Role of the Platelets and Nitric Oxide Biotransformation in Ischemic Stroke: A Translative Review from Bench to Bedside

被引:41
作者
Bladowski, Maciej [1 ]
Gawrys, Jakub [1 ]
Gajecki, Damian [1 ]
Szahidewicz-Krupska, Ewa [1 ]
Sawicz-Bladowska, Anna [1 ]
Doroszko, Adrian [1 ]
机构
[1] Wroclaw Med Univ, Fac Med, Dept Internal Med Hypertens & Clin Oncol, Wroclaw, Poland
关键词
VON-WILLEBRAND-FACTOR; TRANSDERMAL GLYCERYL TRINITRATE; CEREBRAL-ARTERY OCCLUSION; FREE-RADICAL SCAVENGER; ST-SEGMENT ELEVATION; EARLY ASPIRIN USE; ACTIVATING-FACTOR; ASYMMETRIC DIMETHYLARGININE; L-ARGININE; IN-VIVO;
D O I
10.1155/2020/2979260
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ischemic stroke remains the fifth cause of death, as reported worldwide annually. Endothelial dysfunction (ED) manifesting with lower nitric oxide (NO) bioavailability leads to increased vascular tone, inflammation, and platelet activation and remains among the major contributors to cardiovascular diseases (CVD). Moreover, temporal fluctuations in the NO bioavailability during ischemic stroke point to its key role in the cerebral blood flow (CBF) regulation, and some data suggest that they may be responsible for the maintenance of CBF within the ischemic penumbra in order to reduce infarct size. Several years ago, the inhibitory role of the platelet NO production on a thrombus formation has been discovered, which initiated the era of extensive studies on the platelet-derived nitric oxide (PDNO) as a platelet negative feedback regulator. Very recently, Radziwon-Balicka et al. discovered two subpopulations of human platelets, based on the expression of the endothelial nitric oxide synthase (eNOS-positive or eNOS-negative platelets, respectively). The e-NOS-negative ones fail to produce NO, which attenuates their cyclic guanosine monophosphate (cGMP) signaling pathway and-as result-promotes adhesion and aggregation while the e-NOS-positive ones limit thrombus formation. Asymmetric dimethylarginine (ADMA), a competitive NOS inhibitor, is an independent cardiovascular risk factor, and its expression alongside with the enzymes responsible for its synthesis and degradation was recently shown also in platelets. Overproduction of ADMA in this compartment may increase platelet activation and cause endothelial damage, additionally to that induced by its plasma pool. All the recent discoveries of diverse eNOS expression in platelets and its role in regulation of thrombus formation together with studies on the NOS inhibitors have opened a new chapter in translational medicine investigating the onset of acute cardiovascular events of ischemic origin. This translative review briefly summarizes the role of platelets and NO biotransformation in the pathogenesis and clinical course of ischemic stroke.
引用
收藏
页数:18
相关论文
共 209 条
[21]   Inhibition of L-arginine transport in platelets by asymmetric dimethylarginine and NG-monomethyl-L-arginine:: Effects of arterial hypertension [J].
Brunini, TMC ;
Moss, MB ;
Siqueira, MAS ;
Meirelles, LR ;
Rozentul, AL ;
Mann, GE ;
Ellory, JC ;
de Moura, RS ;
Mendes-Ribeiro, AC .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2004, 31 (10) :738-740
[22]   The relationship between mean platelet volume, stroke subtype and clinical outcome [J].
Butterworth, RJ ;
Bath, PMW .
PLATELETS, 1998, 9 (06) :359-364
[23]   Decreased nitric oxide levels and increased calcium content in platelets of hypertensive patients [J].
Camilletti, A ;
Moretti, N ;
Giacchetti, G ;
Faloia, E ;
Martarelli, D ;
Mantero, F ;
Mazzanti, L .
AMERICAN JOURNAL OF HYPERTENSION, 2001, 14 (04) :382-386
[24]   Platelet glycoprotein receptor Ib blockade ameliorates experimental cerebral ischemia-reperfusion injury by strengthening the blood-brain barrier function and anti-thrombo-inflammatory property [J].
Chen, Chunyan ;
Li, Tingting ;
Zhao, Yuchen ;
Qian, Yinfeng ;
Li, Xiaoyi ;
Dai, Xiangrong ;
Huang, Dake ;
Pan, Tianzhong ;
Zhou, Lanlan .
BRAIN BEHAVIOR AND IMMUNITY, 2018, 69 :255-263
[25]  
CHEN T, 1994, ARCH INT PHARMACOD T, V327, P266
[26]   CAST: Randomised placebo-controlled trial of early aspirin use in 20,000 patients with acute ischaemic stroke [J].
Chen, ZM ;
Hui, JM ;
Liu, LS ;
Liu, ZM ;
Peto, R ;
Sandercock, P ;
Wang, WQ ;
Wang, YX ;
Wang, ZB ;
Xie, JX ;
You, GX ;
Zhang, FL ;
Zhang, HQ ;
Zhao, ZY .
LANCET, 1997, 349 (9066) :1641-1649
[27]   Indications for early aspirin use in acute ischemic stroke - A combined analysis of 40 000 randomized patients from the Chinese Acute Stroke Trial and the International Stroke Trial [J].
Chen, ZM ;
Sandercock, P ;
Pan, HC ;
Counsell, C ;
Collins, R ;
Liu, LS ;
Xie, JX ;
Warlow, C ;
Peto, R .
STROKE, 2000, 31 (06) :1240-1249
[28]   Impact of selective platelet inhibition in reducing cardiovascular risk - role of vorapaxar [J].
Cheng, Judy W. M. .
VASCULAR HEALTH AND RISK MANAGEMENT, 2016, 12 :263-268
[29]   Reduced microvascular thrombosis and improved outcome in acute murine stroke by inhibiting GP IIb/IIIa receptor-mediated platelet aggregation [J].
Choudhri, TF ;
Hoh, BL ;
Zerwes, HG ;
Prestigiacomo, CJ ;
Kim, SC ;
Connolly, ES ;
Kottirsch, G ;
Pinsky, DJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (07) :1301-1310
[30]   Platelet-leukocyte aggregation induced by PAR agonists: regulation by nitric oxide and matrix metalloproteinases [J].
Chung, AWY ;
Radomski, A ;
Alonso-Escolano, D ;
Jurasz, P ;
Stewart, MW ;
Malinski, T ;
Radomski, MW .
BRITISH JOURNAL OF PHARMACOLOGY, 2004, 143 (07) :845-855