Horm Metab Res 2013; 45(12): 845-848
DOI: 10.1055/s-0033-1348265
Original Basic
© Georg Thieme Verlag KG Stuttgart · New York

Kinetics of Oxytocin Response to Repeated Restraint Stress and/or Chronic Cold Exposure

V. Danevova
1   Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia
2   Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University, Bratislava, Slovakia
,
R. Kvetnansky
1   Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia
,
D. Jezova
1   Institute of Experimental Endocrinology, Slovak Academy of Sciences, Bratislava, Slovakia
2   Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University, Bratislava, Slovakia
› Author Affiliations
Further Information

Publication History

received 26 March 2013

accepted 27 May 2013

Publication Date:
25 July 2013 (online)

Abstract

Recently, several new atypical actions of circulating oxytocin are emerging, which may be of importance for the physiological effects of oxytocin released during stress. However, little information is available on oxytocin response to chronic stress stimuli. The aim of the present study is to deepen the knowledge on oxytocin secretion during chronic and repeated stress. The main hypothesis to be tested was that oxytocin release in response to single and to repeated or chronic stress is of different kinetics. Adult male Sprague-Dawley rats were exposed to 2 different stress stimuli or their combination. Restraint (immobilization) of different duration (10–120 min) and number of repetitions (1 or 7 times) as well as chronic exposure (28 days) to cold temperature were used. Concentrations of oxytocin in plasma and posterior pituitary were measured by a radioimmunoassay. Concentrations of oxytocin in plasma increased significantly in response to both single and repeated immobilization. Acute immobilization caused rapid increase already after 10 min of restraint, while the recovery occurred only after 24 h. Repeated restraint caused delayed onset of increased oxytocin release and a more rapid recovery to prestress levels after 3 h. In conclusion, the results of the present study show that though with a different kinetics, increased oxytocin release is preserved during repeated exposure to an intensive stressor, namely immobilization for 120 min. During repeated exposure to shorter stressors, an adaptation in oxytocin responses may occur. This should be taken into account with respect to cardiovascular and metabolic effects of stress-induced oxytocin.

 
  • References

  • 1 Jezova D, Skultetyova I, Tokarev DI, Bakos P, Vigas M. Vasopressin and oxytocin in stress. Ann N Y Acad Sci 1995; 771: 192-203
  • 2 Gutkowska J, Jankowski M. Oxytocin revisited: its role in cardiovascular regulation. J Neuroendocrinol 2012; 24: 599-608
  • 3 Gutkowska J, Jankowski M. Oxytocin revisited: It is also a cardiovascular hormone. J Am Soc Hypertens 2008; 2: 318-325
  • 4 Ondrejcakova M, Ravingerova T, Bakos J, Pancza D, Jezova D. Oxytocin exerts protective effects on in vitro myocardial injury induced by ischemia and reperfusion. Can J Physiol Pharmacol 2009; 87: 137-142
  • 5 Ondrejcakova M, Barancik M, Bartekova M, Ravingerova T, Jezova D. Prolonged oxytocin treatment in rats affects intracellular signaling and induces myocardial protection against infarction. Gen Physiol Biophys 2012; 31: 261-270
  • 6 Houshmand F, Faghihi M, Zahediasl S. Biphasic protective effect of oxytocin on cardiac ischemia/reperfusion injury in anaesthetized rats. Peptides 2009; 30: 2301-2308
  • 7 Faghihi M, Alizadeh AM, Khori V, Latifpour M, Khodayari S. The role of nitric oxide, reactive oxygen species, and protein kinase C in oxytocin-induced cardioprotection in ischemic rat heart. Peptides 2012; 37: 314-319
  • 8 Grewen KM, Light KC. Plasma oxytocin is related to lower cardiovascular and sympathetic reactivity to stress. Biol Psychol 2011; 87: 340-349
  • 9 Takayanagi Y, Kasahara Y, Onaka T, Takahashi N, Kawada T, Nishimori K. Oxytocin receptor-deficient mice developed late-onset obesity. Neuroreport 2008; 19: 951-955
  • 10 Eckertova M, Ondrejcakova M, Krskova K, Zorad S, Jezova D. Subchronic treatment of rats with oxytocin results in improved adipocyte differentiation and increased gene expression of factors involved in adipogenesis. Br J Pharmacol 2011; 162: 452-463
  • 11 Deblon N, Veyrat-Durebex C, Bourgoin L, Caillon A, Bussier AL, Petrosino S, Piscitelli F, Legros JJ, Geenen V, Foti M, Wahli W, Di Marzo V, Rohner-Jeanrenaud F. Mechanisms of the anti-obesity effects of oxytocin in diet-induced obese rats. PLoS One 2011; 6: e25565
  • 12 Szeto A, Nation DA, Mendez AJ, Dominguez-Bendala J, Brooks LG, Schneiderman N, McCabe PM. Oxytocin attenuates NADPH-dependent superoxide activity and IL-6 secretion in macrophages and vascular cells. Am J Physiol Endocrinol Metab 2008; 295: E1495-E1501
  • 13 Fekete EM, Antoni MH, Lopez C, Mendez AJ, Szeto A, Fletcher MA, Klimas N, Kumar M, Schneiderman N. Stress buffering effects of oxytocin on HIV status in low-income ethnic minority women. Psychoneuroendocrinology 2011; 36: 881-890
  • 14 Gouin JP, Carter CS, Pournajafi-Nazarloo H, Glaser R, Malarkey WB, Loving TJ, Stowell J, Kiecolt-Glaser JK. Marital behavior, oxytocin, vasopressin, and wound healing. Psychoneuroendocrinology 2010; 35: 1082-1090
  • 15 Ondrejcakova M, Bakos J, Garafova A, Kovacs L, Kvetnansky R, Jezova D. Neuroendocrine and cardiovascular parameters during simulation of stress-induced rise in circulating oxytocin in the rat. Stress 2010; 13: 314-322
  • 16 Neumann ID, Landgraf R. Balance of brain oxytocin and vasopressin: implications for anxiety, depression, and social behaviors. Trends Neurosci 2012; 35: 649-659
  • 17 Zheng J, Babygirija R, Bülbül M, Cerjak D, Ludwig K, Takahashi T. Hypothalamic oxytocin mediates adaptation mechanism against chronic stress in rats. Am J Physiol Gastrointest Liver Physiol 2010; 299: G946-G953
  • 18 Kvetnansky R, Mikulaj L. Adrenal and urinary catecholamines in rats during adaptation to repeated immobilization stress. Endocrinology 1970; 87: 738-743
  • 19 Grinevich V, Jezova D, Gambaryan S, Illarionova A, Kolleker A, Seeburg PH, Schwarz MK. Hypertrophy and altered activity of the adrenal cortex in Homer 1 knockout mice. Horm Metab Res 2011; 43: 551-556
  • 20 Repcekova D, Mikulaj L. Plasma testosterone of rats subjected to immobilization stress and/or HCG administration. Horm Res 1977; 8: 51-57
  • 21 Robinson IC. The development and evaluation of a sensitive and specific radioimmunoassay for oxytocin in unextracted plasma. J Immunoassay 1980; 1: 323-347
  • 22 Jezova D, Michajlovskij N, Kvetnansky R, Makara GB. Paraventricular and supraoptic nuclei of the hypothalamus are not equally important for oxytocin release during stress. Neuroendocrinology 1993; 57: 776-781
  • 23 Wotjak CT, Naruo T, Muraoka S, Simchen R, Landgraf R, Engelmann M. Forced swimming stimulates the expression of vasopressin and oxytocin in magnocellular neurons of the rat hypothalamic paraventricular nucleus. Eur J Neurosci 2001; 13: 2273-2281
  • 24 Dubovicky M, Mach M, Key M, Morris M, Paton S, Lucot JB. Diurnal behavioral and endocrine effects of chronic shaker stress in mice. Neuro Endocrinol Lett 2007; 28: 846-853
  • 25 Hashiguchi H, Ye SH, Morris M, Alexander N. Single and repeated environmental stress: effect on plasma oxytocin, corticosterone, catecholamines, and behavior. Physiol Behav 1997; 61: 731-736
  • 26 Suzuki H, Onaka T, Kasai M, Kawasaki M, Ohnishi H, Otsubo H, Saito T, Hashimoto H, Yokoyama T, Fujihara H, Dayanithi G, Murphy D, Nakamura T, Ueta Y. Response of arginine vasopressin-enhanced green fluorescent protein fusion gene in the hypothalamus of adjuvant-induced arthritic rats. J Neuroendocrinol 2009; 21: 183-190
  • 27 Babygirija R, Zheng J, Bülbül M, Cerjak D, Ludwig K, Takahashi T. Sustained delayed gastric emptying during repeated restraint stress in oxytocin knockout mice. J Neuroendocrinol 2010; 22: 1181-1186
  • 28 Aguilera G. Regulation of pituitary ACTH secretion during chronic stress. Front Neuroendocrinol 1994; 15: 321-350
  • 29 Dronjak S, Kvetnansky R, Jezova D. Effect of immobilization and cold stress on sympatho-adrenal system in rats exposed to long-term cold. Yugoslav Med Biochem 2001; 20: 217-222