Molecular Physiology Division, Zoology Department, Faculty of Science, Beni-Suef University, Salah Salem St, 62511, Beni-Suef, Egypt.
Environ Sci Pollut Res Int. 2021 Aug;28(32):43515-43527. doi: 10.1007/s11356-021-13391-x. Epub 2021 Apr 9.
The study examines the prophylactic action of artichoke leaf hydroethanolic extract (ALE) and artichoke flower head hydroethanolic extract (AFE) against diethylnitrosamine (DEN)/acetylaminofluorene (AAF)-induced lung cancer in Wistar rats. To chemically induce lung cancer, DEN was injected intraperitoneally twice a week for a fortnight at a dose of 150 mg/kg body weight (b.w.), followed by oral supplementation of AAF four times a week for 3 weeks at a dose of 20 mg/kg b.w. The DEN/AAF-administered rats were orally supplemented with ALE or AFE at a dose of 100 mg/kg b.w. for 17 weeks starting from the 1st week of DEN injection to the 17th week of the experiment. The lung cancerous injuries resulting from DEN/AAF-administration were significantly improved by the treatment with ALE and AFE as observed in histological examination. In addition, there was a significant reduction in lung lipid peroxidation, with resultant elevation in antioxidant enzymatic activity of glutathione-S-transferase, glutathione peroxidase, glutathione reductase, and superoxide dismutase as well as glutathione content in DEN/AAF-supplemented rats treated with ALE and AFE as compared to DEN/AAF-administered control. The lung tumor suppressor protein (p53) and B-cell lymphoma-2 (Bcl-2) mRNA expression significantly increased in the rats treated with ALE and AFE. In conclusion, the finding showed that ALE and AFE produced anti-cancer prophylactic effects against DEN/AAF-induced lung cancer in rats via suppression of oxidative stress and improved apoptotic signal induction.
该研究考察了朝鲜蓟叶水醇提取物(ALE)和朝鲜蓟花花头水醇提取物(AFE)对二乙基亚硝胺(DEN)/乙酰氨基芴(AAF)诱导的 Wistar 大鼠肺癌的预防作用。为了化学诱导肺癌,每周两次向 DEN 腹腔内注射两次,剂量为 150mg/kg 体重(b.w.),然后每周口服 AAF 四次,剂量为 20mg/kg b.w.,持续 3 周。DEN/AAF 给药大鼠从 DEN 注射的第 1 周开始至实验的第 17 周,每天口服补充 ALE 或 AFE,剂量为 100mg/kg b.w.。用 ALE 和 AFE 治疗可显著改善 DEN/AAF 给药引起的肺癌损伤,如组织学检查所见。此外,DEN/AAF 补充大鼠的肺脂质过氧化显著减少,谷胱甘肽-S-转移酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶和超氧化物歧化酶的抗氧化酶活性以及谷胱甘肽含量升高。与 DEN/AAF 给药的对照组相比,用 ALE 和 AFE 治疗的 DEN/AAF 补充大鼠的肺肿瘤抑制蛋白(p53)和 B 细胞淋巴瘤-2(Bcl-2)mRNA 表达显著增加。总之,该发现表明,ALE 和 AFE 通过抑制氧化应激和改善凋亡信号诱导,对 DEN/AAF 诱导的大鼠肺癌产生了抗癌预防作用。