Neurobiology of Social Behavior

Primate Neuroethology

Volumn , Issue , 2010, Pages

  Maestripieri, Dario ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

Brain lesion studies; Neurobiological regulation; Primates; Social behavior

Indexed keywords

EID: 79954476702     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1093/acprof:oso/9780195326598.003.0019     Document Type: Chapter

References (159)

1. Amaral, D. G. (2002). The primate amygdala and the neurobiology of social behavior: Implications for understanding social anxiety. Biological Psychiatry, 51, 11-17.
2. Amaral, D. G., Capitanio, J. P., Jourdain, M., Mason, W. A., Mendoza, S. P., & Prather, M (2003). The amygdala: Is it an essential component of the neural network for social cognition? Neuropsychologia, 41, 235-240.
3. Aou, S., Oomura, Y., & Yoshimatsu, H. (1988). Neuron activity of the ventromedial hypothalamus and the medial preoptic area of the female monkey during sexual behavior. Brain Research, 455, 65-71.
4. Bachevalier, J., Malkova, L., & Mishkin, M. (2001). Effects of selective neonatal temporal lobe lesions on socioemotional behavior in infant rhesus monkeys (Macaca mulatta). Behavioral Neuroscience, 115, 545-559.
5. Bailey, J. N., Breidenthal, S. E., Jorgensen, M. J., McCracken, J. T., & Fairbanks, L. A. (2007). The association of DRD4 and novelty seeking is found in a nonhuman primate model. Psychiatric Genetics, 17, 23-27.
6. Banki, C. M., & Molnar, G. (1981). Cerebrospinal fluid 5-HIAA as an index of central serotonergic processes. Psychiatry Research, 5, 23-32.
7. Barr, C. S., Newman, T. K., Shannon, C., Parker, C., Dvoskin, R. L., Becker, M. L., et al. (2004b). Rearing condition and rh5-HTTLPR interact to influence limbic-hypothalamicpituitary-adrenal axis response to stress in infant macaques. Biological Psychiatry, 55, 733-738.
8. Barr, C. S., Schwandt, M. L., Lindell, S. G., Higley, J. D., Maestripieri, D., Goldman, D., et al. (2008). Variation at the mu-opioid receptor gene (OPRM1) influences attachment behavior in infant primates. Proceedings of the National Academy of Sciences USA, 105, 5277-5281.
9. Bauman, M. D., Lavenex, P., Mason, W. A., Capitanio, J. P., & Amaral, D. G. (2004). The development of social behavior following neonatal amygdala lesions in rhesus monkeys. Journal of Cognitive Neuroscience, 16, 1388-1411.
10. Bauman, M. D., Toscano, J. E., Mason, W. A., Lavenex, P., Amaral, D. G. (2006). The expression of social dominance following neonatal lesions of the amygdala or hippocampus in rhesus monkeys (Macaca mulatta). Behavioral Neuroscience, 120, 749-760.
11. Bennett, A. J., Lesch, K. P., Heils, A., Long, J. C., Lorenz, J. G., Shoaf, S. E., et al. (2002). Early experience and serotonin transporter gene variation interact to influence primate CNS function. Molecular Psychiatry, 7, 118-122.
12. Boccia, M. L., Goursaud, A. S., Bachevalier, J., Anderson, K. D., & Pedersen, C. A. (2007). Peripherally administered non-peptide oxytocin antagonist, L368,899, accumulates in limbic brain areas: A new pharmacological tool for the study of social motivation in nonhuman primates. Hormones and Behavior, 52, 344-351.
13. Boccia, M. L., Panicker, A. K., Pedersen, C., & Petrusz, P. (2001). Oxytocin receptors in nonhuman primate brain visualized with monoclonal antibody. Neuroreport, 12, 1723-1726.
14. Botchin, M. B., Kaplan, J. R., Manuck, S. B., & Mann, J. J. (1993). Low versus high prolactin responders to fenfluramine challenge: Marker of behavioral differences in adult male cynomolgus macaques. Neuropsychopharmacology, 9, 93-99.
15. Brothers, L. (1996). Brain mechanisms of social cognition. Journal of Psychopharmacology, 10, 2-8.
16. Brown, S., & Schaefer, E. A. (1888). An investigation into the functions of the occipital and temporal lobes of the monkey's brain. Philosophical Transactions of the Royal Society of London Series B, 179, 303-327.
17. Butter, C. M., & Snyder, D. R. (1972). Alterations in aversive and aggressive behaviors following orbital frontal lesions in rhesus monkeys. Acta Neurobiologica Experimentalis, 32, 525-565.
18. Carter, C. S. (1998). Neuroendocrine perspectives on social attachment and love. Psychoneuro-endocrinology, 23, 779-818.
19. Chamberlain, B., Ervin, F. R., Pihl, R. O., & Young, S. N. (1987). The effect of raising of lowering tryptophan levels on aggression in vervet monkeys. Pharmacology, Biochemistry, and Behavior, 28, 503-510.
20. Chambers, K. C., & Phoenix, C. H. (1989). Apomorphine, (-)-deprenyl, and yohimbine fail to increase sexual behavior in rhesus males. Behavioral Neuroscience, 103, 816-823.
21. Champoux, M., Higley, J. D., & Suomi, S. J. (1997). Behavioral and physiological characteristics of Indian and Chinese-Indian hybrid rhesus macaque infants. Developmental Psychobiology, 31, 49-63.
22. Cleveland, A., Westergaard, G. C., Trenkle, M. K., & Higley, J. D. (2004). Physiological predictors of reproductive outcome and mother-infant behaviors in captive rhesus macaque females (Macaca mulatta). Neuropsychopharmacology, 29, 901-910.
23. Cooke, B., Higley, J. D., Shannon, C., Lindell, S. G., Higley, H. M., Suomi, S. J., et al. (1997). Rearing history and CSF oxytocin as predictors of maternal competency in rhesus macaques. American Journal of Primatology, 42, 102.
24. Csiffary, A., Ruttner, Z., Toth, Z., & Palkovits, M. (1992). Oxytocin nerve fibers innervate β-endorphin neurons in the arcuate nucleus of the rat hypothalamus. Neuroendocrinology, 56, 429-435.
25. Depue, R. A., & Morrone-Strupinsky, J. V. (2005). A neurobehavioral model of affiliative bonding: Implications for conceptualizing a human trait of affiliation. Behavioral and Brain Sciences, 28, 313-395.
26. Dicks, D., Myers, R. E., & Kling, A. (1969). Uncus and amygdala lesions: Effects on social behavior in the free ranging rhesus monkey. Science, 165, 69-71.
27. Dix, T. (1991). The affective organization of parenting: Adaptive and maladaptive processes. Psychological Bulletin, 110, 3-25.
28. Dixson, A. F. (1990). Medial hypothalamic lesions and sexual receptivity in the female common marmoset (Callithrix jacchus). Folia Primatologica, 54, 46-56.
29. Dixson, A. F. (1998). Primate sexuality. Oxford: Oxford University Press.
30. Dixson, A. F., & Hastings, M. H. (1992). Effects of ibotenic acid-induced neuronal degeneration in the hypothalamus upon proceptivity and sexual receptivity in the female marmoset. Journal of Neuroendocrinology, 4, 719-726.
31. Dunbar, R. I. M. (1988). Primate social systems. London: Croom Helm.
32. Dunbar, R. I. M. (1992). Neocortex size as a constraint on group size in primates. Journal of Human Evolution, 20, 469-493.
33. Emery, N. J., Capitanio, J. P., Mason, W. A., Machado, C. J., Mendoza, S. P., & Amaral, D. G. (2001). The effects of bilateral lesions of the amygdala on dyadic social interactions in rhesus monkeys (Macaca mulatta). Behavioral Neuroscience, 115, 515-544.
34. Fabre-Nys, C., Meller, R. E., & Keverne, E. B. (1982). Opiate antagonists stimulate affiliative behaviour in monkeys. Pharmacology, Biochemistry, and Behavior, 16, 653-659.
35. Fairbanks, L. A., Fontenot, M. B., Phillips-Conroy, J. E., Jolly, C. J., Kaplan, J. R., & Mann, J. J. (1999). CSF monoamines, age and impulsivity in wild grivet monkeys (Cercopithecus aethiops aethiops). Brain, Behavior, and Evolution, 53, 305-312.
36. Fairbanks, L. A., Jorgensen, M. J., Huff, A., Blau, K., Hung, Y., & Mann, J. J. (2004). Adolescent impulsivity predicts adult dominance attainment in male vervet monkeys. American Journal of Primatology, 64, 1-17.
37. Fairbanks, L. A., Melega, W. P., Jorgensen, M. J., Kaplan, J. R., & McGuire, M. T. (2001). Social impulsivity inversely associated with CSF 5-HIAA and fluoxetine exposure in vervet monkeys. Neuropsychopharmacology, 24, 370-378.
38. Fairbanks, L. A., Melega, W. P., & McGuire, M. T. (1998). CSF 5-HIAA is associated with individual differences in maternal protectiveness in vervet monkeys. American Journal of Primatology, 45, 179-180.
39. Freimer, N. B., Service, S. K., Ophoff, R. A., Jasinska, A. J., Villeneuve, A., Belisle, A., et al. (2007). A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using rference sequences from related species. Proceedings of the National Academy of Sciences USA, 104, 15811-15816.
40. Gimpl, G., & Fahrenholz, F. (2001). The oxytocin receptor system: Structure, function, and regulation. Physiological Reviews, 81, 629-683.
41. Gothard, K. M., Battaglia, F. P., Erickson, C. A., Spitler, K. M., & Amaral, D. G. (2007). Neural responses to facial expression and facial identity in the monkey amygdala. Journal of Neurophysiology, 97, 1671-1683.
42. Goursaud, A. S., & Bachevalier, J. (2007). Social attachment in juvenile monkeys with neonatal lesion of the hippocampus, amygdala and orbital frontal cortex. Behavioral Brain Research, 176, 75-93.
43. Goursaud, A. S., Mendoza, S. P., & Capitanio, J. P. (2006). Do neonatal bilateral ibotenic acid lesions of the hippocampal formation or of the amygdala impair HPA axis responsiveness and regulation in infant rhesus macaques (Macaca mulatta)? Brain Research, 1071, 97-104.
44. Gradwell, P. B., Everitt, B. J., & Herbert, J. (1975). 5-hydroxytryptamine in the central nervous system and sexual receptivity of female rhesus monkeys. Brain Research, 88, 281-293.
45. Grant, K. A., Shively, C. A., Nader, M. A., Ehrenkaufer, R. L., Line, S. W., Morton, T. E., et al. (1998). Effect of social status on striatal dopamine D2 receptor binding characteristics in cynomolgus monkeys assessed with positron emission tomography. Synapse, 29, 80-83.
46. Graves, F. C., Wallen, K., & Maestripieri, D. (2002). Opioids and attachment in rhesus macaque abusive mothers. Behavioral Neuroscience, 116, 489-493.
47. Guard, H. J., Newman, J. D., & Roberts, R. L. (2002). Morphine administration selectively facilitates social play in common marmosets. Developmental Psychobiology, 41, 37-49.
48. Hammock, E. A. D., & Young, L. J. (2005). Micro-satellite instability generates diversity in brain and sociobehavioral traits. Science, 308, 1630-1634.
49. Heinrichs, M., Baumgartner, T., Kirschbaum, C., & Ehlert, U. (2003). Social support and oxytocin interact to suppress cortisol and subjective responses to psychosocial stress. Biological Psychiatry, 54, 1389-1398.
50. Higley, J. D. (2003). Aggression. In: D. Maestripieri (Ed.), Primate psychology (pp. 17-40). Cambridge, MA: Harvard University Press.
51. Higley, J. D., King, S. T., Hasert, M. F., Champoux, M., Suomi, S. J., & Linnoila, M. (1996a). Stability of interindividual differences in serotonin function and its relationship to aggressive wounding and competent social behavior in rhesus macaque females. Neuropsychopharmacology, 14, 67-76.
52. Higley, J. D., Mehlman, P. T., Higley, S. B., Fernald, B., Vickers, S., Lindell, S. G., et al. (1996b). Excessive mortality in young male nonhuman primates with low CSF 5-HIAA concentrations. Archives of General Psychiatry, 53, 537-543.
53. Higley, J. D., Mehlman, P. T., Poland, R. E., Taub, D. M., Vickers, J., Suomi, S. J., et al. (1996c). CSF testosterone and CSF 5-HIAA correlate with different types of aggressive behaviors. Biological Psychiatry, 40, 1067-1082.
54. Higley, J. D., Mehlman, P. T., Taub, D. M., Higley, S. B., Suomi, S. J., Linnoila, M., et al. (1992b). Cerebrospinal fluid monoamine and adrenal correlates of aggression in freeranging rhesus monkeys. Archives of General Psychiatry, 49, 436-441.
55. Higley, J. D., Suomi, S. J., & Linnoila, M. (1991). CSF monoamine metabolite concentrations vary according to age, rearing, and sex, and are influenced by the stressor of social separation in rhesus monkeys. Psychopharmacology, 103, 551-556.
56. Higley, J. D., Suomi, S. J., & Linnoila, M. (1992a). A longitudinal assessment of CSF monoamine metabolite and plasma cortisol concentrations in young rhesus monkeys. Biological Psychiatry, 32, 127-145.
57. Higley, J. D., Thompson, W. W., Champoux, M., Goldman, D., Hasert, M. F., Kraemer, G. W., et al. (1993). Paternal and maternal genetic and environmental contributions to cerebrospinal fluid monoamine metabolites in rhesus monkeys (Macaca mulatta). Archives of General Psychiatry, 50, 615-623.
58. Holman, S. D., & Goy, R. W. (1995). Experiential and hormonal correlates of care-giving in rhesus macaques. In: C. R. Pryce, R. D. Martin, & D. Skuse (Eds.), Motherhood in Human and Nonhuman Primates. Biosocial Determinants (pp. 87-93). Basel: Karger.
59. Howell, S., Westergaard, G., Hoos, B., Chavanne, T. J., Shoaf, S. E., Cleveland, A., et al. (2007). Serotonergic influences on life-history outcomes in free-ranging male rhesus macaques. American Journal of Primatology, 69, 1-15.
60. Insel, T. R. (1992). Oxytocin and the neurobiology of attachment. Behavioral and Brain Sciences, 15, 515-516.
61. Insel, T. R., & Winslow, J. T. (1998). Serotonin and neuropeptides in affiliative behaviors. Biological Psychiatry, 44, 207-219.
62. Kalin, N. H., Shelton, S. E., & Barksdale, C. M. (1988). Opiate modulation of separationinduced distress in non-human primates. Brain Research, 440, 285-292.
63. Kalin, N. H., Shelton, S. E., & Lynn, D. E. (1995). Opiate systems in mother and infant primates coordinate intimate contact during reunion. Psychoneuroendocrinology, 20, 735-742.
64. Kaplan, J. R., Fontenot, M. B., Berard, J. D., Manuck, S. B., & Mann, J. J. (1995). Delayed dispersal and elevated monoaminergic activity in free-ranging rhesus monkeys. American Journal of Primatology, 35, 229-234.
65. Kaplan, J. R., Phillips-Conroy, J., Fontenot, M. B., Jolly, C. J., Fairbanks, L. A., & Mann, J. J. (1999). Cerebrospinal fluid monoaminergic metabolites differ in wild anubis and hybrid (Anubis hamadryas) baboons: Possible relationships to life history and behavior. Neuropsychopharmacology, 20, 517-524.
66. Kaplan, J. R., Manuck, S. B., Fontenot, B., & Mann, J. J. (2002). Central nervous system monoamine correlates of social dominance in cynomolgus monkeys (Macaca fascicularis). Neuropsychopharmacology, 26, 431-443.
67. Kendrick, K. M., & Dixson, A. F. (1986). Anteromedial hypothalamic lesions block proceptivity but not receptivity in the female common marmoset (Callithrix jacchus). Brain Research, 375, 221-229.
68. Keverne, E. B., Martensz, N. D., & Tuite, B. (1989). β-endorphin concentrations in cerebrospinal fluid of monkeys are influenced by grooming relationships. Psychoneuroendocrinology, 14, 155-161.
69. Kling, A., & Brothers, L. A. (1992). The amygdala and social behavior. In: J. Aggleton (Ed.), The amygdala: Neurobiological aspects of emotion, memory, and mental dysfunction (pp. 353-377). New York: Wiley-Liss..
70. Kling, A., & Cornell, R. (1971). Amygdalectomy and social behavior in the caged stumptailed macaque (Macaca speciosa). Folia Primatologica, 14, 190-208.
71. Kling, A., Lancaster, J., & Benitone, J. (1970). Amygdalectomy in the free-ranging vervet (Cercopithecus aethiops). Journal of Psychiatric Research, 7, 191-199.
72. Kling, A., & Steklis, H. D. (1976). A neural substrate for affiliative behavior in nonhuman primates. Brain, Behavior, and Evolution, 13, 216-238.
73. Kluver, H., & Bucy, P. C. (1937). "Psychic blindness" and other symptoms following bilateral temporal lobectomy in rhesus monkeys. American Journal of Physiology, 119, 352-353.
74. Kluver, H., & Bucy, P. C. (1939). Preliminary analysis of functions of the temporal lobes in monkeys. Archives of Neurology and Psychiatry, 42, 979-1000.
75. Koyama, Y., Fujita, I., Aou, S., & Oomura, Y. (1988). Proceptive presenting elicited by electrical stimulation of the female monkey hypothalamus. Brain Research, 446, 199-203.
76. Kozorovitskiy, Y., Hughes, M., Lee, K., & Gould, E. (2006). Fatherhood affects dendritic spines and vasopressin V1a receptors in the primate prefrontal cortex. Nature Neuroscience, 9, 1094-1095.
77. Kraemer, G. W. (1992). A psychobiological theory of attachment. Behavioral and Brain Sciences, 15, 493-451.
78. Kraemer, G. W., Ebert, M. H., Schmidt, D. E., & McKinney, W. T. (1989). A longitudinal study of the effect of different social rearing conditions on cerebrospinal fluid norepinephrine and biogenic amine metabolites in rhesus monkeys. Neuropsychopharmacology, 2, 175-189.
79. Kyes, R. C., Botchin, M. B., Kaplan, J. R., Manuck, S. B., & Mann, J. J. (1995). Aggression and brain serotonergic responsivity: Response to slides in male macaques. Physiology and Behavior, 57, 205-208.
80. Lesch, K. P., Bengel, D., Heils, A., Sabol, S. Z., Greenberg, B. D., Petri, S., et al. (1996). Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science, 274, 1527-1531.
81. Lindell, S. G., Higley, J. D., Shannon, C., & Linnoila, M. (1997). Low levels of CSF 5-HIAA in female rhesus macaques predict mother-infant interaction patterns and mother's CSF 5-HIAA correlates with infant's CSF 5-HIAA. American Journal of Primatology, 2, 129.
82. Maestripieri, D. (1993a). Maternal anxiety in rhesus macaques (Macaca mulatta). I. Measurement of anxiety and identification of anxiety-eliciting situations. Ethology, 95, 19-31.
83. Maestripieri, D. (1993b). Maternal anxiety in rhesus macaques (Macaca mulatta). II. Emotional bases of individual differences in mothering style. Ethology, 95, 32-42.
84. Maestripieri, D. (1994). Infant abuse associated with psychosocial stress in a group-living pigtail macaque (Macaca nemestrina) mother. American Journal of Primatology, 32, 41-49.
85. Maestripieri, D. (1999). The biology of human parenting: Insights from nonhuman primates. Neuroscience and Biobehavioral Reviews, 23, 411-422.
86. Maestripieri, D. (2005). Early experience affects the intergenerational transmission of infant abuse in rhesus monkeys. Proceedings of the National Academy of Sciences USA, 102, 9726-9729.
87. Maestripieri, D. (2008). The role of the brain serotonergic system in the origin and transmission of adaptive and maladaptive variations in maternal behavior in rhesus macaques. In: R. Bridges (Ed.), Neurobiology of the parental brain (pp. 163-173). Amsterdam: Elsevier.
88. Maestripieri, D., Higley, J. D., Lindell, S. G., Newman, T. K., McCormack, K. M., & Sanchez,M. M. (2006a). Early maternal rejection affects the development of monoaminergic systems and adult abusive parenting in rhesus macaques. Behavioral Neuroscience, 120, 1017-1024.
89. Maestripieri, D., Lindell, S. G., Ayala, A., Gold, P. W., & Higley, J. D. (2005). Neurobiological characteristics of rhesus macaque abusive mothers and their relation to social and maternal behavior. Neuroscience and Biobehavioral Reviews, 29, 51-57.
90. Maestripieri, D., Lindell, S. G., & Higley, J. D. (2007). Intergenerational transmission of maternal behavior in rhesus monkeys and its underlying mechanisms. Developmental Psychobiology, 49, 165-171.
91. Maestripieri, D., McCormack, K. M., Lindell, S. G., Higley, J. D., & Sanchez, M. M. (2006b). Influence of parenting style on the offspring's behavior and CSF monoamine metabolite levels in crossfostered and noncrossfostered female rhesus macaques. Behavioral Brain Research, 175, 90-95.
92. Maestripieri, D., Schino, G., Aureli, F., & Troisi, A. (1992). A modest proposal: Displacement activities as an indicator of emotions in primates. Animal Behaviour, 44, 967-979.
93. Manuck, S. B., Kaplan, J. R., & Lotrich, F. E. (2006). Brain serotonin and aggressive disposition in humans and nonhuman primates. In: R. J. Nelson (Ed.), Biology of aggression (pp. 65-113). Oxford: Oxford University Press.
94. Manuck, S. B., Kaplan, J. R., Rymeski, B. A., Fairbanks, L. A., & Wilson, M. E. (2003). Approach to a social stranger is associated with low central nervous system serotonergic responsivity in female cynomolgus monkeys (Macaca fascicularis). American Journal of Primatology, 61, 187-194.
95. Martel, F. L., Nevison, C. M., Rayment, F. D., Simpson, M. J. A., & Keverne, E. B. (1993). Opioid receptor blockade reduces maternal affect and social grooming in rhesus monkeys. Psychoneuroendocrinology, 18, 307-321.
96. Martel, F. L., Nevison, C. M., Simpson, M. J. A., & Keverne, E. B. (1995). Effects of opioid receptor blockade on the social behavior of rhesus monkeys living in large family groups. Developmental Psychobiology, 28, 71-84.
97. Martensz, N. D., Vellucci, S. V., Keverne, E. B., & Herbert, J. (1986). β-endorphins levels in the cerebrospinal fluid of male talapoin monkeys in social groups related to dominance status and the luteinizing hormone response to naloxone. Neuroscience, 18, 651-658.
98. Mason, W. A., Capitanio, J. P., Machado, C. J., Mendoza, S. P., & Amaral, D. G. (2006). Amygdalectomy and responsiveness to novelty in rhesus monkeys (Macaca mulatta): Generality and individual consistency of effects. Emotion, 6, 73-81.
99. McCormack, K., Newman, T. K., Higley, J. D., Maestripieri, D., & Sanchez, M. M.'(2009). Serotonin transporter gene variation, infant abuse, and responsiveness to stress in rhesus acaque mothers and infants. Hormones and Behavior, 55, 538-547.
100. Mehlman, P. T., Higley, J. D., Faucher, I., Lilly, A. A., Taub, D. M., Suomi, S. J., et al. (1994). Low CSF 5-HIAA concentrations and severe aggression and impaired impulse control in nonhuman primates. American Journal of Psychiatry, 151, 1485-1491.
101. Mehlman, P. T., Higley, J. D., Faucher, I., Lilly, A. A., Taub, D. M., Vickers, J. H., et al. (1995). Correlation of CSF 5-HIAA concentrations with sociality and the timing of emigration in free-ranging primates. American Journal of Psychiatry, 152, 907-913.
102. Mehlman, P. T., Higley, J. D., Fernald, B. J., Sallee, F. R., Suomi, S. J., & Linnoila, M. (1997). CSF 5-HIAA, testosterone, and sociosexual behaviors in free-ranging male rhesus macaques in the mating season. Psychiatry Research, 72, 89-102.
103. Meller, R. E., Keverne, E. B., & Herbert, J. (1980). Behavioural and endocrine effects of naltrexone in male talapoin monkeys. Pharmacology, Biochemistry, and Behavior, 13, 663-672.
104. Miczek, K. A., & Fish, E. W. (2006). Monoamines, GABA, glutamate, and aggression. In: R. J. Nelson (Ed.), Biology of aggression (pp. 114-149). Oxford: Oxford University Press.
105. Miczek, K. A., Woolley, J., Schlisserman, S., & Yoshimura, H. (1981). Analysis of amphetamine effects on agonistic and affiliative behavior in squirrel monkeys (Saimiri sciureus). Pharmacology, Biochemistry, and Behavior, 14, 103-107.
106. Nelson, E., & Panksepp, J. (1998). Brain substrates of infant-mother attachment: Contributions of opioids, oxytocin, and norepinephrine. Neuroscience and Biobehavioral Reviews, 22, 437-452.
107. Numan, M., & Insel, T. R. (2003). The neurobiology of parental behavior. Berlin: Springer.
108. Panksepp, J., Herman, B. H., Vilberg, T., Bishop, P., & DeEskinazi, F. G. (1980). Endogenous opioids and social behavior. Neuroscience and Biobehavioral Reviews, 4, 473-487.
109. Panksepp, J., Nelson, E., & Bekkedal, M. (1999). Brain systems for the mediation of social separation-distress and social-reward: Evolutio-nary antecedents and neuropeptide intermedi-aries. In: C. S. Carter, I. I. Lederhendler, & B. Kirkpatrick (Eds.), The integrative neurobiology of affiliation (pp. 221-243). Cambridge, MA: MIT Press.
110. Parker, K. J., Buckmaster, C. L., Schatzberg, A. F., & Lyons, D. M. (2005). Intranasal oxytocin administration attenuates the ACTH stress response in monkeys. Psychoneuroendocrinology, 30, 924-929.
111. Pomerantz, S. M. (1990). Apomorphine facilitates male sexual behavior of rhesus monkeys. Pharmacology, Biochemistry, and Behavior, 35, 659-664.
112. Pomerantz, S. M. (1991). Quinelorane (LY163502), a D2 dopamine receptor agonist, acts centrally to facilitate penile erections of male rhesus monkeys. Pharmacology, Biochemistry, and Behavior, 39, 123-128.
113. Pomerantz, S. M., Hepner, B. C., & Wertz, J. M. (1991). 5-HT1A and 5-HT1C/1D receptor agonists produce reciprocal effects on male sexual behavior of rhesus monkeys. European Journal of Pharmacology, 243, 227-234.
114. Prather, M. D., Lavenex, P., Mauldin-Jordan, M. L., Mason, W. A., Capitanio, J. P.,Mendoza, S. P., et al. (2001). Increased social fear and decreased fear of objects in monkeys with neonatal amygdala lesions. Neuroscience, 106, 653-658.
115. Pryce, C. R. (1992). A comparative systems model of the regulation of maternal motivation in mammals. Animal Behaviour, 43, 417-441.
116. Raleigh, M. J., Brammer, G. L., Yuwiler, A., Flannery, J. W., & McGuire, M. T. (1980). Serotonergic influences on the social behavior of vervet monkeys (Cercopithecus aethiops sabaeus). Experimental Neurology, 68, 322-334.
117. Raleigh, M. J., Brammer, G. L., & McGuire, M. T. (1983). Male dominance, serotonergic systems, and the behavioral and physiological effects of drugs in vervet monkeys (Cercopithecus aethiops sabaeus). In: K. A. Miczek (Ed.), Ethopharmacology: Primate models of neuropsychiatric disorders (pp. 185-197). New York: Alan R. Liss.
118. Raleigh, M. J., Brammer, G. L., McGuire, M. T., & Yuwiler, A. (1985). Dominant social status facilitates behavioral effects of serotonergic agonists. Brain Research, 348, 274-282.
119. Raleigh, M. J., Brammer, G. L., Ritvo, E. R., Geller, E., McGuire, M. T., & Yuwiler, A. (1986). Effects of chronic fenfluramine on blood serotonin, cerebrospinal fluid metabolites, and behavior in monkeys. Psychopharmacology, 90, 503-508.
120. Raleigh, M. J., & McGuire, M. T. (1986). Animal analogues of ostracism: Biological mechanisms and social consequences. Ethology and Sociobiology, 7, 53-66.
121. Raleigh, M. J., & McGuire, M. T. (1990). Social influences on endocrine function in male vervet monkeys. In: T. E. Ziegler & F. B. Bercovitch (Eds.), Socioendocrinology of primate reproduction (pp. 95-111). New York: Wiley-Liss.
122. Raleigh, M. J., McGuire, M. T., Brammer, G. L., Pollack, D. B., & Yuwiler, A. (1991). Serotonergic mechanisms promote dominance acquisition in adult male vervet monkeys. Brain Research, 559, 181-190.
123. Raleigh, M. J., & Steklis, H. D. (1981). Effects of orbital frontal and temporal neocortical lesions on affiliative behavior of vervet monkeys (Cercopithecus aethiops sabaeus). Experimental Neurology, 73, 378-389.
124. Rendall, D., & Di Fiore, A. (1995). The road less traveled: Phylogenetic perspectives in primatology. Evolutionary Anthropology, 4, 43-52.
125. Rilling, J. K., & Insel, T. R. (1999). The primate neocortex in comparative perspective using magnetic resonance imaging. Journal of Human Evolution, 37, 191-223.
126. Rilling, J. K., Sanfey, A. G., Nystrom, L. E., Cohen, J. D., Gutman, D. A., Zeh, T. R., et al. (2004b). Imaging the social brain with fMRI and interactive games. International Journal of Neuropsychopharmacology, 7, S477-S478.
127. Rilling, J. K., Winslow, J. T., & Kilts, C. D. (2004a). The neural correlates of mate competition in dominant male rhesus macaques. Biological Psychiatry, 56, 364-375.
128. Rilling, J. K., Winslow, J. T., O'Brien, D., Gutman, D. A., Hoffman, J. M., & Kilts, C. D. (2001). Neural correlates of maternal separation in rhesus monkeys. Biological Psychiatry, 49, 146-157.
129. Rogers, J., Martin, L. J., Comuzzie, A. G., Mann, J. J., Manuck, S. B., Leland, M., et al. (2004). Genetics of monoamine metabolites in baboons: Overlapping sets of genes influence levels of 5-hydroxyindolacetic acid, 3-hydroxy-4-methoxyphenylglycol, and homovanillic acid. Biological Psychiatry, 55, 739-744.
130. Rosenblum, L. A., Smith, E. L. P., Altemus, M., Scharf, B. A., Owens, M. J., Nemeroff, C. B., et al. (2002). Differing concentrations of corticotropin-releasing factor and oxytocin in the cerebrospinal fluid of bonnet and pigtail macaques. Psychoneuroendocrinology, 27, 651-660.
131. Rosvold, H. E., Mirsky, A. F., & Pribram, K. H. (1954). Influence of amygdalectomy on social behavior in monkeys. Journal of Comparative Physiology and Psychology, 47, 173-178.
132. Schino, G., & Troisi, A. (1992). Opiate receptor blockade in juvenile macaques: Effect on affiliative interactions with their mothers and group companions. Brain Research, 576, 125-130.
133. Schino, G., Troisi, A., Perretta, G., & Monaco, V. (1991). Measuring anxiety in nonhuman primates: Effect of lorazepam on macaque scratching. Pharmacology, Biochemistry, and Behavior, 38, 889-891.
134. Schwandt, M. L., Howell, S., Bales, K., Jaffe, B. D., Westergaard, G. C., & Higley, J. D. (2007). Associations between the neuropeptides oxytocin and vasopressin and the behavior of free-ranging female rhesus macaques (Macaca mulatta). American Journal of Physical Anthropology Supplement, 44, 210-211.
135. Shannon, C., Schwandt, M. L., Champoux, M., Shoaf, S. E., Suomi, S. J., Linnoila, M., et al. (2005). Maternal absence and stability of individual differences in CSF 5-HIAA concentrations in rhesus monkey infants. American Journal of Psychiatry, 162, 1658-1664.
136. Sheese, B. E., Voelker, P. M., Rothbart, M. K., & Posner, M. I. (2007). Parenting quality interacts with genetic variation in dopamine receptor D4 to influence temperament in early childhood. Development and Psychopathology, 19, 1039-1046.
137. Shively, C. A. (1998). Social subordination stress, behavior, and central monoaminergic function in female cynomolgus monkeys. Biological Psychiatry, 44, 882-891.
138. Shively, C. A., Fontenot, B., & Kaplan, J. R. (1995). Social status, behavior, and central serotonergic responsivity in female cynomolgus monkeys. American Journal of Primatology, 37, 333-350.
139. Skuse, D. (2006). Genetic influences on the neural basis on social cognition. Philosophical Transactions of the Royal Society of London Series B, 361, 2129-2141.
140. Smith, E. O., & Byrd, L. D. (1983). Studying the behavioral effects of drugs in group-living nonhuman primates. In: K. A. Miczek (Ed.), Ethopharmacology: Primate models of neuropsychiatric disorders (pp. 1-31). New York: Alan Liss.
141. Smuts, B. B., Cheney, D. L., Seyfarth, R. M., Wrangham, R. W., & Struhsaker, T. T. (Eds.). (1987). Primate societies. Chicago: University of Chicago Press.
142. Snowdon, C. T., Ziegler, T. E., Schultz-Darken, N. J., & Ferris, C. F. (2006). Social odours, sexual arousal and pairbonding in primates. Philosophical Transactions of the Royal Society of London Series B, 361, 2079-2089.
143. Spies, H. G., Norman, R. L., Clifton, D. K., Ochsner, A. J., Jensen, J. N., & Phoenix, C. H. (1976). Effects of bilateral amygdaloid lesions on gonadal hormones in serum and on sexual behavior in female rhesus monkeys. Physiology and Behavior, 17, 985-992.
144. Thierry, B., Singh, M., & Kaumanns, W. (Eds.). (2004). Macaque societies: A model for the evolution of social organization. Cambridge: Cambridge University Press.
145. Toloczko, D. M., Young, L., & Insel, T. R. (1997). Are there oxytocin receptors in the primate brain? Annals of the New York Academy of Sciences, 807, 506-509.
146. Trefilov, A., Berard, J., Krawczak, M., & Schmidtke, J. (2000). Natal dispersal in rhesus macaques is related to serotonin transporter gene promoter variation. Behaviour Genetics, 30, 295-301.
147. Troisi, A., & D'Amato, F. R. (1991). Anxiety in the pathogenesis of primate infant abuse: A pharmacological study. Psychopharmacology, 103, 571-572.
148. Uvnas-Moberg, K. (1998). Oxytocin may mediate the benefits of positive social interaction and emotions. Psychoneuroendocrinology, 23, 819-835.
149. Wallen, K. (1990). Desire and ability: Hormones and the regulation of female sexual behavior. Neuroscience and Biobehavioral Reviews, 14, 233-241.
150. Way, B. M., Lacan, G., Fairbanks, L. A., & Melega, W. P. (2007). Architectonic distribution of the serotonin transporter within the orbitofrontal cortex of the vervet monkey. Neuroscience, 148, 937-948.
151. Wendland, J. R., Lesch, K. P., Newman, T. K., Timme, A., Gachot-Neveu, H., Thierry, B., et al. (2005). Differential functional variability of serotonin transporter and monoamine oxidase A genes in macaque species displaying contrasting levels of aggression-related behavior. Behaviour Genetics, 36, 163-172.
152. Wester, P., Bergstrom, U., Eriksson, A., Gezelius, C., Hardy, J., & Winblad, B. (1990). Ventricular cerebrospinal fluid monoamine transmitter and metabolic concentrations reflect human brain neurochemistry in autopsy cases. Journal of Neurochemistry, 54, 1148-1156.
153. Westergaard, G. C., Mehlman, P. T., Shoaf, S. E., Suomi, S. J., & Higley, J. D. (1999). CSF 5-HIAA and aggression in female macaque monkeys: Species and individual differences. Psychopharmacology, 145, 440-446.
154. Westergaard, G. C., Suomi, S. J., Chavanne, T. J., Houser, L., Hurley, A., Cleveland, A., et al. (2003). Physiological correlates of aggression and impulsivity in free-ranging female primates. Neuropsychopharmacology, 28, 1045-1055.
155. Winslow, J. T. (2005). Neuropeptides and non-human primate social deficits associated with pathogenic rearing experience. International Journal of Developmental Neuroscience, 23, 245-251.
156. Winslow, J. T., & Insel, T. R. (1991). Social status in pairs of male squirrel monkeys determines the behavioral response to central oxytocin adminis-tration. Journal of Neuroscience, 11, 2032-2038.
157. Winslow, J. T., Noble, P. L., Lyons, C. K., Sterk, S. M., & Insel, T. R. (2003). Rearing effects on cerebrospinal fluid oxytocin concentration on social buffering in rhesus monkeys. Neuropsychopharmacology, 28, 910-918.
158. Yodyingyuad, U., de La Riva, C., Abbott, D. H., Herbert, J., & Keverne, E. B. (1985). Relationship between dominance hierarchy, cerebrospinal fluid levels of amine transmitter metabolites (5-hydroxy-indoleacetic acid and homovanillic acid) and plasma cortisol levels in monkeys. Neuroscience, 16, 851-858.
159. Young, L. J. (2002). The neurobiology of social recognition, approach, and avoidance. Biological Psychiatry, 51, 18-26.