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Licensed Unlicensed Requires Authentication Published by De Gruyter October 1, 2020

Caffeic and chlorogenic acids modulate altered activity of key enzymes linked to hypertension in cyclosporine-induced hypertensive rats

  • Odunayo M. Agunloye EMAIL logo , Ganiyu Oboh , Gbemisola T. Bello and Ademola A. Oyagbemi

Abstract

Objectives

This study aimed to explore the protective mechanism of caffeic acid (CAA) and chlorogenic acid (CHA) on cyclosporine (CSA) induced hypertensive rats.

Methods

Effect of CAA and CHA on diastolic blood pressure (DBP), mean arterial pressure (MAP), angiotensin-converting enzyme (ACE), e-nucleotide triphosphate dephosphorylase (e-NTPDase), 5′ nucleotidase and adenosine deaminase (ADA) activity in CSA-induced hypertensive rats were determined.

Results

CAA and CHA administration stabilized hypertensive effect caused by CSA administration. Also, altered activity of ACE (lung), e-NTPDase, 5′ nucleotidase, ADA as well as elevated malondiadehyde (MDA) level was restored in all the treated hypertensive rats in comparison with the untreated hypertensive rats.

Conclusion

Hence, these observed results could underlie some of the mechanisms through which CAA and CHA could offer antihypertensive effect.


Corresponding author: Odunayo M. Agunloye PhD, Department of Biochemistry, Federal University of Technology, Akure, Nigeria, Phone: +2348067998394, E-mail:

  1. Research funding: None declared.

  2. Author contributions: Ganiyu Oboh designed the research work, proof read the manuscript and provided technical supports. Odunayo M Agunloye co-ordinated the laboratory works, performed some bioassays, wrote the manuscript and provides technical supports. Gbemisola T Bello carried out the set out experiments details and data analysis. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: Research involving animals complied with all relevant National regulations and Institutional policies (Federal University of Technology, Akure Research Policy) for the care and use of animals and guidelines for animal protection and welfare were followed strictly (NIH Publications No. 8023, revised 1978).

References

1. Lopez-Sendon, J, Swedberg, K, McMurray, J, Tamargo, J, Maggioni, AP, Dargie, H, et al. Expert consensus document on angiotensin converting enzyme inhibitors in cardiovascular disease: the task force on ACE-inhibitors of the European society of cardiology. Eur Heart J 2004;25:1454−70. https://doi.org/10.1016/j.ehj.2004.06.003.Search in Google Scholar

2. Tarasola, OS, Golubinskaya, VO, Kosiakov, AN, Borovik, AS, Timin, EN, Rodionov, IM. The role of purinergic and adrenergic transmitters of the sympathetic system in the control of arterial blood pressure variability. J Auton Nerv Syst 1998;70:66–70. https://doi.org/10.1016/s0165-1838(98)00031-9.Search in Google Scholar

3. Vaziri, ND, Ni, Z, Oveisi, F, Trnavsky-Hobbs, DL. Effect of antioxidant therapy on blood pressure and no synthase expression in hypertensive rats. Hypertension 2000;36:957–64. https://doi.org/10.1161/01.hyp.36.6.957.Search in Google Scholar

4. Rajagopalan, S, Kurz, S, Munzel, T, Tarpey, M, Freeman, BA, Griendling, KK, 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. https://doi.org/10.1172/jci118623.Search in Google Scholar

5. Jackson, EK. Adenosine: a physiological brake on renin release. Annu Rev Pharmacol 1991;31:1–35. https://doi.org/10.1146/annurev.pa.31.040191.000245.Search in Google Scholar

6. Chan, CM, Unwin, RJ, Bardini, M, Oglesby, IB, Ford, AP, Townsend-Nicholson, A, et al. Localization of P2X1 purinoceptors by autoradiography and immunohistochemistry in rat kidneys. Am J Physiol 1998;274:799–804. https://doi.org/10.1152/ajprenal.1998.274.4.f799.Search in Google Scholar

7. Inscho, EW, Cook, AK, Imig, JD, Vial, C, Evans, RJ. Renal autoregulation in P2X1 knockout mice. Acta Physiol Scand 2004;181:445–53. https://doi.org/10.1111/j.1365-201x.2004.01317.x.Search in Google Scholar

8. Agunloye, OM, Oboh, G. Caffeic acid and chlorogenic acid: evaluation of antioxidant effect and inhibition of key enzymes linked with hypertension. J Food Biochem 2018;42:e1254. https://doi.org/10.1111/jfbc.12541. [Accessed 2018].Search in Google Scholar

9. Duncker, DJ, Laxson, DD, Lindstrom, P, Bache, RJ. Endogenous adenosine and coronary vasoconstriction in hypoperfused myocardium during exercise. Cardiovasc Res 1993;27:1592–7. https://doi.org/10.1093/cvr/27.9.1592.Search in Google Scholar

10. Edlund, A, Sollevi, A. Theophylline increases coronary vascular tone in humans: evidence for a role of endogenous adenosine in flow regulation. Acta Physiol Scand 1995;155:303–11. https://doi.org/10.1111/j.1748-1716.1995.tb09978.x.Search in Google Scholar

11. Hein, TW, Kuo, L. cAMP-independent dilation of coronary arterioles to adenosine: role of nitric oxide, G proteins, and KATP channels. Circ Res 1999;85:634–42. https://doi.org/10.1161/01.res.85.7.634.Search in Google Scholar

12. Nasser, SA, Sabra, R, Elmallah, AI, Mohy El-Din, MM, Khedr, MM, et al. Facilitation by the renin-angiotensin system of cyclosporine-evoked hypertension in rats: role of arterial baro reflexes and vasoreactivity. Life Sci 2016;163:1–10. https://doi.org/10.1016/j.lfs.2016.08.024.Search in Google Scholar

13. Agunloye, OM, Oboh, G, Ademiluyi, AO, Ademosun, AO, Akindahunsi, AA, Oyagbemi, AA, et al. Cardio-protective and antioxidant properties of caffeic acid and chlorogenic acid: mechanistic role of angiotensin converting enzyme, cholinesterase and arginase activities in cyclosporine induced hypertensive rats. Biomed Pharmacothe 2019;109:450–8. 2019. https://doi.org/10.1016/j.biopha.2018.10.044.Search in Google Scholar

14. AlShukor, N, Camp, JV, Gonzales, GB, Staljanssens, D, Struijs, K, Shanker, N, et al. Hypolipidemic effect of purslane (Portulaca oleracea L.) in rats fed on high cholesterol diet. J Sci Food Agric 2016;6:558–65. 2016. https://doi.org/10.4172/2155-9600.100557.Search in Google Scholar

15. Andriantsitohaina, R, Auger, C, Chataigneau, T, E´tienne-Selloum, N, Li, H, Martınez, CM, et al. Molecular mechanisms of the cardiovascular protective effects of polyphenols. Br J Nutr 2012;108:1532–49. 2012. https://doi.org/10.1017/s0007114512003406.Search in Google Scholar

16. Cushman, DW, Cheung, HS. Spectrophotometric assay and properties of the Angiotensin I- converting enzyme of rabbit lung. Biochem Pharmacol 1981;20:1637–48.10.1016/0006-2952(71)90292-9Search in Google Scholar

17. Schetinger, MRC, Morsch, VM, Bonan, C, Wyse, AT. NTPDase and 5′- nucleotidase activities in physiological and disease conditions: new perspectives for human health. Biofactors 2007;31:77–98. https://doi.org/10.1002/biof.5520310205.Search in Google Scholar

18. Heymann, D, Reddington, M, Kreutzberg, GW. Subcellular localization of 5′- nucleotidase in rat brain. J Neurochem 1984;43:971–8. https://doi.org/10.1111/j.1471-4159.1984.tb12832.x.Search in Google Scholar

19. Guisti, G, Galanti, B. Colorimetric method. In: Bergmeyer, HU, editor. Methods of enzymatic analysis. Germany: Verlag Chemie Weinheim; 1984. 315–23 pp.Search in Google Scholar

20. Ohkawa, H, Ohishi, N, Yagi, K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351–8. https://doi.org/10.1016/0003-2697(79)90738-3.Search in Google Scholar

21. Bradford, MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248–54. https://doi.org/10.1016/0003-2697(76)90527-3.Search in Google Scholar

22. Barba de la Rosa, AP, Barba Montoya, A, Martinez-Cuevas, P, Hernandez-Ledesma, B, Leon-Galvan, MF, De Leon-Rodriguez, A, et al. Tryptic amaranth glutelin digests induce endothelial nitric oxide production through inhibition of ACE: antihypertensive role of amaranth peptides. Nitric Oxide 2010;23:106–11. https://doi.org/10.1016/j.niox.2010.04.006.Search in Google Scholar

23. Akinyemi, AJ, Thome, GR, Morsch, VM, Stefanello, N, Goularte, JF, Belló-Klein, A, et al. Effect of dietary supplementation of ginger and turmeric rhizomes on angiotensin-1 converting enzyme (ACE) and arginase activities in L-NAME induced hypertensive rats. J Funct Foods 2015;17:792–801. 2015. https://doi.org/10.1016/j.jff.2015.06.011.Search in Google Scholar

24. Ko, SC, Jung, WK, Kang, SM, Lee, SH, Kang, MC, Heo, S, Kang, KH, et al. Angiotensin I-converting enzyme (ACE) inhibition and nitric oxide (NO)-mediated antihypertensive effect of octaphlorethol a isolated from Ishige sinicola: in vitro molecular mechanism and in vivo SHR model. J Funct Foods 2015;18:289–99. https://doi.org/10.1016/j.jff.2015.07.003.Search in Google Scholar

25. Jung, C, Gonon, AT, Sjoquist, PO. Arginase inhibition mediates cardioprotection during ischaemia-reperfusion. Cardiovasc Res 2010;85:147–54. 2010. https://doi.org/10.1093/cvr/cvp303.Search in Google Scholar

26. Scacchi, R, Ruggeri, M, Corbo, R.M. Variation of the butyrylcholinesterase (BChE) and acetylcholinesterase (AChE) genes in coronary artery disease. Clin Chim Acta 2011;412:1341–4. 2011. https://doi.org/10.1016/j.cca.2011.03.033.Search in Google Scholar

27. Tarasova, OS, Golubinskaya, VO, Kosiakov, AN, Borovik, AS, Timin, EN, Rodionov, IM. The role of purinergic and adrenergic transmitters of the sympathetic system in the control of arterial blood pressure variability. J Auton Nerv Syst 1998;70:66–70.10.1016/S0165-1838(98)00031-9Search in Google Scholar

28. Bhullar, KS, Lassalle-Claux, G, Touaibia, M, Rupasinghe, HPV. Antihypertensive effect of caffeic acid and its analogs through dual renin–angiotensin–aldosterone system inhibition. Eur J Pharmacol 2014;730:125–32. https://doi.org/10.1016/j.ejphar.2014.02.038.Search in Google Scholar

29. Burnstock, G, Kennedy, C. A dual function for adenosine 5′-triphosphate in the regulation of vascular tone. Excitatory cotransmitter with noradrenaline from perivascular nerves and locally released inhibitory intravascular agent. Circ Res 1986;58:319–30. https://doi.org/10.1161/01.res.58.3.319.Search in Google Scholar

30. Korchazhkina, O, Wright, G, Exley, C. Intravascular ATP and coronary vasodilation in the isolated working rat heart. Br J Pharmacol 1999;127:701–8. https://doi.org/10.1038/sj.bjp.0702610.Search in Google Scholar

31. Martin, F, Gorman, MW, Savage, MV, Feigl, EO. Plasma ATP during exercise: possible role in regulation of coronary blood flow. Am J Physiol Heart Circ Physiol 2005;288:1586–90.10.1152/ajpheart.00983.2004Search in Google Scholar PubMed

32. Abbracchio, MP, Ceruti, S. P1 receptors and cytokine secretion. Purinergic Signal 2007;3:13–25. https://doi.org/10.1007/s11302-006-9033-z.Search in Google Scholar

33. Oboh, G, Agunloye, OM, Akinyemi, AJ, Ademiluyi, AO, Adefegba, SA. Comparative study on the inhibitory effect of caffeic and chlorogenic acids on key enzymes linked to Alzheimer’s disease and some pro-oxidant induced oxidative stress in rats’ brain-in vitro. Neurochem J 2013;38:413–19. 2013. https://doi.org/10.1007/s11064-012-0935-6.Search in Google Scholar

Received: 2019-12-19
Accepted: 2020-06-29
Published Online: 2020-10-01

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