Publications by authors named "Portero-Otin M"

This study aimed to assess differences in the enteral microbiome of relatively recent-onset amyotrophic lateral sclerosis (ALS) patients (< 6-15 months since symptom onset) compared to healthy individuals, focusing on short-chain fatty acids (SCFAs) as potential mediators of host metabolism. We included 28 volunteers (16 ALS, 12 controls) with informed consent. No significant effect of ALS on alpha diversity (measuring the variety and abundance of species within a single sample, and indicating the health and complexity of the microbiome) was observed, but ALS patients had higher abundances of Fusobacteria and Acidobacteria.

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  • - Amyotrophic lateral sclerosis (ALS) is a severe motor neuron disease with about a three-year average survival time, primarily characterized by TDP-43 protein issues that affect gene stability and autophagy processes.
  • - Research on ALS mice revealed that reducing ATG4B worsens survival and autophagy, while an increase in LC3ylation was observed in both ALS patients and mouse models, suggesting a link between these processes.
  • - Antisense oligonucleotides (ASOs) targeting TDP-43 genes have been developed, showing potential for non-invasive treatments that can effectively distribute in the brain after administration.
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The dysfunction of TAR DNA-binding protein 43 (TDP-43) is implicated in various neurodegenerative diseases, though the specific contributions of its toxic gain-of-function versus loss-of-function effects remain unclear. This study investigates the impact of TARDBP loss on cellular metabolism and viability using human-induced pluripotent stem cell-derived motor neurons and HeLa cells. TARDBP silencing led to reduced metabolic activity and cell growth, accompanied by neurite degeneration and decreased oxygen consumption rates in both cell types.

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  • Obesity contributes to age-related neurodegenerative diseases by causing mitochondrial dysfunction and oxidative damage to proteins, mainly through lipoxidation due to high unsaturated fatty acid levels.
  • In a study using a pig model, researchers found that obesity increased the biomarker malondialdehyde-lysine (MDAL) by 34% in the brain, with positive correlations to body weight and LDL cholesterol levels.
  • Including omega-3 fatty acids and probiotics in a high-fat diet can prevent oxidative changes in the brain, indicating that dietary choices may play a role in preventing neurodegenerative conditions.
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  • - The study focuses on understanding how different disease patterns are related to human lifespan and health span, utilizing data from over 482,000 individuals in Catalonia who died after age 50.
  • - Key findings reveal that as lifespan increases, the onset of diseases is delayed, the prevalence of individuals living without diseases is lower around life expectancy, and long-lived women are less prone to multisystem diseases.
  • - The research indicates that the relationship between health span and lifespan varies depending on the specific organ systems affected, and there are notable differences in how these factors play out between men and women.
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One of the challenges facing science/biology today is uncovering the molecular bases that support and determine animal and human longevity. Nature, in offering a diversity of animal species that differ in longevity by more than 5 orders of magnitude, is the best 'experimental laboratory' to achieve this aim. Mammals, in particular, can differ by more than 200-fold in longevity.

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The use of garlic () for treating arterial hypertension has been recognized as effective for several decades. However, tolerance to treatment is low, and several technological modifications have been developed to improve its tolerability, such as the aging process at controlled temperature and humidity. This study aims to validate the antihypertensive effects of an optimized extract of aged black garlic with low doses of s-allyl-cysteine (SAC) in a Grade I hypertensive population with drug treatment.

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  • Insulin resistance (IR) becomes more common with age and is linked to various chronic diseases, with diet playing a significant role in its development.
  • Advanced glycation end products (AGEs) in food are emphasized as major contributors to IR, supported by both animal and human studies.
  • While small clinical trials indicate that lowering dietary AGEs can improve insulin sensitivity, further large-scale studies are needed to confirm their harmful effects in chronic diseases.
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Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterized by the progressive loss of motor neurons in the spinal cord. Glial cells, including astrocytes and microglia, have been shown to contribute to neurodegeneration in ALS, and metabolic dysfunction plays an important role in the progression of the disease. Glycogen is a soluble polymer of glucose found at low levels in the central nervous system that plays an important role in memory formation, synaptic plasticity, and the prevention of seizures.

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  • A lipidomic analysis using non-targeted LC-MS/MS was performed on post-mortem human brain samples from middle-aged individuals, including those with and without Alzheimer’s disease (AD) symptoms, to identify lipid fingerprints.
  • The study found that white matter (WM) exhibits a unique lipid profile that is more resistant to damage compared to grey matter (GM), displaying lower fatty acid unsaturation and higher ether lipid content.
  • As Alzheimer's disease progresses, significant changes in lipid profiles occur, particularly in the WM, affecting functions related to cell membranes, energy production, antioxidant defense, and bioactive lipids, which may worsen the condition of neurons and glial cells.
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Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease leading to selective and progressive motor neuron (MN) death. Despite significant heterogeneity in pathogenic and clinical terms, MN demise ultimately unifies patients. Across the many disturbances in neuronal biology present in the disease and its models, two common trends are loss of calcium homeostasis and dysregulations in lipid metabolism.

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Sphingolipids function as membrane constituents and signaling molecules, with crucial roles in human diseases, from neurodevelopmental disorders to cancer, best exemplified in the inborn errors of sphingolipid metabolism in lysosomes. The dihydroceramide desaturase Δ4-dihydroceramide desaturase 1 (DEGS1) acts in the last step of a sector of the sphingolipid pathway, de novo ceramide biosynthesis. Defects in DEGS1 cause the recently described hypomyelinating leukodystrophy-18 (HLD18) (OMIM #618404).

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Aging biology entails a cell/tissue deregulated metabolism that affects all levels of biological organization. Therefore, the application of "omic" techniques that are closer to phenotype, such as metabolomics, to the study of the aging process should be a turning point in the definition of cellular processes involved. The main objective of the present study was to describe the changes in plasma metabolome associated with biological aging and the role of sex in the metabolic regulation during aging.

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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is an enveloped positive stranded RNA virus which has caused the recent deadly pandemic called COVID-19. The SARS-CoV-2 virion is coated with a heavily glycosylated Spike glycoprotein which is responsible for attachment and entry into target cells. One, as yet unexploited strategy for preventing SARS-CoV-2 infections, is the targeting of the glycans on Spike.

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  • * Glycerophospholipids, particularly ether lipids, are crucial for maintaining the structure and function of neural cell membranes, influencing processes like membrane trafficking and cell signaling.
  • * The research explores the important role of ether lipids in brain health, their antioxidant effects, and how changes in their levels are linked to the pathology of sAD, suggesting a vicious cycle that exacerbates the disease.
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It is assumed that the human brain is especially susceptible to oxidative stress, based on specific traits such as a higher rate of mitochondrial free radical production, a high content in peroxidizable fatty acids, and a low antioxidant defense. However, it is also evident that human neurons, although they are post-mitotic cells, survive throughout an entire lifetime. Therefore, to reduce or avoid the impact of oxidative stress on neuron functionality and survival, they must have evolved several adaptive mechanisms to cope with the deleterious effects of oxidative stress.

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  • Dipeptidyl peptidase 9 (DPP9) is linked to activating the NLRP1 inflammasome, which is important in immune responses against viral infections like SARS-CoV-2.
  • Recent studies suggested that DPP9's activity is influenced by oxidative stress, affecting gastrointestinal inflammation and playing a role in lung issues during severe COVID-19.
  • Analysis of biopsies and plasma revealed DPP9 expression is associated with oxidative stress markers and antiviral pathways, leading to potential drug targets for treatment.
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  • The study investigates senescence mechanisms in the hSOD1-G93A motor neuron disease model by measuring markers like p16, p21, and SA-β-gal in nervous tissue.
  • Researchers found elevated p16 and p21 levels in glial cells but no expected increase in SA-β-gal activity, suggesting a unique senescence profile.
  • Additionally, they noted changes in SASP-related mRNA levels and TDP-43 splicing activity, while certain drugs had varied effects on these senescence markers and disease progression.
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  • * In a study of 541 AIS patients, 40 (7.4%) had experienced a TIA within the week prior, and those patients showed less severe strokes, better recovery outcomes, and reduced brain damage compared to those without recent TIAs.
  • * Analysis revealed that these patients also had a distinct metabolomic/lipidomic profile, indicating higher levels of structural and bioactive lipids, which could enhance neuronal survival and improve the immune response, ultimately contributing to better adaptation
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Aberrant endocannabinoid signaling accompanies several neurodegenerative disorders, including multiple sclerosis. Here, we report altered endocannabinoid signaling in X-linked adrenoleukodystrophy (X-ALD), a rare neurometabolic demyelinating syndrome caused by malfunction of the peroxisomal ABCD1 transporter, resulting in the accumulation of very long-chain fatty acids (VLCFAs). We found abnormal levels of cannabinoid receptor 2 (CB2r) and related endocannabinoid enzymes in the brain and peripheral blood mononuclear cells (PBMCs) of X-ALD patients and in the spinal cord of a murine model of X-ALD.

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Growing evidence implicates the gut microbiome in cognition. Blastocystis is a common gut single-cell eukaryote parasite frequently detected in humans but its potential involvement in human pathophysiology has been poorly characterized. Here we describe how the presence of Blastocystis in the gut microbiome was associated with deficits in executive function and altered gut bacterial composition in a discovery (n = 114) and replication cohorts (n = 942).

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The microbiota-gut-brain axis has emerged as a novel target in depression, a disorder with low treatment efficacy. However, the field is dominated by underpowered studies focusing on major depression not addressing microbiome functionality, compositional nature, or confounding factors. We applied a multi-omics approach combining pre-clinical models with three human cohorts including patients with mild depression.

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This study aimed to determine how the microbiota profile might be predisposed to a better response in blood lipid profiles due to dietary fibre supplementation. A three-arm intervention study that included three different fibre types (mainly insoluble, soluble, and antioxidant fibre) supplemented (19.2 g/day) during 2 months in individuals with hypercholesterolemia was developed.

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