Short-term perinatal hypoxia does not affect the functioning of skeletal muscle arteries in adult rats
- Autores: Shvetsova A.A.1, Simonenko S.D.1, Kabiolsky I.A.1, Gaynullina D.K.1
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Afiliações:
- M.V. Lomonosov Moscow State University
- Edição: Volume 111, Nº 9 (2025)
- Páginas: 1545-1557
- Seção: EXPERIMENTAL ARTICLES
- URL: https://stomuniver.ru/0869-8139/article/view/696702
- DOI: https://doi.org/10.7868/S2658655X25090082
- ID: 696702
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Resumo
Perinatal hypoxia is one of the most common pathologies in early ontogenesis, which can have a programming effect on the functioning of the vascular system. The latter has been shown for the pulmonary arteries, as well as in several studies on systemic arteries. However, there are no data on the delayed effect of perinatal hypoxia on the functioning of the hemodynamically important vascular region of skeletal muscles. In this regard, the aim of this work was to study the delayed effects of a short-term normobaric hypoxia in early ontogenesis on the functioning of skeletal muscle arteries in adulthood. In this work, normobaric hypoxia (8% O2) was applied for 2 hours in 2-day-old male rats, after which they were raised to adulthood (11-12 weeks) and the functional activity of the sural arteries and the level of systolic blood pressure were assessed. Contractile responses of the sural arteries to an α1-adrenoceptor agonist, endothelium-dependent relaxation responses of arteries to acetylcholine and endothelium-independent relaxation responses to an NO-donor did not differ between the Hypoxia and Control groups. The anticontractile effects of NO and Ca2+-activated potassium channels of large conductance, as well as the procontractile effect of Rho-kinase in arteries were not changed in rats that underwent perinatal hypoxia. Systolic blood pressure levels did not differ between the groups. Thus, according to the results presented in this work, short-term normobaric perinatal hypoxia does not lead to delayed changes in the regulation of sural artery tone and blood pressure in rats in adulthood.
Sobre autores
A. Shvetsova
M.V. Lomonosov Moscow State UniversityМосква, Россия
S. Simonenko
M.V. Lomonosov Moscow State UniversityМосква, Россия
I. Kabiolsky
M.V. Lomonosov Moscow State UniversityМосква, Россия
D. Gaynullina
M.V. Lomonosov Moscow State University
Email: Dina.Gaynullina@gmail.com
Москва, Россия
Bibliografia
- Barker DJP (2002) Fetal programming of coronary heart disease. Trends Endocrinol Metab 13: 364–368. https://doi.org/10.1016/S1043-2760(02)00689-6
- Miranda JO, Ramalho C, Henriques-Coelho T, Areias JC (2017) Fetal programming as a predictor of adult health or disease: the need to reevaluate fetal heart function. Heart Fail Rev 22: 861–877. https://doi.org/10.1007/s10741-017-9638-z
- Thornburg KL (2015) The programming of cardiovascular disease. J Dev Orig Health Dis 6: 366–376. https://doi.org/10.1017/S2040174415001300
- Moshiro R, Mdoe P, Perlman JM (2019) A Global View of Neonatal Asphyxia and Resuscitation. Front Pediatr 7: 489. https://doi.org/10.3389/fped.2019.00489
- Lawn JE, Blencowe H, Oza S, You D, Lee ACC, Waiswa P, Lalli M, Bhutta Z, Barros AJD, Christian P, Mathers C, Cousens SN (2014) Every newborn: Progress, priorities, and potential beyond survival. Lancet 384: 189–205. https://doi.org/10.1016/S0140-6736(14)60496-7
- Sartori C, Allemann Y, Trueb L, Delabays A, Nicod P, Scherrer U (1999) Augmented vasoreactivity in adult life associated with perinatal vascular insult. Lancet 353: 2205–2207. https://doi.org/10.1016/S0140-6736(98)08352-4
- Peyter AC, Muehlethaler V, Liaudet L, Marino M, Di Bernardo S, Diaceri G, Tolsa JF (2008) Muscarinic receptor M1 and phosphodiesterase 1 are key determinants in pulmonary vascular dysfunction following perinatal hypoxia in mice. Am J Physiol – Lung Cell Mol Physiol 295: 201–213. https://doi.org/10.1152/ajplung.00264.2007
- Jones RD, Morice AH, Emery CJ (2004) Effects of Perinatal Exposure to Hypoxia upon the Pulmonary Circulation of the Adult Rat. Physiol Res 53: 11–17. https://doi.org/10.33549/physiolres.930421
- Marino M, Bény JL, Peyter AC, Bychkov R, Diaceri G, Tolsa JF (2007) Perinatal hypoxia triggers alterations in K+ channels of adult pulmonary artery smooth muscle cells. Am J Physiol – Lung Cell Mol Physiol 293: 1171–1182. https://doi.org/10.1152/ajplung.00126.2007
- Marino M, Bény JL, Peyter AC, Diaceri G, Tolsa JF (2011) Perinatal hypoxia enhances cyclic adenosine monophosphate-mediated BK Ca channel activation in adult murine pulmonary artery. J Cardiovasc Pharmacol 57: 154–165. https://doi.org/10.1097/FJC.0b013e3182016adf
- Peyter AC, Delhaes F, Diaceri G, Menétrey S, Tolsa JF (2014) Perinatal nitric oxide therapy prevents adverse effects of perinatal hypoxia on the adult pulmonary circulation. Biomed Res Int 2014: 949361. https://doi.org/10.1155/2014/949361
- Liu B, Liu Y, Shi R, Feng X, Li X, Zhang W, Wu J, Li N, Zhou X, Sun M, Xu Z (2018) Chronic Prenatal Hypoxia Down-Regulated BK Channel Β1 Subunits in Mesenteric Artery Smooth Muscle Cells of the Offspring. Cell Physiol Biochem 45: 1603–1616. https://doi.org/10.1159/000487727
- Chen X, Qi L, Su H, He Y, Li N, Gao Q, Li H, Xu T, Lu L, Xu Z, Tang J (2020) Prenatal hypoxia attenuated contraction of offspring coronary artery associated with decreased PKCβ Ser660 phosphorylation and intracellular calcium. Life Sci 261: 118364. https://doi.org/10.1016/j.lfs.2020.118364
- Štulcová B (1977) Postnatal Development of Cardiac Output Distribution Measured by Radioactive Microspheres in Rats. Neonatology 32: 119–124. https://doi.org/10.1159/000241004
- Shimokawa H, Sunamura S, Satoh K (2016) RhoA/Rho-Kinase in the Cardiovascular System. Circ Res 118(2): 352–366. https://doi.org/10.1161/CIRCRESAHA.115.306532
- Тарасова ОС, Гайнуллина ДК (2017) Rho-киназа как ключевой участник регуляции тонуса сосудов в норме и при сосудистых расстройствах. Артер гипертен 23: 383–394. [Tarasova OS, Gainullina DK (2017) Rho-kinase as a key participant in the regulation of vascular tone in normal conditions and in vascular disorders. Arter Hyperten 23: 383–394. https://doi.org/10.18705/1607-419X-2017-23-5-383-394
- Gaynullina DK, Sofronova SI, Shvetsova AA, Selivanova EK, Sharova AP, Martyanov AA, Tarasova OS (2018) Antenatal/early postnatal hypothyroidism increases the contribution of Rho-kinase to contractile responses of mesenteric and skeletal muscle arteries in adult rats. Pediatr Res 84: 112–117. https://doi.org/10.1038/s41390-018-0029-5
- Ortiz M, Loidl F, Vázquez-Borsetti P (2022) Transition to extrauterine life and the modeling of perinatal asphyxia in rats. WIREs Mech Dis 14: 1–16. https://doi.org/10.1002/wsbm.1568
- Shateeva VS, Simonenko SD, Khlystova MA, Selivanova EK, Borzykh AA, Gaynullina DK, Shvetsova AA (2025) Perinatal hypoxia augments contractile impact of NADPH oxidase-derived ROS in early postnatal rat arteries. Pediatr Res 97(3): 1220–1261. https://doi.org/10.1038/s41390-024-03466-z
- Shvetsova AA, Khukhareva DD, Simonenko SD, Khlystova MA, Borzykh AA, Gaynullina DK (2024) Perinatal hypoxia weakens anticontractile influence of NO in rat arteries during early postnatal period. Pediatr Res 95(7): 1758–1763. https://doi.org/10.1038/s41390-024-03062-1
- Mulvany MJ, Halpern W (1977) Contractile properties of small arterial resistance vessels in spontaneously hypertensive and normotensive rats. Circ Res 41: 19–26. https://doi.org/10.1161/01.RES.41.1.19
- Faul F, Erdfelder E, Lang A-G, Buchner A (2007) G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods 39: 175–191. https://doi.org/10.3758/bf03193146
- Tarasova O, Sjöblom-Widfeldt N, Nilsson H (2003) Transmitter characteristics of cutaneous, renal and skeletal muscle small arteries in the rat. Acta Physiol Scand 177: 157–166. https://doi.org/10.1046/J.1365-201X.2003.01057.X
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