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Adrenal Medulla Chemo Sensitivity Does Not Compensate the Lack of Hypoxia Driven Carotid Body Chemo Reflex in Guinea Pigs

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 1071))

Abstract

Guinea pigs (GP), originally from the Andes, have absence of hypoxia-driven carotid body (CB) reflex. Neonatal mammals have an immature CB chemo reflex and respond to hypoxia with metabolic changes arising from direct effects of hypoxia on adrenal medulla (AM). Our working hypothesis is that adult GP would mimic neonatal mammals. Plasma epinephrine (E) has an AM origin, while norepinephrine (NE) is mainly originated in sympathetic endings, implying that specific GP changes in plasma E/NE ratio, and in blood glucose and lactate levels during hypoxia would be observed. Experiments were performed on young adult GP and rats. Hypoxic ventilation (10% O2) increased E and NE plasma levels similarly in both species but PaO2 was lower in GP than in rats. Plasma E/NE ratio in GP was higher (≈1.0) than in rats (≈0.5). The hypoxia-evoked increases in blood glucose and lactate were smaller in GP than in the rat. The AM of both species contain comparable E content, but NE was four times lower in GP than in rats. GP superior cervical ganglion also had lower NE content than rats and an unusual high level of dopamine, a negative modulator of sympathetic transmission. Isolated AM from GP released half of E and one tenth of NE than the rat AM, and hypoxia did not alter the time course of CA outflow. These data indicate the absence of direct effects of hypoxia on AM in the GP, and a lower noradrenergic tone in this species. Pathways for hypoxic sympatho-adrenal system activation in GP are discussed.

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References

  • Eränkö O (1978) Small intensely fluorescent (SIF) cells and nervous transmission in sympathetic ganglia. Annu Rev Pharmacol Toxicol 18:417–430

    Article  Google Scholar 

  • Goldstein DS, McCarty R, Polinsky RJ, Kopin IJ (1983) Relationship between plasma norepinephrine and sympathetic neural activity. Hypertension 5(4):552–559

    Article  CAS  Google Scholar 

  • Goldstein DS, Eisenhofer G, Kopin IJ (2003) Sources and significance of plasma levels of catechols and their metabolites in humans. J Pharmacol Exp Ther 305(3):800–811

    Article  CAS  Google Scholar 

  • Gonzalez C, Almaraz L, Obeso A, Rigual R (1994) Carotid body chemoreceptors: from natural stimuli to sensory discharges. Physiol Rev 74:829–898

    Article  CAS  Google Scholar 

  • Gonzalez-Obeso E, Docio I, Olea E, Cogolludo A, Obeso A, Rocher A, Gomez-Niño A (2017) Guinea pig oxygen-sensing and carotid body functional properties. Front Physiol 8:285

    Article  Google Scholar 

  • Guyenet PG (2000) Neural structures that mediate sympathoexcitation during hypoxia. Respir Physiol 121(2–3):147–162

    Article  CAS  Google Scholar 

  • Inoue M, Fujishiro N, Imanaga I (1998) Hypoxia and cyanide induce depolarization and catecholamine release in dispersed guinea-pig chromaffin cells. J Physiol 507(3):807–818

    Article  CAS  Google Scholar 

  • Kumar GK, Rai V, Sharma SD, Ramakrishnan DP, Peng YJ, Souvannakitti D, Prabhakar NR (2006) Chronic intermittent hypoxia induces hypoxia-evoked catecholamine efflux in adult rat adrenal medulla via oxidative stress. J Physiol 575(Pt 1):229–239

    Article  CAS  Google Scholar 

  • Macquin-Mavier I, Clerici C, Franco-Montoya ML, Harf A (1988) Mechanism of histamine-induced epinephrine release in guinea pig. J Pharmacol Exp Ther 247(2):706–709

    CAS  PubMed  Google Scholar 

  • Marina N, Ang R, Machhada A, Kasymov V, Karagiannis A, Hosford PS, Mosienko V, Teschemacher AG, Vihko P, Paton JF, Kasparov S, Gourine AV (2015) Brainstem hypoxia contributes to the development of hypertension in the spontaneously hypertensive rat. Hypertension 65(4):775–783

    Article  CAS  Google Scholar 

  • Marshall JM (1994) Peripheral chemoreceptors and cardiovascular regulation. Physiol Rev 74(3):543–594

    Article  CAS  Google Scholar 

  • Obeso A, Almaraz L, Gonzalez C (1989) Effects of cyanide and uncouplers on chemoreceptor activity and ATP content of the cat carotid body. Brain Res 481(2):250–257

    Article  CAS  Google Scholar 

  • Olea E, Agapito MT, Gallego-Martin T, Rocher A, Gomez-Niño A, Obeso A, Gonzalez C, Yubero S (2014) Intermittent hypoxia and diet-induced obesity: effects on oxidative status, sympathetic tone, plasma glucose and insulin levels, and arterial pressure. J Appl Physiol 117(7):706–719

    Article  CAS  Google Scholar 

  • Padbury J, Agata Y, Ludlow J, Ikegami M, Baylen B, Humme J (1987) Effect of fetal adrenalectomy on catecholamine release and physiologic adaptation at birth in sheep. J Clin Invest 80(4):1096–1103

    Article  CAS  Google Scholar 

  • Rico AJ, Prieto-Lloret J, Gonzalez C, Rigual R (1987) Hypoxia and acidosis increase the secretion of catecholamines in the neonatal rat adrenal medulla: an in vitro study. Am J Physiol Cell Physiol 289:C1417–C1425. 2005

    Article  Google Scholar 

  • Schwenke DO, Bolter CP, Cragg PA (2007) Are the carotid bodies of the guinea-pig functional? Comp Biochem Physiol A Mol Integr Physiol 146(2):180–188

    Article  Google Scholar 

  • Seidler FJ, Slotkin TA (1985) Adrenomedullary function in the neonatal rat: responses to acute hypoxia. J Physiol 358:1–16

    Article  CAS  Google Scholar 

  • Seidler FJ, Slotkin TA (1986) Ontogeny of adrenomedullary responses to hypoxia and hypoglycemia: role of splanchnic innervation. Brain Res Bull 16:11–14

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by Grants BFU2015-63706R (MINECO, FEDER-UE) and CIBER CB06/06/0050 from ISCiii (Spain).

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Correspondence to Asuncion Rocher .

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Olea, E. et al. (2018). Adrenal Medulla Chemo Sensitivity Does Not Compensate the Lack of Hypoxia Driven Carotid Body Chemo Reflex in Guinea Pigs. In: Gauda, E., Monteiro, M., Prabhakar, N., Wyatt, C., Schultz, H. (eds) Arterial Chemoreceptors. Advances in Experimental Medicine and Biology, vol 1071. Springer, Cham. https://doi.org/10.1007/978-3-319-91137-3_21

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