Targeting of adenosine receptors in ischemia-reperfusion injury

被引:51
作者
Laubach, Victor E. [1 ]
French, Brent A. [2 ,3 ]
Okusa, Mark D. [3 ]
机构
[1] Univ Virginia Hlth Syst, Dept Surg, Charlottesville, VA 22908 USA
[2] Univ Virginia Hlth Syst, Dept Biomed Engn & Med, Charlottesville, VA 22908 USA
[3] Univ Virginia Hlth Syst, Dept Med, Charlottesville, VA 22908 USA
关键词
inflammation; innate immunity; preconditioning; therapeutic targets; transplantation; ACUTE KIDNEY INJURY; NEUTROPHIL-MEDIATED INJURY; MURINE SEPTIC PERITONITIS; ALVEOLAR EPITHELIAL-CELLS; MYOCARDIAL INFARCT SIZE; MARROW-DERIVED CELLS; NO-REFLOW PHENOMENON; INDUCED LUNG INJURY; PROTEIN-KINASE-C; A(2A) RECEPTOR;
D O I
10.1517/14728222.2011.541441
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Importance of the field: Ischemia-reperfusion (IR) injury is a common problem after transplantation as well as myocardial infarction and stroke. IR initiates an inflammatory response leading to rapid tissue damage. Adenosine, produced in response to IR, is generally considered a protective signaling molecule and elicits its physiological responses through four distinct adenosine receptors. The short half-life, lack of specificity and rapid metabolism limits the use of adenosine as a therapeutic agent. Thus, intense research efforts have focused on the synthesis and implementation of specific adenosine receptor agonists and antagonists as potential therapeutic agents for a variety of inflammatory conditions including IR injury. Areas covered in this review: Current knowledge on IR injury with a focus on lung, heart and kidney and studies that have advanced our understanding of the role of adenosine receptors and the therapeutic potential of adenosine receptor agonists and antagonists for the prevention of IR injury. What the reader will gain: Insight into the role of adenosine receptor signaling in IR injury. Take home message: No therapies are currently available that specifically target IR injury; however, targeting of specific adenosine receptors may offer therapeutic strategies in this regard.
引用
收藏
页码:103 / 118
页数:16
相关论文
共 163 条
[11]  
Blackburn Michael R, 2009, Handb Exp Pharmacol, P215, DOI 10.1007/978-3-540-89615-9_8
[12]  
BREDA MA, 1989, J THORAC CARDIOV SUR, V97, P654
[13]   Adenosine A2B receptors are highly expressed on murine type II alveolar epithelial cells [J].
Cagnina, Rebecca E. ;
Ramos, Susan I. ;
Marshall, Melissa A. ;
Wang, Guoquan ;
Frazier, C. Renea ;
Linden, Joel .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2009, 297 (03) :L467-L474
[14]   Preactivation of NKT cells with α-GalCer protects against hepatic ischemia-reperfusion injury in mouse by a mechanism involving IL-13 and adenosine A2A receptor [J].
Cao, Zongxian ;
Yuan, Youzhong ;
Jeyabalan, Geetha ;
Du, Qiang ;
Tsung, Allan ;
Geller, David A. ;
Billiar, Timothy R. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2009, 297 (02) :G249-G258
[15]   Systemic adenosine A2A agonist ameliorates ischemic reperfusion injury in the rabbit spinal cord [J].
Cassada, DC ;
Gangemi, JJ ;
Rieger, JM ;
Linden, J ;
Kaza, AK ;
Long, SM ;
Kron, IL ;
Tribble, CG ;
Kern, JA .
ANNALS OF THORACIC SURGERY, 2001, 72 (04) :1245-1250
[16]   Modulation of ischemic brain injury and neuroinflammation by adenosine A2A receptors [J].
Chen, Jiang-Fan ;
Pedata, Felicita .
CURRENT PHARMACEUTICAL DESIGN, 2008, 14 (15) :1490-1499
[17]   Adenosine A2A Agonist Administration Improves Islet Transplant Outcome: Evidence for the Role of Innate Immunity in Islet Graft Rejection [J].
Chhabra, Preeti ;
Wang, Kunjie ;
Zeng, Qiang ;
Jecmenica, Mladen ;
Langman, Linda ;
Linden, Joel ;
Ketchum, Robert J. ;
Brayman, Kenneth L. .
CELL TRANSPLANTATION, 2010, 19 (05) :597-612
[18]   Complement activation following oxidative stress [J].
Collard, CD ;
Lekowski, R ;
Jordan, JE ;
Agah, A ;
Stahl, GL .
MOLECULAR IMMUNOLOGY, 1999, 36 (13-14) :941-948
[19]   THE ADENOSINE NEUTROPHIL PARADOX RESOLVED - HUMAN NEUTROPHILS POSSESS BOTH A1 AND A2 RECEPTORS THAT PROMOTE CHEMOTAXIS AND INHIBIT O-2- GENERATION, RESPECTIVELY [J].
CRONSTEIN, BN ;
DAGUMA, L ;
NICHOLS, D ;
HUTCHISON, AJ ;
WILLIAMS, M .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (04) :1150-1157
[20]   ATL 313, A Selective A(2A) Adenosine Receptor Agonist, Reduces Myocardial Infarct Size in a Rat Ischemia/Reperfusion Model [J].
Dai, Wangde ;
Hale, Sharon L. ;
Nayak, Rohith ;
Kloner, Robert A. .
OPEN CARDIOVASCULAR MEDICINE JOURNAL, 2009, 3 :166-172