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Low molecular weight fucoidan increases VEGF165-induced endothelial cell migration by enhancing VEGF165 binding to VEGFR-2 and NRP1.低分子量岩藻依聚糖通过增强VEGF165与VEGFR-2和神经纤毛蛋白1(NRP1)的结合来增加VEGF165诱导的内皮细胞迁移。
J Biol Chem. 2006 Dec 8;281(49):37844-52. doi: 10.1074/jbc.M600686200. Epub 2006 Oct 6.
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Transpl Immunol. 2006 Jun;16(1):14-9. doi: 10.1016/j.trim.2006.03.003. Epub 2006 Apr 5.
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Fucoidan a sulfated polysaccharide from brown algae is a potent modulator of connective tissue proteolysis.
Arch Biochem Biophys. 2006 Jan 1;445(1):56-64. doi: 10.1016/j.abb.2005.11.001. Epub 2005 Nov 28.
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Effects of middle molecular weight fucoidans on in vitro and ex vivo angiogenesis of endothelial cells.中分子量岩藻聚糖对内皮细胞体外和体内外血管生成的影响。
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9
Sulfated fucans, fresh perspectives: structures, functions, and biological properties of sulfated fucans and an overview of enzymes active toward this class of polysaccharide.硫酸化岩藻聚糖:新视角——硫酸化岩藻聚糖的结构、功能和生物学特性以及作用于这类多糖的酶概述
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10
A fucoidan fraction from Ascophyllum nodosum.一种来自泡叶藻的岩藻聚糖组分。
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低分子岩藻聚糖对小鼠的口服单剂量毒性研究

Oral Single Dose Toxicity Study of Low Molecular Fucoidan in Mice.

作者信息

Jung Young-Mi, Yoo Kang Min, Park Dong-Chan, Kim Tae-Kwon, Lee Hyeung-Sik, Ku Sae-Kwang

机构信息

ENZ Bio Co., Ltd., Daegu, 702-832 Korea.

211Department of Genetic Engineering, College of Natural Sciences, Kyungpook National University, Daegu, 702-701 Korea.

出版信息

Toxicol Res. 2008 Mar;24(1):79-86. doi: 10.5487/TR.2008.24.1.079. Epub 2008 Mar 1.

DOI:10.5487/TR.2008.24.1.079
PMID:32038780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7006321/
Abstract

This study was conducted to obtain information of the oral dose toxicity of low molecular fucoidan (LMF) in male and female mice. In order to calculate 50% lethal dose (LD) and approximate lethal dose (LD), test material was once orally administered to male and female ICR mice at dose levels of 2000, 1000, 500, 250, 125 and 0 (vehicle control) mg/kg (body wt.). The mortality and the changes on body weight, clinical signs, gross observation and organ weight and histopathology of principle organs were monitored 14 days after LMF treatment. We could not find any mortalities, clinical signs, body weight changes and gross findings. In addition, significant changes in the organ weight and histopathology of principal organs were not observed except for some sporadic findings. The results obtained in this study suggest that LMF may not be toxic in mice and may be therefore safe for clinical use. The LD and approximate LD in mice after single oral dose of LMF were considered over 2000 mg/kg in both female and male mice.

摘要

本研究旨在获取低分子岩藻聚糖(LMF)对雄性和雌性小鼠的经口剂量毒性信息。为了计算半数致死剂量(LD)和近似致死剂量(LD),将受试物以2000、1000、500、250、125和0(溶剂对照)mg/kg(体重)的剂量水平一次性经口给予雄性和雌性ICR小鼠。在LMF处理14天后,监测死亡率以及体重、临床体征、大体观察、主要器官重量和组织病理学的变化。我们未发现任何死亡、临床体征、体重变化和大体检查结果。此外,除了一些散在发现外,未观察到主要器官的器官重量和组织病理学有显著变化。本研究获得的结果表明,LMF对小鼠可能无毒,因此临床使用可能是安全的。单次经口给予LMF后,雌性和雄性小鼠的LD和近似LD均被认为超过2000 mg/kg。