Yıl: 2020 Cilt: 58 Sayı: 1 Sayfa Aralığı: 1 - 8 Metin Dili: İngilizce DOI: 10.4274/haseki.galenos.2019.5525 İndeks Tarihi: 06-10-2020

Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats

Öz:
Aim: The imbalance between production of reactive oxygen species and antioxidant defense determines the degree of oxidative toxicity and severity of subsequent myocardial damage.We aimed to evaluate the anti-oxidative effects of neprilysin and angiotensin inhibition on cardiovascular target tissues in dexhamethasone-induced hypertensive rats.Methods: Thirty-six Wistar rats were divided into six groups. Three groups received 30 μg/kg/day dexamethasone for 14 days to induce arterial hypertension. Mean arterial blood pressures were verified by carotid artery cannulation. Ramipril (10 mg/kg), and sacubitril/valsartan (80 mg/kg) were administered for 18 days to the hypertensive and normotensive groups. Glutathione peroxidase, superoxide dismutase and malondialdehyde levels were evaluated in cardiovascular target tissues.Results: Serum and cardiac malondialdehyde levels were lower, while cardiac glutathione peroxidase and superoxide dismutase were higher in treatment groups than in control groups. Aortic malondialdehyde in sacubitril/valsartan group was lower; aortic and renal superoxide dismutase in sacubitril/valsartan and ramipril groups were significantly higher than in control group. Serum glutathione peroxidase was higher in hypertensive sacubitril/valsartan group than in hypertensive control group.Conclusion: We demonstrated that neprilysin and/or angiotensin inhibition had protective properties against oxidative stress exerted by dexhamethasone-induced hypertension in cardiovascular target organs, which may be mediated by reversal of natriuretic peptides degradation.
Anahtar Kelime:

Neprilisin ve Anjiyotensin Blokajı, Deksametazonla Indüklenen Hipertansif Ratların Kardiyovasküler Hedef Dokularındaki Oksidatif Stresi Hafifletmektedir

Öz:
Amaç: Reaktif oksijen türlerinin aşırı üretimi ile antioksidan savunma arasındaki dengesizlik, oksidatif toksisite derecesini ve sonraki dönemde miyokart hasarının ciddiyetini belirler. Biz bu çalışmada deksametazonun indüklediği hipertansif ratlarda, neprilisin ve anjiyotensin inhibisyonunun kardiyovasküler hedef dokulardaki anti-oksidatif etkilerini değerlendirmeyi amaçladık. Yöntemler: Otuz altı Wistar rat altı gruba ayrıldı. Arteriyel hipertansiyonu indüklemek için üç gruba 14 gün boyunca 30 μg/kg/gün deksametazon uygulandı. Ortalama arter kan basıncı, karotis arter kanülasyonu ile ölçüldü. Hipertansif ve normotansif gruplara ramipril (10 mg/kg) ve sakubitril/valsartan (80 mg/kg) 18 gün boyunca uygulandı. Kardiyovasküler hedef dokularda glutatyon peroksidaz, süperoksit dismutaz ve malondialdehit düzeyleri değerlendirildi. Bulgular: Tedavi gruplarında kontrol grubuna göre serum ve kardiyak malondialdehit düzeyleri düşükken, kardiyak glutatyon peroksidaz ve süperoksit dismutaz düzeyleri daha yüksek bulundu. Sacubitril/valsartan grubunda aortic malondialdehit düzeyi düşük; sacubitril/valsartan ve ramipril gruplarında aortik ve renal süperoksit dismutaz kontrol grubundan anlamlı olarak yüksek saptandı. Serum glutatyon peroksidaz düzeyi, hipertansif sakubitril/valsartan grubunda hipertansif kontrol grubuna göre daha yüksek bulundu. Sonuç: Neprilisin ve/veya anjiyotensin inhibisyonunun, kardiyovasküler hedef organlarda deksametazonla indüklenen hipertansiyondan kaynaklanan oksidatif strese karşı koruyucu özelliklere sahip olduğunu gösterdik. Bu etkinin, natriüretik peptitlerin degradasyonunun tersine çevrilmesiyle ilişkili olabileceğini düşünmekteyiz.
Anahtar Kelime:

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  • Sousa-Uva M, Neumann FJ, Ahlsson A, et al; ESC Scientific Document Group. 2018 ESC/EACTS Guidelines on myocardial revascularization. Eur J Cardiothorac Surg 2019;55:4-90.
  • Turan T, Menteşe Ü, Ağaç MT, et al. The relation between intensity and complexity of coronary artery lesion and oxidative stress in patients with acute coronary syndrome. Anatol J Cardiol 2015;15:795-800.
  • Menteşe U, Turan I, Usta S, et al. Systemic oxidant/antioxidant balance in human abdominal aortic aneurysm. Perfusion 2016;31:288-94.
  • Dugas TR. Unraveling mechanisms of toxicant-induced oxidative stress in cardiovascular disease. Curr Opin Toxicol 2018;7:1-8.
  • Hubers SA, Brown NJ. Combined Angiotensin Receptor Antagonism and Neprilysin Inhibition. Circulation 2016;133:1115-24.
  • Volpe M. Natriuretic peptides and cardio-renal disease. Int J Cardiol 2014;176:630-9.
  • Solomon SD, Zile M, Pieske B, et al. The angiotensin receptor neprilysin inhibitor LCZ696 in heart failure with preserved ejection fraction: a phase 2 double-blind randomised controlled trial. Lancet 2012;380:1387-95.
  • Ruilope LM, Dukat A, Böhm M, Lacourcière Y, Gong J, Lefkowitz MP. Blood-pressure reduction with LCZ696, a novel dual-acting inhibitor of the angiotensin II receptor and neprilysin: a randomised, double-blind, placebo-controlled, active comparator study. Lancet 2010;375:1255-66.
  • Manni ME, Rigacci S, Borchi E, et al. Monoamine Oxidase Is Overactivated in Left and Right Ventricles from Ischemic Hearts: An Intriguing Therapeutic Target. Oxid Med Cell Longev 2016;2016:4375418.
  • Shiomi T, Tsutsui H, Matsusaka H, et al. Overexpression of glutathione peroxidase prevents left ventricular remodeling and failure after myocardial infarction in mice. Circulation 2004;109:544-9.
  • Kinugawa S, Tsutsui H, Hayashidani S, et al. Treatment with dimethylthiourea prevents left ventricular remodeling and failure after experimental myocardial infarction in mice: role of oxidative stress. Circ Res 2000;87:392-8.
  • Toussaint O, Houbion A, Remacle J. Relationship between the critical level of oxidative stresses and the glutathione peroxidase activity. Toxicology 1993;81:89-101.
  • Dubey H, Singh A, Patole AM, Tenpe CR. Antihypertensive effect of allicin in dexamethasone-induced hypertensive rats. Integr Med Res 2017;6:60-5.
  • Aykan DA, Koca TT, Yaman S, Eser N. Angiotensin converting enzyme and neprilysin inhibition alter pain response in dexhamethasone-induced hypertensive rats. Pharmacol Rep 2019;71:306-10.
  • d’Emmanuele di Villa Bianca R, Mitidieri E, Donnarumma E, et al. Hydrogen sulfide is involved in dexamethasone-induced hypertension in rat. Nitric Oxide 2015;46:80-6.
  • Peng X, Su H, Liang D, et al. Ramipril and resveratrol co-treatment attenuates RhoA/ROCK pathway-regulated early-stage diabetic nephropathy-associated glomerulosclerosis in streptozotocin-induced diabetic rats. Environ Toxicol 2019;34:861-8.
  • Bilanda DC, Dimo T, Dzeufiet Djomeni PD, et al. Antihypertensive and antioxidant effects of Allanblackiafloribunda Oliv. (Clusiaceae) aqueous extract in alcohol- and sucrose-induced hypertensive rats. J Ethnopharmacol 2010;128:634-40.
  • Buege JA, Aust SD. Microsomal lipid peroxidation. Methods Enzymol 1978;52:302.
  • Beyer WF Jr, Fridovich I. Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Anal Biochem 1987;161:559-66.
  • Beutler E, Beutler B, Matsumoto J. Glutathione peroxidase activity of inorganic selenium and seleno-DL-cysteine. Experientia 1975;31:769-70.
  • McMurray JJ, Packer M, Desai AS, et al; PARADIGM-HF Investigators and Committees. Angiotensin-neprilysin inhibition versus enalapril in heart failure. New Engl J Med 2014;371:993-1004.
  • Maric C, Zheng W, Walther T. Interactions between angiotensin ll and atrial natriuretic peptide in renomedullary interstitial cells: the role of neutral endopeptidase. Nephron Physiol 2006;103:149-56.
  • Solomon SD, Zile M, Pieske B, et al; Prospective comparison of ARNI with ARB on Management Of heart failUre with preserved ejectioN fracTion (PARAMOUNT) Investigators. The angiotensin receptor neprilysin inhibitor LCZ696 in heart failure with preserved ejection fraction: a phase 2 double blind randomised controlled trial. Lancet. 2012;380:1387-95.
  • Taniyama Y, Griendling KK. Reactive oxygen species in the vasculature: molecular and cellular mechanisms. Hypertension 2003;42:1075-81.
  • Mueller CF, Laude K, McNally JS, Harrison DG. ATVB in focus: redox mechanisms in blood vessels. Arterioscler Thromb Vasc Biol 2005;25:274-8.
  • Mehta PK, Griendling KK. Angiotensin II cell signaling: physiological and pathological effects in the cardiovascular system. Am J Physiol Cell Physiol 2007;292:C82-97.
  • do Vale GT, Leoni D, Sousa AH, et al. Acute restraint stress increases blood pressure and oxidative stress in the cardiorenal system of rats: a role for AT(1) receptors. Stress 2019:1-10.
  • Chabrashvili T, Tojo A, Onozato ML, et al. Expression and cellular localization of classic NADPH oxidase subunits in the spontaneously hypertensive rat kidney. Hypertension 2002;39:269-74.
  • Wang D, Chen Y, Chabrashvili T, et al. Role of oxidative stress in endothelial dysfunction and enhanced responses to angiotensin II of afferent arterioles from rabbits infused with angiotensin II. J Am Soc Nephrol 2003;14:2783-9.
  • Fellner SK, Arendshorst WJ. Angiotensin II, reactive oxygen species, and Ca21signaling in afferent arterioles. Am J Physiol Renal Physiol 2005;289:F1012-9.
  • Kopkan L, Castillo A, Navar LG, Majid DS. Enhanced superoxide generation modulates renal function in ANG II-induced hypertensive rats. Am J Physiol Renal Physiol 2006;290:F80-6.
  • Pagano PJ, Ito Y, Tornheim K, Gallop PM, Tauber AI, Cohen RA. An NADPH oxidase superoxide-generating system in the rabbit aorta. Am J Physiol 1995;268:H2274-80.
  • Rajagopalan S, Kurz S, Münzel T, et al. Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NADH/NADPH oxidase activation. Contribution to alterations of vasomotor tone. J Clin Invest 1996;97:1916-23.
  • Landmesser U, Dikalov S, Price SR, et al. Oxidation of tetrahydrobiopterin leads to uncoupling of endothelial cell nitric oxide synthase in hypertension. J Clin Invest 2003;111:1201-9.
  • Schnackenberg CG, Wilcox CS. The SOD mimetic tempol restores vasodilation in afferent arterioles of experimental diabetes. Kidney Int 2001;59:1859-64.
  • Gongora MC, Qin Z, Laude K, et al. Role of extracellular superoxide dismutase in hypertension. Hypertension 2006;48:473-81.
  • Zafari AM, Ushio-Fukai M, Akers M, et al. Role of NADH/NADPH oxidase-derived H2O2 in angiotensin II-induced vascular hypertrophy. Hypertension 1998;32:488-95.
  • Weber DS, Rocic P, Mellis AM, et al. Angiotensin II-induced hypertrophy is potentiated in mice overexpressing p22phox in vascular smooth muscle. Am J Physiol Heart Circ Physiol 2005;288:H37-42.
  • Patel R, Cardneau JD, Colles SM, Graham LM. Synthetic smooth muscle cell phenotype is associated with increased nicotinamide adenine dinucleotide phosphate oxidase activity: effect on collagen secretion. J Vasc Surg 2006;43:364-71.
APA Altıntaş Aykan D, seyithanoğlu m, ESER N, TANRIVERDİ B, YAMAN S (2020). Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. , 1 - 8. 10.4274/haseki.galenos.2019.5525
Chicago Altıntaş Aykan Duygun,seyithanoğlu muhammed,ESER Nadire,TANRIVERDİ BURAK,YAMAN Selma Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. (2020): 1 - 8. 10.4274/haseki.galenos.2019.5525
MLA Altıntaş Aykan Duygun,seyithanoğlu muhammed,ESER Nadire,TANRIVERDİ BURAK,YAMAN Selma Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. , 2020, ss.1 - 8. 10.4274/haseki.galenos.2019.5525
AMA Altıntaş Aykan D,seyithanoğlu m,ESER N,TANRIVERDİ B,YAMAN S Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. . 2020; 1 - 8. 10.4274/haseki.galenos.2019.5525
Vancouver Altıntaş Aykan D,seyithanoğlu m,ESER N,TANRIVERDİ B,YAMAN S Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. . 2020; 1 - 8. 10.4274/haseki.galenos.2019.5525
IEEE Altıntaş Aykan D,seyithanoğlu m,ESER N,TANRIVERDİ B,YAMAN S "Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats." , ss.1 - 8, 2020. 10.4274/haseki.galenos.2019.5525
ISNAD Altıntaş Aykan, Duygun vd. "Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats". (2020), 1-8. https://doi.org/10.4274/haseki.galenos.2019.5525
APA Altıntaş Aykan D, seyithanoğlu m, ESER N, TANRIVERDİ B, YAMAN S (2020). Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. Haseki Tıp Bülteni, 58(1), 1 - 8. 10.4274/haseki.galenos.2019.5525
Chicago Altıntaş Aykan Duygun,seyithanoğlu muhammed,ESER Nadire,TANRIVERDİ BURAK,YAMAN Selma Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. Haseki Tıp Bülteni 58, no.1 (2020): 1 - 8. 10.4274/haseki.galenos.2019.5525
MLA Altıntaş Aykan Duygun,seyithanoğlu muhammed,ESER Nadire,TANRIVERDİ BURAK,YAMAN Selma Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. Haseki Tıp Bülteni, vol.58, no.1, 2020, ss.1 - 8. 10.4274/haseki.galenos.2019.5525
AMA Altıntaş Aykan D,seyithanoğlu m,ESER N,TANRIVERDİ B,YAMAN S Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. Haseki Tıp Bülteni. 2020; 58(1): 1 - 8. 10.4274/haseki.galenos.2019.5525
Vancouver Altıntaş Aykan D,seyithanoğlu m,ESER N,TANRIVERDİ B,YAMAN S Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats. Haseki Tıp Bülteni. 2020; 58(1): 1 - 8. 10.4274/haseki.galenos.2019.5525
IEEE Altıntaş Aykan D,seyithanoğlu m,ESER N,TANRIVERDİ B,YAMAN S "Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats." Haseki Tıp Bülteni, 58, ss.1 - 8, 2020. 10.4274/haseki.galenos.2019.5525
ISNAD Altıntaş Aykan, Duygun vd. "Blockade of the Neprilysin and Angiotensin Ameliorates Oxidative Stress in the Cardiovascular Target Tissues of Dexamethasone-induced Hypertensive Rats". Haseki Tıp Bülteni 58/1 (2020), 1-8. https://doi.org/10.4274/haseki.galenos.2019.5525