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Neuropeptidase activities in plasma after acute restraint stress. Interaction with cortico-limbic areas

Published online by Cambridge University Press:  17 February 2016

Ana Belén Segarra
Affiliation:
Unit of Physiology, University of Jaén, Jaén, Spain
Joaquín Hernández
Affiliation:
Unit of Physiology, University of Jaén, Jaén, Spain
Isabel Prieto
Affiliation:
Unit of Physiology, University of Jaén, Jaén, Spain
Marc de Gasparo
Affiliation:
Cardiovascular and Metabolic Syndrome Adviser, Rossemaison, Switzerland
Manuel Ramírez-Sánchez*
Affiliation:
Unit of Physiology, University of Jaén, Jaén, Spain
*
Manuel Ramírez-Sánchez, Unit of Physiology, University of Jaén, Bldg B3-263, 23071 Jaén, Spain. Tel: +34 953 212302; Fax: +34 953 212943; E-mail: [email protected]

Abstract

Objective

To evaluate the influence of acute restraint stress (ARS) on plasma enkephalinase and oxytocinase activities. ARS modifies basal activities in cortico-limbic regions of rats and induces changes in the correlations observed between these regions. The interactions between plasma and cortico-limbic activities will be also evaluated.

Methods

Enkephalinase (AlaAP and LeuAP) and oxytocinase (P-LeuAP) activities were fluorometrically determined in plasma of control and stressed rats using aminoacyl-β-naphthylamides (aaNNap), AlaNNap and LeuNNap as substrates.

Results

No differences in enzymatic activities were observed between control and stressed animals in plasma. In contrast, highly significant positive and negative correlations between plasma and cortico-limbic regions were demonstrated in controls. Stress conditions significantly alter the pattern of these correlations.

Conclusion

The present results clearly support a connection between plasma and brain involving certain neuropeptidase activities that change under stress conditions.

Type
Short Communication
Copyright
© Scandinavian College of Neuropsychopharmacology 2016 

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References

1. Goldstein, DS, Kopin, IJ. Evolution of concepts of stress. Stress 2007;10:109120.CrossRefGoogle ScholarPubMed
2. Sterling, P. Allostasis: a model of predictive regulation. Physiol Behav 2012;106:515.CrossRefGoogle Scholar
3. Thayer, JF, Lane, RD. Claude Bernard and the heart-brain connection: further elaboration of a model of neurovisceral integration. Neurosci Biobehav Rev 2009;33:8188.CrossRefGoogle Scholar
4. Prieto, I, Villarejo, AB, Segarra, AB et al. Brain, heart and kidney correlate for the control of blood pressure and water balance: role of angiotensinases. Neuroendocrinology 2014;100:198208.CrossRefGoogle ScholarPubMed
5. Hernández, J, Segarra, AB, Ramírez, M et al. Stress influences brain enkephalinase, oxytocinase and angiotensinase activities: a new hypothesis. Neuropsychobiology 2009;59:184189.CrossRefGoogle ScholarPubMed
6. Hernández, J, Prieto, I, Segarra, AB et al. Interaction of neuropeptidase activities in cortico-limbic regions after acute restraint stress. Behav Brain Res 2015;287:4248.CrossRefGoogle ScholarPubMed
7. Ramírez, M, Prieto, I, Banegas, I et al. Neuropeptidases. Methods Mol Biol 2011;789:287294.CrossRefGoogle ScholarPubMed
8. Segarra, AB, Prieto, I, Banegas, I et al. Asymmetrical effect of captopril on the angiotensinase activity in frontal cortex and plasma of the spontaneously hypertensive rats: expanding the model of neuroendocrine integration. Behav Brain Res 2012;230:423427.CrossRefGoogle ScholarPubMed
9. Segarra, AB, Prieto, I, Banegas, I et al. The brain-heart connection: frontal cortex and left ventricle angiotensinase activities in control and captopril-treated hypertensive rats-a bilateral study. Int J Hypertens 2013;2013:156179.CrossRefGoogle ScholarPubMed
10. Bradford, MM. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 1976;72:248254.CrossRefGoogle Scholar
11. Prieto, I, Villarejo, AB, Segarra, AB et al. Tissue distribution of CysAP activity and its relationship to blood pressure and water balance. Life Sci 2015;134:7378.CrossRefGoogle ScholarPubMed
12. Pierzchala, K, Van Loon, GR. Plasma native and peptidase-derivable Met-enkephalin responses to restraint stress in rats. Adaptation to repeated restraint. J Clin Invest 1990;85:861873.CrossRefGoogle ScholarPubMed
13. Saravia, F, Padros, MR, Ase, A et al. Differential response to a stress stimulus of proenkephalin peptide content in immune cells of naive and chronically stressed rats. Neuropeptides 1998;32:351359.CrossRefGoogle ScholarPubMed
14. Barron, BA, Pierzchala, K, Loon, GR. Source of stress-induced increase in plasma met-enkephalin in rats: contribution of adrenal medulla and/or sympathetic nerves. J Neuroendocrinol 1990;2:381388.CrossRefGoogle ScholarPubMed
15. Sánchez, MM, Aguado, F, Sánchez-Toscano, F et al. Neuroendocrine and immunocytochemical demonstrations of decreased hypothalamo-pituitary-adrenal axis responsiveness to restraint stress after long-term social isolation. Endocrinology 1998;139:579587.CrossRefGoogle ScholarPubMed
16. Babygirija, R, Bülbül, M, Yoshimoto, S et al. Central and peripheral release of oxytocin following chronic homotypic stress in rats. Auton Neurosci 2012;167:5660.CrossRefGoogle ScholarPubMed
17. Laguna-Abreu, MT, Koenigkam-Santos, M, Colleta, AM et al. Time course of vasopressin and oxytocin secretion after stress in adrenalectomized rats. Horm Metab Res 2005;37:8488.CrossRefGoogle ScholarPubMed
18. Lang, RE, Heil, JW, Ganten, D et al. Oxytocin unlike vasopressin is a stress hormone in the rat. Neuroendocrinology 1983;37:314316.CrossRefGoogle ScholarPubMed
19. Carrasco, GA, Van De Kar, LD. Neuroendocrine pharmacology of stress. Eur J Pharmacol 2003;463:235272.CrossRefGoogle ScholarPubMed
20. Loyens, E, De Bundel, D, Demaegdt, H et al. Antidepressant-like effects of oxytocin in mice are dependent on the presence of insulin-regulated aminopeptidase. Int J Neuropsychopharmacol 2013;16:11531163.CrossRefGoogle ScholarPubMed
21. Banegas, I, Prieto, I, Vives, F et al. Asymmetrical response of aminopeptidase A and nitric oxide in plasma of normotensive and hypertensive rats with experimental hemiparkinsonism. Neuropharmacology 2009;56:573579.CrossRefGoogle ScholarPubMed
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