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糖酵解及其关键限速酶在急性肺损伤中的研究进展

Advances in glycolysis and its key rate-limiting enzymes in acute lung injury
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摘要 急性肺损伤是一种以肺部炎症和微血管通透性增加为特征的临床综合征,但其发生机制尚未阐明.糖酵解及其关键限速酶己糖激酶、磷酸果糖激酶1和丙酮酸激酶M2,以及间接限速酶6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶3,均被认为参与了急性肺损伤的发生.本文总结糖酵解相关限速酶在急性肺损伤中的病理生理特征及其相关性,通过抑制糖酵解相关限速酶抑制糖酵解可缓解急性肺损伤.因此,靶向糖酵解相关限速酶开发急性肺损伤治疗药物具有极大的临床意义. Acute lung injury is a clinical syndrome characterized by pulmonary inflammation and increased microvascular permeability,but the mechanism of its occurrence is still unclear.Glycolysis and its key rate-limiting enzymes hexokinase,phosphofructokinase 1,and pyruvate kinase M2,as well as the indirect rate-limiting enzyme 6-phosphofructose-2-kinase/fructose-2,6-biphosphatase 3,are thought to be involved in the development of acute lung injury.This article summarizes the pathophysiological characteristics and correlation of glycolysis related rate-limiting enzymes in acute lung injury.Inhibition of glycolysis can alleviate acute lung injury by inhibiting glycolysis related rate-limiting enzymes.Therefore,it is of great clinical significance to develop therapeutic drugs for acute lung injury by targeting rate-limiting enzymes related to glycolysis.
作者 李强 王博 林慧庆 Li Qiang;Wang Bo;Lin Huiqing(Department of Thoracic Surgery,Renmin Hospital of Wuhan University,Wuhan 430060,China;The First Clinical College of Wuhan University,Wuhan 430060,China)
出处 《中华实验外科杂志》 CAS 北大核心 2023年第11期2420-2426,共7页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金面上项目(82170106) 中国器官移植发展基金会(2020HX0011)。
关键词 急性肺损伤 糖酵解 糖酵解关键限速酶 Acute Lung Injury Glycolysis Key rate-limiting enzymes of glycolysis
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  • 1Tracey KJ. The inflammatory reflex. Nature ,2002,420:853-859.
  • 2Bernik TR, Friedman SG, Ochani M, et al. Pharmacological stimulation of the cholinergic antiinflammatory pathway. Exp Med, 2002,195:781- 788.
  • 3Borovikova LV, Ivanova S, Zhang M, et al. Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin. Nature, 2000,405:458-462.
  • 4Borovikova LV, Ivanova S, Nardi D, et al. Role of vagus nerve signaling in CNI-1493-mediated suppression of acute inflammation. Auton Neurosci, 2000,85 : 141-147.
  • 5Wang H, Yu M, Ochani M, et al. Nicotinic acetyleholine receptor α7 subunit is an essential regulator of inflammation. Nature, 2003,421 : 384-388.
  • 6Janeway CA Jr, Medzhitov R. Innate immune recognition. Annu Rev Immuno12002; 20:197-216.
  • 7Chen GY, Nunez G. Sterile inflammation: sensing and react- ing to damage. Nat Rev lmmuno12010; 10:826-837.
  • 8Warburg O, Wind F, Negelein E. The metabolism of tumors in the body. JGen Physiol 1927; 8:519-530.
  • 9Sbarra AJ, Karnovsky ML. The biochemical basis of phago- cytosis. I. Metabolic changes during the ingestion of parti- cles by polymorphonuclear leukocytes. J Biol Chem 1959; 234:1355-1362.
  • 10Guthrie LA, McPhail LC, Henson PM, Johnston Jr RB. Prim- ing of neutrophils for enhanced release of oxygen metabolites by bacterial lipopolysaccharide. Evidence for increased ac- tivity of the superoxide-producing enzyme. J Exp Med 1984; 160:1656-1671.

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