Therapeutic perspectives on PDE4B inhibition in adipose tissue dysfunction and chronic liver injury.

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY Expert Opinion on Therapeutic Targets Pub Date : 2024-07-01 Epub Date: 2024-06-19 DOI:10.1080/14728222.2024.2369590
Dalton W Staller, Robert G Bennett, Ram I Mahato
{"title":"Therapeutic perspectives on PDE4B inhibition in adipose tissue dysfunction and chronic liver injury.","authors":"Dalton W Staller, Robert G Bennett, Ram I Mahato","doi":"10.1080/14728222.2024.2369590","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Chronic liver disease (CLD) is a complex disease associated with profound dysfunction. Despite an incredible burden, the first and only pharmacotherapy for metabolic-associated steatohepatitis was only approved in March of this year, indicating a gap in the translation of preclinical studies. There is a body of preclinical work on the application of phosphodiesterase 4 inhibitors in CLD, none of these molecules have been successfully translated into clinical use.</p><p><strong>Areas covered: </strong>To design therapies to combat CLD, it is essential to consider the dysregulation of other tissues that contribute to its development and progression. As such, proper therapies must combat this throughout the body rather than focusing only on the liver. To detail this, literature characterizing the pathogenesis of CLD was pulled from PubMed, with a particular focus placed on the role of PDE4 in inflammation and metabolism. Then, the focus is shifted to detailing the available information on existing PDE4 inhibitors.</p><p><strong>Expert opinion: </strong>This review gives a brief overview of some of the pathologies of organ systems that are distinct from the liver but contribute to disease progression. The demonstrated efficacy of PDE4 inhibitors in other human inflammatory diseases should earn them further examination for the treatment of CLD.</p>","PeriodicalId":12185,"journal":{"name":"Expert Opinion on Therapeutic Targets","volume":" ","pages":"545-573"},"PeriodicalIF":4.6000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11305103/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Expert Opinion on Therapeutic Targets","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/14728222.2024.2369590","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Chronic liver disease (CLD) is a complex disease associated with profound dysfunction. Despite an incredible burden, the first and only pharmacotherapy for metabolic-associated steatohepatitis was only approved in March of this year, indicating a gap in the translation of preclinical studies. There is a body of preclinical work on the application of phosphodiesterase 4 inhibitors in CLD, none of these molecules have been successfully translated into clinical use.

Areas covered: To design therapies to combat CLD, it is essential to consider the dysregulation of other tissues that contribute to its development and progression. As such, proper therapies must combat this throughout the body rather than focusing only on the liver. To detail this, literature characterizing the pathogenesis of CLD was pulled from PubMed, with a particular focus placed on the role of PDE4 in inflammation and metabolism. Then, the focus is shifted to detailing the available information on existing PDE4 inhibitors.

Expert opinion: This review gives a brief overview of some of the pathologies of organ systems that are distinct from the liver but contribute to disease progression. The demonstrated efficacy of PDE4 inhibitors in other human inflammatory diseases should earn them further examination for the treatment of CLD.

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
PDE4B抑制剂在脂肪组织功能障碍和慢性肝损伤中的治疗前景。
简介慢性肝病(CLD)是一种与严重功能障碍相关的复杂疾病。尽管慢性肝病给患者带来了巨大的负担,但第一种也是唯一一种治疗代谢相关性脂肪性肝炎的药物疗法直到今年 3 月才获得批准,这表明临床前研究的转化还存在差距。关于磷酸二酯酶 4 抑制剂在慢性肝病中的应用已有大量临床前研究工作,但这些分子还没有一个成功应用于临床:要设计抗慢性淋巴细胞白血病的疗法,就必须考虑到导致该病发展和恶化的其他组织的失调。因此,适当的疗法必须在全身范围内防治这种疾病,而不是仅仅关注肝脏。为了详细说明这一点,我们从 PubMed 上检索了有关慢性肝病发病机制的文献,其中特别关注 PDE4 在炎症和新陈代谢中的作用。然后,重点转向详细介绍现有 PDE4 抑制剂的可用信息:本综述简要概述了一些器官系统的病理变化,这些病理变化不同于肝脏,但会导致疾病进展。PDE4抑制剂在其他人类炎症性疾病中的疗效已得到证实,这为它们治疗CLD赢得了进一步的研究机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
8.90
自引率
1.70%
发文量
58
审稿时长
3 months
期刊介绍: The journal evaluates molecules, signalling pathways, receptors and other therapeutic targets and their potential as candidates for drug development. Articles in this journal focus on the molecular level and early preclinical studies. Articles should not include clinical information including specific drugs and clinical trials. The Editors welcome: Reviews covering novel disease targets at the molecular level and information on early preclinical studies and their implications for future drug development. Articles should not include clinical information including specific drugs and clinical trials. Original research papers reporting results of target selection and validation studies and basic mechanism of action studies for investigative and marketed drugs. The audience consists of scientists, managers and decision makers in the pharmaceutical industry, academic researchers working in the field of molecular medicine and others closely involved in R&D.
期刊最新文献
Therapeutic approaches targeting oncogenic proteins in myeloid leukemia: challenges and perspectives. An update on the role of ferroptosis in ischemic stroke: from molecular pathways to Neuroprotection. Druggable genes for therapeutic targeting in PTH signaling for osteoporosis. Is Cav1.3 a feasible therapeutic target for a rare neurodevelopmental disorder? The emerging role of TIM-3 in colorectal cancer: a promising target for immunotherapy.
×
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