首页 | 本学科首页   官方微博 | 高级检索  
     

微胶珠化胰岛肌肉内移植治疗小鼠1型糖尿病
引用本文:李 慧,傅红兴,朱雁林,李校堃. 微胶珠化胰岛肌肉内移植治疗小鼠1型糖尿病[J]. 中国组织工程研究, 2013, 17(25): 4637-4643. DOI: 10.3969/j.issn.2095-4344.2013.25.011
作者姓名:李 慧  傅红兴  朱雁林  李校堃
作者单位:温州医学院药学院,浙江省温州市 350025
基金项目:国家自然科学基金资助项目(81071277);浙江省自然科学基金资助项目(Y2080915);浙江省大学生科技创新活动资助项目(2011R413006)。
摘    要:背景:前期实验证明海藻酸钡微胶珠具有免疫隔离作用,并且不会引起免疫排斥反应。目的:观察包裹胰岛海藻酸钡微胶珠对1型糖尿病小鼠的治疗作用。方法:分离纯化SD大鼠胰腺单个胰岛细胞团,并包裹于海藻酸钡微胶珠内。以腹腔注射链脲佐菌素诱导建立C57BL/6小鼠1型糖尿病模型,随机分组:实验组小鼠股二头肌内多点注射包裹胰岛的海藻酸钡微胶珠,对照组小鼠股二头肌内多点注射胰岛,糖尿病对照组及正常对照组小鼠股二头肌内多点注射生理盐水。术后观察小鼠血糖及胰岛微胶珠在肌肉内存在状况。结果与结论:分离纯化后获得高纯度胰岛,每只供体可获得(905.4±34.5)个,并具有良好生物活性。实验组小鼠血糖降为正常的时间约为6.3 d,移植胰岛存活时间大于30 d,对照组小鼠血糖一直未降至正常,移植胰岛存活时间约为4 d。实验组降糖速率明显快于对照组和糖尿病对照组(P < 0.05)。表明包裹胰岛的海藻酸钡微胶珠镶嵌在肌肉组织中可良好存活,治疗小鼠1型糖尿病。

关 键 词:生物材料  生物材料与药物控释  异种胰岛  海藻酸钡  微胶珠化  移植  1型糖尿病  血糖  C57BL/6小鼠  国家自然科学基金  
收稿时间:2012-10-17

Intramuscular transplantation of macroencapsulated islets for type 1 diabetes mellitus in mice
Li Hui,Fu Hong-xing,Zhu Yan-lin,Li Xiao-kun. Intramuscular transplantation of macroencapsulated islets for type 1 diabetes mellitus in mice[J]. Chinese Journal of Tissue Engineering Research, 2013, 17(25): 4637-4643. DOI: 10.3969/j.issn.2095-4344.2013.25.011
Authors:Li Hui  Fu Hong-xing  Zhu Yan-lin  Li Xiao-kun
Affiliation:School of Pharmacy, Wenzhou Medical College, Wenzhou  325035, Zhejiang Province, China
Abstract:BACKGROUND:Alginate-barium chloride microbeads confer immune isolation and prevent graft rejection in preliminary experiments.OBJECTIVE:To assess the role of alginate- barium chloride microbead encapsulation in the treatment of type 1 diabetes mellitus in mice.METHODS:The single islet cell group was isolated from the pancreas of Sprague-Dawley rats and purified. And cells were encapsulated into alginate-barium chloride microbeads. Type 1 diabetes mellitus was induced with streptozotocin into C57BL/6 mice via intraperitoneal injection, and randomly divided into four groups. The pure islets encapsulated in alginate-barium chloride microbeads were transplanted into the biceps femoris in the mice with type 1 diabetes mellitus, as experimental group. The pure islets were transplanted into diabetic recipients at biceps femoris, as control group. Normal C57BL/6 mice were injected with saline into biceps femoris, as normal control group. Diabetic C57BL/6 mice were injected with saline into biceps femoris, as diabetes control group. Then the blood glucose levels and macroencapsulated islets at the transplantation site were observed.RESULTS AND CONCLUSION:After isolation and purification, (905.4±34.5) islets per mouse were obtained and possessed excellent activity. Duration of normal blood glucose after operation in experimental group was approximately 6.3 days. The islet graft survival duration was longer than 30 days. The blood glucose levels in control group were not recovered to normal, and the islet graft survival duration was 4 days. The glucose-lowering rate in experimental group was significantly faster than that in control group and diabetes control group (P < 0.05). Experimental findings indicate that, islets encapsulated in alginate-barium chloride microbeads could survive in the muscles and treat type 1 diabetes mellitus.
Keywords:biomaterials   biomaterials and controlled drug release   islet xenograft   alginate-barium chloride   microbead   transplantation   type 1 diabetes mellitus   blood glucose   C57BL/6 mice   National Natural Science Foundation of China  
点击此处可从《中国组织工程研究》浏览原始摘要信息
点击此处可从《中国组织工程研究》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号