Barbosa Maiara M C, Vicentini Fernando A, Castro-Ghizoni Cristiane V, Lameira Osmar A, Sa-Nakanishi Anacharis B, Bracht Livia, Peralta Rosane M, Natali Maria R M, Bracht Adelar, Comar Jurandir F
Department of Biochemistry, University of Maringa, 87020900 Maringa, Brazil.
Department of Morphological Sciences, University of Maringa, 87020900 Maringa, Brazil.
Endocr Metab Immune Disord Drug Targets. 2018;18(3):268-280. doi: 10.2174/1871530318666180215102029.
TNBS-induced colitis is an experimental immunopathology in rats that shares many features with human inflammatory bowel diseases. Copaiba oleoresin is extracted from plants of the genus Copaifera and is shown to reduce inflammation.
The aim of this study was to investigate the action of copaiba oil (C. reticulata Ducke) on inflammation and oxidative status in the distal colon of colitic rats.
Acute and subchronic colitis were induced in Wistar rats by an intracolonic enema with 2,4,6-trinitrobenzenesulfonic acid (TNBS). The colonic morphology was assessed by histological analysis and the oxidative stress parameters were measured in the intestinal homogenate. The liver damage markers were measured in the plasma. Control and colitic rats were orally treated either with one single dose (acute colitis) of copaiba oil (1.15 g Kg-1) or once a day during seven days (subchronic colitis).
The intestinal morphology was severely modified by acute and subchronic colitis, as indicated by the intramural infiltration of polymorphonuclear cells and the increased thickness of all colon layers. The levels of TBARS, protein carbonyl groups and reactive oxygen species (ROS) were increased in the intestine of colitic rats. Copaiba oil did not attenuate the inflammatory damage in acute and subchronic colitis, but it decreased the activity of myeloperoxidase, leukocyte infiltration and oxidative stress in the colon. The level of plasma bilirubin and the activity of alkaline phosphatase were both increased in treated healthy and colitic rats.
Copaiba oil decreased oxidative stress and inflammation but did not prevent intestinal damage in the colon of colitic rats. The alterations of plasma markers of hepatic damage caused by the oil seem to be associated to its harmful action on the liver.
三硝基苯磺酸(TNBS)诱导的结肠炎是一种大鼠实验性免疫病理学模型,与人类炎症性肠病有许多共同特征。巴西香脂树脂从巴西香脂属植物中提取,已证明具有抗炎作用。
本研究旨在探讨巴西香脂油(C. reticulata Ducke)对结肠炎大鼠远端结肠炎症和氧化状态的影响。
通过向Wistar大鼠结肠内注入2,4,6-三硝基苯磺酸(TNBS)诱导急性和亚慢性结肠炎。通过组织学分析评估结肠形态,并在肠道匀浆中测量氧化应激参数。在血浆中测量肝损伤标志物。对照组和结肠炎大鼠口服单剂量(急性结肠炎)巴西香脂油(1.15 g Kg-1)或连续7天每天一次(亚慢性结肠炎)。
急性和亚慢性结肠炎严重改变了肠道形态,表现为多形核细胞壁内浸润和所有结肠层厚度增加。结肠炎大鼠肠道中丙二醛、蛋白质羰基和活性氧(ROS)水平升高。巴西香脂油在急性和亚慢性结肠炎中并未减轻炎症损伤,但降低了结肠中髓过氧化物酶活性、白细胞浸润和氧化应激。治疗后的健康大鼠和结肠炎大鼠血浆胆红素水平和碱性磷酸酶活性均升高。
巴西香脂油降低了氧化应激和炎症,但并未预防结肠炎大鼠结肠的肠道损伤。该油引起的肝损伤血浆标志物改变似乎与其对肝脏的有害作用有关。