This article represents the proceedings of a symposium at the 2001 Research Society on Alcoholism meeting in Montreal, Canada. The chairs were Alan Cahill and Carol C. Cunningham. The presentations were (1) Mitochondrial regulation of ethanol-induced hepatocyte apoptosis: possible involvement of proapoptotic Bcl-2 family protein Bax, by Masayuki Adachi and Hiromasa Ishii; (2) Effects of ethanol on mitochondrial reactive oxygen species production and oxidative protein modification, by Shannon M. Bailey; (3) Acute ethanol binges elicit widespread oxidative mitochondrial DNA damage and depletion: protective effects of antioxidants and inhibitors of ethanol metabolism, by Bernard Fromenty; and (4) Effects of chronic ethanol consumption upon hepatic mtDNA oxidative modification and depletion, by Alan Cahill and Adrian Davies.
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Eur J Public Health
July 2024
Department of Health Sciences, College of Life Sciences, University of Leicester, Leicester, UK.
Background: Despite concerns about worsening pregnancy outcomes resulting from healthcare restrictions, economic difficulties and increased stress during the COVID-19 pandemic, preterm birth (PTB) rates declined in some countries in 2020, while stillbirth rates appeared stable. Like other shocks, the pandemic may have exacerbated existing socioeconomic disparities in pregnancy, but this remains to be established. Our objective was to investigate changes in PTB and stillbirth by socioeconomic status (SES) in European countries.
View Article and Find Full Text PDFEur J Public Health
July 2024
Health Information, Sciensano, Belgium.
Background: Timely and high-quality population-level health information is needed to support evidence-informed decision-making, for planning and evaluation of prevention, care and cure activities as well as for research to generate new knowledge. FAIR (Findable, Accessible, Interoperable and Reusable) principles are one of the key elements supporting health research and making it more cost-effective through the reuse of already existing data. Currently, health data are in many countries dispersed and difficult to find and access.
View Article and Find Full Text PDFN Engl J Med
October 2022
From the Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia (R.D.G., I.Y., S.C., A.C.), and the Department of Pediatrics, University of Pennsylvania Perelman School of Medicine (R.D.G.) - both in Philadelphia; and Howard Hughes Medical Institute and Department of Molecular Biology, Massachusetts General Hospital, Boston (A.L.M., H.S., Z.G., T.-L.T., V.K.M.), and the Metabolism Program, Broad Institute, Cambridge (A.L.M., H.S., Z.G., T.L.T., V.K.M.) - both in Massachusetts.
We describe the case of identical twin boys who presented with low body weight despite excessive caloric intake. An evaluation of their fibroblasts showed elevated oxygen consumption and decreased mitochondrial membrane potential. Exome analysis revealed a de novo heterozygous variant in , which encodes the β subunit of mitochondrial ATP synthase (also called complex V).
View Article and Find Full Text PDFAm J Physiol Gastrointest Liver Physiol
May 2011
Dept. of Pathology, Anatomy and Cell Biology, Thomas Jefferson Univ., Philadelphia, PA 19107, USA.
Chronic ethanol feeding is known to negatively impact hepatic energy metabolism. Previous studies have indicated that the underlying lesion responsible for this may lie at the level of the mitoribosome. The aim of this study was to characterize the structure of the hepatic mitoribosome in alcoholic male rats and their isocalorically paired controls.
View Article and Find Full Text PDFAlcohol Clin Exp Res
January 2009
Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Background: Chronic ethanol feeding to male rats has been shown to result in decreased mitochondrial translation, depressed respiratory complex levels and mitochondrial respiration rates. In addition, ethanol consumption has been shown to result in an increased dissociation of mitoribosomes. S-adenosyl-L-methionine (SAM) is required for the assembly and subsequent stability of mitoribosomes and is depleted during chronic ethanol feeding.
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