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. 2013 Jun;88(3):282-8.
doi: 10.1016/j.ijpsycho.2012.04.008. Epub 2012 Apr 27.

The influence of social environment on endocrine, cardiovascular and tissue responses in the rabbit

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The influence of social environment on endocrine, cardiovascular and tissue responses in the rabbit

Crystal M Noller et al. Int J Psychophysiol. 2013 Jun.

Abstract

Previous work from our lab demonstrated that social environment influences the progression of atherosclerosis in genetically hyperlipidemic rabbits. The purpose of the current study was to examine behavioral and physiological responses associated with these distinct chronic social conditions. Normolipidemic rabbits were exposed to one of three social environments for 4 hours/day over 20 weeks: 1) an Unstable Group in which animals were paired weekly with a different unfamiliar rabbit, 2) a Stable Group in which rabbits were paired with the same littermate for the entire study, and 3) an Individually Caged Group in which animals were socially isolated. It was found that the Unstable Group, characterized by increased agonistic behavior and relatively less affiliative behavior, exhibited physiological responses indicative of chronic stress (increased urinary norepinephrine, plasma cortisol, splenic weight, and decreased visceral fat and body weight compared to the other groups). These animals also had increased acute plasma oxytocin responses relative to the other groups 10 minutes into the social pairing. In contrast, the Stable Group exhibited more affiliative behavior and less stressful physiological and tissue responses. The Individually Caged Group had elevated urinary norepinephrine relative to the Stable Group, and they exhibited higher heart rates at the end of the study compared to the other groups, suggesting that this social environment is also associated with chronic sympathetic arousal. It was concluded that distinct social contexts lead to different patterns of behavioral and physiological responses, and these responses are relevant to the pathophysiology of atherosclerosis and cardiovascular disease.

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Figures

Figure 1
Figure 1
Urinary catecholamines, plasma cortisol, plasma oxytocin, C-reactive protein, and body weight at baseline, midpoint, and endpoint as a function of social environment. Panel A, urinary norepinephrine (NE). Note the elevated NE level in the Unstable Group at baseline, and the significantly lower NE in the Stable Group collapsed over time. Panel B, urinary epinephrine. Panel C, plasma cortisol. Note the elevated cortisol level in the Unstable Group at midpoint. Panels D & E, plasma oxytocin and C-reactive protein, respectively. Panel F, body weight. Note the lower body weight in the Unstable Group relative to the other groups.
Figure 2
Figure 2
Acute changes in plasma oxytocin as a function of behavioral pairing. Blood was drawn just prior to, 10 minutes into, and 2 hours into the 4-hour social pairing of animals. The results are collapsed across the 7 time points of data collection. Note the increased oxytocin levels in the Unstable Group at 10 minutes. In addition, both the Unstable and Stable Groups exhibited significant oxytocin elevations from baseline at 10 minutes and 120 minutes.

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References

    1. Azpiroz A, Fano E, Garmendia L, Arregi A, Cacho R, Beitia G, Brain PF. Effects of chronic mild stress (CMS) and imipramine administration, on spleen mononuclear cell proliferative response, serum corticosterone level and brain norepinephrine content in male mice. Psychoneuroendocrinology. 1999;24:345–361. - PubMed
    1. Berkman LF, Orth-Gomer K. Prevention of cardiovascular morbidity and mortality: role of social relations. In: Orth-Gomer K, Schneiderman N, editors. Behavioral Medicine Approaches to Cardiovascular Disease Prevention. New York: Lawrence Erlbaum Associates, Inc.; 1996. pp. 51–67.
    1. Blackburn P, Després JP, Lamarche B, Tremblay A, Bergeron J, Lemieux I, Couillard C. Postprandial variations of plasma inflammatory markers in abdominally obese men. Obesity (Silver Spring) 2006;14:1747–1754. - PubMed
    1. Buja LM, Kita T, Goldstein JL, Watanabe Y, Brown MS. Cellular pathology of progressive atherosclerosis in the WHHL rabbit. An animal model of familial hypercholesterolemia. Arteriosclerosis. 1983;3:87–101. - PubMed
    1. Callahan MF, Kirby RF, Cunningham JT, Eskridge-Sloop SL, Johnson AK, McCarty R, Gruber KA. Central oxytocin systems may mediate a cardiovascular response to acute stress in rats. Am J Physiol. 1989;256:H1369–H1377. - PubMed

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