ascorbic-acid has been researched along with tin-mesoporphyrin* in 2 studies
2 other study(ies) available for ascorbic-acid and tin-mesoporphyrin
Article | Year |
---|---|
Prevention of Barrier Disruption by Heme Oxygenase-1 in Intestinal Bleeding Model.
In this study we investigated the effect of free heme, the local level of which was increased by bleeding, on the intestinal barrier function, using human epithelial colorectal adenocarcinoma cells (Caco-2). Our results show that the addition of hemin to the culture medium markedly disrupted the barrier function, which was significantly improved by glutamine supplementation. Although hemin treatment caused the increased expression of heme oxygenase (HO)-1, the inhibition of HO activity resulted in the aggravation of hemin-induced barrier dysfunction. Up-regulation of HO-1 by pretreatment with a low concentration of hemin almost completely prevented hemin-induced barrier dysfunction. Taken together, these observations indicate that an abnormally high level of intracellular free heme causes barrier dysfunction, probably through the modulation of proteins forming tight junctions. Topics: Ascorbic Acid; Caco-2 Cells; Gastrointestinal Hemorrhage; Glutamine; Heme Oxygenase-1; Hemin; Humans; Intestinal Mucosa; Malondialdehyde; Metalloporphyrins | 2016 |
Astroglia overexpressing heme oxygenase-1 predispose co-cultured PC12 cells to oxidative injury.
The mechanisms responsible for the progressive degeneration of dopaminergic neurons and pathologic iron deposition in the substantia nigra pars compacta of patients with Parkinson's disease (PD) remain unclear. Heme oxygenase-1 (HO-1), the rate-limiting enzyme in the oxidative degradation of heme to ferrous iron, carbon monoxide, and biliverdin, is upregulated in affected PD astroglia and may contribute to abnormal mitochondrial iron sequestration in these cells. To determine whether glial HO-1 hyper-expression is toxic to neuronal compartments, we co-cultured dopaminergic PC12 cells atop monolayers of human (h) HO-1 transfected, sham-transfected, or non-transfected primary rat astroglia. We observed that PC12 cells grown atop hHO-1 transfected astrocytes, but not the astroglia themselves, were significantly more susceptible to dopamine (1 microM) + H(2)O(2) (1 microM)-induced death (assessed by nuclear ethidium monoazide bromide staining and anti-tyrosine hydroxylase immunofluorescence microscopy) relative to control preparations. In the experimental group, PC12 cell death was attenuated significantly by the administration of the HO inhibitor, SnMP (1.5 microM), the antioxidant, ascorbate (200 microM), or the iron chelators, deferoxamine (400 microM), and phenanthroline (100 microM). Exposure to conditioned media derived from HO-1 transfected astrocytes also augmented PC12 cell killing in response to dopamine (1 microM) + H(2)O(2) (1 microM) relative to control media. In PD brain, overexpression of HO-1 in nigral astroglia and accompanying iron liberation may facilitate the bioactivation of dopamine to neurotoxic free radical intermediates and predispose nearby neuronal constituents to oxidative damage. Topics: Animals; Antioxidants; Ascorbic Acid; Astrocytes; Cell Death; Cells, Cultured; Coculture Techniques; Culture Media, Conditioned; Dopamine; Drug Synergism; Enzyme Inhibitors; Heme Oxygenase-1; Humans; Hydrogen Peroxide; Iron Chelating Agents; Metalloporphyrins; Oxidative Stress; PC12 Cells; Rats; Rats, Sprague-Dawley; Transfection | 2007 |