Structure and expression of the mouse oxytocin receptor gene. Mating alters topography and content of oxytocin immunoreactivity in male mouse brain. Jirikowski, G.F., Caldwell, J.D., Haussler, H.U. Olfactory bulb norepinephrine depletion abolishes vasopressin and oxytocin preservation of social recognition responses in rats. Endogenous oxytocin is involved in short-term olfactory memory in female rats. Oxytocin but not vasopressin facilitates social recognition following injection into the medial preoptic area of the rat brain. Vasopressin, gonadal steroids and social recognition. Modulation of social memory in male rats by neurohypophyseal peptides. Neurohypophyseal peptides and social recognition in rats. Oxytocin, vasopressin, and the neuroendocrine basis of pair bond formation. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) disrupts social memory/recognition processes in the male mouse.
Cholinergic modulation of a decrement in social investigation following repeated contacts between mice. Social and individual recognition in rodents: methodological aspects and neurobiological bases. Jr Persistence of social investigatory behavior in the male rat: Evidence for long-term memory of initial copulatory experience. Neural control of maternal behaviour and olfactory recognition of offspring. Our data indicate that OT is necessary for the normal development of social memory in mice and support the hypothesis that social memory has a neural basis distinct from other forms of memory. Treatment with OT but not AVP rescued social memory in Oxt −/− mice, and treatment with an OT antagonist produced a social amnesia-like effect in Oxt +/+ mice. Spatial memory and behavioural inhibition measured in a Morris water-maze, Y-maze, or habituation of an acoustic startle also seemed intact. Measurement of both olfactory foraging and olfactory habituation tasks indicated that olfactory detection of non-social stimuli is intact in Oxt −/− mice. We found that male mice mutant for the oxytocin gene ( Oxt −/−) failed to develop social memory, whereas wild-type ( Oxt +/+) mice showed intact social memory. Pharmacological studies indicate that AVP administration may enhance social memory 8, 9, 10, whereas OT administration may either inhibit or facilitate social memory depending on dose, route or paradigm 1, 11, 12, 13.
Brain oxytocin (OT) and vasopressin (AVP) seem to modulate a range of social behaviour from parental care to mate guarding 7. Researchers have operationally defined this memory by a reliable decrease in olfactory investigation in repeated or prolonged encounters with a conspecific 3, 4, 5, 6. Building on the theory of memory making and its role in reconciliation, the paper sketches a typology of postnational citizenship that encourages more flexible forms of belonging.The development of social familiarity in rodents depends predominantly on olfactory cues and can critically influence reproductive success 1, 2. Conversely, memories that are rejected as unimportant or unworthy silence the groups and individuals for whom those memories are cosmopolitan and outward looking and simultaneously displays evidence of exclusionary nationalism which negates collective momories of minority groups such as Aboriginal people. In this way what is remembered and memorialised through collective processes of memory-making binds those who are part of that collective memory together. What is remembered becomes a marker of the past forming part of the reconstruction of the social world. Language eng Summary "This paper explores collective memory and national projects of remembrance and institutional amnesia or forgetting in assessing reconciliation processes between Indigenous and non-Indigenous people. Politics and Government - National symbols and events - Memorials and commemorations.
Label Memories and reconciled futures : social amnesia and the politics of remembering Title Memories and reconciled futures Title remainder social amnesia and the politics of remembering Statement of responsibility by Claudia Tazreiter Creator
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