2016 Fiscal Year Final Research Report
A new strategy for the treatment of rett syndrome with ghrelin and bone marrow transplantation
Project/Area Number |
25461570
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Pediatrics
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Research Institution | Kurume University |
Principal Investigator |
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Co-Investigator(Renkei-kenkyūsha) |
KOJIMA Masayasu 久留米大学, 分子生命科学研究所, 教授 (20202062)
SATOU Motoyasu 獨協医科大学, 生化学, 助教 (20418891)
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Research Collaborator |
NASU Saori 久留米大学, 医学部・放射線同元素施設, 研究員 (90754359)
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Project Period (FY) |
2013-04-01 – 2017-03-31
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Keywords | グレリン / レット症候群 / 骨髄移植 / 放射線障害 |
Outline of Final Research Achievements |
Rett syndrome(RTT) is a congenital neurodeveropmental disease with glial disfunction. Derecki NC reported that, in RTT-model mice (RTT mice), an exchange of abnorlmal glial cells to normal ones by bone marrow transplantation (BMT) partially ameliorated neuronal disoders together with an elongation of thier life-span. Ghrelin, a brain-and-gut hormone, has been reported to calm down the hyper-excited glial cells through the functional ghrelin-receptor on them. In this study, we injected ghrelin once a day for 14 days to BMT-treated or non-BMT-tereated RTT mice and checked thier neuronal phenotype according to the method of Derecki NC. We also checked their life-span. In BMT-RTT mice with or without ghrelin-injection, we could find out no significant evidence for the elongation of life-span nor amelioration of neuronal condition in comparison to non-BMT RTT mice. Although, in non-BMT RTT mice with ghrelin-treatment, significant improvement of their neuronal condition was revealed.
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Free Research Field |
内分泌・代謝
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