Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters










Database
Publication year range
1.
J Intern Med ; 288(1): 103-115, 2020 07.
Article in English | MEDLINE | ID: mdl-32112487

ABSTRACT

OBJECTIVE: The goal of this study was to characterize a Swedish family with members affected by spinocerebellar ataxia 27 (SCA27), a rare autosomal dominant disease caused by mutations in fibroblast growth factor 14 (FGF14). Despite normal structural neuroimaging, psychiatric manifestations and intellectual disability are part of the SCA27 phenotype raising the need for functional neuroimaging. Here, we used clinical assessments, structural and functional neuroimaging to characterize these new SCA27 patients. Since one patient presents with a psychotic disorder, an exploratory study of markers of schizophrenia associated with GABAergic neurotransmission was performed in fgf14-/- mice, a preclinical model that replicates motor and learning deficits of SCA27. METHODS: A comprehensive characterization that included clinical assessments, cognitive tests, structural neuroimaging studies, brain metabolism with 18 F-fluorodeoxyglucose PET ([18F] FDG PET) and genetic analyses was performed. Brains of fgf14-/- mice were studied with immunohistochemistry. RESULTS: Nine patients had ataxia, and all affected patients harboured an interstitial deletion of chromosome 13q33.1 encompassing the entire FGF14 and integrin subunit beta like 1 (ITGBL1) genes. New features for SCA27 were identified: congenital onset, psychosis, attention deficit hyperactivity disorder and widespread hypometabolism that affected the medial prefrontal cortex (mPFC) in all patients. Hypometabolism in the PFC was far more pronounced in a SCA27 patient with psychosis. Reduced expression of VGAT was found in the mPFC of fgf14-/- mice. CONCLUSIONS: This is the second largest SCA27 family identified to date. We provide new clinical and preclinical evidence for a significant psychiatric component in SCA27, strengthening the hypothesis of FGF14 as an important modulator of psychiatric disease.


Subject(s)
Brain/diagnostic imaging , Pedigree , Prefrontal Cortex/metabolism , Spinocerebellar Degenerations/genetics , Adolescent , Adult , Animals , Attention Deficit Disorder with Hyperactivity/complications , Chromosome Deletion , Chromosomes, Human, Pair 13 , Cognition Disorders/genetics , Fibroblast Growth Factors/genetics , Fluorodeoxyglucose F18 , Genotype , Humans , Immunohistochemistry , Integrin beta1/genetics , Magnetic Resonance Imaging , Mice, Knockout , Neuroimaging , Neuropsychological Tests , Phenotype , Positron-Emission Tomography , Psychotic Disorders/complications , Radiopharmaceuticals , Spinocerebellar Degenerations/diagnostic imaging , Sweden , Vesicular Inhibitory Amino Acid Transport Proteins/metabolism , Young Adult
2.
Int J Dev Neurosci ; 64: 48-53, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28373023

ABSTRACT

There is growing evidence that over consumption of high-fat foods and insulin resistance may alter hippocampal-dependent cognitive function. To study the individual contributions of diet and peripheral insulin resistance to learning and memory, we used a transgenic mouse line that overexpresses ecto-nucleotide pyrophosphatase phosphodiesterase-1 in adipocytes, which inhibits the insulin receptor. Here, we demonstrate that a model of peripheral insulin resistance exacerbates high-fat diet induced deficits in performance on the Morris Water Maze task. This finding was then reviewed in the context of the greater literature to explore potential mechanisms including triglyceride storage, adiponectin, lipid composition, insulin signaling, oxidative stress, and hippocampal signaling. Together, these findings further our understanding of the complex relationship among peripheral insulin resistance, diet and memory.


Subject(s)
Brain/metabolism , Cognition Disorders/metabolism , Diet, High-Fat , Insulin Resistance/physiology , Phosphoric Diester Hydrolases/metabolism , Pyrophosphatases/metabolism , Animals , Cognition Disorders/genetics , Mice , Mice, Transgenic , Oxidative Stress/physiology , Phosphoric Diester Hydrolases/genetics , Pyrophosphatases/genetics
3.
Transl Psychiatry ; 6: e806, 2016 05 10.
Article in English | MEDLINE | ID: mdl-27163207

ABSTRACT

Cognitive processing is highly dependent on the functional integrity of gamma-amino-butyric acid (GABA) interneurons in the brain. These cells regulate excitability and synaptic plasticity of principal neurons balancing the excitatory/inhibitory tone of cortical networks. Reduced function of parvalbumin (PV) interneurons and disruption of GABAergic synapses in the cortical circuitry result in desynchronized network activity associated with cognitive impairment across many psychiatric disorders, including schizophrenia. However, the mechanisms underlying these complex phenotypes are still poorly understood. Here we show that in animal models, genetic deletion of fibroblast growth factor 14 (Fgf14), a regulator of neuronal excitability and synaptic transmission, leads to loss of PV interneurons in the CA1 hippocampal region, a critical area for cognitive function. Strikingly, this cellular phenotype associates with decreased expression of glutamic acid decarboxylase 67 (GAD67) and vesicular GABA transporter (VGAT) and also coincides with disrupted CA1 inhibitory circuitry, reduced in vivo gamma frequency oscillations and impaired working memory. Bioinformatics analysis of schizophrenia transcriptomics revealed functional co-clustering of FGF14 and genes enriched within the GABAergic pathway along with correlatively decreased expression of FGF14, PVALB, GAD67 and VGAT in the disease context. These results indicate that Fgf14(-/-) mice recapitulate salient molecular, cellular, functional and behavioral features associated with human cognitive impairment, and FGF14 loss of function might be associated with the biology of complex brain disorders such as schizophrenia.


Subject(s)
Cognitive Dysfunction/genetics , Fibroblast Growth Factors/genetics , Schizophrenia/genetics , Schizophrenic Psychology , Animals , CA1 Region, Hippocampal/pathology , Cognitive Dysfunction/physiopathology , Cognitive Dysfunction/psychology , Gamma Rhythm/physiology , Gene Deletion , Glutamate Decarboxylase/metabolism , Interneurons/pathology , Male , Memory, Short-Term/physiology , Mice , Parvalbumins/metabolism , Phenotype , Schizophrenia/physiopathology , Vesicular Inhibitory Amino Acid Transport Proteins/metabolism
4.
Math Model Nat Phenom ; 9(5): 177-193, 2014.
Article in English | MEDLINE | ID: mdl-28804225

ABSTRACT

Recent advances in high-resolution fluorescence microscopy have enabled the systematic study of morphological changes in large populations of cells induced by chemical and genetic perturbations, facilitating the discovery of signaling pathways underlying diseases and the development of new pharmacological treatments. In these studies, though, due to the complexity of the data, quantification and analysis of morphological features are for the vast majority handled manually, slowing significantly data processing and limiting often the information gained to a descriptive level. Thus, there is an urgent need for developing highly efficient automated analysis and processing tools for fluorescent images. In this paper, we present the application of a method based on the shearlet representation for confocal image analysis of neurons. The shearlet representation is a newly emerged method designed to combine multiscale data analysis with superior directional sensitivity, making this approach particularly effective for the representation of objects defined over a wide range of scales and with highly anisotropic features. Here, we apply the shearlet representation to problems of soma detection of neurons in culture and extraction of geometrical features of neuronal processes in brain tissue, and propose it as a new framework for large-scale fluorescent image analysis of biomedical data.

5.
Minerva Cardioangiol ; 56(5): 571-3, 573-4, 2008 Oct.
Article in English, Italian | MEDLINE | ID: mdl-18813190

ABSTRACT

This report describes a rare case of concurrent abdominal aortic aneurysm and bilateral renal ectopia. Preoperative work-up included intravenous pyelography and angiography to assess renal function, renal artery anatomy, and ureter position. Conventional surgery was performed without renal protection. No deterioration in postoperative renal function was observed.


Subject(s)
Aortic Aneurysm, Abdominal/complications , Kidney/abnormalities , Aged , Aortic Aneurysm, Abdominal/surgery , Humans , Male
6.
Science ; 285(5432): 1411-4, 1999 Aug 27.
Article in English | MEDLINE | ID: mdl-10464102

ABSTRACT

Long-term depression (LTD) is a well-known form of synaptic plasticity of principal neurons in the mammalian brain. Whether such changes occur in interneurons is still controversial. CA3 hippocampal interneurons expressing Ca2+-permeable AMPA receptors exhibited LTD after tetanic stimulation of CA3 excitatory inputs. LTD was independent of NMDA receptors and required both Ca2+ influx through postsynaptic AMPA receptors and activation of presynaptic mGluR7-like receptors. These results point to the capability of interneurons to undergo plastic changes of synaptic strength through joint activation of pre- and postsynaptic glutamate receptors.


Subject(s)
Hippocampus/physiology , Interneurons/physiology , Neuronal Plasticity , Receptors, AMPA/metabolism , Receptors, Metabotropic Glutamate/metabolism , Synapses/physiology , Animals , Calcium/metabolism , Egtazic Acid/analogs & derivatives , Egtazic Acid/pharmacology , Electric Stimulation , Hippocampus/cytology , In Vitro Techniques , Male , Patch-Clamp Techniques , Pyramidal Cells/physiology , Rats , Rats, Sprague-Dawley , Receptors, AMPA/drug effects , Receptors, Metabotropic Glutamate/drug effects , Synaptic Transmission , Tetany
7.
Eur J Neurosci ; 7(3): 516-20, 1995 Mar 01.
Article in English | MEDLINE | ID: mdl-7773448

ABSTRACT

In order to investigate the action of basic fibroblast growth factor (bFGF) in the nervous system, we have studied the ionic signals elicited by this peptide in cultured quail mesencephalic neural crest neurons using patch-clamp and cytofluorimetric techniques. In this preparation stimulation with bFGF induced, with a delay of some tens of seconds, an inward cationic current. Single-channel experiments provided evidence for the activation of a calcium-permeable channel. In single-cell cytofluorimetric measurements, a sustained rise in [Ca2+]i was observed, which was dependent on the presence of external calcium. These events may play a role in the developmental effects of bFGF.


Subject(s)
Calcium Channels/drug effects , Fibroblast Growth Factor 2/pharmacology , Mesencephalon/embryology , Neural Crest/metabolism , Animals , Cells, Cultured , Mesencephalon/cytology , Neural Crest/cytology , Neurons/metabolism , Neurons/physiology , Patch-Clamp Techniques , Quail/embryology
SELECTION OF CITATIONS
SEARCH DETAIL
...