2004
DOI: 10.1016/s1054-3589(04)50003-0
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De Wied and Colleagues II: Further Clarification of the Roles of Vasopressin and Oxytocin in Memory Processing

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Cited by 6 publications
(8 citation statements)
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“…Considerable evidence from the mid-twentieth century demonstrated that OT and VP affect the process of learning and memory, either directly or indirectly by altering arousal (c.f., McEwen, 2004). The original work in this area focused on the impact of VP and OT in passive or active avoidance learning (Bohus et al, 1972, 1978b; de Wied, 1991), but has also expanded to understanding navigation (i.e., hippocampal-dependent cognition; e.g., Engelmann et al, 1992; Everts and Koolhaas, 1999), retrieval and relearning in visual discrimination (Alescio-Lautier et al, 1987), and social recognition and social memory (e.g., Ferguson et al, 2002; Albers, 2012; Stevenson and Caldwell, 2012).…”
Section: Nonapeptides Monogamy and Memorymentioning
confidence: 99%
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“…Considerable evidence from the mid-twentieth century demonstrated that OT and VP affect the process of learning and memory, either directly or indirectly by altering arousal (c.f., McEwen, 2004). The original work in this area focused on the impact of VP and OT in passive or active avoidance learning (Bohus et al, 1972, 1978b; de Wied, 1991), but has also expanded to understanding navigation (i.e., hippocampal-dependent cognition; e.g., Engelmann et al, 1992; Everts and Koolhaas, 1999), retrieval and relearning in visual discrimination (Alescio-Lautier et al, 1987), and social recognition and social memory (e.g., Ferguson et al, 2002; Albers, 2012; Stevenson and Caldwell, 2012).…”
Section: Nonapeptides Monogamy and Memorymentioning
confidence: 99%
“…The original work in this area focused on the impact of VP and OT in passive or active avoidance learning (Bohus et al, 1972, 1978b; de Wied, 1991), but has also expanded to understanding navigation (i.e., hippocampal-dependent cognition; e.g., Engelmann et al, 1992; Everts and Koolhaas, 1999), retrieval and relearning in visual discrimination (Alescio-Lautier et al, 1987), and social recognition and social memory (e.g., Ferguson et al, 2002; Albers, 2012; Stevenson and Caldwell, 2012). The main neural targets on which VP and OT assert effects on memory include the hippocampus, the cingulate and retrosplenial cortices, septum, several subunits of the thalamus, hypothalamus, and other limbic structures such as the amygdala and medial preoptic area (e.g., Popik and Van Ree, 1998; Ferguson et al, 2001; McEwen, 2004; Ophir et al, 2008b). More recently, increasing attention has been dedicated to understanding the roles of nonapeptides in the hippocampus and hippocampal-dependent memory.…”
Section: Nonapeptides Monogamy and Memorymentioning
confidence: 99%
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“…It convincingly improved LTP and long-term (but not short-term) spatial memory within the eight-arm radial maze task [194]. However, the role of oxytocin on memory storage and retrieval seems not as clear-cut as for vasopressin since its effect depends highly on the type of learning tasks presented, the dose of oxytocin injected and in the case of central administration, the specific brain site injected [197][198][199][200][201][202]. Indeed, in aversive learning situations or in learning contexts based on emotionally arousing and stressful situations, oxytocin exerts amnesic actions [200,202].…”
Section: Mechanism(s) Of Action Of Angiotensin IV Through Interactionmentioning
confidence: 99%