The basolateral amygdala (BLA), hippocampal ventral subiculum, and nucleus accumbens (NAc) comprise the amygdala-hippocampus-NAc (AHN) circuit, which is implicated in drug seeking and reward. The goal of this study was to evaluate microstructural changes and relevant clinical features of the AHN circuit gray matter (GM) in methamphetamine (MA) users using diffusion tensor imaging (DTI). Thirty MA users and 30 age-matched normal volunteers underwent 3-T MR imaging to obtain structural T1-weighted images and DTI data. Freesurfer software was used to automatically segment the NAc and subiculum. A Jülich probability map was employed to parcellate the BLA. Fractional anisotropy (FA) and mean diffusivity (MD) maps were generated and non-linearly coregistered to structural space. DTI measures of the AHN circuit GM were compared between MA users and controls using repeated measures analysis of variance. Correlation analyses were performed between DTI measures and clinical characteristics. Anatomical correlations between the NAc and BLA/subiculum in both groups were assessed using correlation analyses. The MA group had significant lower FA in the bilateral BLA, subiculum, and NAc. Higher total MA dose corresponded with lower FA in all three structures. Hamilton Anxiety Rating Scale scores negatively correlated with the right subiculum FA. Lower left BLA FA was associated with higher thinking disorder and hostile-suspicion factor scores. Left BLA FA was significantly associated with bilateral NAc FA in MA users. Those findings provided neuroimaging evidence of MA-induced microstructural impairment in the AHN circuit GM. Enhanced anatomical correlations between the left BLA and bilateral NAc may be part of the mechanism of MA intake relapse and for development of psychosis.
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January 2025
Department of Physics, Pukyong National University, Busan, 48513, Republic of Korea.
Improving the interface characteristics between the hole-transport layer (HTL) and perovskite absorber layer is crucial for achieving maximum efficiency in inverted perovskite solar cells (PSCs). This paper presents an effective functional compensation layer (FCL) composed of benzothiophene derivatives, particularly 5-(trifluoromethyl)-1-benzothiophene-2-carboxylic acid (TFMBTA); this layer is introduced between the MeO-2PACz HTL and perovskite absorber layer to improve the interfacial characteristics between them. This FCL improves charge transfer, hole extraction, and perovskite deposition by improving the surface morphology of the HTL and optimizing the energy level alignment.
View Article and Find Full Text PDFEcotoxicol Environ Saf
November 2024
College of Veterinary Medicine, Hunan Agricultural University, Changsha 410125, China. Electronic address:
The T-2 toxin is a frequent contaminant in the global environment and agricultural production. Existing evidence suggests that the ingested T-2 toxin can enter the brain and exhibit neurotoxicity. However, it is still unknown whether T-2 toxin causes the depression-like behaviors.
View Article and Find Full Text PDFbioRxiv
October 2024
Nash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai.
Prior adversity increases susceptibility to subsequent stressful events, but the causal underlying changes in brain circuitry are poorly understood. We harnessed unbiased whole-brain activity mapping to identify circuits that are functionally remodeled by prior adversity. This revealed that the anterior hypothalamic nucleus (AHN) displays heightened stress reactivity in previously stressed mice.
View Article and Find Full Text PDFCurr Biol
November 2024
McGovern Institute for Brain Research and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA. Electronic address:
Balanced activity of canonical direct D1 and indirect D2 basal ganglia pathways is considered a core requirement for normal movement, and their imbalance is an etiologic factor in movement and neuropsychiatric disorders. We present evidence for a conceptually equivalent pair of direct D1 and indirect D2 pathways that arise from striatal projection neurons (SPNs) of the striosome compartment rather than from SPNs of the matrix, as do the canonical pathways. These striosomal D1 (S-D1) and D2 (S-D2) pathways target substantia nigra dopamine-containing neurons instead of basal ganglia motor output nuclei.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
October 2024
Department of Pharmacology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599.
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