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哺乳仔猪口服甘氨酸亚铁螯合物导致的致死性胃黏膜坏死

Lethal Gastric Mucosal Necrosis due to Administration of Oral Ferrous Bisglycinate Chelate to Suckling Piglets.

作者信息

Stokar-Regenscheit N, Sydler T, Bürgi E, Lippuner A, Naegeli H, Sidler X

机构信息

Institute of Animal Pathology, Vetsuisse Faculty, University of Bern, Bern, Switzerland.

Institute of Veterinary Pathology, Switzerland.

出版信息

J Comp Pathol. 2017 Jul;157(1):39-45. doi: 10.1016/j.jcpa.2017.04.004. Epub 2017 Jun 9.

Abstract

The oral application of a newly developed ferrous bisglycinate paste for suckling piglets at a dose of 180 mg/kg body weight led to increased death rates in 10% (n = 10) of Swiss test pig breeding farms (n = 100). Necropsy examination of suckling piglets (n = 12), selected randomly from the test farms with increased death rates, demonstrated severe gastric mucosal ulceration and necrosis. Due to the presence of crystalline iron surface coating within the gastric lesions, the iron was considered as the toxic principle and cause of death. To demonstrate the direct toxicity of ferrous bisglycinate, the paste was administered experimentally to a litter of suckling piglets (n = 11). Different time points (24, 48 and 72 h post partum) and doses (180 mg/kg and 360 mg/kg) were investigated. The manufacturer's recommended dose of 180 mg/kg corresponded to approximately 36 mg Fe/kg and to 6.4 % of the acute lethal dose of oral iron in rats. In all piglets the lesions were reproduced and most severe at the earliest time point (24 h post partum) and with the highest applied dose (360 mg/kg). The lesions were in accordance with those described from oral iron intoxication in man, suggesting pigs as an ideal animal model for oral iron toxicity studies.

摘要

对哺乳仔猪口服一种新开发的甘氨酸亚铁糊剂,剂量为180毫克/千克体重,在10%(n = 10)的瑞士试验猪场(n = 100)中导致死亡率上升。从死亡率上升的试验猪场中随机挑选12只哺乳仔猪进行尸检,结果显示存在严重的胃黏膜溃疡和坏死。由于胃部病变处存在结晶状铁表面涂层,铁被认为是有毒成分和死亡原因。为证明甘氨酸亚铁的直接毒性,将该糊剂以不同时间点(产后24、48和72小时)和剂量(180毫克/千克和360毫克/千克)对一窝哺乳仔猪(n = 11)进行实验性给药。制造商推荐的180毫克/千克剂量相当于约36毫克铁/千克,相当于大鼠口服铁急性致死剂量的6.4%。在所有仔猪中都再现了病变,且在最早时间点(产后24小时)和最高给药剂量(360毫克/千克)时最为严重。这些病变与人类口服铁中毒所描述的病变一致,表明猪是口服铁毒性研究的理想动物模型。

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