Zalewska Anna, Zięba Sara, Kostecka-Sochoń Paula, Kossakowska Agnieszka, Żendzian-Piotrowska Małgorzata, Matczuk Jan, Maciejczyk Mateusz
Laboratory of Experimental Dentistry, Medical University of Bialystok, Poland.
Student of the Faculty of Medicine with the Division of Dentistry at the Medical University of Bialystok, Poland; Students Scientific Club "Biochemistry of Civilization Diseases" at the Department of Hygiene, Epidemiology and Ergonomics, Medical University of Bialystok, Poland.
Oxid Med Cell Longev. 2020 Nov 14;2020:8831855. doi: 10.1155/2020/8831855. eCollection 2020.
Previous studies based on animal models demonstrated that N-acetylcysteine (NAC) prevents oxidative stress and improves salivary gland function when the NAC supplementation starts simultaneously with insulin resistance (IR) induction. This study is the first to evaluate the effect of a 4-week NAC supply on the antioxidant barrier and oxidative stress in Wistar rats after six weeks of high-fat diet (HFD) intake. Redox biomarkers were evaluated in the parotid (PG) and submandibular (SMG) salivary glands and stimulated whole saliva (SWS), as well as in the plasma and serum. We demonstrated that the activity of salivary peroxidase and superoxide dismutase and total antioxidant capacity were significantly higher in PG, SMG, and SWS of IR rats treated with NAC. It appears that in PG and SMG of rats fed an HFD, N-acetylcysteine supplementation abolishes oxidative modifications to proteins (evidenced by decreased content of advanced oxidation protein products (AOPP) and advanced glycation end products (AGE)). Simultaneously, it does not reverse oxidative modifications of lipids (as seen in increased concentration of 8-isoprostanes and 4-hydroxynonenal vs. the control), although it reduces the peroxidation of salivary lipids in relation to the group fed a high-fat diet alone. NAC administration increased protein levels in PG and SMG but did not affect saliva secretion, which was significantly lower compared to the controls. To sum up, the inclusion of NAC supplementation after six weeks of HFD feeding was effective in improving the general and salivary gland antioxidant status. Nevertheless, NAC did not eliminate salivary oxidative stress and only partially prevented salivary gland dysfunction.
以往基于动物模型的研究表明,当N-乙酰半胱氨酸(NAC)补充与胰岛素抵抗(IR)诱导同时开始时,它可预防氧化应激并改善唾液腺功能。本研究首次评估了在高脂饮食(HFD)摄入六周后,为期4周的NAC供应对Wistar大鼠抗氧化屏障和氧化应激的影响。在腮腺(PG)、下颌下腺(SMG)和刺激后的全唾液(SWS)以及血浆和血清中评估氧化还原生物标志物。我们证明,用NAC治疗的IR大鼠的PG、SMG和SWS中唾液过氧化物酶和超氧化物歧化酶的活性以及总抗氧化能力显著更高。似乎在喂食HFD的大鼠的PG和SMG中,补充N-乙酰半胱氨酸可消除蛋白质的氧化修饰(通过晚期氧化蛋白产物(AOPP)和晚期糖基化终产物(AGE)含量降低证明)。同时,它不会逆转脂质的氧化修饰(与对照组相比,8-异前列腺素和4-羟基壬烯醛浓度增加),尽管与仅喂食高脂饮食的组相比,它可减少唾液脂质的过氧化。给予NAC可提高PG和SMG中的蛋白质水平,但不影响唾液分泌,与对照组相比,唾液分泌显著降低。总之,在HFD喂养六周后补充NAC可有效改善全身和唾液腺的抗氧化状态。然而,NAC并未消除唾液氧化应激,仅部分预防了唾液腺功能障碍。