Khalil Ayman, Al-Massarani Ghassan, Aljapawe Abdulmunim, Ekhtiar Adnan, Bakir M Adel
Human Nutrition Laboratory, Department of Radiation Medicine, Atomic Energy Commission of Syria (AECS), Damascus, Syria.
Biomarkers Laboratory, Radiation Medicine Department, Atomic Energy Commission of Syria (AECS), Damascus, Syria.
Front Pharmacol. 2020 Sep 4;11:528400. doi: 10.3389/fphar.2020.528400. eCollection 2020.
Wistar rats were whole body irradiated with a single dose of 2 Gy post administration with 10 or 100 mg/kg of resveratrol (RSV) intraperitoneally for 30 days. Rats' livers were dissected and processed to analyze immune response profiles of Th1, Th2, Th9, Th17, and Th22 by flow cytometry. In addition, peripheral blood samples were collected and circulating endothelial cells (CECs) were counted as an indicator for endothelial damage. Results demonstrated that resveratrol at 100 mg/kg enhanced liver immunological response influenced by irradiation by inducing Th2 immune response that was revealed by an increase in IL-10 secretion to more than 5,000 pmol/ml post irradiation. Results also indicated that RSV, at a dose of 100 mg/kg, decreased levels of the main pro-inflammatory cytokines such as INF-, IL-22, IL-17A, and GM-CSF post irradiation. In addition, the same RSV was bound to upregulate the expression of IL-10 mRNA in isolated Kupffer cells (KCs) and their secretion of IL-10 post irradiation. The result demonstrated that KCs were the central source of this anti-inflammatory response mediated mainly by IL10. These results, proposed for the first time, clearly states that RSV promotes IL-10 mediated immune resolution by Kupffer cells and not by hepatocytes. This implies that KCs have a crucial role in radiotherapy. Additionally, this study showed that RSV had an anti-apoptotic effect through re-increasing the number of CECs, which is implicated in irradiation damage. Result of the current work discloses novel findings about the potential of RSV as a radio-protector agent of a natural origin and suggests novel roles of KCs as a pharmacological target during radiation exposure.
将Wistar大鼠腹腔注射10或100mg/kg白藜芦醇(RSV)30天,之后给予单次2Gy的全身照射。解剖大鼠肝脏并进行处理,通过流式细胞术分析Th1、Th2、Th9、Th17和Th22的免疫反应谱。此外,采集外周血样本,计数循环内皮细胞(CEC)作为内皮损伤的指标。结果表明,100mg/kg的白藜芦醇通过诱导Th2免疫反应增强了受辐射影响的肝脏免疫反应,照射后IL-10分泌增加至5000pmol/ml以上即可表明这一点。结果还表明,100mg/kg剂量的RSV在照射后降低了主要促炎细胞因子如INF-、IL-22、IL-17A和GM-CSF的水平。此外,相同剂量的RSV在照射后可上调分离的库普弗细胞(KC)中IL-10 mRNA的表达及其IL-10的分泌。结果表明,KC是主要由IL10介导的这种抗炎反应的核心来源。首次提出的这些结果清楚地表明,RSV通过库普弗细胞而非肝细胞促进IL-10介导的免疫消退。这意味着KC在放射治疗中起关键作用。此外,本研究表明,RSV通过重新增加与辐射损伤有关的CEC数量而具有抗凋亡作用。当前工作的结果揭示了关于RSV作为天然来源的放射保护剂潜力的新发现,并提出了KC在辐射暴露期间作为药理学靶点的新作用。