Institute of Molecular Pathology Biomarkers, University of Extremadura, Caceres, Spain; Laboratoire de Physiologie de la Nutrition et de Sécurité Alimentaire - Université d'Oran1, Ahmed BenBella, Algeria.
Laboratoire de Physiologie de la Nutrition et de Sécurité Alimentaire - Université d'Oran1, Ahmed BenBella, Algeria.
Food Chem Toxicol. 2018 Oct;120:71-80. doi: 10.1016/j.fct.2018.07.001. Epub 2018 Jul 3.
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 (1 μM) after treatment with sulfanilic acid (1 mM) induced a smaller Ca response compared with that obtained with thapsigargin alone. Sulfanilic acid induced a concentration-dependent production of reactive oxygen species; however, this effect was not Ca-dependent. Depolarization of mitochondrial membrane potential was observed at the concentration of 1 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 (100 μM) reduced the effect of sulfanilic acid on trypsin secretion. We conclude that sulfanilic acid might induce oxidative stress, which could alter Ca signaling and enzyme secretion in pancreatic AR42J cells. This creates a situation potentially leading to damage of the exocrine pancreas.
我们研究了食用柠檬黄代谢物磺胺酸对胰腺 AR42J 细胞生理功能的影响。磺胺酸(1 μM-1 mM)可缓慢且逐渐增加细胞内游离钙浓度,并达到平台期。磺胺酸的作用与浓度无关。在用磺胺酸(1 mM)处理细胞后用他普西醇(1 μM)刺激细胞,与单独用他普西醇相比,Ca 反应较小。磺胺酸诱导产生与浓度相关的活性氧;然而,这种作用与 Ca 无关。在 1 mM 磺胺酸的浓度下观察到线粒体膜电位去极化。在存在该化合物的情况下,观察到 GSH/GSSG 比值降低。注意到超氧化物歧化酶 2 的表达减少。最后,用 CCK-8 刺激细胞可导致胰蛋白酶分泌浓度依赖性增加,而用磺胺酸预处理细胞可损害该作用。细胞用抗氧化剂褪黑素(100 μM)预孵育可降低磺胺酸对胰蛋白酶分泌的作用。我们得出结论,磺胺酸可能会诱导氧化应激,从而改变胰腺 AR42J 细胞中的 Ca 信号和酶分泌。这可能导致外分泌胰腺受损。