交通医学
交通醫學
교통의학
MEDICAL JOURNAL OF COMMUNICATIONS
2013年
3期
213-216,220
,共5页
武冰馨%凌勇%赵亚红%杨宇民
武冰馨%凌勇%趙亞紅%楊宇民
무빙형%릉용%조아홍%양우민
红景天苷类似物%低糖低血清损伤%神经保护作用%PC12细胞
紅景天苷類似物%低糖低血清損傷%神經保護作用%PC12細胞
홍경천감유사물%저당저혈청손상%신경보호작용%PC12세포
Salidroside analogues%Hypoglycemia and serum limitation%Neuroprotective effect%PC12 cell
目的:通过在红景天苷及类似物的苯环上引入乙酰基,合成新型红景天苷类似物,以期获得神经保护活性更好的化合物。方法:以4-甲氧基苯乙醇对芳环进行傅克乙酰化反应,得到关键中间体3-乙酰基-4-羟基苯乙醇,再分别与糖基供体(四乙酰基溴代葡萄糖、四乙酰基氯代氨基葡萄糖)进行糖苷化反应,制备新型红景天苷类似物,并采用PC12细胞低糖低血清损伤模型来测定目标化合物对于低糖低血清损伤PC12细胞活力的影响。结果:合成的红景天苷类似物糖苷均经过质谱,核磁和元素分析的结构确证,红景天苷类似物预保护对低糖低血清损伤引起的PC12细胞活力的下降曾剂量依赖性地拮抗作用,尤其是化合物8a对低糖低血清损伤的拮抗作用显著高于红景天苷组。结论:所合成含有乙酰基的红景天苷类似物具有较好的对PC12细胞低糖低血清损伤的神经保护作用,将为今后进一步研究红景天苷类似物用于治疗神经退行性疾病打下坚实的基础。
目的:通過在紅景天苷及類似物的苯環上引入乙酰基,閤成新型紅景天苷類似物,以期穫得神經保護活性更好的化閤物。方法:以4-甲氧基苯乙醇對芳環進行傅剋乙酰化反應,得到關鍵中間體3-乙酰基-4-羥基苯乙醇,再分彆與糖基供體(四乙酰基溴代葡萄糖、四乙酰基氯代氨基葡萄糖)進行糖苷化反應,製備新型紅景天苷類似物,併採用PC12細胞低糖低血清損傷模型來測定目標化閤物對于低糖低血清損傷PC12細胞活力的影響。結果:閤成的紅景天苷類似物糖苷均經過質譜,覈磁和元素分析的結構確證,紅景天苷類似物預保護對低糖低血清損傷引起的PC12細胞活力的下降曾劑量依賴性地拮抗作用,尤其是化閤物8a對低糖低血清損傷的拮抗作用顯著高于紅景天苷組。結論:所閤成含有乙酰基的紅景天苷類似物具有較好的對PC12細胞低糖低血清損傷的神經保護作用,將為今後進一步研究紅景天苷類似物用于治療神經退行性疾病打下堅實的基礎。
목적:통과재홍경천감급유사물적분배상인입을선기,합성신형홍경천감유사물,이기획득신경보호활성경호적화합물。방법:이4-갑양기분을순대방배진행부극을선화반응,득도관건중간체3-을선기-4-간기분을순,재분별여당기공체(사을선기추대포도당、사을선기록대안기포도당)진행당감화반응,제비신형홍경천감유사물,병채용PC12세포저당저혈청손상모형래측정목표화합물대우저당저혈청손상PC12세포활력적영향。결과:합성적홍경천감유사물당감균경과질보,핵자화원소분석적결구학증,홍경천감유사물예보호대저당저혈청손상인기적PC12세포활력적하강증제량의뢰성지길항작용,우기시화합물8a대저당저혈청손상적길항작용현저고우홍경천감조。결론:소합성함유을선기적홍경천감유사물구유교호적대PC12세포저당저혈청손상적신경보호작용,장위금후진일보연구홍경천감유사물용우치료신경퇴행성질병타하견실적기출。
Objective: In an attempt to improve its neuroprotective effects, novel salidroside analogues was synthe-sized by coupling the benzene ring of salidroside with acetyl group. Method: 4-Methoxyl phenethanol was treated with acetyl chloride and AlCl3 to form key intermediate 3-acetyl-4-methoxyl phenethanol by Friedel-Crafts acetylation reac-tion, the target compounds were prepared by glycosylation reaction of the key intermediate and tetraacetyl glucosyl bromide or tetraacetyl glucosamine chloride, and their neuroprotective activities have been evaluated against the hypoglycemia and serum limitation-induced cell death in differentiated PC12 cells. Results:Novel salidroside analogues were synthesized and their structures were confirmed by MS, 1H NMR, and elemental analysis. Target compounds displayed protective effects on the cell viability, especially for compound 8a, which had a great potency superior to salidroside. Conclusion: The synthe-sized salidroside analogues containing acetyl group exhibited strong neuroprotective activities against the hypoglycemia and serum limitation-induced cell death in differentiated PC12 cells, which may provide potentially important information for further development of salidroside analogues and lay the basis for further studies on the neurodegenerative diseases for hu-man clinical treatment.