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本文引用的文献

1
Daily administration of the GIP-R antagonist (Pro3)GIP in streptozotocin-induced diabetes suggests that insulin-dependent mechanisms are critical to anti-obesity-diabetes actions of (Pro3)GIP.在链脲佐菌素诱导的糖尿病模型中每日给予GIP-R拮抗剂(Pro3)GIP表明,胰岛素依赖机制对于(Pro3)GIP的抗肥胖 - 糖尿病作用至关重要。
Diabetes Obes Metab. 2008 Apr;10(4):336-42. doi: 10.1111/j.1463-1326.2007.00712.x.
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Liposomal formulation of 5-fluorocytosine in suicide gene therapy with cytosine deaminase--for colorectal cancer.在使用胞嘧啶脱氨酶进行自杀基因治疗中,5-氟胞嘧啶的脂质体制剂——用于结直肠癌治疗
Cancer Lett. 2008 Apr 18;262(2):164-72. doi: 10.1016/j.canlet.2007.12.006. Epub 2008 Mar 4.
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Gene transfection efficacies of novel cationic gemini lipids possessing aromatic backbone and oxyethylene spacers.具有芳香主链和氧乙烯间隔基的新型阳离子双子脂质的基因转染效率
Biomacromolecules. 2008 Mar;9(3):991-9. doi: 10.1021/bm700930y. Epub 2008 Feb 14.
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An efficient liposomal gene delivery vehicle using Sendai F/HN proteins and protamine.一种使用仙台病毒F/HN蛋白和鱼精蛋白的高效脂质体基因递送载体。
Cancer Gene Ther. 2008 Apr;15(4):214-24. doi: 10.1038/sj.cgt.7701121. Epub 2008 Feb 8.
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Nicotinamide induces differentiation of embryonic stem cells into insulin-secreting cells.烟酰胺诱导胚胎干细胞分化为胰岛素分泌细胞。
Exp Cell Res. 2008 Mar 10;314(5):969-74. doi: 10.1016/j.yexcr.2007.11.019. Epub 2007 Dec 4.
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Nanoparticles as nonviral gene delivery vectors.纳米颗粒作为非病毒基因递送载体。
IEEE Trans Nanobioscience. 2007 Dec;6(4):319-30. doi: 10.1109/tnb.2007.908996.
7
Treatment of streptozotocin-induced diabetes mellitus in mice by intra-bone marrow bone marrow transplantation plus portal vein injection of beta cells induced from bone marrow cells.通过骨髓内骨髓移植加门静脉注射骨髓细胞诱导的β细胞治疗链脲佐菌素诱导的小鼠糖尿病。
Int J Hematol. 2007 Dec;86(5):438-45. doi: 10.1007/BF02984002.
8
Effects of gastric inhibitory polypeptide (GIP) and related analogues on glucagon release at normo- and hyperglycaemia in Wistar rats and isolated islets.胃抑制多肽(GIP)及相关类似物对正常血糖和高血糖状态下Wistar大鼠及分离胰岛胰高血糖素释放的影响。
Biol Chem. 2008 Feb;389(2):189-93. doi: 10.1515/BC.2008.019.
9
Betacellulin and nicotinamide sustain PDX1 expression and induce pancreatic beta-cell differentiation in human embryonic stem cells.β细胞ulin和烟酰胺维持人胚胎干细胞中PDX1的表达并诱导胰腺β细胞分化。
Biochem Biophys Res Commun. 2008 Feb 1;366(1):129-34. doi: 10.1016/j.bbrc.2007.11.112. Epub 2007 Dec 4.
10
Differential effect of activin on mouse embryonic stem cell differentiation in insulin-secreting cells under nestin-positive selection and spontaneous differentiation protocols.在巢蛋白阳性选择和自发分化方案下,激活素对小鼠胚胎干细胞向胰岛素分泌细胞分化的差异作用。
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通过胃肠道给予含人胰岛素基因的壳聚糖纳米粒对大鼠1型糖尿病进行基因治疗。

Gene therapy for type 1 diabetes mellitus in rats by gastrointestinal administration of chitosan nanoparticles containing human insulin gene.

作者信息

Niu Li, Xu Yan-Cheng, Dai Zhe, Tang Hui-Qin

机构信息

Department of Endocrinology, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan 430071, Hubei Province, China.

出版信息

World J Gastroenterol. 2008 Jul 14;14(26):4209-15. doi: 10.3748/wjg.14.4209.

DOI:10.3748/wjg.14.4209
PMID:18636668
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2725384/
Abstract

AIM

To study the expression of human insulin gene in gastrointestinal tracts of diabetic rats.

METHODS

pCMV.Ins, an expression plasmid of the human insulin gene, wrapped with chitosan nanoparticles, was transfected to the diabetic rats through lavage and coloclysis, respectively. Fasting blood glucose and plasma insulin levels were measured for 7 d. Reverse transcription polymerase chain reaction (RT-PCR) analysis and Western blot analysis were performed to confirm the expression of human insulin gene.

RESULTS

Compared with the control group, the fasting blood glucose levels in the lavage and coloclysis groups were decreased significantly in 4 d (5.63 +/- 0.48 mmol/L and 5.07 +/- 0.37 mmol/L vs 22.12 +/- 1.31 mmol/L, respectively, P < 0.01), while the plasma insulin levels were much higher (32.26 +/- 1.81 microIU/mL and 32.79 +/- 1.84 microIU/mL vs 14.23 +/- 1.38 microIU/mL, respectively, P < 0.01). The human insulin gene mRNA and human insulin were only detected in the lavage and coloclysis groups.

CONCLUSION

Human insulin gene wrapped with chitosan nanoparticles can be successfully transfected to rats through gastrointestinal tract, indicating that chitosan is a promising non-viral vector.

摘要

目的

研究人胰岛素基因在糖尿病大鼠胃肠道中的表达。

方法

将包裹有壳聚糖纳米粒的人胰岛素基因表达质粒pCMV.Ins,分别通过灌胃和结肠灌注转染至糖尿病大鼠体内。连续7天测量空腹血糖和血浆胰岛素水平。采用逆转录聚合酶链反应(RT-PCR)分析和蛋白质免疫印迹分析来证实人胰岛素基因的表达。

结果

与对照组相比,灌胃组和结肠灌注组的空腹血糖水平在第4天显著降低(分别为5.63±0.48 mmol/L和5.07±0.37 mmol/L,而对照组为22.12±1.31 mmol/L,P<0.01),而血浆胰岛素水平则高得多(分别为32.26±1.81 μIU/mL和32.79±1.84 μIU/mL,而对照组为14.23±1.38 μIU/mL,P<0.01)。仅在灌胃组和结肠灌注组中检测到人胰岛素基因mRNA和人胰岛素。

结论

包裹有壳聚糖纳米粒的人胰岛素基因可通过胃肠道成功转染至大鼠体内,表明壳聚糖是一种有前景的非病毒载体。