15 results match your criteria: "Biocenter-Innsbruck Medical University[Affiliation]"

Plasma soluble P-selectin correlates with triglycerides and nitrite in overweight/obese patients with schizophrenia.

Pteridines

January 2020

Michael E. DeBakey VA Medical Center, Houston, TX, USA, Menninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, TX, USA.

Background: Soluble P-selectin (sP-selectin) is associated with risk factors for cardiovascular disease (CVD) but this association has not been evaluated in patients with schizophrenia. This study primarily evaluated the association of sP-selectin with plasma lipids and nitrite (NO-) respectively in overweight/obese adults with schizophrenia.

Methods: One-hundred and six patients with schizophrenia (mean age 32.

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The impairment of regulatory T cells (Tregs) is a characteristic feature of autoimmune hepatitis (AIH), and the degradation of tryptophan (Trp) to kynurenine (Kyn), by gamma interferon-induced indoleamine-2,3-dioxygenase-1 (IDO-1), is a central metabolomics check point in the differentiation of Tregs. For this reason, we investigate whether or not Kyn and IDO activity is potentially useful biomarkers in pediatric AIH.Between January 2016 and January 2017, children of AIH type-1 (AIH-1, n = 37), AIH type-2 with liver kidney microsome-1 autoantibodies (AIH-2-LKM-1, n = 8), and autoantibody-negative Wilsons Disease (WD, n = 8) and alpha-1 anti-trypsin deficiency (AATD, n = 10), were enrolled in a cross-sectional survey of Kyn and Trp levels and Kyn/Trp ratios (IDO activity) by HPLC, and neopterin levels by ELISA.

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Objectives: Plasma nitrite is a metabolite of nitric oxide and reflects endogenous nitric oxide synthase (NOS) activity. Although plasma nitrites were previously linked with obesity and metabolic syndrome (MetS), the direction of association remains inconsistent, possibly due to sample heterogeneity. In a relatively homogeneous population, we hypothesized that nitrite levels will be positively associated with overweight/obesity and MetS.

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HIV-1 causes chronic inflammation and AIDS in humans, whereas related simian immunodeficiency viruses (SIVs) replicate efficiently in their natural hosts without causing disease. It is currently unknown to what extent virus-specific properties are responsible for these different clinical outcomes. Here, we incorporate two putative HIV-1 virulence determinants, i.

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Background: Increased monocyte activation and intestinal damage have been shown to be predictive for the increased morbidity and mortality observed in treated people living with human immunodeficiency virus (PLHIV).

Methods: A cross-sectional analysis of cellular and soluble markers of monocyte activation, coagulation, intestinal damage, and inflammation in plasma and cerebrospinal fluid (CSF) of PLHIV with suppressed plasma viremia on combination antiretroviral therapy and age and demographically comparable HIV-negative individuals participating in the Comorbidity in Relation to AIDS (COBRA) cohort and, where appropriate, age-matched blood bank donors (BBD).

Results: People living with HIV, HIV-negative individuals, and BBD had comparable percentages of classical, intermediate, and nonclassical monocytes.

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Autoimmunity to HSP60 during diet induced obesity in mice.

Int J Obes (Lond)

February 2017

School of Clinical Sciences and Bristol Heart Institute, Bristol Royal Infirmary, University of Bristol, Bristol, UK.

Adaptive immunity has been implicated in adipose tissue inflammation, obesity and its adverse metabolic consequences. No obesity-related autoantigen has yet been identified, although heat shock protein 60 (HSP60) has been implicated in other autoimmune diseases. We investigated whether feeding a high-fat diet to C57BL/6J mice would cause autoimmunity to HSP60 and whether immunomodulation with peptides from HSP60 would reverse the resulting obesity or metabolic dysfunction.

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Kynurenine and Tryptophan Levels in Patients With Schizophrenia and Elevated Antigliadin Immunoglobulin G Antibodies.

Psychosom Med

October 2016

From the Mood and Anxiety Program (Okusaga, Postolache) and Child and Adolescent Psychiatry Division, Department of Psychiatry (Reeves), University of Maryland School of Medicine, Baltimore, Maryland; Department of Psychiatry and Behavioral Sciences (Okusaga), The University of Texas Health Science Center at Houston, Houston, Texas; Division of Biological Chemistry (Fuchs), Biocenter Innsbruck Medical University, Innsbruck, Austria; Department of Psychiatry (Hartmann, Rujescu), University of Halle-Wittenberg, Germany; University of South Florida (Groer), Tampa, Florida; Department of Public Health (Cook), Mercyhurst University, Erie, Pennsylvania; Rocky Mountain Mental Illness Research Education and Clinical Center (MIRECC; Stearns-Yoder; Hoisington, Brenner, Postolache), Denver, Colorado; Military and Veteran Microbiome Consortium for Research and Education (Stearns-Yoder, Hoisington, Lowry, Brenner, Postolache), Denver, Colorado; Department of Microbiology and Immunology (Pandey), Medical University of South Carolina, Charleston, South Carolina; Maryland Psychiatric Research Center, Department of Psychiatry (Kelly), University of Maryland School of Medicine, Baltimore, Maryland; Johns Hopkins University (Eaton), Baltimore, Maryland; Civil and Environmental Engineering Department (Hoisington), United States Air Force Academy, Colorado Springs, Colorado; Department of Integrative Physiology and Center for Neuroscience (Lowry), University of Colorado Boulder, Boulder, Colorado; Departments of Psychiatry, Neurology, and Physical Medicine and Rehabilitation (Brenner), University of Colorado, Anschutz Medical Campus, Aurora, Colorado; Veterans Integrated Service Network (VISN) 5, Mental Illness Research Education and Clinical Center (MIRECC; Postolache), Baltimore, Maryland.

Objective: Several studies have reported an association between nonceliac gluten sensitivity and schizophrenia. Immune and kynurenine (KYN) pathways have also been implicated in the pathophysiology of schizophrenia, and certain proinflammatory immune mediators may increase KYN and reduce tryptophan (TRP) levels.

Methods: We measured serum antigliadin immunoglobulin G (IgG), KYN, and TRP in 950 patients with schizophrenia.

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Inflammatory, endocrine and metabolic correlates of fatigue in obese children.

Psychoneuroendocrinology

December 2016

Univ Bordeaux, Nutrition and Integrative Neurobiology, F-33076 Bordeaux, France; INRA, Nutrition and Integrative Neurobiology, F-33076 Bordeaux, France.

Alterations in endocrine functions and low-grade systemic inflammation represent fundamental characteristics of obesity. These biological systems have been repeatedly linked to fatigue symptoms. The aim of the study was to assess the relationship between fatigue dimensions and metabolic/inflammatory markers in a sample of non-diabetic obese children.

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Blood Levels of Monoamine Precursors and Smoking in Patients with Schizophrenia.

Front Public Health

September 2016

Mood and Anxiety Program, University of Maryland School of Medicine, Baltimore, MD, USA; VISN 5 Capitol Health Care Network Mental Illness Research Education and Clinical Center (MIRECC), Baltimore, MD, USA; Rocky Mountain MIRECC, Denver, CO, USA.

Smoking is highly prevalent in patients with schizophrenia and exerts a negative impact on cardiovascular mortality in these patients. Smoking has complex interactions with monoamine metabolism through the ability of cigarette smoke to suppress Type 1 T helper cell (Th1) type immunity, the immunophenotype that is implicated in phenylalanine hydroxylase (PAH) dysfunction and tryptophan (Trp) breakdown to kynurenine (Kyn) via indoleamine 2,3-dioxygenase. Nicotine also induces tyrosine hydroxylase (TH) gene expression, leading to increased synthesis of catecholamines.

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Ewing sarcoma (ES) is an aggressive pediatric tumor driven by the fusion protein EWS-FLI1. We report that EWS-FLI1 suppresses TDO2-mediated tryptophan (TRP) breakdown in ES cells. Gene expression and metabolite analyses reveal an EWS-FLI1-dependent regulation of TRP metabolism.

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Objectives: Health, disease, and immune function are key areas of research in studies of ecology and evolution, but work on free-ranging primates has been inhibited by a lack of direct noninvasive measures of condition. Here, we evaluate the potential usefulness of noninvasive measurement of three biomarkers, the acute-phase proteins C-reactive protein (CRP) and haptoglobin, and neopterin, a by-product of macrophage activity.

Materials And Methods: We took advantage of veterinary checks on captive rhesus (24) and long-tailed (3) macaques at the German Primate Center (DPZ) to analyze serum marker measures, before measuring concentrations in feces and urine, and evaluating relationships between matched serum, urine, and fecal concentrations.

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Elevated levels of plasma phenylalanine in schizophrenia: a guanosine triphosphate cyclohydrolase-1 metabolic pathway abnormality?

PLoS One

October 2014

Mood and Anxiety Program, University of Maryland School of Medicine, Baltimore, Maryland, United States of America ; University of Maryland Child and Adolescent Mental Health Innovations Center, Baltimore, Maryland, United States of America ; VISN 5 Capitol Health Care Network Mental Illness Research Education and Clinical Center (MIRECC), Baltimore, Maryland, United States of America ; VISN 19 MIRECC, Denver, Colorado, United States of America.

Background: Phenylalanine and tyrosine are precursor amino acids required for the synthesis of dopamine, the main neurotransmitter implicated in the neurobiology of schizophrenia. Inflammation, increasingly implicated in schizophrenia, can impair the function of the enzyme Phenylalanine hydroxylase (PAH; which catalyzes the conversion of phenylalanine to tyrosine) and thus lead to elevated phenylalanine levels and reduced tyrosine levels. This study aimed to compare phenylalanine, tyrosine, and their ratio (a proxy for PAH function) in a relatively large sample of schizophrenia patients and healthy controls.

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Testing for immunomodulatory properties of nanoparticles.

J Biomed Nanotechnol

February 2011

Division of Biological Chemistry, Biocenter Innsbruck Medical University, 6020 Innsbruck, Austria.

Immune activation and inflammation can precipitate a variety of diseases. A screening assay for immunomodulatory properties is described. It is based on freshly isolated human peripheral blood mononuclear cells and allows testing for effects of nanoparticles on the human immune system.

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Bovine colostrum (BC) is the thick yellow fluid a lactating cow gives to a suckling calf during its first days of life to support the growth of the calf and prevent gastrointestinal infections until the calf has synthesized its own active immune defense system. BC contains a complex system of immune factors and has a long history of use in traditional medicine. In an approach to evaluate the effects of bovine colostrum (BC) on the T-cell/macrophage interplay, we investigated and compared the capacity of BC containing low and high amounts of lactose and lactoferrin to modulate tryptophan degradation and neopterin formation in unstimulated and mitogen-stimulated human peripheral blood mononuclear cells (PBMC).

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Protein arginine methylation has been implicated in different cellular processes including transcriptional regulation by the modification of histone proteins. Here we demonstrate significant in vitro activities and multifaceted specificities of Aspergillus protein arginine methyltransferases (PRMTs) and we provide evidence for a role of protein methylation in mechanisms of oxidative stress response. We have isolated all three Aspergillus PRMTs from fungal extracts and could assign significant histone specificity to RmtA and RmtC.

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