Suppr超能文献

二氯醋酸二异丙胺,一种新型丙酮酸脱氢酶激酶4抑制剂,作为重症流感中代谢紊乱和多器官功能衰竭的潜在治疗药物。

Diisopropylamine dichloroacetate, a novel pyruvate dehydrogenase kinase 4 inhibitor, as a potential therapeutic agent for metabolic disorders and multiorgan failure in severe influenza.

作者信息

Yamane Kazuhiko, Indalao Irene L, Chida Junji, Yamamoto Yoshikazu, Hanawa Masaaki, Kido Hiroshi

机构信息

Division of Enzyme Chemistry, Institute for Enzyme Research, The University of Tokushima, Tokushima, Japan.

R&D Department, Daiichi Sankyo Healthcare Co., Ltd., Tokyo, Japan.

出版信息

PLoS One. 2014 May 27;9(5):e98032. doi: 10.1371/journal.pone.0098032. eCollection 2014.

Abstract

Severe influenza is characterized by cytokine storm and multiorgan failure with metabolic energy disorders and vascular hyperpermeability. In the regulation of energy homeostasis, the pyruvate dehydrogenase (PDH) complex plays an important role by catalyzing oxidative decarboxylation of pyruvate, linking glycolysis to the tricarboxylic acid cycle and fatty acid synthesis, and thus its activity is linked to energy homeostasis. The present study tested the effects of diisopropylamine dichloroacetate (DADA), a new PDH kinase 4 (PDK4) inhibitor, in mice with severe influenza. Infection of mice with influenza A PR/8/34(H1N1) virus resulted in marked down-regulation of PDH activity and ATP level, with selective up-regulation of PDK4 in the skeletal muscles, heart, liver and lungs. Oral administration of DADA at 12-h intervals for 14 days starting immediately after infection significantly restored PDH activity and ATP level in various organs, and ameliorated disorders of glucose and lipid metabolism in the blood, together with marked improvement of survival and suppression of cytokine storm, trypsin up-regulation and viral replication. These results indicate that through PDK4 inhibition, DADA effectively suppresses the host metabolic disorder-cytokine cycle, which is closely linked to the influenza virus-cytokine-trypsin cycle, resulting in prevention of multiorgan failure in severe influenza.

摘要

重症流感的特征是细胞因子风暴和多器官功能衰竭,并伴有代谢能量紊乱和血管通透性增加。在能量稳态调节中,丙酮酸脱氢酶(PDH)复合物通过催化丙酮酸的氧化脱羧反应,将糖酵解与三羧酸循环及脂肪酸合成联系起来,发挥着重要作用,因此其活性与能量稳态相关。本研究测试了新型PDH激酶4(PDK4)抑制剂二氯醋酸二异丙胺(DADA)对重症流感小鼠的影响。用甲型PR/8/34(H1N1)流感病毒感染小鼠后,PDH活性和ATP水平显著下调,骨骼肌、心脏、肝脏和肺中的PDK4选择性上调。感染后立即开始每隔12小时口服DADA,持续14天,可显著恢复各器官的PDH活性和ATP水平,改善血液中的葡萄糖和脂质代谢紊乱,同时显著提高生存率,抑制细胞因子风暴、胰蛋白酶上调和病毒复制。这些结果表明,通过抑制PDK4,DADA可有效抑制与流感病毒-细胞因子-胰蛋白酶循环密切相关的宿主代谢紊乱-细胞因子循环,从而预防重症流感中的多器官功能衰竭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1175/4035290/46ce6b6bee97/pone.0098032.g001.jpg

相似文献

2
Erk regulation of pyruvate dehydrogenase flux through PDK4 modulates cell proliferation.
Genes Dev. 2011 Aug 15;25(16):1716-33. doi: 10.1101/gad.16771811.
5
FoxO1 regulates myocardial glucose oxidation rates via transcriptional control of pyruvate dehydrogenase kinase 4 expression.
Am J Physiol Heart Circ Physiol. 2017 Sep 1;313(3):H479-H490. doi: 10.1152/ajpheart.00191.2017. Epub 2017 Jul 7.
8
9
Platelet-activating factor receptor plays a role in lung injury and death caused by Influenza A in mice.
PLoS Pathog. 2010 Nov 4;6(11):e1001171. doi: 10.1371/journal.ppat.1001171.
10
FABP5 deficiency enhances susceptibility to H1N1 influenza A virus-induced lung inflammation.
Am J Physiol Lung Cell Mol Physiol. 2013 Jul 1;305(1):L64-72. doi: 10.1152/ajplung.00276.2012. Epub 2013 Apr 26.

引用本文的文献

2
MAM kinases: physiological roles, related diseases, and therapeutic perspectives-a systematic review.
Cell Mol Biol Lett. 2025 Mar 28;30(1):35. doi: 10.1186/s11658-025-00714-w.
4
Dichloroacetate for Cancer Treatment: Some Facts and Many Doubts.
Pharmaceuticals (Basel). 2024 Jun 6;17(6):744. doi: 10.3390/ph17060744.
6
Oncolytic Virotherapy: A New Paradigm in Cancer Immunotherapy.
Int J Mol Sci. 2024 Jan 18;25(2):1180. doi: 10.3390/ijms25021180.
8
Anemoside B4, a new pyruvate carboxylase inhibitor, alleviates colitis by reprogramming macrophage function.
Inflamm Res. 2024 Mar;73(3):345-362. doi: 10.1007/s00011-023-01840-x. Epub 2023 Dec 29.

本文引用的文献

1
Regulation of energy metabolism by long-chain fatty acids.
Prog Lipid Res. 2014 Jan;53:124-44. doi: 10.1016/j.plipres.2013.12.001. Epub 2013 Dec 18.
2
Obesity, inflammation and diet.
Pediatr Gastroenterol Hepatol Nutr. 2013 Sep;16(3):143-52. doi: 10.5223/pghn.2013.16.3.143. Epub 2013 Sep 30.
3
PPARγ Agonists in Adaptive Immunity: What Do Immune Disorders and Their Models Have to Tell Us?
PPAR Res. 2013;2013:519724. doi: 10.1155/2013/519724. Epub 2013 Aug 1.
5
Blood lactate/ATP ratio, as an alarm index and real-time biomarker in critical illness.
PLoS One. 2013;8(4):e60561. doi: 10.1371/journal.pone.0060561. Epub 2013 Apr 5.
6
Pyruvate dehydrogenase kinase as a novel therapeutic target in oncology.
Front Oncol. 2013 Mar 7;3:38. doi: 10.3389/fonc.2013.00038. eCollection 2013.
8
Activity-based kinase profiling of approved tyrosine kinase inhibitors.
Genes Cells. 2013 Feb;18(2):110-22. doi: 10.1111/gtc.12022. Epub 2012 Dec 26.
9
Transcriptional regulation of pyruvate dehydrogenase kinase.
Diabetes Metab J. 2012 Oct;36(5):328-35. doi: 10.4093/dmj.2012.36.5.328. Epub 2012 Oct 18.
10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验