Division of Biochemistry, Department of Physiology and Biochemistry, University of Veterinary Medicine, István utca 2, H-1078 Budapest, Hungary.
Department of Pharmacology and Toxicology, University of Veterinary Medicine, István utca 2, H-1078 Budapest, Hungary.
Oxid Med Cell Longev. 2020 Dec 8;2020:3181202. doi: 10.1155/2020/3181202. eCollection 2020.
Bioactive compounds such as benzoquinone derivates presented in fermented wheat germ extract (FWGE) have several positive effects on overall health status of humans and animals alike. Since available data regarding the antioxidant activity of FWGE are limited, the aim of our study was to investigate its effects on the cellular redox homeostasis applying primary hepatocyte cell cultures of rat origin. Cultures were challenged to lipopolysaccharide (LPS) treatment for 2 or 8 hours to trigger inflammatory response. Further, culture media were concomitantly supplemented with or without FWGE (Immunovet®, 0.1% and 1%). In order to monitor the metabolic activity of the cell cultures, CCK-8 test was applied, while reactive oxygen species (ROS) production was measured using Amplex Red method. Malondialdehyde concentration of culture media as a specific marker of lipid peroxidation and the activity of glutathione peroxidase in cell lysates were also determined to monitor the redox status of the cultures. Based on our findings, it can be concluded that FWGE did not show cytotoxic effects in any applied concentration in cell cultures. Furthermore, FWGE efficiently decreased cellular ROS production and lipid peroxidation rate in case of LPS-induced inflammatory response. However, without LPS treatment, higher concentration of FWGE increased the rate of both ROS and malondialdehyde synthesis. This observation may refer to the prooxidant activity of high dose FWGE, which is an important beneficial effect regarding tumor cells. However, in case of noninflamed hepatocytes, considering the results of glutathione peroxidase activity, the application of the product did not result in severe oxidative distress. In accordance with the abovementioned findings, FWGE as a redox modulator, applied in the appropriate concentration, can serve as a promising candidate in the supplementary therapy of patients suffering from various inflammatory diseases, decreasing the free radical generation, thus avoiding the occurrence of cytotoxic effects.
生物活性化合物,如苯醌衍生物,存在于发酵小麦胚芽提取物(FWGE)中,对人类和动物的整体健康状况有多种积极影响。由于关于 FWGE 的抗氧化活性的可用数据有限,因此我们的研究目的是应用大鼠原代肝细胞培养物来研究其对细胞氧化还原稳态的影响。培养物受到脂多糖(LPS)处理 2 或 8 小时,以引发炎症反应。此外,培养基同时补充或不补充 FWGE(Immunovet®,0.1%和 1%)。为了监测细胞培养物的代谢活性,应用 CCK-8 试验,同时使用 Amplex Red 法测量活性氧(ROS)的产生。还测定了培养基中丙二醛浓度作为脂质过氧化的特异性标志物以及细胞裂解物中谷胱甘肽过氧化物酶的活性,以监测培养物的氧化还原状态。根据我们的发现,可以得出结论,FWGE 在任何应用浓度的细胞培养物中均未显示细胞毒性作用。此外,FWGE 有效地降低了 LPS 诱导的炎症反应中细胞内 ROS 的产生和脂质过氧化速率。但是,没有 LPS 处理时,较高浓度的 FWGE 增加了 ROS 和丙二醛合成的速率。这种观察结果可能与高剂量 FWGE 的促氧化剂活性有关,这对于肿瘤细胞是一个重要的有益作用。但是,在非炎症性肝细胞的情况下,考虑到谷胱甘肽过氧化物酶活性的结果,该产品的应用并未导致严重的氧化应激。根据上述发现,FWGE 作为一种氧化还原调节剂,在适当的浓度下应用,可以作为患有各种炎症性疾病的患者的补充治疗的有前途的候选物,减少自由基的产生,从而避免细胞毒性作用的发生。