Functional state of arteries and microvasculature at the early stage of metabolic syndrome in male and female rats

Authors

DOI:

https://doi.org/10.33910/2687-1270-2024-5-1-83-93

Keywords:

metabolic syndrome, arteries, microcirculatory vessels, endothelium, laser Doppler flowmetry (LDF), fructose load

Abstract

We studied the mechanisms of artery and vessel dilatation in the microvasculature of young male and female Wistar rats during early modeling of the metabolic syndrome (MS) with fructose load (FrDR, fructose diet rat). Consumption of a fructose solution by rats was accompanied by changes in the biochemical composition of blood plasma: hyperglycemia, increased triglyceride concentrations, decreased HDL-C levels and increased uric acid concentrations. Blood flow in the skin MCR was reduced by 11% in males, 8% in females and 24% in ovariohysterectomized females, and the neurogenic and endothelium-dependent vascular tone of the MCR was increased. Endothelium-dependent and endothelium-independent regulation of microcirculatory blood flow was impaired. In the mesenteric arteries of fructose-fed rats, the contractile response to phenylephrine was increased, and acetylcholine- and nitroprusside-induced dilatations were attenuated: the biggest changes were found in ovariohysterectomized females and males. NO production inhibition was accompanied by a significant decrease in the amplitude of artery dilatation, and the value of residual artery dilatation in male and female FrDRs was reliably higher compared to rats in the control groups. Our conclusion is that fructose consumption by rats in an early age quite quickly leads to the development of MS signs, including to arterial hypertension (AH). Negative changes in the biochemical composition of blood and hypertension were more pronounced in male rats and ovariohysterectomized females. FrDRs showed a reduced NO-mediated dilatation of mesenteric arteries but a bigger amplitude of EDH-mediated dilatation.

References

Colafella, K. M. M., Denton, K. M. (2018) Sex-specific differences in hypertension and associated cardiovascular disease. Nature Reviews Nephrology, vol. 14, no. 3, pp. 185–201. https://doi.org/10.1038/nrneph.2017.189 (In English)

Cracowski, J. L., Roustit, M. (2020) Human skin microcirculation. Comprehensive Physiology, vol. 10, no. 3, pp. 1105–1154. https://doi.org/10.1002/cphy.c190008 (In English)

Crespo, P. S., Prieto Perera, J. A., Lodeiro, F. A., Azuara, L. A. (2007) Metabolic syndrome in childhood. Public Health Nutrition, vol. 10, no. 10A, pp. 1121–1125. https://doi.org/10.1017/s1368980007000596 (In English)

Cruzado, M. C., Risler, N. R., Miatello, R. M. et al. (2005) Vascular smooth muscle cell NAD(P)H oxidase activity during the development of hypertension: Effect of angiotensin II and role of insulin like growth factor-1 receptor transactivation. American Journal of Hypertension, vol. 18, pp. 81–87. https://doi.org/10.1016/j.amjhyper.2004.09.001 (In English)

Després, J. P., Lemieux, I., Bergeron, J. et al. (2008) Abdominal obesity and the metabolic syndrome: Contribution to global cardiometabolic risk. Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 28, no. 6, pp. 1039–1049. https://doi.org/10.1161/atvbaha.107.159228 (In English)

Gonzalez-Chávez, A., Chávez-Fernández, J. A., Elizondo-Argueta, S. (2018) Metabolic syndrome and cardiovascular disease: A health challenge. Archives of Medical Research, vol. 49, no. 8, pp. 516–521. https://doi.org/10.1016/j.arcmed.2018.10.003 (In English)

Hall, J. E. (2012) Guyton and Hall textbook of medical physiology. 12 ed. Philadelphia: Saunders, 1120 p. (In English)

Kauser, K., Rubanyi, G. M. (1994) Gender difference in bioassayable endothelium-derived nitric oxide from isolated rat aortae. American Journal of Physiology, vol. 267, no. 6, pp. 2311–2317. https://doi.org/10.1152/ajpheart.1994.267.6.h2311 (In English)

Krentz, A. J., Clough, G., Byrne, C. D. (2009) Vascular disease in the metabolic syndrome: Do we need to target the microcirculation to treat large vessel disease? Journal of Vascular Research, vol. 46, no. 6, pp. 515–526. https://doi.org/10.1159/000226220 (In English)

Lee, A. M., Gurka, M. J., DeBoer, M. D. (2016) Trends in metabolic syndrome severity and lifestyle factors among adolescents. Pediatrics, vol. 137, no. 3, article e20153177. https://doi.org/10.1542/peds.2015-3177 (In English)

Liu, Y., Kabakov, A. Y., Xie, A. (2020) Metabolic regulation of endothelial SK channels and human coronary microvascular function. International Journal of Cardiology, vol. 312, pp. 1–9. https://doi.org/10.1016/j.ijcard.2020.03.028 (In English)

Matsumoto, T., Goulopoulou, S., Taguchi, K. et al. (2015) Constrictor prostanoids and uridine adenosine tetraphosphate: Vascular mediators and therapeutic targets in hypertension and diabetes. British Journal of Pharmacology, vol. 172, no. 16, pp. 3980 –4001. https://doi.org/10.1111/bph.13205 (In English)

Miller, J. M., Kaylor, M. B., Johannsson, M. et al. (2014) Prevalence of metabolic syndrome and individual criterion in US adolescents: 2001–2010 National Health and Nutrition Examination Survey. Metabolic Syndrome and Related Disorders, vol. 12, no. 10, pp. 527–532. https://doi.org/10.1089/met.2014.0055 (In English)

Mozumdar, A., Liguori, G. (2011) Persistent increase of prevalence of metabolic syndrome among U.S. adults: NHANES III to NHANES 1999–2006. Diabetes Care, vol. 34, no. 1, pp. 216–219. https://doi.org/10.2337/dc10-0879 (In English)

Ndrepepa, G. (2018) Uric acid and cardiovascular disease. Clinica Chimica Acta, vol. 484, pp. 150 –163. https://doi.org/10.1016/j.cca.2018.05.046 (In English)

Pradhan, A. D. (2014) Sex differences in the metabolic syndrome: Implications for cardiovascular health in women. Clinical Chemistry, vol. 60, no. 1, pp. 44–52. https://doi.org/10.1373/clinchem.2013.202549 (In English)

Rendell, M. S., Finnegan, M. F., Healy, J. C. et al. (1998) The relationship of laser-Doppler skin blood flow measurements to the cutaneous microvascular anatomy. Microvascular Research, vol. 55, no. 1, pp. 3–13. https://doi.org/10.1006/mvre.1997.2049 (In English)

Saklayen, M. G. (2018) The global epidemic of the metabolic syndrome. Current Hypertension Reports, vol. 20, no. 2, article 12. https://doi.org/10.1007/s11906-018-0812-z (In English)

Santilli, F., D’Ardes, D., Guagnano, M. T., Davi, G. (2017) Metabolic syndrome: Sex-related cardiovascular risk and therapeutic approach. Current Medicinal Chemistry, vol. 24, no. 24, pp. 2602–2627. https://doi.org/10.2174/0929867324666170710121145 (In English)

Serné, E. H., de Jongh, R. T., Eringa, E. C. et al. (2006) Microvascular dysfunction: Сausative role in the association between hypertension, insulin resistance and the metabolic syndrome? Essays in Biochemistry, no. 42, pp. 163–176. https://doi.org/10.1042/bse0420163 (In English)

Silveira Rossi, J. L., Barbalho, S. M., Reverete de Araujo, R. et al. (2022) Metabolic syndrome and cardiovascular diseases: Going beyond traditional risk factors. Diabetes/Metabolism Research and Reviews, vol. 38, no. 3, article e3502. https://doi.org/10.1002/dmrr.3502 (In English)

Yin, D. D., Wang, Q. C., Zhou, X., Li, Y. (2017) Endothelial dysfunction in renal arcuate arteries of obese Zucker rats: The roles of nitric oxide, endothelium-derived hyperpolarizing factors, and calcium-activated K+ channels. PLoS One, vol. 127, no. 812, article e0183124. https://doi.org/10.1371/journal.pone.0183124 (In English)

Zhang, H., Sun, T., Cheng, Y. et al. (2022) Impact of metabolic syndrome and systemic inflammation on endothelial function in postmenopausal women. Turk Kardiyol Dern Ars, vol. 50, no. 1, pp. 57–65. https://doi.org/10.5543/tkda.2022.47443 (In English)

Published

2024-07-01

Issue

Section

Experimental articles