angiogenin and Metabolic-Syndrome

angiogenin has been researched along with Metabolic-Syndrome* in 2 studies

Other Studies

2 other study(ies) available for angiogenin and Metabolic-Syndrome

ArticleYear
Angiogenin mediates paternal inflammation-induced metabolic disorders in offspring through sperm tsRNAs.
    Nature communications, 2021, 11-29, Volume: 12, Issue:1

    Paternal environmental inputs can influence various phenotypes in offspring, presenting tremendous implications for basic biology and public health and policy. However, which signals function as a nexus to transmit paternal environmental inputs to offspring remains unclear. Here we show that offspring of fathers with inflammation exhibit metabolic disorders including glucose intolerance and obesity. Deletion of a mouse tRNA RNase, Angiogenin (Ang), abolished paternal inflammation-induced metabolic disorders in offspring. Additionally, Ang deletion prevented the inflammation-induced alteration of 5'-tRNA-derived small RNAs (5'-tsRNAs) expression profile in sperm, which might be essential in composing a sperm RNA 'coding signature' that is needed for paternal epigenetic memory. Microinjection of sperm 30-40 nt RNA fractions (predominantly 5'-tsRNAs) from inflammatory Ang

    Topics: Animals; Epigenesis, Genetic; Inflammation; Lipopolysaccharides; Male; Metabolic Syndrome; Mice; Mutation; Paternal Exposure; Phenotype; Ribonuclease, Pancreatic; RNA, Small Untranslated; RNA, Transfer; Spermatozoa

2021
Inflammatory activation in children with primary hypertension.
    Pediatric nephrology (Berlin, Germany), 2010, Volume: 25, Issue:9

    Low-grade inflammation plays a role in the pathogenesis of primary hypertension (PH) and target organ damage (TOD). We evaluated the profile of inflammatory mediators (CRP, RANTES, MIP-1beta, MIP-1alpha, MCP-1, IL-6, angiogenin, adiponectin) in 30 healthy children (12.7 +/- 3.3 years) and 44 patients with untreated PH (13.7 +/- 2.7 years; n.s). Patients had greater concentrations of CRP, MIP-1beta, and RANTES than controls (all p < 0.05). Children with metabolic syndrome (MS) had greater CRP than children without MS (p = 0.007) and CRP correlated with number of MS criteria, body mass index (BMI), visceral fat, deep subcutaneous fat assessed by magnetic resonance imaging, carotid intima-media thickness (cIMT), left ventricular mass index, and markers of oxidative stress. RANTES correlated with cholesterol, LDL cholesterol, ApoB, and ApoB/ApoA1. Angiogenin correlated with BMI, waist circumference, visceral fat, uric acid, and patients with cIMT>2SD had greater concentration of angiogenin than those with normal cIMT (p = 0.03). Adiponectin was lower in patients with cIMT>2SD than in those with normal cIMT (p = 0.02). No model explaining variability of TOD has been built. Elevated RANTES and MIP-1beta and normal IL-6 and TNF-alpha levels indicate a vascular inflammatory process. Lack of correlation between CRP and chemokines suggests that vascular inflammation in PH precedes the systemic inflammatory changes.

    Topics: Adiponectin; Adolescent; Biomarkers; C-Reactive Protein; Cardiovascular Diseases; Case-Control Studies; Chemokine CCL2; Chemokine CCL3; Chemokine CCL4; Chemokine CCL5; Child; Cross-Sectional Studies; Humans; Hypertension; Immunity, Innate; Inflammation; Inflammation Mediators; Interleukin-6; Metabolic Syndrome; Obesity; Poland; Ribonuclease, Pancreatic

2010