Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8546280 | Food and Chemical Toxicology | 2018 | 45 Pages |
Abstract
We studied the effects of the tartrazine-metabolite sulfanilic acid on the physiology of pancreatic AR42J cells. Sulfanilic acid (1 μM-1 mM) induced a slow and progressive increase in intracellular free-calcium concentration that reached a plateau. The effect of sulfanilic acid was not concentration-dependent. Stimulation of cells with thapsigargin (1â¯Î¼M) after treatment with sulfanilic acid (1â¯mM) induced a smaller Ca2+ response compared with that obtained with thapsigargin alone. Sulfanilic acid induced a concentration-dependent production of reactive oxygen species; however, this effect was not Ca2+-dependent. Depolarization of mitochondrial membrane potential was observed at the concentration of 1â¯mM sulfanilic acid. In the presence of the compound a decrease in the GSH/GSSG ratio was observed. A decrease in the expression of superoxide dismutase 2 was noted. Finally, stimulation of cells with CCK-8 led to a concentration-dependent increase of trypsin secretion that was impaired by pretreatment of cells with sulfanilic acid. Preincubation of cells with the antioxidant melatonin (100â¯Î¼M) reduced the effect of sulfanilic acid on trypsin secretion. We conclude that sulfanilic acid might induce oxidative stress, which could alter Ca2+ signaling and enzyme secretion in pancreatic AR42J cells. This creates a situation potentially leading to damage of the exocrine pancreas.
Keywords
AR42J cellsCCK-8sarcoendoplasmic reticulum Ca2+-ATPaseBAPNACM-H2DCFDATMRMSOD2EGTAGSHThapsigarginGSSGFCCPTPsFURA-2/AM5-(and-6)-chloromethyl-2′,7′-dichlorodihydrofluorescein diacetate, acetyl estercholecystokinin octapeptideROS[Ca2+]iHydrogen peroxideFura-2 acetoxymethyl esterSulfanilic acidSuperoxide dismutase 2endoplasmic reticulumintracellular free Ca2+ concentrationSERCAtetramethylrhodamine methyl esterH2O2Pancreasreduced glutathionecarbonyl cyanide 4-(trifluoromethoxy)phenylhydrazoneCalciumoxidized glutathioneReactive oxygen species
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Authors
Fatma Zohra Ameur, Nabila Mehedi, Omar Kheroua, Djamel Saïdi, Gines M. Salido, Antonio Gonzalez,