Skip to main content
Log in

Blood Pressure Changes After Exposures Increasing Angiotensin-Converting Enzyme Activity and After Its Normalization with Dihydroquercetin in Male Wistar Rats

  • Published:
Bulletin of Experimental Biology and Medicine Aims and scope

Changes in BP and HR were assessed after exposures increasing activity of angiotensin-converting enzyme: ionizing radiation, NO synthase inhibitor (L-NAME), and dexamethasone. Effects of dihydroquercetin and angiotensin-converting enzyme inhibitor enalapril on activity of this enzyme, BP, and HR were also evaluated under these exposures. Wistar male rats were subjected to X-ray irradiation in a dose of 2.5 Gy. Angiotensin-converting enzyme activity in the aorta sections was determined by Hip-His-Leu hydrolysis. BP and HR were recorded using a non-invasive tail-cuff method and PowerLab 8/35 software. BP and HR were not altered with the increase in activity of angiotensin-converting enzyme after irradiation. In case of prolonged (7 days) treatment with NO synthase inhibitor and dexamethasone, the increase in enzyme activity was accompanied by elevation of BP and, in the case of NO synthase inhibitor, HR reduction. Dihydroquercetin normalized the enzyme activity and lowered BP, but not to the normal level. Enalapril normalized BP, increased by NO synthase inhibitor solution intake; at the same time, the angiotensinconverting enzyme activity decreased more than 2-fold in comparison with the normal.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Korystova AF, Kublik LN, Kim YA, Levitman MK, Shaposhnikova VV, Korystov YN. Dihydroquercetin and Fucoidin Inhibit the Increase of Angiotensin-Converting Enzyme Activity in the Rat Aorta after Irradiation. Bull. Exp. Biol. Med. 2018;165(3):360-363.

    Article  CAS  Google Scholar 

  2. Korystova AF, Kublik LN, Levitman MK, Samokhvalova TV, Shaposhnikova VV, Korystov YN. Ionizing Radiation Enhances Activity of Angiotensin-Converting Enzyme in Rat Aorta. Bull. Exp. Biol. Med. 2018;165(2):216-219.

    Article  CAS  Google Scholar 

  3. Orlov VA, Gilyarevsky SR, Urusbieva DM, Daurbekova LV. Adverse effects of ACE inhibitors and cardiovascular treatment tactics. Ross. Kardiol. Zh. 2005;10(3):79-90. Russian.

    Google Scholar 

  4. Ackermann A, Fernández-Alfonso MS, Sánchez de Rojas R, Ortega T, Paul M, González C. Modulation of angiotensin-converting enzyme by nitric oxide. Br. J. Pharmacol. 1998;124(2):291-298.

    Article  CAS  Google Scholar 

  5. Arutyunyan TV, Korystova AF, Kublik LN, Levitman MKh, Shaposhnikova VV, Korystov YN. Effects of taxifolin on the activity of angiotensin-converting enzyme and reactive oxygen and nitrogen species in the aorta of aging rats and rats treated with the nitric oxide synthase inhibitor and dexamethasone. Age (Dordr). 2013;35(6):2089-2097.

    Article  CAS  Google Scholar 

  6. Bader M. Tissue renin-angiotensin-aldosterone systems: Targets for pharmacological therapy. Annu. Rev. Pharmacol. Toxicol. 2010;50:439-465.

    Article  CAS  Google Scholar 

  7. Fitzgerald S.M, Brands M.W. Hypertension in L-NAMEtreated diabetic rats depends on an intact sympathetic nervous system. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2002;282(4):R1070-R1076.

    Article  CAS  Google Scholar 

  8. Kim S, Iiwao H. Molecular and cellular mechanisms of angiotensin II-mediated cardiovascular and renal diseases. Pharmacol. Rev. 2000;52(1):12-34.

    Google Scholar 

  9. Linz W, Wohlfart P, Schölkens BA, Malinski T, Wiemer G. Interactions among ACE, kinins and NO. Cardiovasc. Res. 1999;43(3):549-561.

    Article  CAS  Google Scholar 

  10. Mehta PK, Griendling KK. Angiotensin II cell signaling: physiological and pathological effects in the cardiovascular system. Am. J. Physiol. Cell Physiol. 2007;292(1):C82-C97.

    Article  CAS  Google Scholar 

  11. Touyz RM. Blood Pressure Regulation and Pathology. Cellular and Molecular Pathobiology of Cardiovascular Disease. Willis MS, Homeister JW, Stone JR, eds. Glasgow, 2014. P. 257-275.

  12. Schäfer SC, Wallerath T, Closs EI, Schmidt C, Schwarz PM, Förstermann U, Lehr HA. Dexamethasone suppresses eNOS and CAT-1 and induces oxidative stress in mouse resistance arterioles. Am. J. Physiol. Heart Circ. Physiol. 2005;288(1):H436-H444.

    Article  Google Scholar 

  13. Zanzinger J, Czachurski J, Seller H. Inhibition of sympathetic vasoconstriction is a major principle of vasodilation by nitric oxide in vivo. Circ. Res. 1994;75(6):1073-1077.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. F. Korystova.

Additional information

Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 166, No. 7, pp. 36-40, July, 2018

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Korystova, A.F., Kublik, L.N., Levitman, M.K. et al. Blood Pressure Changes After Exposures Increasing Angiotensin-Converting Enzyme Activity and After Its Normalization with Dihydroquercetin in Male Wistar Rats. Bull Exp Biol Med 166, 31–34 (2018). https://doi.org/10.1007/s10517-018-4282-8

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10517-018-4282-8

Key Words

Navigation