基于GLP-1的治疗和外分泌胰腺:加速发育不良和癌症?

IF 0.1 Q4 GASTROENTEROLOGY & HEPATOLOGY Journal of the Pancreas Pub Date : 2014-09-28 DOI:10.6092/1590-8577/2775
P. Butler
{"title":"基于GLP-1的治疗和外分泌胰腺:加速发育不良和癌症?","authors":"P. Butler","doi":"10.6092/1590-8577/2775","DOIUrl":null,"url":null,"abstract":"Type 2 diabetes (T2DM) is characterized by a deficit in pancreatic beta cell mass with increased beta cell apoptosis. Abnormalities of the exocrine pancreas have also been reported in T2DM, including a decreased overall pancreas size and increased pancreatitis. A promising therapy for T2DM emerged from an old observation that ingested glucose enhances insulin secretion to a greater extent than intravenously infused glucose, an observation termed the incretin effect. The hormone glucagon like peptide one (GLP-1) released from endocrine cells in the gut in response to food ingestion was identified as one of the incretin factors. GLP-1 based therapy has been marked for treatment of T2DM, either as injected GLP-1 mimetics or as orally active inhibitors of the enzyme that degrades endogenously secreted GLP-1 (Dipeptidyl peptidase 4, DPP-4). DPP-4 inhibitors and GLP-1 mimetics are effective at lowering blood glucose in T2DM. The concern as regards the unintended actions of GLP-1 based therapy on the exocrine pancreas was first noted in case reports of pancreatitis in individuals treated with the GLP-1 mimetic exenatide, and this was followed by a caution from the Federal Drug Administration (FDA) based on increased reports of pancreatitis noted in the FDA adverse event reporting system (AERS). Subsequent reports of the actions of GLP-1 on the exocrine pancreas have been controversial. Some, but not all studies, have reported an increase in pancreatic size in animal treated with GLP-1 based therapies. In one human study (of brain dead organ donors) we reported an increase in pancreas weight and pancreatic dysplasia in individuals with T2DM exposed to prior therapy with GLP-1 based therapy (7 DPP-4 inhibitors, 1 GLP-1 mimetic). Others have contested those findings. It is our view that the matter is not resolved and that additional studies are required to establish the safety of this widely prescribed class of drugs. Image: Gila monster ( Heloderma suspectum ) venom contains a substance that shares much of its chemistry with human GLP-1. (Author: Blueag9 ,  Wikimedia Commons )","PeriodicalId":47280,"journal":{"name":"Journal of the Pancreas","volume":"15 1","pages":"527-527"},"PeriodicalIF":0.1000,"publicationDate":"2014-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"GLP-1 Based Therapy and the Exocrine Pancreas: Accelerated Dysplasia and Cancer?\",\"authors\":\"P. Butler\",\"doi\":\"10.6092/1590-8577/2775\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Type 2 diabetes (T2DM) is characterized by a deficit in pancreatic beta cell mass with increased beta cell apoptosis. Abnormalities of the exocrine pancreas have also been reported in T2DM, including a decreased overall pancreas size and increased pancreatitis. A promising therapy for T2DM emerged from an old observation that ingested glucose enhances insulin secretion to a greater extent than intravenously infused glucose, an observation termed the incretin effect. The hormone glucagon like peptide one (GLP-1) released from endocrine cells in the gut in response to food ingestion was identified as one of the incretin factors. GLP-1 based therapy has been marked for treatment of T2DM, either as injected GLP-1 mimetics or as orally active inhibitors of the enzyme that degrades endogenously secreted GLP-1 (Dipeptidyl peptidase 4, DPP-4). DPP-4 inhibitors and GLP-1 mimetics are effective at lowering blood glucose in T2DM. The concern as regards the unintended actions of GLP-1 based therapy on the exocrine pancreas was first noted in case reports of pancreatitis in individuals treated with the GLP-1 mimetic exenatide, and this was followed by a caution from the Federal Drug Administration (FDA) based on increased reports of pancreatitis noted in the FDA adverse event reporting system (AERS). Subsequent reports of the actions of GLP-1 on the exocrine pancreas have been controversial. Some, but not all studies, have reported an increase in pancreatic size in animal treated with GLP-1 based therapies. In one human study (of brain dead organ donors) we reported an increase in pancreas weight and pancreatic dysplasia in individuals with T2DM exposed to prior therapy with GLP-1 based therapy (7 DPP-4 inhibitors, 1 GLP-1 mimetic). Others have contested those findings. It is our view that the matter is not resolved and that additional studies are required to establish the safety of this widely prescribed class of drugs. Image: Gila monster ( Heloderma suspectum ) venom contains a substance that shares much of its chemistry with human GLP-1. (Author: Blueag9 ,  Wikimedia Commons )\",\"PeriodicalId\":47280,\"journal\":{\"name\":\"Journal of the Pancreas\",\"volume\":\"15 1\",\"pages\":\"527-527\"},\"PeriodicalIF\":0.1000,\"publicationDate\":\"2014-09-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Pancreas\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.6092/1590-8577/2775\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Pancreas","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6092/1590-8577/2775","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 2

摘要

2型糖尿病(T2DM)的特点是胰腺β细胞数量减少,细胞凋亡增加。外分泌胰腺的异常在T2DM中也有报道,包括胰腺总尺寸减小和胰腺炎增加。一个有希望的治疗T2DM的方法来自于一个古老的观察,即摄入葡萄糖比静脉输注葡萄糖更能促进胰岛素分泌,这一观察结果被称为肠促胰岛素效应。胰高血糖素样肽1 (glucagon like peptide one, GLP-1)是肠道内分泌细胞对食物摄取反应所释放的激素之一。基于GLP-1的治疗已被标记为治疗T2DM,无论是作为注射GLP-1模拟物,还是作为降解内源性分泌GLP-1(二肽基肽酶4,DPP-4)的酶的口服活性抑制剂。DPP-4抑制剂和GLP-1模拟物可有效降低T2DM患者的血糖。关于基于GLP-1的治疗对外分泌胰腺的意外作用的担忧首先在使用GLP-1模拟艾塞那肽治疗的个体胰腺炎的病例报告中被注意到,随后联邦药物管理局(FDA)基于FDA不良事件报告系统(AERS)中胰腺炎报告的增加而发出警告。随后关于GLP-1对外分泌胰腺作用的报道一直存在争议。一些,但不是所有的研究都报道了GLP-1治疗动物胰腺大小的增加。在一项人类研究(脑死亡器官供体)中,我们报道了先前接受GLP-1治疗(7种DPP-4抑制剂,1种GLP-1模拟物)的T2DM患者胰腺重量增加和胰腺发育不良。其他人对这些发现提出了质疑。我们认为,问题尚未解决,需要进一步的研究来确定这类广泛使用的药物的安全性。图片:吉拉怪物(Heloderma susectum)的毒液含有一种与人类GLP-1化学成分相似的物质。(作者:Blueag9,维基共享资源)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
GLP-1 Based Therapy and the Exocrine Pancreas: Accelerated Dysplasia and Cancer?
Type 2 diabetes (T2DM) is characterized by a deficit in pancreatic beta cell mass with increased beta cell apoptosis. Abnormalities of the exocrine pancreas have also been reported in T2DM, including a decreased overall pancreas size and increased pancreatitis. A promising therapy for T2DM emerged from an old observation that ingested glucose enhances insulin secretion to a greater extent than intravenously infused glucose, an observation termed the incretin effect. The hormone glucagon like peptide one (GLP-1) released from endocrine cells in the gut in response to food ingestion was identified as one of the incretin factors. GLP-1 based therapy has been marked for treatment of T2DM, either as injected GLP-1 mimetics or as orally active inhibitors of the enzyme that degrades endogenously secreted GLP-1 (Dipeptidyl peptidase 4, DPP-4). DPP-4 inhibitors and GLP-1 mimetics are effective at lowering blood glucose in T2DM. The concern as regards the unintended actions of GLP-1 based therapy on the exocrine pancreas was first noted in case reports of pancreatitis in individuals treated with the GLP-1 mimetic exenatide, and this was followed by a caution from the Federal Drug Administration (FDA) based on increased reports of pancreatitis noted in the FDA adverse event reporting system (AERS). Subsequent reports of the actions of GLP-1 on the exocrine pancreas have been controversial. Some, but not all studies, have reported an increase in pancreatic size in animal treated with GLP-1 based therapies. In one human study (of brain dead organ donors) we reported an increase in pancreas weight and pancreatic dysplasia in individuals with T2DM exposed to prior therapy with GLP-1 based therapy (7 DPP-4 inhibitors, 1 GLP-1 mimetic). Others have contested those findings. It is our view that the matter is not resolved and that additional studies are required to establish the safety of this widely prescribed class of drugs. Image: Gila monster ( Heloderma suspectum ) venom contains a substance that shares much of its chemistry with human GLP-1. (Author: Blueag9 ,  Wikimedia Commons )
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of the Pancreas
Journal of the Pancreas GASTROENTEROLOGY & HEPATOLOGY-
自引率
0.00%
发文量
0
期刊最新文献
Why do we need to be focused on pancreatic cancer Pediatric Pancreatic Lymphadenitis Tuberculosis Causing IVC Thrombosis in Syria: A Case Report Tumor-related paraneoplastic disorder creating a bogus synapse? A Case Report of Undifferentiated Pancreatic Carcinoma The Effect of Non-Steroidal Anti-Inflammatory Drugs on Acute Pancreatitis: A Retrospective Study at a London District General Hospital
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1