Christophe Camillerapp , David B. Mayfield , Sabitha Papineni , Antoine Leroux , Jean-François Jeanne
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引用次数: 0
摘要
s -乙酰谷胱甘肽(SAG)是一种谷胱甘肽前体,以生物可利用的形式作为食物或膳食成分,用于恢复或维持循环谷胱甘肽(GSH)水平。谷胱甘肽是一种抗氧化应激的有效防御化合物,也是许多其他生理功能的关键决定因素。通过体外细菌反向突变试验、体外微核试验、急性口服毒性研究和重复给药(13周)毒性研究来评估SAG补充的安全性。体外实验没有发现任何基因毒性或诱变活性。急性口服毒性研究(LD50 ~ 2000 mg/kg)未导致死亡或发病。服用13周以上的SAG耐受性良好,没有导致任何神经行为改变或运动活动、眼科、血液学、凝血、血液生化、尿液分析、甲状腺激素或男性生殖系统的影响。肝、肾和脾重量轻度增加,无不良反应,且在历史控制范围内,任何器官未见与治疗相关的大体或组织病理学发现。结果,NOAEL被确定为1500 mg/kg/天,这是测试的最高剂量。因此,这些毒理学研究的结果支持在食品或膳食补充剂中安全使用SAG。
Safety assessment of S-Acetyl Glutathione for use in foods and dietary supplements
S-Acetyl Glutathione (SAG) is a glutathione precursor used as a food or dietary ingredient in a bioavailable form to restore or maintain circulating glutathione (GSH) levels. GSH is a potent defense compound against oxidative stress and a key determinant of many other physiological functions. The safety of SAG supplementation was assessed in an in vitro bacterial reverse mutation assay, an in vitro micronucleus test, an acute oral toxicity study, and a repeated dose (13 week) toxicity study. The in vitro assays did not reveal any genotoxic or mutagenic activity. No mortality or morbidity resulted from the acute oral toxicity study (LD50 > 2000 mg/kg). Administration of SAG over 13 weeks was well tolerated and did not result in any neurobehavioral alterations or effects on locomotor activity, ophthalmology, hematology, coagulation, blood biochemistry, urinalysis, thyroid hormones or the male reproductive system. Mild increases noted in liver, kidney and spleen weights were non-adverse and within historical control ranges, and no treatment-related gross or histopathology findings were observed in any organs. As a result, the NOAEL was determined to be 1500 mg/kg/day, the highest dose tested. Therefore, the results of these toxicological studies support the safe use of SAG in foods or dietary supplements.
期刊介绍:
Food and Chemical Toxicology (FCT), an internationally renowned journal, that publishes original research articles and reviews on toxic effects, in animals and humans, of natural or synthetic chemicals occurring in the human environment with particular emphasis on food, drugs, and chemicals, including agricultural and industrial safety, and consumer product safety. Areas such as safety evaluation of novel foods and ingredients, biotechnologically-derived products, and nanomaterials are included in the scope of the journal. FCT also encourages submission of papers on inter-relationships between nutrition and toxicology and on in vitro techniques, particularly those fostering the 3 Rs.
The principal aim of the journal is to publish high impact, scholarly work and to serve as a multidisciplinary forum for research in toxicology. Papers submitted will be judged on the basis of scientific originality and contribution to the field, quality and subject matter. Studies should address at least one of the following:
-Adverse physiological/biochemical, or pathological changes induced by specific defined substances
-New techniques for assessing potential toxicity, including molecular biology
-Mechanisms underlying toxic phenomena
-Toxicological examinations of specific chemicals or consumer products, both those showing adverse effects and those demonstrating safety, that meet current standards of scientific acceptability.
Authors must clearly and briefly identify what novel toxic effect (s) or toxic mechanism (s) of the chemical are being reported and what their significance is in the abstract. Furthermore, sufficient doses should be included in order to provide information on NOAEL/LOAEL values.