A 90-day preclinical toxicological evaluation in rats of a highly purified and concentrated mulberry leaf extract

IF 2.7 4区 医学 Q3 TOXICOLOGY Journal of Applied Toxicology Pub Date : 2024-06-04 DOI:10.1002/jat.4644
Timothy S. Murbach, Róbert Glávits, John R. Endres, Gábor Hirka, Ilona Pasics Szakonyiné
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Abstract

Mulberry (genus Morus) leaves have long been used as a human food, especially in Asia, and animal feed. More recently, mulberry leaf extracts have been introduced as a convenient way to consume mulberry for non-nutritional functional effects. Reducose® 5% is an Morus alba leaf extract that has been highly purified and standardized to a content of 5 ± 0.5% 1-deoxynojirimycin, a naturally present polyhydroxylated piperidine alkaloid analog of D-glucose. This extract has previously been evaluated in acute and subacute (28-day) oral toxicity studies in which no adverse effects of the test item were observed in mice or rats, respectively. Due to continued and growing interest in the extract in multinational markets, we have now further investigated potential toxic effects in subchronic (90-day) oral toxicity study in male and female Han:WIST rats. The test item was administered at doses of 850, 1700, and 2550 mg/kg bw/day, and did not cause adverse effects in clinical signs, body weight development, clinical pathology, gross pathology, or histopathology in comparison to the vehicle-control group. The no-observed-adverse-effect-level was determined to be 2550 mg/kg bw/day. These results add to the existing body of both preclinical and clinical work relevant to the safety of the extract and of interest to regulators in various global markets.

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在大鼠体内进行为期 90 天的高纯度浓缩桑叶提取物临床前毒理学评估。
桑叶(桑属)长期以来一直被用作人类食品(尤其是在亚洲)和动物饲料。最近,桑叶提取物作为一种方便的食用桑叶的方法被引入,以获得非营养的功能效果。Reducose® 5% 是一种桑叶提取物,经过高度纯化和标准化处理,其含量为 5 ± 0.5% 1-脱氧野尻霉素,这是一种天然存在的 D-葡萄糖的多羟基哌啶生物碱类似物。该提取物曾在急性和亚急性(28 天)口服毒性研究中进行过评估,结果表明小鼠和大鼠分别未观察到试验品的不良影响。由于跨国市场对该提取物的兴趣持续增长,我们现在进一步在亚慢性(90 天)口服毒性研究中对雄性和雌性 Han:WIST 大鼠的潜在毒性作用进行了调查。与药物对照组相比,受试物的剂量分别为 850、1700 和 2550 毫克/千克体重/天,在临床症状、体重发育、临床病理学、大体病理学和组织病理学方面均未造成不良影响。无观测不良效应水平被确定为 2550 毫克/千克体重/天。这些结果丰富了现有的与该提取物安全性相关的临床前和临床研究成果,也引起了全球各市场监管部门的关注。
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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