Department of Biomedical Sciences, State University of Rio Grande do Norte, Mossoró, Brazil.
Cancer Chemother Pharmacol. 2011 May;67(5):1085-100. doi: 10.1007/s00280-010-1409-7. Epub 2010 Jul 27.
PURPOSE: Oral mucositis (OM) is a frequent side effect in patients with cancer. We investigate the effect of atorvastatin (ATV), a cholesterol-lowering drug, on OM induced by 5-fluorouracil (5-FU) in hamsters. METHODS: OM was induced by the i.p. administration of 5-FU, with excoriations of the cheek pouch mucosa. The animals were pretreated with i.p. ATV 1, 5 or 10 mg/kg or vehicle (saline and 5% (vol/vol) ethanol) 30 min before 5-FU injection and daily for 5 or 10 days. Samples of cheek pouches and main organs were removed for histopathological analysis, determination of TNF-α, IL-1β, nitrite, non-protein sulfhydryl group (NP-SH) levels, myeloperoxidase (MPO) assay and immunohistochemistry for induced nitric oxide synthase (iNOS). Blood was collected for a leukogram analysis of biochemical parameters and analysis of bacteremia. RESULTS: ATV at doses of 1 and 5 mg/kg reduced mucosal damage and inflammation, as well as the levels of cytokines, nitrite and myeloperoxidase activity on the 5th and 10th day of OM and immunostaining for iNOS on the 5th day of OM.ATV at 1 mg/kg increased cheek pouch NP-SH when compared to 5-FU groups on the 10th day of OM. The association between ATV 5 mg/kg and 5-FU decreased the survival rate, amplified the leukopenia of animals, increased transaminase serum levels and caused liver lesions. We also detected the presence of Gram-negative bacillus in the blood of 100% of the animals treated with ATV 5 mg/kg + 5-FU. CONCLUSIONS: Atorvastatin prevented mucosal damage and inflammation associated with 5-FU-induced OM, but the association of a higher dose of ATV with 5-FU induced hepatotoxicity and amplified leukopenia.
目的:口腔黏膜炎(OM)是癌症患者常见的副作用。我们研究了降脂药阿托伐他汀(ATV)对氟尿嘧啶(5-FU)诱导的仓鼠 OM 的影响。
方法:通过腹腔注射 5-FU 引起 OM,使颊囊黏膜擦伤。动物在 5-FU 注射前 30 分钟腹腔注射 ATV 1、5 或 10 mg/kg 或载体(生理盐水和 5%(体积/体积)乙醇),并在第 5 天或第 10 天每天注射一次。切除颊囊和主要器官的样本进行组织病理学分析、TNF-α、IL-1β、亚硝酸盐、非蛋白巯基(NP-SH)水平、髓过氧化物酶(MPO)测定和诱导型一氧化氮合酶(iNOS)免疫组化。采集血液进行白细胞计数分析生化参数和菌血症分析。
结果:ATV 1 和 5 mg/kg 剂量在第 5 和第 10 天减轻了 OM 时的黏膜损伤和炎症以及细胞因子、亚硝酸盐和 MPO 活性水平,并在第 5 天减轻了 iNOS 免疫染色。与 5-FU 组相比,ATV 1 mg/kg 在第 10 天增加了颊囊 NP-SH。ATV 5 mg/kg 与 5-FU 联合使用降低了存活率,加重了动物的白细胞减少症,增加了血清转氨酶水平并导致肝脏病变。我们还检测到 100%用 ATV 5 mg/kg+5-FU 治疗的动物血液中存在革兰氏阴性杆菌。
结论:阿托伐他汀预防了与 5-FU 诱导的 OM 相关的黏膜损伤和炎症,但较高剂量的 ATV 与 5-FU 联合使用会引起肝毒性并加重白细胞减少症。
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