Hypertension and cardiovascular remodelling in rats exposed to continuous light: protection by ACE-inhibition and melatonin
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25110398
PubMed Central
PMC4106091
DOI
10.1155/2014/703175
Knihovny.cz E-zdroje
- MeSH
- antihypertenziva terapeutické užití MeSH
- hypertenze farmakoterapie MeSH
- inhibitory ACE terapeutické užití MeSH
- kaptopril terapeutické užití MeSH
- krevní tlak účinky léků MeSH
- krysa rodu Rattus MeSH
- melatonin terapeutické užití MeSH
- oxidační stres účinky léků MeSH
- potkani Wistar MeSH
- světlo * MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antihypertenziva MeSH
- inhibitory ACE MeSH
- kaptopril MeSH
- melatonin MeSH
Exposure of rats to continuous light attenuates melatonin production and results in hypertension development. This study investigated whether hypertension induced by continuous light (24 hours/day) exposure induces heart and aorta remodelling and if these alterations are prevented by melatonin or angiotensin converting enzyme inhibitor captopril. Four groups of 3-month-old male Wistar rats (10 per group) were treated as follows for six weeks: untreated controls, exposed to continuous light, light-exposed, and treated with either captopril (100 mg/kg/day) or melatonin (10 mg/kg/day). Exposure to continuous light led to hypertension, left ventricular (LV) hypertrophy and fibrosis, and enhancement of the oxidative load in the LV and aorta. Increase in systolic blood pressure by continuous light exposure was prevented completely by captopril and partially by melatonin. Both captopril and melatonin reduced the wall thickness and cross-sectional area of the aorta and reduced the level of oxidative stress. However, only captopril reduced LV hypertrophy development and only melatonin reduced LV hydroxyproline concentration in insoluble and total collagen in rats exposed to continuous light. In conclusion, captopril prevented LV hypertrophy development in the continuous light-induced hypertension model, while only melatonin significantly reduced fibrosis. This antifibrotic action of melatonin may be protective in hypertensive heart disease.
3rd Clinic of Medicine School of Medicine Comenius University 83305 Bratislava Slovakia
Department of Physiology School of Medicine Charles University 50038 Hradec Kralove 1 Czech Republic
Institute of Molecular Biomedicine School of Medicine Comenius University 81372 Bratislava Slovakia
Zobrazit více v PubMed
Reiter RJ, Manchester LC, Fuentes-Broto L, Tan D. Cardiac hypertrophy and remodelling: pathophysiological consequences and protective effects of melatonin. Journal of Hypertension. 2010;28(1):S7–S12. PubMed
Simko F, Pechanova O. Remodelling of the heart and vessels in experimental hypertension: advances in protection. Journal of Hypertension. 2010;28(supplement 1):S1–S6. PubMed
Simko F, Matuskova J, Luptak I, et al. Effect of simvastatin on remodeling of the left ventricle and aorta in L-NAME-induced hypertension. Life Sciences. 2004;74(10):1211–1224. PubMed
Simko F, Pelouch V, Torok J, et al. Protein remodeling of the heart ventricles in hereditary hypertriglyceridemic rat: effect of ace-inhibition. Journal of Biomedical Science. 2005;12(1):103–111. PubMed
Mandarim-de-Lacerda CA, Pereira LMM. Effect of telmisartan on preexistent cardiac and renal lesions in spontaneously hypertensive mature rats. Histology and Histopathology. 2004;19(3):727–733. PubMed
Simko F. Statins: a perspective for left ventricular hypertrophy treatment. European Journal of Clinical Investigation. 2007;37(9):681–691. PubMed
Kyselovic J, Krenek P, Wibo M, Godfraind T. Effects of amlodipine and lacidipine on cardiac remodelling and renin production in salt-loaded stroke-prone hypertensive rats. The British Journal of Pharmacology. 2001;134(7):1516–1522. PubMed PMC
Simko F, Reiter RJ, Pechanova O, Paulis L. Experimental models of melatonin-deficient hypertension. Frontiers in Bioscience. 2013;18(2):616–625. PubMed
Ozturk M, Ozler M, Kurt YG, et al. Efficacy of melatonin, mercaptoethylguanidine and 1400W in doxorubicin- and trastuzumab-induced cardiotoxicity. Journal of Pineal Research. 2011;50(1):89–96. PubMed
Grossini E, Molinari C, Uberti F, Mary DASG, Vacca G, Caimmi PP. Intracoronary melatonin increases coronary blood flow and cardiac function through β-adrenoreceptors, MT1/MT2 receptors, and nitric oxide in anesthetized pigs. Journal of Pineal Research. 2011;51(2):246–257. PubMed
Samimi-Fard S, Abreu-Gonzalez P, Dominguez-Rodriguez A, Jimenez-Sosa A. A case-control study of melatonin receptor type 1A polymorphism and acute myocardial infarction in a Spanish population. Journal of Pineal Research. 2011;51(4):400–404. PubMed
Zeman M, Herichova I. Melatonin and clock genes expression in the cardiovascular system. Frontiers in Bioscience. 2013;1(5):743–753. PubMed
Simko F, Paulis L. Melatonin as a potential antihypertensive treatment. Journal of Pineal Research. 2007;42(4):319–322. PubMed
Tengattini S, Reiter RJ, Tan D, Terron MP, Rodella LF, Rezzani R. Cardiovascular diseases: protective effects of melatonin. Journal of Pineal Research. 2008;44(1):16–25. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Sanchez-Sanchez JJ, Kaski JC, Reiter RJ. Melatonin and circadian biology in human cardiovascular disease. Journal of Pineal Research. 2010;49(1):14–22. PubMed
Paulis L, Šimko F. Blood pressure modulation and cardiovascular protection by melatonin: potential mechanisms behind. Physiological Research. 2007;56(6):671–684. PubMed
Hoffman RA, Reiter RJ. Rapid pinealectomy in hamsters and other small rodents. The Anatomical Record. 1965;153(1):19–21. PubMed
Cunnane SC, Manku MS, Oka M, Horrobin DF. Enhanced vascular reactivity to various vasoconstrictor agents following pinealectomy in the rat: role of melatonin. Canadian Journal of Physiology and Pharmacology. 1980;58(3):287–293. PubMed
Zanoboni A, Zanoboni-Muciaccia W. Experimental hypertension in pinealectomized rats. Life Sciences. 1967;6(21):2327–2331. PubMed
Brown GM, Bar-Or A, Grossi D, Kashur S, Johannson E. Urinary 6-sulphatoxymelatonin, an index of pineal function in the rat. Journal of Pineal Research. 1991;10(3):141–147. PubMed
Tan DX, Chen LD, Poeggeler B, et al. Melatonin: a potent, endogenous hydroxyl radical scavenger. Endocrine Journal. 1993;1:157–160.
Reiter RJ, Tan DX, Terron MP, Flores LJ, Czarnocki Z. Melatonin and its metabolites: new findings regarding their production and their radical scavenging actions. Acta Biochimica Polonica. 2007;54(1):1–9. PubMed
Galano A, Tan DX, Reiter RJ. Melatonin as a natural ally against oxidative stress: a physicochemical examination. Journal of Pineal Research. 2011;51(1):1–16. PubMed
Reiter RJ, Tan DX. Melatonin: a multitasking molecule. Progress in Brain Research. 2010;181:127–151. PubMed
Rezzani R, Porteri E, de Ciuceis C, et al. Effects of melatonin and pycnogenol on small artery structure and function in spontaneously hypertensive rats. Hypertension. 2010;55(6):1373–1380. PubMed
Reiter RJ, Tan D, Korkmaz A. The circadian melatonin rhythm and its modulation: possible impact on hypertension. Journal of Hypertension. 2009;27(supplement 6):S17–S20. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Reiter RJ. Melatonin and cardiovascular disease: myth or reality? Revista Espanola de Cardiologia. 2012;65(3):215–218. PubMed
Paulis L, Matuskova J, Adamcova M, et al. Regression of left ventricular hypertrophy and aortic remodelling in NO-deficient hypertensive rats: effect of L-arginine and spironolactone. Acta Physiologica. 2008;194(1):45–55. PubMed
Benova T, Viczenczova C, Radosinska J, et al. Melatonin attenuates hypertension-related proarrhythmic myocardial maladaptation of connexin-43 and propensity of the heart to lethalarrhythmias. Canadian Journal of Physiology and Pharmacology. 2013;91(8):633–639. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Garcia-Gonzalez M, Reiter RJ. Prognostic value of nocturnal melatonin levels as a novel marker in patients with ST-segment elevation myocardial infarction. The American Journal of Cardiology. 2006;97(8):1162–1164. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Reiter RJ. Clinical aspects of melatonin in the acute coronary syndrome. Current Vascular Pharmacology. 2009;7(3):367–373. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Arroyo-Ucar E, Reiter RJ. Decreased level of melatonin in serum predicts left ventricular remodelling after acute myocardial infarction. Journal of Pineal Research. 2012;53(3):319–323. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Arroyo-Ucar E, Avanzas P, Reiter RJ. Global left ventricular longitudinal strain is associated with decreased melatonin levels in patients with acute myocardial infarction: a two-dimensional speckle tracking study. Biomarkers. 2013;18(4):310–313. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Garcia-Gonzalez MJ, Kaski JC, Reiter RJ, Jimenez-Sosa A. A unicenter, randomized, double-blind, parallel-group, placebo-controlled study of Melatonin as an Adjunct in patients with acute myocaRdial Infarction undergoing primary Angioplasty. The Melatonin Adjunct in the acute myocaRdial Infarction treated with Angioplasty (MARIA) trial: study design and rationale. Contemporary Clinical Trials. 2007;28(4):532–539. PubMed
Dominguez-Rodriguez A, Abreu-Gonzalez P, Reiter RJ. Melatonin and cardioprotection in the acute myocardial infarction: a promising cardioprotective agent. International Journal of Cardiology. 2012;158(2):309–310. PubMed
Repova-Bednarova K, Aziriova S, Hrenak J. Effect of captopril and melatonin on fibrotic rebuilding of the aorta in 24 hour light-induced hypertension. Physiological Research. 2013;62(supplement 1):S135–S141. PubMed
Bernátová I, Pecháňová O, Pelouch V, Šimko F. Regression of chronic L-NAME-treatment-induced left ventricular hypertrophy: effect of captopril. Journal of Molecular and Cellular Cardiology. 2000;32(2):177–185. PubMed
Simko F, Pechanova O, Pelouch V, et al. Effect of melatonin, captopril, spironolactone and simvastatin on blood pressure and left ventricular remodelling in spontaneously hypertensive rats. Journal of Hypertension. 2009;27(supplement 6):S5–S10. PubMed
Pelouch V, Milerova M, Ostadal B, Samánek M, Hucín B. Protein profiling of human atrial and ventricular musculature: the effect of normoxaemia and hypoxaemia in congenital heart diseases. Physiological Research. 1993;42(4):235–242. PubMed
Pelouch V, Milerova M, Ostadal B, Hucin B, Samanek M. Differences between atrial and ventricular protein profiling in children with congenital heart disease. Molecular and Cellular Biochemistry. 1995;147(1–4):43–49. PubMed
Reddy GK, Enwemeka CS. A simplified method for the analysis of hydroxyproline in biological tissues. Clinical Biochemistry. 1996;29(3):225–229. PubMed
Munch G, Keis R, Wessels A, et al. Determination of advanced glycation end products in serum by fluorescence spectroscopy and competitive ELISA1. European Journal of Clinical Chemistry and Clinical Biochemistry. 1997;35(9):669–677. PubMed
Bhatwadekar AD, Ghole VS. Rapid method for the preparation of an AGE-BSA standard calibrator using thermal glycation. Journal of Clinical Laboratory Analysis. 2005;19(1):11–15. PubMed PMC
Witko-Sarsat V, Friedlander M, Capeillère-Blandin C, et al. Advanced oxidation protein products as a novel marker of oxidative stress in uremia. Kidney International. 1996;49(5):1304–1313. PubMed
Lang JK, Gohil K, Packer L. Simultaneous determination of tocopherols, ubiquinols, and ubiquinones in blood, plasma, tissue homogenates, and subcellular fractions. Analytical Biochemistry. 1986;157(1):106–116. PubMed
Kucharská J, Gvozdjáková A, Šimko F. Simvastatin decreased coenzyme Q in the left ventricle and skeletal muscle but not in the brain and liver in L-NAME-induced hypertension. Physiological Research. 2007;56(supplement 2):S49–S54. PubMed
Zeman M, Dulková K, Bada V, Herichová I. Plasma melatonin concentrations in hypertensive patients with the dipping and non-dipping blood pressure profile. Life Sciences. 2005;76(16):1795–1803. PubMed
Buijs RM, Kalsbeek A. Hypothalamic integration of central and peripheral clocks. Nature Reviews Neuroscience. 2001;2(7):521–526. PubMed
Scheer FAJL, van Montfrans GA, van Someren EJW, Mairuhu G, Buijs RM. Daily nighttime melatonin reduces blood pressure in male patients with essential hypertension. Hypertension. 2004;43(2):192–197. PubMed
Jonas M, Garfinkel D, Zisapel N, Laudon M, Grossman E. Impaired nocturnal melatonin secretion in non-dipper hypertensive patients. Blood Pressure. 2003;12(1):19–24. PubMed
Simko F, Pechanova O, Pelouch V, et al. Continuous light and L-NAME-induced left ventricular remodelling: different protection with melatonin and captopril. Journal of Hypertension. 2010;28(supplement 1):S13–S18. PubMed
Pechánová O, Zicha J, Paulis L, et al. The effect of N-acetylcysteine and melatonin in adult spontaneously hypertensive rats with established hypertension. European Journal of Pharmacology. 2007;561(1–3):129–136. PubMed
Paulis L, Pechanova O, Zicha J, et al. Melatonin prevents fibrosis but not hypertrophy development in the left ventricle of NG-nitro-L-arginine-methyl ester hypertensive rats. Journal of Hypertension. 2009;27(supplement 6):S11–S16. PubMed
Weber KT. From inflammation to fibrosis: a stiff stretch of highway. Hypertension. 2004;43(4):716–719. PubMed
Simko F, Simko J. The potential role of nitric oxide in the hypertrophic growth of the left ventricle. Physiological Research. 2000;49(1):37–46. PubMed
Simko F. Is NO the king? Pathophysiological benefit with uncertain clinical impact [editorial] Physiological Research. 2007;56(supplement 2):S1–S6. PubMed
Karppanen H, Lahovaara S, Männistö P, Vapaatalo H. Plasma renin activity and in vitro synthesis of aldosterone by the adrenal glands of rats with spontaneous, renal, or pinealectomy induced hypertension. Acta Physiologica Scandinavica. 1975;94(2):184–188. PubMed
Milosievic V, Trifunovic S, Sekulic M, et al. Chronic exposure to constant light affects morphology and secretion of adrenal zona fascikulata cells in female rats. General Physiology and Biophysics. 2005;24(3):299–309. PubMed
Li H, Kang Y, Yu L, Xu H, Zhao H. Melatonin reduces blood pressure in rats with stress-induced hypertension viaGABAA receptors. Clinical and Experimental Pharmacology and Physiology. 2009;36(4):436–440. PubMed
Reiter RJ, Tan DX, Manchester LC, Pilar Terron M, Flores LJ, Koppisepi S. Medical implications of melatonin: receptor-mediated and receptor-independent actions. Advances in Medical Sciences. 2007;52:11–28. PubMed
Koziróg M, Poliwczak AR, Duchnowicz P, Koter-Michalak M, Sikora J, Broncel M. Melatonin treatment improves blood pressure, lipid profile, and parameters of oxidative stress in patients with metabolic syndrome. Journal of Pineal Research. 2011;50(3):261–266. PubMed
Simko F, Simko J, Fabryova M. ACE-inhibition and angiotensin II receptor blockers in chronic heart failure: pathophysiological consideration of the unresolved battle. Cardiovascular Drugs and Therapy. 2003;17(3):287–290. PubMed
Lactacystin-induced kidney fibrosis: Protection by melatonin and captopril
The Impact of microRNAs in Renin-Angiotensin-System-Induced Cardiac Remodelling
Effect of Melatonin on the Renin-Angiotensin-Aldosterone System in l-NAME-Induced Hypertension
Lactacystin-Induced Model of Hypertension in Rats: Effects of Melatonin and Captopril