Marks S L, Cook A K, Reader R, Kass P H, Théon A P, Greve C, Rogers Q R
Department of Medicine and Epidemiology, University of California, Davis 95616, USA.
Am J Vet Res. 1999 Jun;60(6):755-63.
To determine effects of glutamine-supplemented and glutamine-free amino acid-based purified diets, compared with a dry expanded diet, on intestinal structure and function in a model that used cats with methotrexate-induced enteritis.
18 adult specific-pathogen-free cats.
12 cats were given intragastric feedings of an amino acid-based purified diet supplemented with glutamine (7% [wt:wt]) or an isonitrogenous amount of glycine and alanine; 6 cats consumed a dry expanded diet. After 21 days, cats received methotrexate (MTX; 11 mg/kg of body weight, IV). Intestinal permeability testing was performed immediately before and 66 hours after MTX administration. Celiotomy was performed 72 hours after MTX administration for aseptic removal of mesenteric lymph nodes, collection of full-thickness intestinal biopsy specimens, determination of intestinal cellular proliferation, and collection of aortic and portal venous blood samples for determination of arteriovenous amino acid concentrations across the intestine.
Administration of MTX was associated with severe enterotoxicosis manifested as diarrhea (8/12 cats), vomiting (12/12), and positive results for bacterial culture of mesenteric lymph nodes (12/12) in cats receiving the purified diets, independent of glutamine supplementation. Diet did not affect villus tip length and villus surface area in the small intestine or cellular proliferation. Administration of MTX was associated with significantly increased intestinal permeability, which was not attenuated by glutamine supplementation.
Feeding of a glutamine-supplemented amino acid-based purified diet was unable to preserve intestinal function in cats with MTX-induced enteritis.
Intestinal morphologic alterations correlate poorly with intestinal function as measured by means of bacterial translocation and intestinal permeability.
在甲氨蝶呤诱导肠炎的猫模型中,确定补充谷氨酰胺和不含谷氨酰胺的氨基酸基纯化日粮与干膨化日粮相比,对肠道结构和功能的影响。
18只成年无特定病原体猫。
12只猫经胃给予补充谷氨酰胺(7%[重量比])的氨基酸基纯化日粮或等氮量的甘氨酸和丙氨酸;6只猫食用干膨化日粮。21天后,猫接受甲氨蝶呤(MTX;11mg/kg体重,静脉注射)。在MTX给药前和给药后66小时立即进行肠道通透性测试。MTX给药后72小时进行剖腹术,无菌切除肠系膜淋巴结,收集全层肠道活检标本,测定肠道细胞增殖,并采集主动脉和门静脉血样以测定肠道动静脉氨基酸浓度。
在接受纯化日粮的猫中,MTX给药与严重的肠中毒相关,表现为腹泻(8/12只猫)、呕吐(12/12)和肠系膜淋巴结细菌培养阳性(12/12),与谷氨酰胺补充无关。日粮不影响小肠绒毛顶端长度和绒毛表面积或细胞增殖。MTX给药与肠道通透性显著增加相关,补充谷氨酰胺并未使其减弱。
在甲氨蝶呤诱导肠炎的猫中,饲喂补充谷氨酰胺的氨基酸基纯化日粮无法维持肠道功能。
肠道形态学改变与通过细菌移位和肠道通透性测量的肠道功能相关性较差。