Volumes of the mesiotemporal structures (hippocampus-amygdala complex) were measured in 19 men who were chronic multiepisode schizophrenics and 18 age-matched healthy controls using T1-weighted contiguous coronal magnetic resonance images of 3.1-mm width. Using the level of the mammillary bodies as an anatomical landmark, the whole hippocampus-amygdala complex was divided into an anterior section (mainly containing amygdaloid tissue) and a posterior section (mainly containing the hippocampal formation). Total mesiotemporal tissue volume was reduced significantly in the patient group compared to controls (-11%), with significant reductions in both left (-20%) and right (-15%) hippocampal sections. Reduced limbic tissue volume was associated with increased severity of psychopathology. Severity of positive psychotic symptoms (Brief Psychiatric Rating Scale [BPRS] psychosis factor) was correlated significantly with right and left total mesiotemporal volumes (Spearman rho's = -0.61 p < 0.01). Negative symptom scores (BPRS anergia factor, Scale for Assessment of Negative Symptoms [SANS] global items) were not significantly correlated with any mesiotemporal tissue volumes. The data corroborate and extend previous findings of temporolimbic structure volume reduction in schizophrenia, and suggest that the positive psychotic symptoms of schizophrenia are associated with anatomic anomalies in mesiotemporal structure.
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http://dx.doi.org/10.1016/0006-3223(93)90289-p | DOI Listing |
Nat Commun
October 2024
Department of Neurobiology & Anatomy, Drexel University College of Medicine, Philadelphia, PA, 19129, USA.
Memories are crucial for daily life, yet the network-level organizing principles governing neural representations of experiences remain unknown. Employing dual-site in vivo recording in freely behaving male mice, here we show that hippocampal dorsal CA1 (dCA1) and basolateral amygdala (BLA) utilize distinct coding strategies for novel experiences. A small assembly of BLA neurons emerged active during memory acquisition and persisted through consolidation, whereas most dCA1 neurons were engaged in both processes.
View Article and Find Full Text PDFBrain Commun
October 2024
Neurosciences and Mental Health, Hospital for Sick Children Research Institute, Toronto, ON, Canada M5G 0A4.
J Headache Pain
October 2024
Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome Polo Pontino ICOT, Latina, Italy.
Background: This study investigated for a possible contributing role of hippocampus in the different clinical phenotypic manifestations of migraine aura.
Methods: Herein, patients were categorized as those with pure visual aura (MwAv), those who reported additional somatosensory and dysphasic symptoms (MwAvsd), and healthy controls (HCs). Neuroimaging data obtained using FreeSurfer-based segmentation of hippocampal subfields were compared between HCs and patients with migraine with aura, as well as between HCs and those with MwAv and MwAvsd.
Comput Methods Programs Biomed
December 2024
Department of Computer Science and Engineering, Gyeongsang National University, Jinju 52828, South Korea; Department of AI Convergence Engineering, Gyeongsang National University, Jinju 52828, South Korea. Electronic address:
Nature
August 2024
Department of Neurosurgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Humans have the remarkable cognitive capacity to rapidly adapt to changing environments. Central to this capacity is the ability to form high-level, abstract representations that take advantage of regularities in the world to support generalization. However, little is known about how these representations are encoded in populations of neurons, how they emerge through learning and how they relate to behaviour.
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