Behavioural NeuroscienceCorticotropin releasing factor influences aggression and monoamines: Modulation of attacks and retreats
Section snippets
Subjects and housing
Juvenile rainbow trout (Oncorhynchus mykiss; raised from eggs) weighing 150±30 g were housed indoors in a 6-foot diameter circular tank under natural light conditions prior to experimentation (Gavins Point National Fish Hatchery, Yankton, SD, USA). Fish were fed daily with sinking trout feed (Nelson’s Silver Cup, Murray, Utah, USA) at a rate of 1% body weight per day. All experiments were conducted in a manner that minimized suffering and the number of animals used, in accordance with the
Behavior
Social interaction was initially tested between sized-paired fish, one injected icv with aCSF and the other with CRF (either 500 or 2000 ng doses). A greater percentage of fights was won by fish treated with CRF, regardless of dose (Fisher exact, P<0.022; Fig. 2). However, the most meaningful results are revealed by examining the effects of CRF on specific types of behavior.
Discussion
Trout treated icv with either of two doses CRF tended to win aggressive interactions when paired with size-matched fish injected icv with saline (Fig. 2). However, the CRF-treated trout did not win all such interactions. Nonetheless, CRF treatment did influence specific behaviors that control the fight outcome, such as total attacks, latency to attack, retreats and ratio of attacks to retreats (Fig. 3, Fig. 4, Fig. 5). Treatment with CRF suppressed plasma cortisol concentrations elevated by the
Conclusion
While icv CRF treatment did influence aggressive interactions, the results may be more easily understood as an effect on anxious and motivated behaviors. The outcome of an aggressive interaction is complex. Central CRF influenced overall attacks, latency to first attack, and retreat behavior, but only in winners. The icv injection procedure is stressful, and stimulated an increase in plasma cortisol, an effect that was suppressed by treatment with icv CRF. Aggressive social interaction had a
Acknowledgments
We would like to thank the Gavin's Point National Fish Hatchery in Yankton, South Dakota for their gracious donation of fish, time and effort, without which this experiment would not have been possible. This work was supported by NIH Grant P20 RR15567, and a South Dakota Board of Regents Fellowship (to R.E.C.).
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2023, Behavioural Brain ResearchCitation Excerpt :These CRF1 receptors are also found in limbic brain regions (including preoptic area, amygdala (Dm and Vc/Vl), hippocampus (Dl), and raphé ) [32,38], such that intracerebroventricular (icv) CRF treatment in rainbow trout stimulates locomotion, anxiogenic behavior, and influences the nature and outcome of aggressive interactions [33,39]. Additionally, while CRF has been demonstrated to elevate anxiety and indecision [21,33,39,40], and to induce a stereotypical behavior, snap shake [21,33,40,41], that is associated with indecision regarding escape, the selective anxiolytic (anxiety reducing) CRF type 1 (CRF1) receptor antagonist Antalarmin not only blocks snap shake, but in doing so appears to facilitate decision-making and faster escape [21]. To investigate the role of CRF1 antagonism directly on learned escape in our Rainbow trout model, both Escape and Stay fish were administered Antalarmin (or saline) orally on day 4 of the 7-day training period.
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2021, Neurobiology of StressCitation Excerpt :Studies in all types of species demonstrate that aggressive interaction promotes stress responses from neuroendocrine systems (Blanchard et al., 1995; Lucas et al., 2004; Monder et al., 1994; Øverli et al., 2004b; Smith et al., 2016; Summers, 2001, 2002; Summers et al., 2005b, 2005c; Summers and Winberg, 2006). Importantly, the activity of those neural and endocrine responses also modifies social aggression (Backström et al., 2011a; Blanchard et al., 2005; Carpenter et al., 2009; Farrokhi et al., 2004; Griebel et al., 1995; Lepage et al., 2005; Øverli et al., 2002a, 2002b; Schjolden et al., 2009; Wall et al., 2004a; Winberg et al., 2001). While the transmitter systems and brain regions active during social interaction/rank development stress are recapitulated in any listing related to aggression, since these two behavioral elements are typically coincidental, there are studies that examine stress responsiveness specifically during aggression.
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2021, Neuroscience and Biobehavioral ReviewsCitation Excerpt :Phenotype commitment occurs at the end of the second day of interaction, allowing us to use days 3 and 4 to test behavioral alterations as a result of pharmacological manipulation. When introducing a single treatment of an Orx1 antagonist (SB-674042) into the BLA of vulnerable mice, behavioral adaptation took place with approximately 65 % of the animals shifting to the resilient phenotype (Yaeger et al., 2020)(Fig. 1), similar to the effect of the CRF1 receptor antagonist antalarmin (Yaeger et al., 2019; Smith et al., 2016b; Carpenter et al., 2009b; Summers et al., 2017). This suggests Orx1 activity within the BLA modulates the development of resilient or susceptible phenotypes.
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2021, Journal of Chemical NeuroanatomyCitation Excerpt :In general, occurrence of GR in both TH and GnRH neurons in the hypothalamic areas indicates an affiliation between cortisol and GnRH/TH activity, whereas existence of a putative binding site for GR in the promoter of DA-D2 receptor gene in the grey mullet (Nocillado et al., 2005) suggests the possibility that GR may regulate DA-D2 receptors during stress. Besides, direct stimulatory influence of CRH treatement on DA content in the POA (Carpenter et al., 2009) also cannot be ruled out. The opioidergic system is well conserved during the course of evolution and is found in invertebrates as well as vertebrates.
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