Ishii Masaki, Matsumoto Yasuhiko, Sekimizu Kazuhisa
Genome Pharmaceuticals Institute Co., Ltd.
Teikyo University Institute of Medical Mycology.
Drug Discov Ther. 2018;12(3):122-125. doi: 10.5582/ddt.2018.01028.
Cyclodextrins (CyDs) are cyclic oligosaccharides consisting of six to eight glucose residues. Administration of α-CyD (six glucose residues) inhibits sucrose-induced hyperglycemia in humans. Here we show that oral administration of α-CyD and dimethyl α-CyD suppresses sucrose-induced hyperglycemia in an in vivo evaluation system using silkworms. On the other hand, β-CyD (seven glucose residues), γ-CyD (eight glucose residues), and their derivatives did not show the suppressive effect. These findings suggest that dimethyl α-CyD is a new inhibitor against sucrose-induced hyperglycemia and the silkworm system is useful for evaluation of suppressive activities of α-CyD derivatives against postprandial hyperglycemia.
环糊精(CyDs)是由六至八个葡萄糖残基组成的环状寡糖。给予α-环糊精(六个葡萄糖残基)可抑制人类因蔗糖诱导的高血糖症。在此我们表明,在使用家蚕的体内评估系统中,口服α-环糊精和二甲基α-环糊精可抑制蔗糖诱导的高血糖症。另一方面,β-环糊精(七个葡萄糖残基)、γ-环糊精(八个葡萄糖残基)及其衍生物未显示出抑制作用。这些发现表明,二甲基α-环糊精是一种针对蔗糖诱导的高血糖症的新型抑制剂,并且家蚕系统可用于评估α-环糊精衍生物对餐后高血糖症的抑制活性。