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通过玻璃化法对大鼠胰岛进行冷冻保存。

Cryopreservation of rat islets of Langerhans by vitrification.

作者信息

Sasamoto Hiromi, Futami Midori, Ando Yusuke, Nakaji Shuhei

机构信息

Department of Biomedical Engineering, Faculty of Engineering, Okayama University of Science, 1-1 Ridaicho Kitaku, Okayama, Okayama 700-0005, Japan.

出版信息

J Artif Organs. 2012 Sep;15(3):283-9. doi: 10.1007/s10047-012-0635-7. Epub 2012 Mar 2.

Abstract

Cryopreservation could be a possible means of addressing the shortage of islets of Langerhans. We investigated the effects of EDT324 solution on the vitrification of isolated rat islets of Langerhans. Rat pancreatic islets were cryopreserved in 10% DMSO by a slow-rate freezing method or were cryopreserved in EDT324 solution by vitrification. The cryopreserved islets were compared in terms of viability, stimulation index and metabolic function after transplantation. After cryopreservation, the viability and stimulation of islets stored in EDT324 were 92.4% and 6.4, respectively, and were higher than islets stored by slow freezing (72.5% and 1.5, respectively). Streptozotocin-induced diabetic rats were transplanted with islets cryopreserved in EDT324, which corrected diabetes and achieved euglycemia within 2 days after transplantation. These results indicate that EDT324 allows successful cryopreservation of rat islets for long-term storage as an alternative solution to traditionally used solutions, such as 10% DMSO. Transplantation of cryopreserved islets into diabetic rats can achieve euglycemia.

摘要

低温保存可能是解决胰岛短缺问题的一种可行方法。我们研究了EDT324溶液对分离的大鼠胰岛玻璃化的影响。大鼠胰岛通过慢速冷冻法在10%二甲基亚砜(DMSO)中进行低温保存,或通过玻璃化法在EDT324溶液中进行低温保存。对低温保存后的胰岛在移植后的活力、刺激指数和代谢功能方面进行比较。低温保存后,EDT324溶液中保存的胰岛活力和刺激指数分别为92.4%和6.4,高于慢速冷冻保存的胰岛(分别为72.5%和1.5)。将EDT324溶液中低温保存的胰岛移植到链脲佐菌素诱导的糖尿病大鼠体内,移植后2天内纠正了糖尿病并实现了血糖正常。这些结果表明,EDT324能够成功地对大鼠胰岛进行低温保存以长期储存,作为传统使用的溶液(如10% DMSO)的替代解决方案。将低温保存的胰岛移植到糖尿病大鼠体内可实现血糖正常。

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