Pharmacology of Ischemia-Reperfusion. Translational Research Considerations

被引:14
|
作者
Prieto-Moure, Beatriz [2 ]
Lloris-Carsi, Jose M. [1 ]
Barrios-Pitarque, Carlos [2 ]
Toledo-Pereyra, Luis-H. [3 ,4 ]
Maria Lajara-Romance, Jose [2 ]
Berda-Antoli, M. [2 ]
Lloris-Cejalvo, J. M. [2 ]
Cejalvo-Lapena, Dolores [2 ]
机构
[1] Univ Valencia, Dept Surg, Valencia, Spain
[2] Catholic Univ Valencia, Expt Surg, Valencia, Spain
[3] Western Michigan Univ, Homer Stryker MD Sch Med, Kalamazoo, MI 49008 USA
[4] Michigan State Univ, Coll Human Med, Kalamazoo, MI USA
关键词
ischemia-reperfusion; pharmacology; more common therapies; preconditioning; antioxidants; reduction of inflammatory cytokines; macrophage; neutrophil reduction; NITRIC-OXIDE SYNTHASE; NECROSIS-FACTOR-ALPHA; RANDOMIZED-CONTROLLED-TRIAL; HEME OXYGENASE-1 PROTECTS; ACTIVATED RECEPTOR-GAMMA; PERFUSED RAT-KIDNEY; FACTOR-KAPPA-B; ISCHEMIA/REPERFUSION INJURY; LUNG ISCHEMIA; ISCHAEMIA/REPERFUSION INJURY;
D O I
10.3109/08941939.2015.1119219
中图分类号
R61 [外科手术学];
学科分类号
摘要
Ischemia-reperfusion (IRI) is a complex physiopathological mechanism involving a large number of metabolic processes that can eventually lead to cell apoptosis and ultimately tissue necrosis.Treatment approaches intended to reduce or palliate the effects of IRI are varied, and are aimed basically at: inhibiting cell apoptosis and the complement system in the inflammatory process deriving from IRI, modulating calcium levels, maintaining mitochondrial membrane integrity, reducing the oxidative effects of IRI and levels of inflammatory cytokines, or minimizing the action of macrophages, neutrophils, and other cell types. This study involved an extensive, up-to-date review of the bibliography on the currently most widely used active products in the treatment and prevention of IRI, and their mechanisms of action, in an aim to obtain an overview of current and potential future treatments for this pathological process. The importance of IRI is clearly reflected by the large number of studies published year after year, and by the variety of pathophysiological processes involved in this major vascular problem. A quick study of the evolution of IRI-related publications in PubMed shows that in a single month in 2014, 263 articles were published, compared to 806 articles in the entire 1990.
引用
收藏
页码:234 / 249
页数:16
相关论文
共 50 条
  • [41] The potential of translational bioinformatics approaches for pharmacology research
    Li, Lang
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2015, 80 (04) : 862 - 867
  • [42] Translational research into sexual disorders: pharmacology and behavior
    Chan, J.
    Oosting, R. S.
    Kooijman, E.
    van Hasselt, F. N.
    Snoeren, E. M. S.
    Waldinger, M. D.
    Olivier, B.
    [J]. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2008, 18 : S47 - S48
  • [43] Expression of cytokines in lung injury after intervention with anti-L-selectin in experimental ischemia-reperfusion.
    van Griensven, M
    Stalp, M
    Lehmann, U
    Seekamp, A
    [J]. SHOCK, 1999, 11 : 85 - 86
  • [44] Nitric oxide differently influences non-phagocytic neutrophil reactions during myocardial ischemia-reperfusion.
    Portnychenko, AG
    Tumanovs'ka, LV
    Voznesens'ka, TY
    Moybenko, OO
    [J]. CLINICAL IMMUNOLOGY, 2002, 103 (03) : S11 - S11
  • [45] Nitric oxide donor, nitroprusside, improved short-term survival after intestinal ischemia-reperfusion.
    Haglind, E
    Nilsson, B
    [J]. SHOCK, 1999, 12 : 44 - 44
  • [46] PHARMACOLOGY OF AZAPROPAZONE - POTENTIAL UTILITY IN THE TREATMENT OF ISCHEMIA REPERFUSION INJURY
    MOUSA, SA
    RAINSFORD, KD
    TIMMERMANS, PBMWM
    [J]. CARDIOVASCULAR DRUG REVIEWS, 1992, 10 (03): : 323 - 332
  • [47] Expression of cytokines in lung injury after intervention with anti-L-selectin in experimental ischemia-reperfusion.
    van Griensven, M
    Stalp, M
    Lehmann, U
    Seekamp, A
    [J]. SHOCK, 1999, 12 : 32 - 32
  • [48] ICAM-1 and ailopurinol inhibited TNF-a and MPO response after intestinal ischemia-reperfusion.
    Alatas, Ö
    Çolak, Ö
    Ilhan, H
    Tokar, B
    [J]. CLINICAL CHEMISTRY, 2002, 48 (06) : A77 - A77
  • [49] Myocardial ischemia/reperfusion: Translational pathophysiology of ischemic heart disease
    Heusch, Gerd
    [J]. MED, 2024, 5 (01): : 10 - 31
  • [50] Lung-Specific Extracellular Superoxide Dismutase Blocks Neutrophil-Mediated Toxicity in Brain Ischemia-Reperfusion.
    Mai Nguyen
    Gates, Kathleen
    Prifti, Landa
    Lim, Kihong
    O'Reilly, Michael
    Kim, Minsoo
    Halterman, Marc W.
    [J]. STROKE, 2019, 50