School of Animal and Veterinary Sciences, Roseworthy Campus, University of Adelaide, Roseworthy, SA, Australia.
Br J Nutr. 2010 Aug;104(4):513-9. doi: 10.1017/S000711451000084X. Epub 2010 Apr 9.
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.
癌症化疗引起的粘膜炎是一种严重的消化道疾病。鸸鹋油在关节炎和伤口愈合的动物模型中表现出抗炎特性;然而,其对肠道的影响尚不清楚。我们研究了鸸鹋油在大鼠模型中减轻粘膜炎严重程度的潜力。雌性 Dark Agouti 大鼠(110-150 g)经口灌胃给予鸸鹋油(0.5 或 1 ml)或水(1 ml),连续 5 天,然后腹腔注射 5-氟尿嘧啶(5-FU,150 mg/kg)或生理盐水(对照),并持续至处死日(5-FU 给药后 48、72 和 96 小时)。处死时采集肠组织,测定组织学(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测定体内蔗糖酶活性。与 5-FU 处理的对照组(1724 (sem 431) U/g)相比,1 毫升鸸鹋油(451 (sem 168) U/g 和 1 毫升,503 (sem 213) U/g)可显著降低 96 小时时 5-FU 处理大鼠空肠的中性粒细胞活性(MPO)。在接受 1 毫升鸸鹋油的大鼠中,空肠 CD 也显著增加(96 小时时 152 (sem 8) μm),与 5-FU 处理的对照组相比(106 (sem 12) μm)。鸸鹋油不影响蔗糖酶活性。鸸鹋油可降低化疗恢复期间大鼠急性空肠炎症,并改善肠道粘膜结构。需要进一步研究鸸鹋油作为治疗肠道疾病的营养补充剂的潜在益处。