Academic literature on the topic 'Emotions. Rhesus monkey'

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Journal articles on the topic "Emotions. Rhesus monkey"

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Xiao, D. "Pathways for emotions and memory I. Input and output zones linking the anterior thalamic nuclei with prefrontal cortices in the rhesus monkey." Thalamus & Related Systems 2, no. 1 (December 2002): 21–32. http://dx.doi.org/10.1016/s1472-9288(02)00031-6.

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Xiao, D., and H. Barbas. "Pathways for emotions and memory I. Input and output zones linking the anterior thalamic nuclei with prefrontal cortices in the rhesus monkey." Thalamus and Related Systems 2, no. 01 (December 2002): 21. http://dx.doi.org/10.1017/s1472928802000316.

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Xiao, D. "Pathways for emotions and memory II. Afferent input to the anterior thalamic nuclei from prefrontal, temporal, hypothalamic areas and the basal ganglia in the rhesus monkey." Thalamus & Related Systems 2, no. 1 (December 2002): 33–48. http://dx.doi.org/10.1016/s1472-9288(02)00030-4.

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Xiao, D., and H. Barbas. "Pathways for emotions and memory II. Afferent input to the anterior thalamic nuclei from prefrontal, temporal, hypothalamic areas and the basal ganglia in the rhesus monkey." Thalamus and Related Systems 2, no. 01 (December 2002): 33. http://dx.doi.org/10.1017/s1472928802000304.

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Raper, Jessica, Maria C. Alvarado, Kathy L. Murphy, and Mark G. Baxter. "Multiple Anesthetic Exposure in Infant Monkeys Alters Emotional Reactivity to an Acute Stressor." Anesthesiology 123, no. 5 (November 1, 2015): 1084–92. http://dx.doi.org/10.1097/aln.0000000000000851.

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Abstract Background Retrospective studies in humans have shown a higher prevalence of learning disabilities in children that received multiple exposures to general anesthesia before the age of 4 yr. Animal studies, primarily in rodents, have found that postnatal anesthetic exposure causes neurotoxicity and neurocognitive deficits in adulthood. The authors addressed the question of whether repeated postnatal anesthetic exposure was sufficient to cause long-term behavioral changes in a highly translationally relevant rhesus monkey model, allowing study of these variables against a background of protracted nervous system and behavioral development. Methods Rhesus monkeys of both sexes underwent either three 4-h exposures to sevoflurane anesthesia (anesthesia group n = 10) or brief maternal separations (control group n = 10) on postnatal day 6 to 10 that were repeated 14 and 28 days later. Monkeys remained with their mothers in large social groups at all times except for overnight observation after each anesthetic/control procedure. At 6 months of age, each monkey was tested on the human intruder paradigm, a common test for emotional reactivity in nonhuman primates. Results The frequency of anxiety-related behaviors was significantly higher in monkeys that were exposed to anesthesia as neonates as compared with controls: anesthesia 11.04 ± 1.68, controls 4.79 ± 0.77, mean ± SEM across all stimulus conditions. Conclusion Increased emotional behavior in monkeys after anesthesia exposure in infancy may reflect long-term adverse effects of anesthesia.
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Izquierdo, Alicia, and Elisabeth A. Murray. "Combined Unilateral Lesions of the Amygdala and Orbital Prefrontal Cortex Impair Affective Processing in Rhesus Monkeys." Journal of Neurophysiology 91, no. 5 (May 2004): 2023–39. http://dx.doi.org/10.1152/jn.00968.2003.

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The amygdala and orbital prefrontal cortex (PFo) interact as part of a system for affective processing. To assess whether there is a hemispheric functional specialization for the processing of emotion or reward or both in nonhuman primates, rhesus monkeys ( Macaca mulatta) with combined lesions of the amygdala and PFo in one hemisphere, either left or right, were compared with unoperated controls on a battery of tasks that tax affective processing, including two tasks that tax reward processing and two that assess emotional reactions. Although the two operated groups did not differ from each other, monkeys with unilateral lesions, left and right, showed altered reward-processing abilities as evidenced by attenuated reinforcer devaluation effects and an impairment in object reversal learning relative to controls. In addition, both operated groups showed blunted emotional reactions to a rubber snake. By contrast, monkeys with unilateral lesions did not differ from controls in their responses to an unfamiliar human (human “intruder”). Although the results provide no support for a hemispheric specialization of function, they yield the novel finding that unilateral lesions of the amygdala-orbitofrontal cortical circuit in monkeys are sufficient to significantly disrupt affective processing.
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Laine, Christopher M., Kevin M. Spitler, Clayton P. Mosher, and Katalin M. Gothard. "Behavioral Triggers of Skin Conductance Responses and Their Neural Correlates in the Primate Amygdala." Journal of Neurophysiology 101, no. 4 (April 2009): 1749–54. http://dx.doi.org/10.1152/jn.91110.2008.

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The amygdala plays a crucial role in evaluating the emotional significance of stimuli and in transforming the results of this evaluation into appropriate autonomic responses. Lesion and stimulation studies suggest involvement of the amygdala in the generation of the skin conductance response (SCR), which is an indirect measure of autonomic activity that has been associated with both emotion and attention. It is unclear if this involvement marks an emotional reaction to an external stimulus or sympathetic arousal regardless of its origin. We recorded skin conductance in parallel with single-unit activity from the right amygdala of two rhesus monkeys during a rewarded image viewing task and while the monkeys sat alone in a dimly lit room, drifting in and out of sleep. In both experimental conditions, we found similar SCR-related modulation of activity at the single-unit and neural population level. This suggests that the amygdala contributes to the production or modulation of SCRs regardless of the source of sympathetic arousal.
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Patterson, Amanda, Jessica Taubert, Reza Azadi, Susan G. Wardle, Arash Afraz, and Leslie G. Ungerleider. "Emotional valence mediates attention to illusory facial features in rhesus monkeys." Journal of Vision 20, no. 11 (October 20, 2020): 1329. http://dx.doi.org/10.1167/jov.20.11.1329.

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Arce, Marilyn, Vasiliki Michopoulos, Kathryn N. Shepard, Quynh-Chau Ha, and Mark E. Wilson. "Diet choice, cortisol reactivity, and emotional feeding in socially housed rhesus monkeys." Physiology & Behavior 101, no. 4 (November 2010): 446–55. http://dx.doi.org/10.1016/j.physbeh.2010.07.010.

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Nakayama, Katsura, Shunji Goto, Koji Kuraoka, and Katsuki Nakamura. "Decrease in nasal temperature of rhesus monkeys (Macaca mulatta) in negative emotional state." Physiology & Behavior 84, no. 5 (April 2005): 783–90. http://dx.doi.org/10.1016/j.physbeh.2005.03.009.

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Dissertations / Theses on the topic "Emotions. Rhesus monkey"

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King, Hanna M. "The Effects of Testosterone on Emotional Processing in Male Rhesus Monkeys (Macaca Mulatta)." 2010. https://scholarworks.umass.edu/theses/534.

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The effects of testosterone (T) extend beyond reproductive behavior to the areas of cognitive and emotional functioning. While T effects on cognition have been extensively investigated, less is known about the role of T in the processing of emotional stimuli. Considering the role that T plays in aggressive behavior and dominance status, it is of particular interest to determine whether T modulates the processing of social threat. Due to their similarities to humans in brain organization, reproductive endocrinology and affective regulation, rhesus monkeys (macaca mulatta) provide an excellent model to investigate this relationship. In a within-subjects design, six male rhesus monkeys underwent treatment to suppress endogenous T and received either T or oil replacement. Tests of anxiety, attention and memory for social and non-social emotional stimuli, and risk-taking were administered to animals during both treatments. Data analyses indicate that T treatment resulted in faster response times, but had no effect on anxiety, attention or memory for emotional stimuli, or on risk-taking behavior. There are several limitations to this study that may account for the lack of effect of T and therefore, further investigation of the relationship between T and emotional processing is warranted.
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Erlanger, Pamela. "The effect of prenatal alcohol exposure on emotion regulation during maternal separation in rhesus monkeys." 1999. http://catalog.hathitrust.org/api/volumes/oclc/43981943.html.

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Thesis (M.S.)--University of Wisconsin--Madison, 1999.
Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 62-70).
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Book chapters on the topic "Emotions. Rhesus monkey"

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Michopoulos, Vasiliki. "Emotional Eating in Socially Subordinate Female Rhesus Monkeys." In Developments in Primatology: Progress and Prospects, 141–58. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30872-2_7.

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Suomi, Stephen J. "Early Stress and Adult Emotional Reactivity in Rhesus Monkeys." In Novartis Foundation Symposia, 171–88. Chichester, UK: John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470514047.ch11.

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Michopoulos, Vasiliki, Carla Moore, and Mark E. Wilson. "Psychosocial Stress and Diet History Promote Emotional Feeding in Female Rhesus Monkeys." In Neuromethods, 109–25. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-104-2_8.

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Michopoulos, Vasiliki, Kelly Ethun, and Mark E. Wilson. "Psychosocial Stress and Dietary Environment Promote Emotional Feeding in Female Rhesus Monkeys." In Neuromethods, 95–114. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0924-8_6.

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Kalin, Ned H., and Steven E. Shelton. "The Regulation of Defensive Behaviors in Rhesus Monkeys." In Anxiety, Depression, and Emotion, 50–68. Oxford University Press, 2000. http://dx.doi.org/10.1093/acprof:oso/9780195133585.003.0003.

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"The Development of Affect in Rhesus Monkeys." In The Psychobiology of Affective Development (PLE: Emotion), 135–76. Psychology Press, 2014. http://dx.doi.org/10.4324/9781315745695-10.

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