Distribution of neuropeptides in the limbic system of the rat: The hippocampus
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Adolescent morphine exposure impairs dark avoidance memory and synaptic potentiation of ventral hippocampal CA1 during adulthood in rats
2023, Life SciencesCitation Excerpt :Although the longitudinal axis of the hippocampus has many similarities, the dorsal and ventral regions have separate distinct internal and external connections. This explains the functional difference between these two regions [19–21]. The dorsal hippocampus is responsible for processing spatial memory [19,22,23], and the ventral hippocampus mediates avoidance memory and emotional processing [19,24].
Neuropeptides in learning and memory
2013, NeuropeptidesCitation Excerpt :VIP and its receptors are expressed in several regions of the brain responsible for learned behaviors (hippocampus, amygdala, cortex; Loren et al., 1979). The importance of VIP can be demonstrated by the fact that it is expressed in three different types of interneurons in the hippocampal formation (Ammon’s horn, dentate gyrus; Acsády et al., 1996; Roberts et al., 1984). The presence of VIP in these regions suggest a crucial role for this peptide in cognitive functions.
The NTSR1 gene modulates the association between hippocampal structure and working memory performance
2013, NeuroImageCitation Excerpt :In addition to our study (Li et al., 2011) linking the NTSR1 gene to WM, a prior rodent study also showed that administration of a NTSR1 antagonist impairs WM in a learning task (Tirado-Santiago et al., 2006). A potential link among the hippocampus, the NTSR1 gene, and WM is further supported by the following evidence: the high distribution of NT and NT receptors in hippocampus regions (Kohler et al., 1987; Quirion et al., 1987; Roberts et al., 1984), the high expression of NTSR1 mRNA (Lepee-Lorgeoux et al., 1999) and protein (Boudin et al., 2000) in the hippocampus, and the effect of NT on the firing of hippocampus CA1 interneurons (Li et al., 2008) and on neurons that project to the hippocampus (Matthews, 1999). In sum, previous research has linked the NTSR1 gene and the hippocampus separately to WM performance, and has found a close connection between the NTSR1 gene and the hippocampus (i.e., the distribution and predominant expression of NTSR1 protein in the hippocampus).
Contacts between medial and lateral perforant pathway fibers and parvalbumin expressing neurons in the subiculum of the rat
2008, NeuroscienceCitation Excerpt :Comparison of the present findings of perforant pathway contacts on parvalbumin positive dendrites (16%) with our previously published, more general EM findings in which the dendritic targets (18%) were not further characterized (Baks te Bulte et al., 2005), indicates that the parvalbumin-positive interneuron population most likely represents the main recipient of entorhinal input. Thus, although a variety of interneurons have been differentiated electrophysiologically (Menendez de la Prida et al., 2003; Menendez de la Prida, 2006) as well as anatomically (Köhler and Chan-Palay, 1982, 1983; Roberts et al.,1984; Seress et al., 1994; Fujise et al., 1995; Lin and Totterdell, 1998), the parvalbumin-positive interneurons should be considered as the most likely mediators for the reported weak inhibitory response of principal neurons in the subiculum upon entorhinal stimulation (dorsal subiculum; Gigg et al., 2000). The latter authors suggested that the inhibition they found was inflicted via a monosynaptic excitatory influence combined with a multisynaptic inhibitory route via CA1 neurons.
The somatostatin receptors in the normal and epileptic hippocampus of the gerbil: Subtype-specific localization and its alteration
2003, Brain ResearchCitation Excerpt :A high concentration of somatostatin (SRIF) is known to be present in the hippocampal areas. SRIF containing neurons have been found mainly in the stratum oriens and pyramidale of CA1, all strata of CA3, the hilus of the dentate area, and the subicular regions [18,33,37]. A recent study has shown that SRIF regulates neurotransmission at excitatory synapses in rat glutamatergic hippocampal neurons [4].