Publications by authors named "Domenico F"

Nuclear factor erythroid 2-related factor 2 (NRF2) is a master regulator of cellular homeostasis, overseeing the expression of a wide array of genes involved in cytoprotective processes such as antioxidant and proteostasis control, mitochondrial function, inflammation, and the metabolism of lipids and glucose. The accumulation of misfolded proteins triggers the release, stabilization, and nuclear translocation of NRF2, which in turn enhances the expression of critical components of both the proteasomal and lysosomal degradation pathways. This process facilitates the clearance of toxic protein aggregates, thereby actively maintaining cellular proteostasis.

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Down Syndrome (DS) is a genetic disorder caused by the presence of an extra copy of chromosome 21, and leading to various developmental and cognitive defects. A critical feature of DS is the occurrence of oxidative distress particularly in the brain, which exacerbates neurodevelopmental processes. Mitochondria play a crucial role in cell energy metabolism and their impairment is one of the major causes of oxidative distress in several pathologies.

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  • Progressive hearing loss often has a genetic basis, with specific mutations like those in the microRNA miR-96 linked to hearing impairments in both humans and mice.
  • This study examines two mouse models with different human mutations in miR-96, utilizing auditory tests and microscopy to analyze impacts on hearing and hair cell structure.
  • Results show that while both mutations cause deafness in homozygous mice, heterozygous effects vary significantly, revealing potential therapeutic targets that could delay hearing loss progression in affected mice.
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Background: Defective mitochondria and aberrant brain mitochondrial bioenergetics are consistent features in syndromic intellectual disability disorders, such as Rett syndrome (RTT), a rare neurologic disorder that severely affects mainly females carrying mutations in the X-linked MECP2 gene. A pool of CB1 cannabinoid receptors (CB1R), the primary receptor subtype of the endocannabinoid system in the brain, is located on brain mitochondrial membranes (mtCB1R), where it can locally regulate energy production, synaptic transmission and memory abilities through the inhibition of the intra-mitochondrial protein kinase A (mtPKA). In the present study, we asked whether an overactive mtCB1R-mtPKA signaling might underlie the brain mitochondrial alterations in RTT and whether its modulation by systemic administration of the CB1R inverse agonist rimonabant might improve bioenergetics and cognitive defects in mice modeling RTT.

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Over the past two decades, there has been a growing scholarly interest in the adoption of technology in healthcare. While numerous studies have delved into the effects of specific technologies on the performance of different organizational units and medical specialties, the findings have often been divergent. Unlike the established literature, our approach focuses on the organization's perspective to analyze how technology impacts process performance in hospital settings.

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Participants in socio-economic systems are often ranked based on their performance. Rankings conveniently reduce the complexity of such systems to ordered lists. Yet, it has been shown in many contexts that those who reach the top are not necessarily the most talented, as chance plays a role in shaping rankings.

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  • Brain insulin resistance connects energy metabolism failure to cognitive decline in type 2 diabetes and Alzheimer's disease, but the early changes leading to insulin resistance are not well understood.
  • Abnormal levels of biliverdin reductase-A (BVR-A) are found in both conditions, linked to insulin resistance and affecting insulin signaling and energy production in the brain.
  • The study reveals that lower BVR-A disrupts insulin response and mitochondrial function, highlighting its importance for potential therapeutic targets to combat brain insulin resistance and neurodegeneration.
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  • Down syndrome (DS), caused by an extra copy of chromosome 21, leads to intellectual disability and is linked to early brain development issues and Alzheimer-like decline in aging.
  • The study analyzed Ts66Yah mice, a newer model for DS, revealing significant behavioral changes related to spatial memory and anxiety as the mice aged from 3 to 9 months.
  • The research identified disruptions in key molecular pathways in the hippocampus, indicating that changes driven by the DS genotype can trigger early brain development problems and facilitate premature aging, while showing only a minor impact from the sex of the mice.
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Redox reactions play a critical role for intracellular processes, including pathways involved in metabolism and signaling. Reactive oxygen species (ROS) act either as second messengers or generators of protein modifications, fundamental mechanisms for signal transduction. Disturbance of redox homeostasis is associated with many disorders.

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Isoflavones are a group of (poly)phenols, also defined as phytoestrogens, with chemical structures comparable with estrogen, that exert weak estrogenic effects. These phytochemical compounds have been targeted for their proven antioxidant and protective effects. Recognizing the increasing prevalence of cardiovascular diseases (CVD), there is a growing interest in understanding the potential cardiovascular benefits associated with these phytochemical compounds.

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The Squat Jump (SJ) test is widely recognized as a reliable test for assessing lower-limb explosive strength. However, uncertainty persists in the literature regarding the optimal starting positions for maximizing vertical jump performance. This uncertainty is exacerbated by a disproportionate focus on athletes in existing studies, with insufficient consideration being given to non-athletic women.

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  • Alzheimer's disease (AD) involves multiple causes and is significantly influenced by oxidative stress (OS), which impacts brain function and contributes to neurodegeneration.
  • The review focuses on the "OS hypothesis of AD," discussing how mechanisms like amyloid beta peptide, lipid, and protein oxidation relate to the disease and exploring antioxidant strategies to potentially slow its progression.
  • A deeper understanding of how oxidative stress affects brain pathways is essential for developing treatments that could mitigate the toxicity related to AD and enhance patients' quality of life.
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Hypertension and derived cardiovascular disease (CVD) are among the leading causes of death worldwide. Increased oxidative stress and inflammatory state are involved in different alterations in endothelial functions that contribute to the onset of CVD. Polyphenols, and in particular anthocyanins, have aroused great interest for their antioxidant effects and their cardioprotective role.

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Countermovement jumping (CMJ) and free-arm countermovement jumping (CMJFA) express the explosive-elastic force of the lower limbs. Strategies to enhance performance in both types of jumping can be categorized into cognitive and ecological-dynamic approaches. However, the effectiveness of these approaches in improving CMJ and CMJFA remains incompletely understood.

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A high-frequency (1.5 kHz) spontaneous Raman spectroscopy measurement technique is developed and applied to measure external fluctuations generated in the local concentration of an isothermal binary gas mixture of methane and air. Raman excitation is provided by a high-frequency laser at 527 nm in dual-pulsed mode.

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Curcumin is a polyphenol compound widely investigated for its potential health benefits. Clinical evidence from randomized controlled trials shows substantial positive effects in healthy individuals but contrasting results for patients with cardio-metabolic disorders. There is growing evidence that the gut microbiota may play a role in curcumin transformation and absorption of more bioactive compounds, suggesting that the baseline health status (or other unmeasured variables) may explain the observed variability of the results.

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Diabetic nephropathy (DN) represents the most common microvascular complication in patients with diabetes. This progressive kidney disease has been recognized as the major cause of end-stage renal disease with higher morbidity and mortality. However, its tangled pathophysiology is still not fully known.

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  • Down syndrome is linked to Alzheimer's disease and involves early brain insulin resistance, which our previous research identified in children with DS before AD symptoms appear.
  • We tested the KYCCSRK peptide in Ts2Cje mice, finding it boosts insulin signaling, enhances mitochondrial function, and lowers oxidative stress.
  • The peptide also reduces levels of proteins associated with Alzheimer's and restores brain health by improving synaptic plasticity, offering potential new treatments for intellectual disability and AD in those with DS.
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The CNS houses naturally occurring pathways that project from the brain to modulate spinal neuronal activity. The noradrenergic locus coeruleus (the A6 nucleus) originates such a descending control whose influence on pain modulation encompasses an interaction with a spinally projecting non-cerulean noradrenergic cell group. Hypothesizing the origin of an endogenous pain inhibitory pathway, our aim was to identify this cell group.

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Nutcracker syndrome (NCS) is a rare pediatric disease caused by left kidney vein compression. Besides the "Triade's symptoms", including hematuria, proteinuria, and flank pain, a wide spectrum of clinical manifestations has been reported. As the significant hemodynamic changes secondary to the dilatation of the left renal vein, serious consequences such as renal vein thrombosis and severe anemia might occur in these children.

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Metformin is the most common anti-diabetic drug and a promising therapy for disorders beyond diabetes, including Rett syndrome (RTT), a rare neurologic disease characterized by severe intellectual disability. A 10-day-long treatment rescued aberrant mitochondrial activity and restrained oxidative stress in a female RTT mouse model. However, this treatment regimen did not improve the phenotype of RTT mice.

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Protein homeostasis or "proteostasis" represent the process that regulates the balance of the intracellular functional and "healthy" proteins. Proteostasis is fundamental to preserve physiological metabolic processes in the cell and it allow to respond to any given stimulus as the expression of components of the proteostasis network is customized according to the proteomic demands of different cellular environments. In conditions that promote unfolding/misfolding of proteins chaperones act as signaling molecules inducing extreme measures to either fix the problem or destroy unfolded proteins.

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Currently, physical inactivity and sedentariness in children are becoming increasingly common, resulting in children’s poor ability to perform basic motor patterns. It is important to find strategies that instructors can adopt to improve awareness of the importance of physical activity for health and wellness, as well as motor efficiency. Two teaching methods can be used: prescriptive teaching and heuristic learning.

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Alterations in intrauterine fetal growth increase the risk of adverse perinatal and neonatal outcomes. In this retrospective study, we analyzed data of 906 pregnancies collected in our maternal fetal medicine center, with different patterns of growth: 655 AGA (Appropriate for Gestational Age), 62 SGA (Small for Gestational Age: fetuses born with a weight less than 10° centile, not diagnosed before delivery), 189 FGR (Fetal Growth Restriction, classified in early and late according to gestational week at diagnosis). For each group, we compared maternal characteristics, gestational age at delivery, and perinatal and neonatal outcomes.

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Article Synopsis
  • Researchers studied mice with targeted mutations to understand gene function and disease, but off-target effects can lead to unexpected mutations, complicating phenotype analysis.
  • They found that of 1,311 mouse lines, 25 displayed independent deafness phenotypes unrelated to the targeted mutation, indicating spontaneous mutations can arise during breeding.
  • The study identified various mutations linked to hearing loss, revealing some involved new genes and others were new versions of known genes, and most mutations likely occurred during breeding rather than in embryonic stem cells.
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