Intermittent hypobaric hypoxia and neuroendocrine reaction of the parvocellular neurons of the paraventricular hypothalamic nucleus

Authors

  • V. O. Shamenko Zaporizhzhia State Medical University, Ukraine,
  • Ye. V. Kadzharian Zaporizhzhia State Medical University, Ukraine,
  • A. V. Abramov Zaporizhzhia State Medical University, Ukraine,

DOI:

https://doi.org/10.14739/2310-1237.2019.3.188834

Keywords:

hypothalamus, neuropeptides, intermittent hypobaric hypoxia, adaptation

Abstract

 

The neuroendocrine system occupies an important place in the systemic mechanisms of the body response to stress. The paraventricular nuclei of the hypothalamus (PVH) are one of the most important links of the brain`s neuroendocrine system which determine the reactivity of the hypothalamic-pituitary-adrenal axis (HPA) in response to the various stressors and thereby ensure the development of adaptive reactions by the formation of body resistance to the stress.

The aim of the research was to study the functional state of the peptidergic neurons of the medial parvocellular nuclei of the paraventricular hypothalamic nucleus (PVHmp) during the multi-day action of intermittent hypobaric hypoxia and in the posthypoxic period.

Materials and methods. The research was conducted on 24 male Wistar rats. Intermittent hypoxia was modeled by a daily 6-hour stay of rats at an altitude of 6000 m (pO2 = 9.8 %) for 15 days, the posthypoxic period lasted for 10 days. The distribution of corticotropin-releasing hormone (CRH), [Arg8]-vasopressin (AVP), β-endorphin, cFos and HIF-1α proteins was studied by quantitative immunofluorescence methods in serial frontal sections of the hypothalamus.

Results. The intermittent hypobaric hypoxia stimulated the developing of mild hypertrophy of PVHmp neurons and increased the concentration of RNA in the cytoplasm by 37 %. An indicator of PVHmp neurons response to hypoxia was 2.5-fold increase in the concentration of the HIF-1α protein in them. IHH elevated the concentration of cFos protein in PVHmp by 37 %, increased the area of immunoreactivity to AVP by 2.5 times, to CRH and β-endorphin by 3 times. There was an increase in the synthesis of neuropeptides in response to hypoxia, which led to the elevation in the concentration of AVP in PVHmp by 6.6 times, β-endorphin by 7 times, and CRH by 8.5 times. The immunoreactivity indicators for the HIF-1α protein and its concentration in PVHmp remained at a high level in the posthypoxic period. At the same time, high immunoreactivity to CRH and β-endorphin in PVHmp was noted, as well as a high concentration of these neuropeptides in neurons against the background of AVP synthesis inhibition in neurons. It is possible that high rates of neurosecretory activity of PVHmp in the posthypoxic period may indicate the formation of neuroendocrine mechanisms of adaptation of the HPA axis to the long-term effect of hypoxia.

Conclusions. Intermittent hypobaric hypoxia stimulates the neurosecretory activity of the PVHmp neurons, increases the synthesis and secretion of CRH and AVP hormones that activate the HPA axis. Synthesis of the secretory response indicator cFos protein and a central regulator of hypoxic responses HIF‑1α protein is also increasing in the peptidergic neurons of the PVHmp. High levels of the PVHmp neurosecretory activity at the posthypoxic period are preserved and indicate the formation of neuroendocrine mechanisms of the HPA axis adaptation to the long term intermittent hypoxia exposures.

 

References

McEwen, B. S. (2009). The brain is the central organ of stress and adaptation. Neuroimage, 47(3), 911-913. https://doi.org/10.1016/j.neuroimage.2009.05.071

McEwen, B. S., Bowles, N. P., Gray, J. D., Hill, M. N., Hunter, R. G., Karatsoreos, I. N., & Nasca, C. (2015). Mechanisms of stress in the brain. Nature Neuroscience, 18(10), 1353-1363. https://doi.org/10.1038/nn.4086

Meerson, F. Z. (1981). Adaptatsiya, stress i profilaktika [Adaptation, stress and prevention]. Moscow: Nauka [in Russian].

McEwen, B. S. (2007). Physiology and neurobiology of stress and adaptation: Central role of the brain. Physiological Reviews, 87(3), 873-904. https://doi.org/10.1152/physrev.00041.2006

Bonfiglio, J. J., Inda, C., Refojo, D., Holsboer, F., Arzt, E., & Silberstein, S. (2011). The Corticotropin-Releasing Hormone Network and the Hypothalamic-Pituitary-Adrenal Axis: Molecular and Cellular Mechanisms Involved. Neuroendocrinology, 94(1), 12-20. https://doi.org/10.1159/000328226

Swanson, L. W., & Sawchenko, P. E. (1983). Hypothalamic integration - organization of the paraventricular and supraoptic nuclei. Annual Review of Neuroscience, 6, 269-324. https://doi.org/10.1146/annurev.ne.06.030183.001413

Reznikov, A. G. (2007). Endokrinologicheskie aspekty stressa [Endocrinological Aspects of Stress]. Mezhdunarodnyi endokrinologicheskii zhurnal, (4), 20-24. [in Russian].

Busnardo, C., Tavares, R. F., Resstel, L. B. M., Elias, L. L. K., & Correa, F. M. A. (2010). Paraventricular nucleus modulates autonomic and neuroendocrine responses to acute restraint stress in rats. Autonomic Neuroscience-Basic & Clinical, 158(1-2), 51-57. https://doi.org/10.1016/j.autneu.2010.06.003

Volpi, S., Rabadan-Diehl, C., & Aguilera, G. (2004). Vasopressinergic regulation of the hypothalamic pituitary adrenal axis and stress adaptation. Stress-the International Journal on the Biology of Stress, 7(2), 75-83. https://doi.org/10.1080/10253890410001733535

Sivukhina, E. V., & Jirikowski, G. F. (2016). Magnocellular hypothalamic system and its interaction with the hypothalamo-pituitary-adrenal axis. Steroids, 111, 21-28. https://doi.org/10.1016/j.steroids.2016.01.008

Kovalitskaya, Y. A., & Navolotskaya, E. V. (2011). Nonopioid effect of beta-endorphin. Biochemistry-Moscow, 76(4), 379-393. https://doi.org/10.1134/s0006297911040018

Berezovskiy, V. A. (2012). Tsvetok Gil'gamesha. Prirodnaya i instrumental'naya oroterapiya : (ocherki o gorakh i ikh vliyanii na organizm cheloveka) [Flower of Gilgamesh. Natural and instrumental orotherapy (essays of the mountains and their effects on the human body)]. Donetsk: Publisher Zaslavsky A.Yu. [in Russian].

Karash, Yu. M., Strelkov, R. B., & Chizhov F. Ya. (1988). Normobaricheskaya gipoksiya v lechenii, profilaktike i reabilitatsii [Intermittent Normobaric Hypoxia for Treatment, Prevention, and Rehabilitation Purposes]. Moscow: Izdatelstvo Meditsina. [in Russian].

Xi, L, & Serebrovskaya, T. V. (2009). Intermittent hypoxia: from molecular mechanisms to clinical applications, 1st ed. New York: Nova Science Publishers, Inc.

Coldren, K. M., Li, D. P., Kline, D. D., Hasser, E. M., & Heesch, C. M. (2017). Acute hypoxia activates neuroendocrine, but not presympathetic, neurons in the paraventricular nucleus of the hypothalamus: differential role of nitric oxide. American Journal of Physiology-Regulatory Integrative and Comparative Physiology, 312(6), R982-R995. https://doi.org/10.1152/ajpregu.00543.2016

Kolesnik, Yu. M., Orestenko, Yu. N., & Abramov, A. V. (1993) Sostoyanie vazopressin-, oksitocin- i kortikoliberinsinteziruyushchikh struktur gipotalamusa u krys s sakharnym diabetom pri gipoksicheskikh vozdejstviyakh [The state of vasopressin-, oxytocin- and corticoliberin-synthesizing structures of the hypothalamus in diabetic rats with hypoxic effects]. Fiziologicheskii zhurnal im. I. M. Sechenova, 79(9), 34-42. [in Russian].

Abramov, A. V. (1998) Vliyanie interval'nykh gipoksicheskikh trenirovok na funktsional'noe sostoyanie peptidergicheskikh neironov paraventrikulyarnogo yadra gipotalamusa i neironov stvola mozga krys [The effect of interval hypoxic training on the functional state of the peptidergic neurons of the paraventricular nucleus of the hypothalamus and rat brainstem neurons]. Rossiiskii fiziologicheskii zhurnal im. I.M. Sechenova, 84(3), 173-181. [in Russian].

Basovich, S. N. (2013). Trends in the use of preconditioning to hypoxia for early prevention of future life diseases. Bioscience Trends, 7(1), 23-32. https://doi.org/10.5582/bst.2013.v7.1.23

Zhang, S. X. L., Wang, Y., & Gozal, D. (2012). Pathological Consequences of Intermittent Hypoxia in the Central Nervous System. Comprehensive Physiology, 2(3), 1767-1777. https://doi.org/10.1002/cphy.c100060

Myers, D. A., & Ducsay, C. A. (2014). Altitude, Attitude and Adaptation. Advances in Fetal and Neonatal Physiology, 814, 147-157. https://doi.org/10.1007/978-1-4939-1031-1_13

Peters, A., McEwen, B. S., & Friston, K. (2017). Uncertainty and stress: Why it causes diseases and how it is mastered by the brain. Progress in Neurobiology, 156, 164-188. https://doi.org/10.1016/j.pneurobio.2017.05.004

Gray, J. M., Wilson, C. D., Lee, T. T. Y., Pittman, Q. J., Deussingh, J. M., Hillard, C. J., . . . Hill, M. N. (2016). Sustained glucocorticoid exposure recruits cortico-limbic CRH signaling to modulate endocannabinoid function. Psychoneuroendocrinology, 66, 151-158. https://doi.org/10.1016/j.psyneuen.2016.01.004

Du, J., Wang, Y., Hunter, R., Wei, Y. L., Blumenthal, R., Falke, C., . . . Manji, H. K. (2009). Dynamic regulation of mitochondrial function by glucocorticoids. Proceedings of the National Academy of Sciences of the United States of America, 106(9), 3543-3548. https://doi.org/10.1073/pnas.0812671106

Chen, Y., Fenoglio, K. A., Dube, C. M., Grigoriadis, D. E., & Baram, T. Z. (2006). Cellular and molecular mechanisms of hippocampal activation by acute stress are age-dependent. Molecular Psychiatry, 11(11), 992-1002. https://doi.org/10.1038/sj.mp.4001863

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Shamenko VO, Kadzharian YV, Abramov AV. Intermittent hypobaric hypoxia and neuroendocrine reaction of the parvocellular neurons of the paraventricular hypothalamic nucleus. Pathologia [Internet]. 2019Dec.23 [cited 2024Nov.2];(3). Available from: http://pat.zsmu.edu.ua/article/view/188834

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