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Orally administered emu oil decreases acute inflammation and alters selected small intestinal parameters in a rat model of mucositis

机译:口服给药的鸸oil油可减少急性炎症并改变粘膜炎大鼠模型中选定的小肠参数

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摘要

Mucositis resulting from cancer chemotherapy is a serious disorder of the alimentary tract. Emu oil has demonstrated anti-inflammatory properties in animal models of arthritis and wound healing; however, its effects on the intestine remain unknown. We investigated emu oil for its potential to decrease the severity of mucositis in a rat model. Female Dark Agouti rats (110-150 g) were orogastrically gavaged with emu oil (0.5 or 1 ml) or water (1 ml) for 5 d before intraperitoneal injection of 5-fluorouracil (5-FU, 150 mg/kg) or saline (control), and this was continued up to the day of sacrifice (48, 72 and 96 h post 5-FU administration). Histological (villus height, crypt depth (CD) and disease severity score) and biochemical (myeloperoxidase (MPO) activity) parameters were determined in intestinal tissues collected at sacrifice. Sucrase activity in vivo was quantified by the sucrose breath test. Activated neutrophil activity (MPO) in the ileum was significantly decreased by emu oil (0.5 ml, 451 (sem 168) U/g and 1 ml, 503 (sem 213) U/g) compared with 5-FU-treated controls (1724 (sem 431) U/g) 96 h post 5-FU administration. There were also significant increases in CD (152 (sem 8) microm) in the ileum of rats that received 1 ml emu oil at 96 h compared with 5-FU-treated controls (CD (106 (sem 12) microm)). Emu oil did not affect sucrase activity. Emu oil decreased acute ileal inflammation, and improved mucosal architecture in the intestine during recovery from chemotherapy in rats. Further studies investigating the potential benefits of emu oil as a nutritional supplement for the treatment of intestinal disorders are indicated.
机译:由癌症化学疗法引起的粘膜炎是严重的消化道疾病。 mu油已在关节炎和伤口愈合的动物模型中显示出抗炎特性。然而,其对肠道的作用仍然未知。我们调查了oil油在大鼠模型中降低粘膜炎严重程度的潜力。在腹腔内注射5-氟尿嘧啶(5-FU,150 mg / kg)或生理盐水之前,对雌性Dark Agouti大鼠(110-150 g)口服e油(0.5或1 ml)或水(1 ml)灌胃5 d。 (对照),并且一直持续到处死之日(5-FU给药后48、72和96小时)。在处死时收集的肠组织中确定组织学(绒毛高度,隐窝深度(CD)和疾病严重程度评分)和生化(髓过氧化物酶(MPO)活性)参数。通过蔗糖呼气试验定量体内蔗糖酶活性。与5-FU处理的对照组相比,451油(0.5 ml,451(sem 168)U / g和1 ml,503(sem 213)U / g)显着降低了回肠中活化的中性粒细胞活性(MPO)(1724) (sem 431)U / g)施用5-FU后96小时。与5-FU处理的对照组(CD(106(sem 12)microm))相比,在96小时接受1 ml mu油的大鼠回肠中CD(152(sem 8)microm)也有显着增加。 mu油不影响蔗糖酶活性。 mu油可减轻大鼠急性回肠炎症,并改善大鼠化疗过程中肠道的黏膜结构。指出有进一步的研究调查e油作为营养补充剂治疗肠道疾病的潜在益处。

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