstract
Background: It is believed that alterations in the functioning of the cytochrome P450 (CYP), which participates in metabolic transformations of endogenous polyunsaturated fatty acids (PUFAs) (with the formation of cardioprotective or cardiotoxic products), affects the development of age-related cardiovascular diseases and reduces the effectiveness of some cardioselective drugs. For example, CYP2J2 activation or CYP1B1 inhibition protects against the cardiovascular toxicity of anticancer drugs. It is currently unclear whether CYPs capable of metabolizing arachidonic acid and ω-3 PUFAs to vasodilatory and vasoconstrictive derivatives are expressed in all heart regions.
Methods: The work was performed on senescence-accelerated OXYS rats featuring elevated blood pressure, OXYSb rats (an OXYS substrain with normal blood pressure), and Wistar rats as a "healthy" control. The mRNA level was determined in the right and left ventricles, the right and left atria, and the aorta of 1-, 3-, and 12-month-old rats.
Results: We showed that all heart regions express CYPs capable of metabolizing arachidonic acid and ω-3 PUFAs and revealed significant differences between heart regions both in the mRNA level of genes CYP1B1, CYP2J3, and CYP1A1 and in the time course of expression changes with age.
Conclusions: We noticed that expression levels of these CYPs in the heart regions and aorta differ between hypertensive OXYS rats, normotensive OXYSb rats, and healthy Wistar rats but could not detect any clear-cut patterns associated with the hypertensive status of OXYS rats.
Keywords: CYP1A1; CYP1B1; CYP2J3; OXYS rats; heart chamber; hypertension.
Conflict of interest statement
The authors declare no conflicts of interest.
Similar articles
-
The influence of changes in expression of redox-sensitive genes on the development of retinopathy in rats.Exp Mol Pathol. 2016 Aug;101(1):124-32. doi: 10.1016/j.yexmp.2016.07.008. Epub 2016 Jul 25. Exp Mol Pathol. 2016. PMID: 27466007
-
The Mitochondria-Targeted Antioxidant SkQ1 Downregulates Aryl Hydrocarbon Receptor-Dependent Genes in the Retina of OXYS Rats with AMD-Like Retinopathy.J Ophthalmol. 2014;2014:530943. doi: 10.1155/2014/530943. Epub 2014 Jul 14. J Ophthalmol. 2014. PMID: 25132985 Free PMC article.
-
Effects of sexually dimorphic growth hormone secretory patterns on arachidonic acid metabolizing enzymes in rodent heart.Toxicol Appl Pharmacol. 2015 Dec 15;289(3):495-506. doi: 10.1016/j.taap.2015.10.011. Epub 2015 Oct 19. Toxicol Appl Pharmacol. 2015. PMID: 26493931
-
Crosstalk between adenosine receptors and CYP450-derived oxylipins in the modulation of cardiovascular, including coronary reactive hyperemic response.Pharmacol Ther. 2022 Dec;240:108213. doi: 10.1016/j.pharmthera.2022.108213. Epub 2022 May 18. Pharmacol Ther. 2022. PMID: 35597366 Review.
-
Cytochrome P450-dependent metabolism of omega-6 and omega-3 long-chain polyunsaturated fatty acids.Pharmacol Rep. 2010 May-Jun;62(3):536-47. doi: 10.1016/s1734-1140(10)70311-x. Pharmacol Rep. 2010. PMID: 20631419 Review.
References
-
- Whelton P.K., Carey R.M., Aronow W.S., Casey D.E., Jr., Collins K.J., Dennison Himmelfarb C., DePalma S.M., Gidding S., Jamerson K.A., Jones D.W., et al. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the Prevention, Detection, Evaluation, and Management of High Blood Pressure in Adults: Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation. 2018;138:e426–e483. doi: 10.1161/CIR.0000000000000597. - DOI - PubMed
Grants and funding
- project No. 1021050601082-2-1.6.4;3.1.6/Government funding of topic No. FGMU-2022-0004 for the Institute of Molecular Biology and Biophysics, the Federal Research Center of Fundamental and Translational Medicine (molecular biological research)
- № FWNR-2022-0016/State Budget Project for Federal State Budgetary Institution of Science Federal Research Center Institute of Cytology and Genetics (maintaining of experimental animal model of premature aging)
LinkOut - more resources
Full Text Sources