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本文引用的文献

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Sensing and responding to hypoxia, molecular and physiological mechanisms.感知和应对缺氧:分子与生理机制。
Integr Comp Biol. 2002 Jul;42(3):463-8. doi: 10.1093/icb/42.3.463.
2
Signaling during platelet adhesion and activation.血小板黏附和激活过程中的信号转导。
Arterioscler Thromb Vasc Biol. 2010 Dec;30(12):2341-9. doi: 10.1161/ATVBAHA.110.207522. Epub 2010 Nov 11.
3
The aging stress response.衰老应激反应。
Mol Cell. 2010 Oct 22;40(2):333-44. doi: 10.1016/j.molcel.2010.10.002.
4
Oxidative stress and aging.氧化应激与衰老。
J Nephrol. 2010 Sep-Oct;23 Suppl 15:S29-36.
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Dynamic regulation of fibrinogen: integrin αIIbβ3 binding.纤维蛋白原的动态调节:整合素 αIIbβ3 结合。
Biochemistry. 2010 Nov 2;49(43):9217-25. doi: 10.1021/bi1009858.
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The role of oxidative stress in the aging process.氧化应激在衰老过程中的作用。
ScientificWorldJournal. 2010 Jun 15;10:1121-8. doi: 10.1100/tsw.2010.94.
7
Oxidative stress and vascular function: implications for pharmacologic treatments.氧化应激与血管功能:对药物治疗的启示。
Curr Hypertens Rep. 2010 Jun;12(3):154-61. doi: 10.1007/s11906-010-0103-9.
8
Oxidative stress and central cardiovascular regulation. - Pathogenesis of hypertension and therapeutic aspects -.氧化应激与心血管中枢调节。——高血压发病机制及治疗学方面——
Circ J. 2010 May;74(5):827-35. doi: 10.1253/circj.cj-10-0153. Epub 2010 Apr 15.
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The thromboxane/endoperoxide receptor (TP): the common villain.血栓素/内过氧化物受体(TP):共同的恶棍。
J Cardiovasc Pharmacol. 2010 Apr;55(4):317-32. doi: 10.1097/fjc.0b013e3181d8bc8a.
10
Thrombin receptor antagonism -the potential of antiplatelet medication SCH 530348.凝血酶受体拮抗剂——抗血小板药物 SCH 530348 的潜力。
Expert Opin Pharmacother. 2010 Apr;11(6):1015-22. doi: 10.1517/14656561003720471.

腺嘌呤核苷和血小板。

Adenosine and blood platelets.

机构信息

Departments of Medicine and Biochemistry, Whitaker Cardiovascular Institute, and Evans Center for Interdisciplinary Biomedical Research, Boston University School of Medicine, CVI, 700 Albany St., Boston, MA, 02118, USA.

出版信息

Purinergic Signal. 2011 Sep;7(3):357-65. doi: 10.1007/s11302-011-9220-4. Epub 2011 Feb 8.

DOI:10.1007/s11302-011-9220-4
PMID:21484090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3166992/
Abstract

Adenosine is an important regulatory metabolite and an inhibitor of platelet activation. Adenosine released from different cells or generated through the activity of cell-surface ectoenzymes exerts its effects through the binding of four different G-protein-coupled adenosine receptors. In platelets, binding of A(2) subtypes (A(2A) or A(2B)) leads to consequent elevation of intracellular cyclic adenosine monophosphate, an inhibitor of platelet activation. The significance of this ligand and its receptors for platelet activation is addressed in this review, including how adenosine metabolism and its A(2) subtype receptors impact the expression and activity of adenosine diphosphate receptors. The expression of A(2) adenosine receptors is induced by conditions such as oxidative stress, a hallmark of aging. The effect of adenosine receptors on platelet activation during aging is also discussed, as well as potential therapeutic applications.

摘要

腺苷是一种重要的调节代谢物和血小板激活抑制剂。不同细胞释放的腺苷或通过细胞表面ectoenzymes 的活性产生的腺苷,通过结合四种不同的 G 蛋白偶联腺苷受体发挥其作用。在血小板中,A(2)亚型(A(2A)或 A(2B))的结合导致细胞内环磷酸腺苷的浓度升高,从而抑制血小板的激活。本综述讨论了这种配体及其受体对血小板激活的意义,包括腺苷代谢及其 A(2)亚型受体如何影响二磷酸腺苷受体的表达和活性。A(2)腺苷受体的表达是由氧化应激等衰老特征的条件诱导的。本文还讨论了在衰老过程中腺苷受体对血小板激活的影响,以及潜在的治疗应用。