Comparative characteristic of the brain natriuretic peptide and angiotensin II expression index in the structure of locus coeruleus of brain stem in rats with arterial hypertension of various origins
DOI:
https://doi.org/10.14739/2310-1237.2019.2.177117Keywords:
brain natriuretic peptide, angiotensin II, locus coeruleus, brain stem, arterial hypertension, ratsAbstract
The aim of our study was to determine the characteristics of the BNP and AT II expression in the LC structure of rat brain stem with experimental (genetically determined essential and secondary endocrine-salt) arterial hypertension and to give a comparative description of the expression pattern of these peptides in etiologically different types of arterial hypertension.
Materials and methods. The study was carried out on adult 30 male rats. 20 Wistar animals were divided into two groups – control (10 rats) and 10 rats with simulated endocrine-salt AH (ESAH) and 10 rats of the SHR line with essential AH (EAH). The expression parameters of neuropeptides, such as the content, concentration, and relative area of the immunoreactive material, were studied using an immunohistochemical method.
Results. It was found that from all BNP expression parameters in the locus coeruleus structure, only relative area increased significantly in both groups. The concentration did not significantly change, and the content of immunoreactive material increased significantly only in animals with ESAH. At the same time, all parameters of angiotensin II expression increased significantly in both experimental groups. Thus, in rats with experimental arterial hypertension in the locus coeruleus structure, more pronounced changes in expression parameters are characteristic for angiotensin II, rather than for BNP. There is a discrepancy between levels of pressor angiotensin II expression and depressor BNP expression in the direction of angiotensin II expression increasing during the arterial hypertension formation. The nature and peculiarities of these neuropeptides expression in the LC structure depend on the key link of the pathogenesis of the modeled arterial hypertension.
Conclusions. In rats of the control group with normal blood pressure in LC structure, AT II is more represented. The content and concentration of IRM to AT II are 2.32 and 2.19 times higher than the corresponding BNP values. Prevalence of AT II in the LC structure of the brainstem remains even when arterial hypertension is formed, regardless of its etiology. However, the etiopathogenetic mechanisms of arterial hypertension development impose their own characteristics. In EAH, the content and concentration of AT II is higher than BNP by 4.58 and 3.59 times; in ESAH – by 2.16 and 2.83 times. In the pathogenesis of essential arterial hypertension formation an important role is played by a change in the central control of blood pressure regulation. It is characterized by a significant predominance of the pressor component AT II over the depressor BNP in the brainstem LC structure.
References
Johnson, A., Zhang, Z., Clayton, S., Beltz, T., Hurley, S., Thunhorst, R., & Xue, B. (2015). The roles of sensitization and neuroplasticity in the long-term regulation of blood pressure and hypertension. American Journal Of Physiology-Regulatory, Integrative And Comparative Physiology, 309(11), R1309-R1325. doi: 10.1152/ajpregu.00037.2015
Samuels, E., & Szabadi, E. (2008). Functional Neuroanatomy of the Noradrenergic Locus Coeruleus: Its Roles in the Regulation of Arousal and Autonomic Function Part II: Physiological and Pharmacological Manipulations and Pathological Alterations of Locus Coeruleus Activity in Humans. Current Neuropharmacology, 6(3), 254–285. doi: 10.2174/157015908785777193
Berrocoso, E., Micó, J., & Ugedo, L. (2006). In vivo effect of tramadol on locus coeruleus neurons is mediated by α2-adrenoceptors and modulated by serotonin. Neuropharmacology, 51(1), 146–153. doi: 10.1016/j.neuropharm.2006.03.013
Chen, C., Yang, Y., & Chiu, T. (1999). Activation of rat locus coeruleus neuron GABAA receptors by propofol and its potentiation by pentobarbital or alphaxalone. European Journal Of Pharmacology, 386(2–3), 201–210. doi: 10.1016/s0014-2999(99)00750-5
Grillon, C., Cordova, J., Levine, L., & Morgan, III, C. (2003). Anxiolytic effects of a novel group II metabotropic glutamate receptor agonist (LY354740) in the fear-potentiated startle paradigm in humans. Psychopharmacology, 168(4), 446–454. doi: 10.1007/s00213-003-1444-8
McKinley, M., Albiston, A., Allen, A., Mathai, M., May, C., McAllen, R. et al. (2003). The brain renin–angiotensin system: location and physiological roles. The International Journal Of Biochemistry & Cell Biology, 35(6), 901–918. doi: 10.1016/s1357-2725(02)00306-0
Hodes, A., & Lichtstein, D. (2014). Natriuretic Hormones in Brain Function. Frontiers In Endocrinology, 5. doi: 10.3389/fendo.2014.00201
Kuzio, N. V., Tishchenko, S. V., Samojlenko, N. Yu., & Nifontova, V. V. (2014). Analiz patofiziologicheskikh modelej arterial'noj gipertenzii u melkikh laboratornykh zhivotnykh [Analysis of pathophysiological models of arterial hypertension in small laboratory animals]. Aktualni problemy suchasnoi medytsyny. Visnyk Ukrainskoi medychnoi stomatolohichnoi akademii, 14(3), 210–213. [in Russian].
Kolesnyk, Y., Hancheva, O., Abramov, A., Ivanenko, T., Tischenko, S., Kuzo, N. (patentee) (2015) Patent Ukrainy 102234. Sposib modeliuvannia symptomatychnoi arterialnoi hypertezii u dribnykh hryzuniv [Ukraine patent 102234. Method of simulation of symptomatic arterial hypertension in small rodents]. [in Ukrainian].
Kolesnyk, Yu. M., Hancheva, O. V., Abramov, A. V., Kolesnyk, M. Yu., Ivanenko, T. V., Tishсhenko, S. V., et al. (2017). Sovremennye podkhody i novye metodicheskie vozmozhnosti v ocenke funkcional'nogo sostoyaniya melkikh laboratornykh zhivotnykh [Modern approaches and new methodological possibilities in the functional state of small laboratory animals assessing]. Pathologia, 3(41), 364–370. doi: 10.14739/2310-1237.2017.3.118770 [in Russian].
Norstrom, A., Hansson, H., & Sjostrand, J. (1971). Effects of colchicine on axonal transport and ultrastructure of the hypothalamo-neurohypophyseal system of the rat. Zeitschrift FoR Zellforschung Und Mikroskopische Anatomie, 113(2), 271–293. doi: 10.1007/bf00339421
Paxinos, G., & Watson, C. H. (1986). Atlas of the rat brain in stereotaxic coordinates. Academic, New York.
Pirs, E (1962). Histokhimiya. Toreticheskaya i prikladnaya [Histochemistry: Theoretical and Applied]. Moscow: Izdatel'stvo inostrannoj literatyry. [in Russian]
Zajcev, V., & Liflyandskij, V. (2003). Prikladnaya medicinskaya statistika [Applied medical statistics]. Saint-Petersburg: Foliant. [in Russian]
Liu, K., Lu, C., Li, D., & Paterson, D. (2015). Effect of B-type natriuretic peptide and phosphodiesterase 2A is coupled to neurotransmitter release in pro-hypertensive rats. Autonomic Neuroscience, 192, 69–70. doi: 10.1016/j.autneu.2015.07.053
Stepniakowski, K., Budzikowski, A., Lon, S., & Szczepanska-Sadowska, E. (1991). Central ANP attenuates pressor responses to central AVP in WKY and SHR. Brain Research Bulletin, 27(2), 247–249. doi: 10.1016/0361-9230(91)90076-v
Cao, L., & Yang, X. (2008). Natriuretic peptides and their receptors in the central nervous system. Progress in Neurobiology, 84(3), 234–248. doi: 10.1016/j.pneurobio.2007.12.003
Nassar, N., & Abdel-Rahman, A. (2015). Brain stem adenosine receptors modulate centrally mediated hypotensive responses in conscious rats: A review. Journal of Advanced Research, 6(3), 331–340. doi: 10.1016/j.jare.2014.12.005
Paterson, D. (2015). Cyclic nucleotides and the neural control of cardiac excitability in cardiovascular disease. Autonomic Neuroscience, 192, 45. doi: 10.1016/j.autneu.2015.07.393
Huber, G., Schuster, F., & Raasch, W. (2017). Brain renin-angiotensin system in the pathophysiology of cardiovascular diseases. Pharmacological Research, 125, 72–90. doi: 10.1016/j.phrs.2017.06.016
Downloads
How to Cite
Issue
Section
License
Authors who publish with this journal agree to the following terms:- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (SeeThe Effect of Open Access).