scispace - formally typeset
R

R. A. Canuto

Researcher at University of Turin

Publications -  18
Citations -  271

R. A. Canuto is an academic researcher from University of Turin. The author has contributed to research in topics: Lipid peroxidation & Aldehyde dehydrogenase. The author has an hindex of 10, co-authored 18 publications receiving 263 citations.

Papers
More filters
Journal Article

Lipid peroxidation in fatty liver induced by caffeine in rats.

TL;DR: Results seem to indicate an increased peroxidability in the liver of caffeine-treated animals, due to an increase in triglyceride content, which might contribute to the lipid peroxidation.
Journal ArticleDOI

Hydroxyapatite paste Ostim®, without elevation of full‐thickness flaps, improves alveolar healing stimulating BMP‐ and VEGF‐mediated signal pathways: an experimental study in humans

TL;DR: Clinical and biomolecular observations of this explorative study evidenced that nanocrystalline hydroxyapatite improves alveolar socket healing, increasing angiogenesis, epithelialization, and osteogenesis, also in absence of elevation of full-thickness flaps.
Journal ArticleDOI

Glutathione-S-transferase, alcohol dehydrogenase and aldehyde reductase activities during diethylnitrosamine-carcinogenesis in rat liver

TL;DR: It is demonstrated that, although to a lesser extent than aldehyde dehydrogenase, aldealdehyde reductase and glutathione-S-transferase also increase during carcinogenesis.
Journal ArticleDOI

Exposing human epithelial cells to zoledronic acid can mediate osteonecrosis of jaw: an in vitro model.

TL;DR: The research evidenced, for the first time, the direct involvement of epithelial cells in zoledronic acid-triggered molecular mechanisms leading to osteonecrosis of the jaw, by modulating both osteoblast and osteoclast properties.
Journal ArticleDOI

Hepatocellular Metabolism of 4-Hydroxy-2,3-Nonenal Is Impaired in Conditions of Chronic Cholestasis

TL;DR: It is reported that viable hepatocytes isolated from cholestatic livers of bile duct-ligated rats (BDL hepatocytes) show a significantly lower rate of HNE metabolism than control cells, likely to be the consequence of a significant inhibition in the activity of H NE-metabolizing cytosolic glutathione-S-transferase and alcohol dehydrogenase in BDL hepatocytes.