Doctoral Studies, Medical University of Bialystok, Poland.
Department of Hygiene, Epidemiology and Ergonomics, Medical University of Bialystok, Poland.
Oxid Med Cell Longev. 2020 Jan 3;2020:9086024. doi: 10.1155/2020/9086024. eCollection 2020.
The aim of our research was to evaluate redox balance parameters and biomarkers of oxidative stress (OS) in nonstimulated and stimulated saliva as well as the blood of patients with plaque psoriasis compared to healthy controls. The study involved 40 patients with plaque psoriasis and 40 generally healthy subjects matched by age and gender to the study group patients. We assayed the concentration/activity of antioxidant enzymes: salivary peroxidase (Px), catalase (CAT), and superoxide dismutase (SOD) measured in unstimulated saliva (NWS), stimulated saliva (SWS), and erythrocytes. In plasma as well as NWS and SWS, we measured the concentration/activity of reduced glutathione (GSH), total antioxidant potential (TAC), total oxidative status (TOS), oxidative stress index (OSI), and markers of oxidative modification of proteins: advanced glycation end products (AGE), advanced oxidation protein products (AOPP), and lipid oxidation products: malondialdehyde (MDA) and total lipid hydroperoxide (LOOH). In NWS and SWS, we also evaluated the rate of reactive oxygen species (ROS) production. The concentration of Px, CAT, and SOD was significantly higher in NWS of patients with plaque psoriasis vs. healthy subjects. In SWS of psoriatic patients, we observed considerably higher concentration of Px and CAT, and in erythrocytes of patients with plaque psoriasis, the concentration of GPx and CAT was significantly higher compared to that in the controls. The levels of AOPP, AGE, MDA, and LOOH were considerably higher in NWS, SWS, and plasma of the study group compared to the controls. The concentration of total protein and salivary amylase was significantly lower in NWS and SWS of psoriatic patients compared to the healthy control. In the course of plaque psoriasis, we observed redox imbalances with prevalence of oxidation reactions. Mechanisms involved in the synthesis/secretion of proteins and activity of amylase were depressed in both glands of psoriatic patients; however, they were more inhibited in the parotid gland compared to the submandibular gland. TOS concentration and OSI value in NWS and SWS may serve as diagnostic biomarkers of plaque psoriasis.
我们的研究目的是评估非刺激和刺激唾液以及斑块型银屑病患者血液中的氧化还原平衡参数和氧化应激(OS)生物标志物,并将其与健康对照组进行比较。该研究纳入了 40 名斑块型银屑病患者和 40 名年龄和性别与研究组患者相匹配的健康对照者。我们检测了非刺激唾液(NWS)、刺激唾液(SWS)和红细胞中抗氧化酶的浓度/活性:唾液过氧化物酶(Px)、过氧化氢酶(CAT)和超氧化物歧化酶(SOD)。我们还在血浆以及 NWS 和 SWS 中测量了还原型谷胱甘肽(GSH)、总抗氧化能力(TAC)、总氧化状态(TOS)、氧化应激指数(OSI)以及蛋白质氧化修饰标志物的浓度/活性:晚期糖基化终产物(AGE)、晚期氧化蛋白产物(AOPP)和脂质氧化产物:丙二醛(MDA)和总脂质过氧化物(LOOH)。我们还在 NWS 和 SWS 中评估了活性氧(ROS)的产生速率。与健康对照组相比,斑块型银屑病患者的 NWS 中 Px、CAT 和 SOD 的浓度明显更高。在银屑病患者的 SWS 中,我们观察到 Px 和 CAT 的浓度明显更高,而在斑块型银屑病患者的红细胞中,GPx 和 CAT 的浓度明显高于对照组。与对照组相比,研究组的 NWS、SWS 和血浆中的 AOPP、AGE、MDA 和 LOOH 水平明显更高。与健康对照组相比,银屑病患者的 NWS 和 SWS 中的总蛋白和唾液淀粉酶浓度明显更低。在斑块型银屑病患者中,我们观察到氧化还原失衡,氧化反应占主导地位。在两个腺体中,涉及蛋白质合成/分泌和淀粉酶活性的机制都受到了抑制;然而,与颌下腺相比,在腮腺中受到的抑制更为明显。NWS 和 SWS 中的 TOS 浓度和 OSI 值可能作为斑块型银屑病的诊断生物标志物。