Jesus Tiago M, Azevedo Tiago, Silva-Reis Rita, Ferreira Tiago, Nascimento-Gonçalves Elisabete, Medeiros Catarina, Ferreira João, Gama Adelina, Gaivão Isabel, Pires Maria João, Lanzarin Germano, Félix Luís, Venâncio Carlos, Medeiros Rui, Bastos Margarida M S M, Finimundy Tiane C, Barros Lillian, Gil DA Costa Rui M, Oliveira Paula A
Centre for the Research and Technology of Agro-Environmental and Biological Sciences (CITAB), Institute for Innovation, Capacity Building and Sustainability of Agri-food Production (Inov4Agro), University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal.
Centre for the Research and Technology of Agro-Environmental and Biological Sciences (CITAB), Institute for Innovation, Capacity Building and Sustainability of Agri-food Production (Inov4Agro), University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal;
In Vivo. 2025 May-Jun;39(3):1303-1313. doi: 10.21873/invivo.13934.
BACKGROUND/AIM: Human papillomavirus (HPV) is the most common sexually transmitted infectious agent and, in cases of persistent infection, may cause cancer. This study evaluated the toxicological and antitumor properties of extract (MSE) in KP14HPV16 mice, which carry HPV16 oncogenes.
Thirty-three female FVB/n mice (), including 17 HPV-transgenic and 16 wild-type (WT) mice, were divided into six groups. The control groups received tap water (WT-C, =5, and HPV-C, =6), while the treatment groups received either 0.50 mg/ml MSE (WT-50 and HPV-50, =6) or 0.55 mg/ml MSE (WT-55 and HPV-55, =5) in drinking water for 28 days. Afterwards, animals were sacrificed, and blood and organs were collected for histopathological and biochemical analysis.
The main phenolic compounds in MSE were rosmarinic acid and luteolin--glucoronide. MSE did not significantly affect weight gain in WT mice; however, WT-55 gained significantly more weight than HPV-55. MSE demonstrated antioxidant activity as indicated by the modulation of hepatic superoxide dismutase and glutathione S-transferase (GST) activity, as well as renal GST activity, in MSE-treated HPV groups. MSE did not reduce histological lesion incidence or systemic inflammation in HPV16-transgenic mice.
In general, while MSE was safe and exhibited antioxidant activity, it did not significantly impact HPV16-induced lesions, warranting further research to assess systemic effects with different concentrations and durations.
背景/目的:人乳头瘤病毒(HPV)是最常见的性传播感染病原体,在持续感染的情况下可能引发癌症。本研究评估了提取物(MSE)对携带HPV16致癌基因的KP14HPV16小鼠的毒理学和抗肿瘤特性。
33只雌性FVB/n小鼠(其中17只为HPV转基因小鼠,16只为野生型(WT)小鼠)被分为六组。对照组饮用自来水(WT-C,n = 5,HPV-C,n = 6),而治疗组在饮用水中分别接受0.50 mg/ml MSE(WT-50和HPV-50,n = 6)或0.55 mg/ml MSE(WT-55和HPV-55,n = 5),持续28天。之后,处死动物,采集血液和器官进行组织病理学和生化分析。
MSE中的主要酚类化合物为迷迭香酸和木犀草素 - 葡萄糖醛酸苷。MSE对WT小鼠的体重增加没有显著影响;然而,WT-55组的体重显著高于HPV-55组。在MSE处理的HPV组中,肝超氧化物歧化酶和谷胱甘肽S-转移酶(GST)活性以及肾GST活性的调节表明MSE具有抗氧化活性。MSE并未降低HPV16转基因小鼠的组织学病变发生率或全身炎症。
总体而言,虽然MSE安全且具有抗氧化活性,但它对HPV16诱导的病变没有显著影响,需要进一步研究以评估不同浓度和持续时间的全身效应。