用含中链甘油三酯的乳剂作为替代热量来源对大鼠和家兔的发育毒性研究

Susan Henwood , Daniel Wilson , Randy White , Susan Trimbo
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引用次数: 11

摘要

含有甘油三酯的脂质乳剂被设计为热量来源,可以静脉注射给那些不能通过传统的肠外治疗满足其营养需求的病人。在这项研究中,我们评估了含有中链甘油三酯(MCT)与长链含脂乳(LCT)比例为3:1的20%脂质乳的发育毒性。该乳剂分别以5 mL/kg和21.4 mL/kg的剂量体积以1 g脂/kg和4.28 g脂/kg的剂量静脉滴注给大鼠和家兔,在器官发生期间每天1次,以评估试验品的潜在发育毒性。对照组给予0.9%生理盐水,剂量体积21.4 mL/kg。观察动物的临床毒性症状以及对体重和饲料消耗的不良影响。在第20天(大鼠)或第29天(家兔),对雌性进行尸检并检查母体和胚胎/胎儿毒性。取出胎儿,称重,检查外部、软组织和骨骼异常。4.28 g脂质/kg的剂量导致大鼠和家兔的饲料消耗量降低,这是基于测试品的高热量特性的预期结果。对于给予4.28 g脂质/kg的大鼠,潜在的与试验物品相关的大体尸检发现,包括淋巴结和脾脏肿大、胸腺小和肾盂肿大,发生率较低。即使存在一些母体毒性,对大鼠的胎儿参数也没有不良影响。然而,给脂量为4.28 g /kg的家兔出现胚胎和胎儿毒性(即再吸收)和骨骼异常。在本研究条件下,发育毒性的无观察效应水平为大鼠≥4.28 g脂质/kg,家兔≥1 g脂质/kg但小于4.28 g脂质/kg。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developmental Toxicity Study in Rats and Rabbits Administered an Emulsion Containing Medium Chain Triglycerides as an Alternative Caloric Source

Triglyceride-containing lipid emulsions have been designed as caloric sources that can be administered intravenously to patients that cannot meet their nutritional needs by conventional parenteral therapies. In this study, we evaluate the developmental toxicity of a 20% lipid emulsion that contains a 3:1 ratio of medium chain triglyceride (MCT) to one long chain containing lipid emulsion (LCT). This emulsion was administered by intravenous infusion to rats and rabbits at dosages of 1 and 4.28 g lipid/kg body weight (g lipid/kg) at dose volumes of 5 and 21.4 mL/kg, respectively, once daily during organogenesis to assess the potential developmental toxicity of the test article. The control group received 0.9% saline at a dose volume of 21.4 mL/kg. Animals were observed for clinical signs of toxicity and adverse effects on body weights and feed consumption. On Day 20 (rats) or Day 29 (rabbits), females were necropsied and examined for maternal and embryo/fetal toxicity. Fetuses were removed, weighed, and examined for external, soft tissue, and skeletal abnormalities. Dosages of 4.28 g lipid/kg resulted in lower feed consumption for rats and rabbits, an expected finding based on the high-caloric nature of the test article. Potentially test article-related gross necropsy findings, including enlarged lymph nodes and spleen, small thymus, and enlarged renal pelvis, for rats given 4.28 g lipid/kg were present at a low incidence. There were no adverse effects on fetal parameters for rats even in the presence of some maternal toxicity. However, embryo and fetal toxicity (i.e., resorptions) and skeletal abnormalities were present for rabbits given 4.28 g lipid/kg. Under the conditions of this study, the no-observable-effect level for developmental toxicity was greater than or equal to 4.28 g lipid/kg for rats and greater than or equal to 1 g lipid/kg but less than 4.28 g lipid/kg for rabbits.

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