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2
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本文引用的文献

1
Fecal Microbiota and Metabolome in a Mouse Model of Spontaneous Chronic Colitis: Relevance to Human Inflammatory Bowel Disease.自发性慢性结肠炎小鼠模型中的粪便微生物群和代谢组:与人类炎症性肠病的相关性
Inflamm Bowel Dis. 2016 Dec;22(12):2767-2787. doi: 10.1097/MIB.0000000000000970.
2
The role of barrier function, autophagy, and cytokines in maintaining intestinal homeostasis.屏障功能、自噬和细胞因子在维持肠道稳态中的作用。
Semin Cell Dev Biol. 2017 Jan;61:51-59. doi: 10.1016/j.semcdb.2016.08.018. Epub 2016 Aug 24.
3
Microbiota: relevant player in thiopurine metabolisation?微生物群:硫嘌呤代谢中的相关参与者?
Gut. 2017 Jan;66(1):1-3. doi: 10.1136/gutjnl-2016-312450. Epub 2016 Aug 24.
4
The Prevalence of Nodular Regenerative Hyperplasia in Inflammatory Bowel Disease Patients Treated with Thioguanine Is Not Associated with Clinically Significant Liver Disease.接受硫鸟嘌呤治疗的炎症性肠病患者中结节性再生性增生的患病率与具有临床意义的肝脏疾病无关。
Inflamm Bowel Dis. 2016 Sep;22(9):2112-20. doi: 10.1097/MIB.0000000000000869.
5
Colonic microbiota can promote rapid local improvement of murine colitis by thioguanine independently of T lymphocytes and host metabolism.结肠微生物群可通过硫鸟嘌呤独立于T淋巴细胞和宿主代谢促进小鼠结肠炎的快速局部改善。
Gut. 2017 Jan;66(1):59-69. doi: 10.1136/gutjnl-2015-310874. Epub 2016 Jul 13.
6
High Fat Diets Induce Colonic Epithelial Cell Stress and Inflammation that is Reversed by IL-22.高脂肪饮食诱导结肠上皮细胞应激和炎症,IL-22 可逆转这种情况。
Sci Rep. 2016 Jun 28;6:28990. doi: 10.1038/srep28990.
7
Genetic Coding Variant in GPR65 Alters Lysosomal pH and Links Lysosomal Dysfunction with Colitis Risk.GPR65基因编码变异改变溶酶体pH值并将溶酶体功能障碍与结肠炎风险相关联。
Immunity. 2016 Jun 21;44(6):1392-405. doi: 10.1016/j.immuni.2016.05.007. Epub 2016 Jun 7.
8
Splitting a therapeutic dose of thioguanine may avoid liver toxicity and be an efficacious treatment for severe inflammatory bowel disease: a 2-center observational cohort study.将硫鸟嘌呤的治疗剂量分开服用可能避免肝毒性,并且是治疗重度炎症性肠病的一种有效方法:一项双中心观察性队列研究。
Inflamm Bowel Dis. 2014 Dec;20(12):2239-46. doi: 10.1097/MIB.0000000000000206.
9
Suppression of p21Rac signaling and increased innate immunity mediate remission in Crohn's disease.抑制 p21Rac 信号和增强固有免疫可介导克罗恩病缓解。
Sci Transl Med. 2014 Apr 23;6(233):233ra53. doi: 10.1126/scitranslmed.3006763.
10
Autophagy at the crossroads of metabolism and cellular defense.自噬:代谢与细胞防御的交汇点
Curr Opin Gastroenterol. 2013 Nov;29(6):588-96. doi: 10.1097/MOG.0b013e328365d34d.

结肠硫鸟嘌呤前药:微生物组和新宿主代谢研究。

Colonic thioguanine pro-drug: Investigation of microbiome and novel host metabolism.

机构信息

a Mater Research - University of Queensland, Translational Research Institute , Queensland , Australia.

b Mater Research - University of Queensland , Queensland , Australia.

出版信息

Gut Microbes. 2018 Mar 4;9(2):175-178. doi: 10.1080/19490976.2017.1387343. Epub 2017 Oct 17.

DOI:10.1080/19490976.2017.1387343
PMID:28976243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5989799/
Abstract

Thiopurines are analogues of endogenous purines. They are pro-drugs which require the purine salvage pathway to convert them to the active drug nucleotides (TGN). These drugs are used to maintain clinical remission in patients with inflammatory bowel diseases. In our recent Gut paper, we showed that thioguanine worked quickly to improve colitis in the absence in the host animal of the key guanine salvage enzyme, hypoxanthine-guanine-phosphoribosyltransferase (HPRT). Current evidence favours the proposition that active drug delivery to the host lacking HPRT requires translocation of TGN-loaded bacteria across the inflamed mucosal barrier, and most likely delivery by phagocytosis. Alternatively, the efficacy of thioguanine in treating colitis could be mediated by modulation of the community of the microbiota in the intestine, or there are novel host pathways for conversion of the thioguanine pro-drug to TGN.

摘要

硫嘌呤是内源性嘌呤的类似物。它们是前体药物,需要嘌呤补救途径将其转化为活性药物核苷酸 (TGN)。这些药物用于维持炎症性肠病患者的临床缓解。在我们最近的 Gut 论文中,我们表明,硫鸟嘌呤在缺乏关键嘌呤补救酶次黄嘌呤-鸟嘌呤-磷酸核糖转移酶 (HPRT) 的宿主动物中迅速发挥作用,改善结肠炎。目前的证据支持这样的观点,即缺乏 HPRT 的宿主中活性药物的递送至需要负载 TGN 的细菌穿过炎症性黏膜屏障的易位,并且很可能通过吞噬作用进行递送。或者,硫鸟嘌呤治疗结肠炎的疗效可能是通过调节肠道微生物群落来介导的,或者存在将硫鸟嘌呤前体药物转化为 TGN 的新的宿主途径。