天然产物研究与开发
天然產物研究與開髮
천연산물연구여개발
NATURAL PRODUCT RESEARCH AND DEVELOPMENT
2007年
4期
568-571
,共4页
杨宁%赵谋明%杨宝%朱邦豪%方芳
楊寧%趙謀明%楊寶%硃邦豪%方芳
양저%조모명%양보%주방호%방방
仙人掌%多糖%糖基化终产物%醛糖还原酶%抑制
仙人掌%多糖%糖基化終產物%醛糖還原酶%抑製
선인장%다당%당기화종산물%철당환원매%억제
Opuntia%polysaccharide%advanced glycation end-products%aldose reductase%inhibition
以仙人掌为原料提取多糖产品,通过超滤浓缩和不同浓度乙醇分级沉淀,分别得到55%乙醇沉淀的多糖(OPMC I),进一步乙醇浓度增至80%沉淀的多糖 (OPMCⅡ),以及一次性80%乙醇沉淀的多糖(OPMCⅢ).比较了三种多糖对蛋白质非酶糖基化反应的终端产物(AGEs)和醛糖还原酶(AR)形成的抑制作用.结果表明,在对AGEs形成的抑制过程中,第四周时OPMC II的抑制作用较强,且强于同剂量的氨基胍;在对AR活性的抑制作用中,OPMC II在三种多糖样品中抑制作用最强,但明显低于阳性对照物依帕司他.
以仙人掌為原料提取多糖產品,通過超濾濃縮和不同濃度乙醇分級沉澱,分彆得到55%乙醇沉澱的多糖(OPMC I),進一步乙醇濃度增至80%沉澱的多糖 (OPMCⅡ),以及一次性80%乙醇沉澱的多糖(OPMCⅢ).比較瞭三種多糖對蛋白質非酶糖基化反應的終耑產物(AGEs)和醛糖還原酶(AR)形成的抑製作用.結果錶明,在對AGEs形成的抑製過程中,第四週時OPMC II的抑製作用較彊,且彊于同劑量的氨基胍;在對AR活性的抑製作用中,OPMC II在三種多糖樣品中抑製作用最彊,但明顯低于暘性對照物依帕司他.
이선인장위원료제취다당산품,통과초려농축화불동농도을순분급침정,분별득도55%을순침정적다당(OPMC I),진일보을순농도증지80%침정적다당 (OPMCⅡ),이급일차성80%을순침정적다당(OPMCⅢ).비교료삼충다당대단백질비매당기화반응적종단산물(AGEs)화철당환원매(AR)형성적억제작용.결과표명,재대AGEs형성적억제과정중,제사주시OPMC II적억제작용교강,차강우동제량적안기고;재대AR활성적억제작용중,OPMC II재삼충다당양품중억제작용최강,단명현저우양성대조물의파사타.
Polysaccharides from Opuntia monacantha Cladode (OPMC) were extracted by distilled water and concentrated by ultrafiltration.OPMC I was obtained by precipitation OPMC extracts with 55% of ethanol solution.The supernatant was added ethanol to final concentration 80% to precipitate OPMCⅡ.OPMCⅢ was obtained by precipitation OPMC extracts with 80% of ethanol solution directly.The inhibition of three OPMC polysaccharides on the development of advanced glycated end product (AGE) of protein non-enzymaticaly glycated reaction and aldose reductase (AR) activity were investigated.OPMCⅡ showed stronger inhibition effect on AGE than aminoguanidine with the same dose at fourth week.Among OPMC Ⅰ-Ⅲ,OPMCⅡ also showed the strongest inhibition effect on AR activity,but lower than epalrestat,the positive control.