Enhancing engraftment of islets using perioperative sodium 4-phenylbutyrate

Brend Ray Sea Hsu*, Szu Tah Chen, Shin Huei Fu

*此作品的通信作者

研究成果: 期刊稿件文章同行評審

6 引文 斯高帕斯(Scopus)

摘要

Primary nonfunction (PNF) adversely impacts islet transplantation. In addition to determining whether sodium 4-phenylbutyrate (4-SPB), an anti-inflammatory agent, reduces PNF, this study investigates how 4-SPB affects PNF. Streptozotocin-induced diabetic C57BL/6 mice, that received 75 syngeneic islets underneath left subrenal space, were fed twice daily of either 4-SPB at 500 mg/kg body weight or isotonic saline (NaCl) from 2 days before through 7 days after transplantation. The graft was removed at days 3, 10 and 84 following transplantation. At 68 h following transplantation, serum levels of interleukin-1β (IL-1β) were 2.2 ± 0.4 and 0.4 ± 0.2 pmol/L (n = 6, p < 0.005) for NaCl and 4-SPB groups, respectively. Graft genetic expression of IL-1β was significantly suppressed in 4-SPB group (p < 0.01). At day 10, the blood glucose levels were 22.7 ± 1.0 and 17.1 ± 1.7 mmol/L (n = 12, p < 0.05) and graft insulin contents (IC) were 35.0 ± 8.3 and 107.6 ± 29.7 pmol (n = 12, p < 0.05) for NaCl and 4-SPB groups, respectively. Moreover, the 4-SPB group had a shorter temporary hyperglycemia (15 ± 2, n = 21 vs. 25 ± 2 days, n = 19, p = 0.001) and a higher cumulative cure rate of diabetes (p < 0.001) than the NaCl group. In-vitro studies indicated that 4-SPB did not impact the islets function. These experimental results demonstrated that perioperative administration of 4-SPB decreased serum level and graft genetic expression of IL-1β and attenuated PNF, which enhanced islet engraftment in a syngeneic transplantation mouse model.

原文英語
頁(從 - 到)1952-1959
頁數8
期刊International Immunopharmacology
6
發行號13-14
DOIs
出版狀態已出版 - 20 12 2006
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