Research Article
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Relaxant Effect of Rosuvastatin in Isolated Rat Aorta with Perivascular Adipose Tissue

Year 2024, Volume: 14 Issue: 4, 1127 - 1132, 29.12.2024
https://doi.org/10.33808/clinexphealthsci.1561664

Abstract

Objective: Rosuvastatin displays favorable pleiotropic effects on vascular system to reduce the risk of cardiovascular events besides providing an intensive reduction in LDL-C levels. The role of perivascular adipose tissue (PVAT) in modulating the vasorelaxant effect of rosuvastatin is not evaluated so far. The present study aimed to investigate the vascular relaxant effect of rosuvastatin in rat aortic rings with intact PVAT, as well as to evaluate the possible mechanisms underlying this effect in relation to nitric oxide (NO) and prostaglandin pathways.
Methods: Thoracic aorta rings with intact PVAT, isolated from male Wistar rats (n=5), were mounted on an isolated organ bath system. Endothelium-dependent responses to acetylcholine (Ach,10-6-10-4M) were obtained in aortic rings precontracted submaximally with phenylephrine (Phe,10-6-3x105M). The concentration-dependent relaxant effect of rosuvastatin (10-7-10-4M) was examined in the absence
and presence of NO inhibitor, L-NOARG (10-4M, 30min.) and cyclooxygenase inhibitor, indomethacin (10-5M, 30min.). Vascular relaxation capacity of aortic rings was checked by the nitrovasodilator, sodium nitroprusside (SNP,10-6 M) at the end of the experiments.
Results: Rosuvastatin (10-7-10-4M) produced concentration-dependent relaxations in Phe-precontracted rat aortic rings with intact PVAT. Pretreatment with L-NOARG significantly attenuated the relaxant responses to rosuvastatin in isolated rat aortic rings with intact PVAT. However, pretreatment with indomethacin did not modify the relaxations to rosuvastatin. In the aortic rings, maximal relaxation responses to Ach and SNP were determined to be 75.87±2.68% and 102.54±2.92%, respectively.
Conclusions: This study will provide a basis for investigating the interaction between PVAT and statins in vascular homeostasis.

Ethical Statement

This study was approved by Ethics Committee of Istanbul University, Local Ethics Committee of Animal Experiments (Approval date:22/11/2023; Number: 226767806 )

References

  • Lefer AM, Scalia R, Lefer DJ. Vascular effects of HMG CoAreductase inhibitors (statins) unrelated to cholesterol lowering: New concepts for cardiovascular disease. Cardiovasc Res. 2001;49(2):281-287. DOI:10.1016/s0008-6363(00)00247-9
  • Liao JK, Laufs U. Pleiotropic effects of statins. The Annual Review of Pharmacology and Toxicology 2004;45(1):89-118. DOI:10.1146/annurev.pharmtox.45.120.403.095748
  • Zhou Q, Liao JK. Pleiotropic effects of statins – Basic research and clinical perspectives. Circulation Journal 2010;74(5):818-826. DOI:10.1253/circj.cj-10-0110
  • Oesterle A, Laufs U, Liao JK. Pleiotropic effects of statins on the cardiovascular system. Circulation Research 2017;120(1):229-243. DOI:10.1161/circresaha.116.308537
  • German CA, Liao JK. Understanding the molecular mechanisms of statin pleiotropic effects. Archives of Toxicology 2023;97(6):1529-1545. DOI:10.1007/s00204.023.03492-6
  • Alvarez De Sotomayor M, Herrera MD, Marhuenda E, Andriantsitohaina R. Characterization of endothelial factors involved in the vasodilatory effect of simvastatin in aorta and small mesenteric artery of the rat. British Journal of Pharmacology 2000;131(6):1179-1187. DOI:10.1038/sj.bjp.0703668
  • Bergdahl A, Persson E, Hellstrand P, Swärd K. Lovastatin induces relaxation and inhibits L‐Type Ca2+ current in the ratbasilar artery. Pharmacology & Toxicology 2003;93(3):128-134. DOI:10.1034/j.1600-0773.2003.930304.x
  • Uydeş-Doğan BS, Topal G, Takır, S, İlkay F, Kaleli D, Özdemir O. Relaxant effects of pravastatin, atorvastatin and cerivastatin on isolated rat aortic rings. Life Sciences 2005;76(15):1771–1786. DOI:10.1016/j.lfs. 2004.11.002
  • López J, Mendoza R, Cleva Villanueva G, Martínez G, Castillo EF, Castillo C. Participation of K+ channels in the endotheliumdependent and endothelium-independent components of the relaxant effect of rosuvastatin in rat aortic rings. Journal of Cardiovascular Pharmacology and Therapeutics 2008;13(3),207–213. DOI:10.1177/107.424.8408321716.
  • López‐Canales JS, Lozano‐Cuenca J, López‐Canales OA, Aguilar‐Carrasco JC, Aranda‐Zepeda L, López‐Sánchez P, Castillo‐Henkel EF, López‐Mayorga RM, Valencia‐Hernández I. Pharmacological characterization of mechanisms involved in the vasorelaxation produced by rosuvastatin in aortic rings from rats with a cafeteria‐style diet. Clinical and Experimental Pharmacology and Physiology 2015;42(6):653-661. DOI:10.1111/1440-1681.12406
  • Yildirim FIA, Kaleli Durman D, Aypar E, Ark M, Özdemir O, Doğan BSU. Atorvastatin acutely reduces the reactivity to spasmogens in rat aorta: implication of the inhibition of geranylgeranylation and MYPT‐1 phosphorylation. Fundamental and Clinical Pharmacology 2015;30(2):96-106. DOI:10.1111/fcp.12173
  • Ali N, Begum R, Faisal MS, Khan A, Nabi M, Shehzadi G, Ullah S, Ali W. Current statins show calcium channel blocking activity through voltage gated channels. BMC Pharmacology and Toxicology 2016;17(1). DOI:10.1186/s40360.016.0086-5
  • Ali N, Ali W, Ullah A, Ahmad S, Hussain H, Ali W. Rosuvastatin and Simvastatin potentiate antihypertensive effect of amlodipine through vasorelaxation phenomenon. Pak J Pharm Sci. 2023;36(3):953-961.
  • Kaleli-Durman D, Alp-Yıldırım Fİ, Özdemir O, Uydeş-Doğan BS. Relaxant effect of atorvastatin on isolated rat gastric fundus strips: implications for Ca2+-signalling mechanisms. Canadian Journal of Physiology and Pharmacology 2019;97(5):413-421. DOI:1139/cjpp-2018-0723
  • Nurullahoglu-Atalik K, Oz M, Shafiyi A. Rosuvastatin-induced responses in calf cardiac vein. Bratislavske Lekarske Listy 2015;116(8):494–498. DOI:10.4149/BLL_2015_095
  • Nurullahoglu-Atalik KE, Yerlikaya H, Oz M, Esen H. Determining the Response to Statins in Rat Aorta Using High Fat Diet. Jordan Journal of Biological Sciences 2020;13(1):1-6.
  • Şahintürk S. Rosuvastatin relaxes rat thoracic aorta, pulmonary artery, and trachea via nitric oxide, prostanoids, and potassium channels. Çukurova Medical Journal 2023;48(2):419-431. DOI:10.17826/cumj.1279122
  • McTaggart F, Buckett L, Davidson R, Holdgate G, McCormick A, Schneck D, Smith G, Warwick M. Preclinical and clinical pharmacology of rosuvastatin, a new 3-hydroxy –3-methylglutaryl coenzyme A reductase inhibitor. The American Journal of Cardiology 2001;87(5):28-32. DOI:10.1016/s0002-9149(01)01454-0
  • Cortese F, Gesualdo M, Cortese A, Carbonara, S, Devito F, Zito A, Ricci G, Scicchitano P Ciccone M. Rosuvastatin: Beyond the cholesterol-lowering effect. Pharmacol Res. 2016;107:1-18.DOI:10.1016/j.phrs.2016.02.012
  • Mostaza JM, Escobar C. Rosuvastatin-Based Lipid-Lowering therapy for the control of LDL cholesterol in patients at highvascular risk. Journal of Clinical Medicine 2024;13(7):1894. DOI:10.3390/jcm13071894
  • Nangle MR, Cotter MA, Cameron NE. Effects of rosuvastatin on nitric oxide–dependent function in aorta and corpus cavernosum of diabetic mice. Diabetes 2003;52(9):2396-2402. DOI:10.2337/diabetes.52.9.2396
  • Sanna F, Margaritis M, Antoniades C. Perivascular adipose tissue as an endocrine organ: The role of statins. Current Pharmaceutical Design 2017;23(46):7055-7060. DOI:10.2174/138.161.2823666.170.926133843
  • Zaborska KE, Wareing M, Austin C. Comparisons between perivascular adipose tissue and the endothelium in their modulation of vascular tone. British Journal of Pharmacology 2016;174(20):3388-3397. DOI:10.1111/bph.13648
  • Balakumar P, Alqahtani A, Khan NA, Alqahtani T, Jagadeesh G. The physiologic and physiopathologic roles of perivascular adipose tissue and its interactions with blood vessels and the renin-angiotensin system. Pharmacological Research 2021;173:105890. DOI:10.1016/j.phrs.2021.105890
  • Ahmed A, Bibi A, Valoti M, Fusi F. Perivascular adipose tissue and vascular smooth muscle tone: friends or foes? Cells 2023;12(8):1196. DOI:10.3390/cells12081196
  • Wójcicka G, Jamroz-Wiśniewska A, Atanasova P, Chaldakov GN, Chylińska-Kula B, Bełtowski J. Differential effects of statins on endogenous H2S formation in perivascular adipose tissue. Pharmacological Research 2010;63(1):68-76. DOI:10.1016/j.phrs.2010.10.011
  • Percie Du Sert N, Hurst V, Ahluwalia A, Alam S, Avey MT, Baker M, Browne WJ, Clark A, Cuthill IC, Dirnagl U, Emerson M, Garner P, Holgate ST, Howells DW, Karp NA, Lazic SE, Lidster K, MacCallum CJ, Macleod M, Pearl EJ, Petersen O, Rawle F, Peynolds P, Rooney K, Sena ES, Silberberg SD, Steckler T, Wurbel H. The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research. PLoS Biology 2020;18(7):e3000410.DOI:10.1371/journal.pbio.3000410
  • Blanco‐Rivero J, De Las Heras N, Martín‐Fernández B, Cachofeiro V, Lahera V, Balfagón G. Rosuvastatin restored adrenergic and nitrergic function in mesenteric arteries from obese rats. British Journal of Pharmacology 2010;162(1):271-285. DOI:10.1111/j.1476-5381.2010.01030.x
  • Zhao Y, Vanhoutte PM, Leung SWS. Vascular nitric oxide: Beyond eNOS. Journal of Pharmacological Sciences 2015;129(2):83-94. DOI:10.1016/j.jphs.2015.09.002
  • Barp CG, Bonaventura D, Assreuy J. NO, ROS, RAS, and PVAT: More Than a Soup of Letters. Frontiers in Physiology 2021;12,640021. DOI:10.3389/fphys.2021.64002
Year 2024, Volume: 14 Issue: 4, 1127 - 1132, 29.12.2024
https://doi.org/10.33808/clinexphealthsci.1561664

Abstract

References

  • Lefer AM, Scalia R, Lefer DJ. Vascular effects of HMG CoAreductase inhibitors (statins) unrelated to cholesterol lowering: New concepts for cardiovascular disease. Cardiovasc Res. 2001;49(2):281-287. DOI:10.1016/s0008-6363(00)00247-9
  • Liao JK, Laufs U. Pleiotropic effects of statins. The Annual Review of Pharmacology and Toxicology 2004;45(1):89-118. DOI:10.1146/annurev.pharmtox.45.120.403.095748
  • Zhou Q, Liao JK. Pleiotropic effects of statins – Basic research and clinical perspectives. Circulation Journal 2010;74(5):818-826. DOI:10.1253/circj.cj-10-0110
  • Oesterle A, Laufs U, Liao JK. Pleiotropic effects of statins on the cardiovascular system. Circulation Research 2017;120(1):229-243. DOI:10.1161/circresaha.116.308537
  • German CA, Liao JK. Understanding the molecular mechanisms of statin pleiotropic effects. Archives of Toxicology 2023;97(6):1529-1545. DOI:10.1007/s00204.023.03492-6
  • Alvarez De Sotomayor M, Herrera MD, Marhuenda E, Andriantsitohaina R. Characterization of endothelial factors involved in the vasodilatory effect of simvastatin in aorta and small mesenteric artery of the rat. British Journal of Pharmacology 2000;131(6):1179-1187. DOI:10.1038/sj.bjp.0703668
  • Bergdahl A, Persson E, Hellstrand P, Swärd K. Lovastatin induces relaxation and inhibits L‐Type Ca2+ current in the ratbasilar artery. Pharmacology & Toxicology 2003;93(3):128-134. DOI:10.1034/j.1600-0773.2003.930304.x
  • Uydeş-Doğan BS, Topal G, Takır, S, İlkay F, Kaleli D, Özdemir O. Relaxant effects of pravastatin, atorvastatin and cerivastatin on isolated rat aortic rings. Life Sciences 2005;76(15):1771–1786. DOI:10.1016/j.lfs. 2004.11.002
  • López J, Mendoza R, Cleva Villanueva G, Martínez G, Castillo EF, Castillo C. Participation of K+ channels in the endotheliumdependent and endothelium-independent components of the relaxant effect of rosuvastatin in rat aortic rings. Journal of Cardiovascular Pharmacology and Therapeutics 2008;13(3),207–213. DOI:10.1177/107.424.8408321716.
  • López‐Canales JS, Lozano‐Cuenca J, López‐Canales OA, Aguilar‐Carrasco JC, Aranda‐Zepeda L, López‐Sánchez P, Castillo‐Henkel EF, López‐Mayorga RM, Valencia‐Hernández I. Pharmacological characterization of mechanisms involved in the vasorelaxation produced by rosuvastatin in aortic rings from rats with a cafeteria‐style diet. Clinical and Experimental Pharmacology and Physiology 2015;42(6):653-661. DOI:10.1111/1440-1681.12406
  • Yildirim FIA, Kaleli Durman D, Aypar E, Ark M, Özdemir O, Doğan BSU. Atorvastatin acutely reduces the reactivity to spasmogens in rat aorta: implication of the inhibition of geranylgeranylation and MYPT‐1 phosphorylation. Fundamental and Clinical Pharmacology 2015;30(2):96-106. DOI:10.1111/fcp.12173
  • Ali N, Begum R, Faisal MS, Khan A, Nabi M, Shehzadi G, Ullah S, Ali W. Current statins show calcium channel blocking activity through voltage gated channels. BMC Pharmacology and Toxicology 2016;17(1). DOI:10.1186/s40360.016.0086-5
  • Ali N, Ali W, Ullah A, Ahmad S, Hussain H, Ali W. Rosuvastatin and Simvastatin potentiate antihypertensive effect of amlodipine through vasorelaxation phenomenon. Pak J Pharm Sci. 2023;36(3):953-961.
  • Kaleli-Durman D, Alp-Yıldırım Fİ, Özdemir O, Uydeş-Doğan BS. Relaxant effect of atorvastatin on isolated rat gastric fundus strips: implications for Ca2+-signalling mechanisms. Canadian Journal of Physiology and Pharmacology 2019;97(5):413-421. DOI:1139/cjpp-2018-0723
  • Nurullahoglu-Atalik K, Oz M, Shafiyi A. Rosuvastatin-induced responses in calf cardiac vein. Bratislavske Lekarske Listy 2015;116(8):494–498. DOI:10.4149/BLL_2015_095
  • Nurullahoglu-Atalik KE, Yerlikaya H, Oz M, Esen H. Determining the Response to Statins in Rat Aorta Using High Fat Diet. Jordan Journal of Biological Sciences 2020;13(1):1-6.
  • Şahintürk S. Rosuvastatin relaxes rat thoracic aorta, pulmonary artery, and trachea via nitric oxide, prostanoids, and potassium channels. Çukurova Medical Journal 2023;48(2):419-431. DOI:10.17826/cumj.1279122
  • McTaggart F, Buckett L, Davidson R, Holdgate G, McCormick A, Schneck D, Smith G, Warwick M. Preclinical and clinical pharmacology of rosuvastatin, a new 3-hydroxy –3-methylglutaryl coenzyme A reductase inhibitor. The American Journal of Cardiology 2001;87(5):28-32. DOI:10.1016/s0002-9149(01)01454-0
  • Cortese F, Gesualdo M, Cortese A, Carbonara, S, Devito F, Zito A, Ricci G, Scicchitano P Ciccone M. Rosuvastatin: Beyond the cholesterol-lowering effect. Pharmacol Res. 2016;107:1-18.DOI:10.1016/j.phrs.2016.02.012
  • Mostaza JM, Escobar C. Rosuvastatin-Based Lipid-Lowering therapy for the control of LDL cholesterol in patients at highvascular risk. Journal of Clinical Medicine 2024;13(7):1894. DOI:10.3390/jcm13071894
  • Nangle MR, Cotter MA, Cameron NE. Effects of rosuvastatin on nitric oxide–dependent function in aorta and corpus cavernosum of diabetic mice. Diabetes 2003;52(9):2396-2402. DOI:10.2337/diabetes.52.9.2396
  • Sanna F, Margaritis M, Antoniades C. Perivascular adipose tissue as an endocrine organ: The role of statins. Current Pharmaceutical Design 2017;23(46):7055-7060. DOI:10.2174/138.161.2823666.170.926133843
  • Zaborska KE, Wareing M, Austin C. Comparisons between perivascular adipose tissue and the endothelium in their modulation of vascular tone. British Journal of Pharmacology 2016;174(20):3388-3397. DOI:10.1111/bph.13648
  • Balakumar P, Alqahtani A, Khan NA, Alqahtani T, Jagadeesh G. The physiologic and physiopathologic roles of perivascular adipose tissue and its interactions with blood vessels and the renin-angiotensin system. Pharmacological Research 2021;173:105890. DOI:10.1016/j.phrs.2021.105890
  • Ahmed A, Bibi A, Valoti M, Fusi F. Perivascular adipose tissue and vascular smooth muscle tone: friends or foes? Cells 2023;12(8):1196. DOI:10.3390/cells12081196
  • Wójcicka G, Jamroz-Wiśniewska A, Atanasova P, Chaldakov GN, Chylińska-Kula B, Bełtowski J. Differential effects of statins on endogenous H2S formation in perivascular adipose tissue. Pharmacological Research 2010;63(1):68-76. DOI:10.1016/j.phrs.2010.10.011
  • Percie Du Sert N, Hurst V, Ahluwalia A, Alam S, Avey MT, Baker M, Browne WJ, Clark A, Cuthill IC, Dirnagl U, Emerson M, Garner P, Holgate ST, Howells DW, Karp NA, Lazic SE, Lidster K, MacCallum CJ, Macleod M, Pearl EJ, Petersen O, Rawle F, Peynolds P, Rooney K, Sena ES, Silberberg SD, Steckler T, Wurbel H. The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research. PLoS Biology 2020;18(7):e3000410.DOI:10.1371/journal.pbio.3000410
  • Blanco‐Rivero J, De Las Heras N, Martín‐Fernández B, Cachofeiro V, Lahera V, Balfagón G. Rosuvastatin restored adrenergic and nitrergic function in mesenteric arteries from obese rats. British Journal of Pharmacology 2010;162(1):271-285. DOI:10.1111/j.1476-5381.2010.01030.x
  • Zhao Y, Vanhoutte PM, Leung SWS. Vascular nitric oxide: Beyond eNOS. Journal of Pharmacological Sciences 2015;129(2):83-94. DOI:10.1016/j.jphs.2015.09.002
  • Barp CG, Bonaventura D, Assreuy J. NO, ROS, RAS, and PVAT: More Than a Soup of Letters. Frontiers in Physiology 2021;12,640021. DOI:10.3389/fphys.2021.64002
There are 30 citations in total.

Details

Primary Language English
Subjects Basic Pharmacology
Journal Section Articles
Authors

Deniz Kaleli Durman 0000-0002-8669-7480

Ruveyda Aktaş 0000-0002-6671-4239

Meryem Aras 0000-0002-5926-0953

B. Sönmez Dogan 0000-0002-6729-8150

Publication Date December 29, 2024
Submission Date October 5, 2024
Acceptance Date December 14, 2024
Published in Issue Year 2024 Volume: 14 Issue: 4

Cite

APA Kaleli Durman, D., Aktaş, R., Aras, M., Dogan, B. S. (2024). Relaxant Effect of Rosuvastatin in Isolated Rat Aorta with Perivascular Adipose Tissue. Clinical and Experimental Health Sciences, 14(4), 1127-1132. https://doi.org/10.33808/clinexphealthsci.1561664
AMA Kaleli Durman D, Aktaş R, Aras M, Dogan BS. Relaxant Effect of Rosuvastatin in Isolated Rat Aorta with Perivascular Adipose Tissue. Clinical and Experimental Health Sciences. December 2024;14(4):1127-1132. doi:10.33808/clinexphealthsci.1561664
Chicago Kaleli Durman, Deniz, Ruveyda Aktaş, Meryem Aras, and B. Sönmez Dogan. “Relaxant Effect of Rosuvastatin in Isolated Rat Aorta With Perivascular Adipose Tissue”. Clinical and Experimental Health Sciences 14, no. 4 (December 2024): 1127-32. https://doi.org/10.33808/clinexphealthsci.1561664.
EndNote Kaleli Durman D, Aktaş R, Aras M, Dogan BS (December 1, 2024) Relaxant Effect of Rosuvastatin in Isolated Rat Aorta with Perivascular Adipose Tissue. Clinical and Experimental Health Sciences 14 4 1127–1132.
IEEE D. Kaleli Durman, R. Aktaş, M. Aras, and B. S. Dogan, “Relaxant Effect of Rosuvastatin in Isolated Rat Aorta with Perivascular Adipose Tissue”, Clinical and Experimental Health Sciences, vol. 14, no. 4, pp. 1127–1132, 2024, doi: 10.33808/clinexphealthsci.1561664.
ISNAD Kaleli Durman, Deniz et al. “Relaxant Effect of Rosuvastatin in Isolated Rat Aorta With Perivascular Adipose Tissue”. Clinical and Experimental Health Sciences 14/4 (December 2024), 1127-1132. https://doi.org/10.33808/clinexphealthsci.1561664.
JAMA Kaleli Durman D, Aktaş R, Aras M, Dogan BS. Relaxant Effect of Rosuvastatin in Isolated Rat Aorta with Perivascular Adipose Tissue. Clinical and Experimental Health Sciences. 2024;14:1127–1132.
MLA Kaleli Durman, Deniz et al. “Relaxant Effect of Rosuvastatin in Isolated Rat Aorta With Perivascular Adipose Tissue”. Clinical and Experimental Health Sciences, vol. 14, no. 4, 2024, pp. 1127-32, doi:10.33808/clinexphealthsci.1561664.
Vancouver Kaleli Durman D, Aktaş R, Aras M, Dogan BS. Relaxant Effect of Rosuvastatin in Isolated Rat Aorta with Perivascular Adipose Tissue. Clinical and Experimental Health Sciences. 2024;14(4):1127-32.

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