Buendía Jefferson Antonio, Justinico Castro José Armando, Vela Laura Joanna Tapia, Sinisterra Denis, Sánchez Villamil Juana Patricia, Zuluaga Salazar Andrés Felipe
Grupo de Investigación en Farmacología y Toxicología, Centro de Información y Estudio de Medicamentos y Tóxicos (CIEMTO), Facultad de Medicina, Universidad de Antioquia, Carrera 51D #62-29, Medellín, Colombia.
Departamento de Patología, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
BMC Res Notes. 2019 Sep 18;12(1):584. doi: 10.1186/s13104-019-4598-0.
The aim of this study was to compare in vivo effect of five pharmacological options on inflammation and pulmonary fibrosis induced by paraquat.
54 Wistar SPF rats were used. After 2 h post-intoxication with paraquat ion, groups of 9 animals were randomly assigned to (1) cyclophosphamide plus dexamethasone (2) low molecular weight heparin (3) unfractionated heparin (4) vitamin C every 24 h, (5) atorvastatin or (6) placebo with intraperitoneal saline. Lung inflammation, alveolar injury, hepatocyte damage, hepatic regeneration, acute tubular necrosis and kidney congestion were evaluated.
In the control group 100% of animals presented moderate and severe lung inflammation, while in the groups with atorvastatin and intratracheal heparin this proportion was lower (55.5%; CI 26.6-81.3%) (p = 0.025). A lower degree of moderate or severe hepatic regeneration was evident in the treatment groups with atorvastatin (p = 0.009). In this study was demonstrated that statins and heparin might have a protective effect in the paraquat-induced destructive phase. More evidence is needed to evaluated of dose-response effects of these drugs before to study in clinical trials.
本研究旨在比较五种药物疗法对百草枯诱导的炎症和肺纤维化的体内作用。
使用54只Wistar无特定病原体大鼠。在百草枯中毒2小时后,将9只动物分为一组,随机分配至(1)环磷酰胺加地塞米松组;(2)低分子量肝素组;(3)普通肝素组;(4)每24小时给予维生素C组;(5)阿托伐他汀组;或(6)腹腔注射生理盐水的安慰剂组。评估肺部炎症、肺泡损伤、肝细胞损伤、肝再生、急性肾小管坏死和肾脏充血情况。
在对照组中,100%的动物出现中度和重度肺部炎症,而在阿托伐他汀组和气管内肝素组中,这一比例较低(55.5%;置信区间26.6 - 81.3%)(p = 0.025)。在阿托伐他汀治疗组中,中度或重度肝再生程度较低(p = 0.009)。本研究表明,他汀类药物和肝素可能在百草枯诱导的破坏期具有保护作用。在进行临床试验研究之前,需要更多证据来评估这些药物的剂量反应效应。