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紫海胆硫酸化多糖的物理化学特性及药理活性

Physico-chemical characterization and pharmacological activities of sulfated polysaccharide from sea urchin, Paracentrotus lividus.

作者信息

Salem Yosra Ben, Amri Safa, Hammi Khaoula Mkadmini, Abdelhamid Amal, Cerf Didier Le, Bouraoui Abderrahman, Majdoub Hatem

机构信息

Laboratoire des Interfaces et des Matériaux Avancés (LIMA), Faculté des Sciences de Monastir, Université de Monastir, Bd. de l'environnement, 5019 Monastir, Tunisie.

Laboratoire de Développement Chimique, Galénique et Pharmacologique des Médicaments, Faculté de Pharmacie de Monastir, Université de Monastir, 5000 Monastir, Tunisie.

出版信息

Int J Biol Macromol. 2017 Apr;97:8-15. doi: 10.1016/j.ijbiomac.2017.01.007. Epub 2017 Jan 3.

Abstract

Sulfated polysaccharide (SP) from the eggs of sea urchin Paracentrotus lividus, extracted by papain digestion, was characterized by size exclusion chromatography coupling on-line with light scattering and viscosity detectors (SEC/MALS/VD/DRI), gas chromatography coupled to mass spectrometer (GC-MS), and Fourier transform infrared spectroscopy (FTIR) analysis. The native molecular mass of the extracted polysaccharide is high (≥22 000 KDa) and it is composed mainly of arabinose, accompanied by other monosaccharides (mostly galactose, glucose and fucose), significant amounts of uronic acids (18.4%) and relatively high proportions of sulfate (22.4%). The pharmacological evaluation of SP showed a significant in vivo anti-inflammatory activity (p<0.001), 3h after injection, the edema inhibition was 75.8% at the dose of 100mg/Kg; a significant peripheral analgesic activity (p<0.001), with 64.9% of writhing inhibition, and a significant increase in the hot plate reaction time in mice indicating central analgesic activity. In addition, an interesting gastroprotective effect was observed with this polysaccharide; the gastric ulcer inhibition was 69.7%, at the dose of 100mg/Kg.

摘要

通过木瓜蛋白酶消化从紫球海胆卵中提取的硫酸化多糖(SP),采用尺寸排阻色谱与光散射和粘度检测器联用(SEC/MALS/VD/DRI)、气相色谱-质谱联用(GC-MS)以及傅里叶变换红外光谱(FTIR)分析进行表征。提取的多糖天然分子量较高(≥22000 kDa),主要由阿拉伯糖组成,伴有其他单糖(主要是半乳糖、葡萄糖和岩藻糖)、大量糖醛酸(18.4%)以及相对较高比例的硫酸盐(22.4%)。SP的药理学评价显示出显著的体内抗炎活性(p<0.001),注射后3小时,剂量为100mg/Kg时水肿抑制率为75.8%;显著的外周镇痛活性(p<0.001),扭体抑制率为64.9%,并且小鼠热板反应时间显著增加表明具有中枢镇痛活性。此外,观察到这种多糖具有有趣的胃保护作用;剂量为100mg/Kg时胃溃疡抑制率为69.7%。

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