The endocannabinoid system: 'NO' longer anonymous in the control of nitrergic signalling?

被引:23
作者
Lipina, Christopher [1 ]
Hundal, Harinder S. [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Sir James Black Ctr, Div Cell Signalling & Immunol, Dundee DD1 5EH, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
endocannabinoid system; reactive nitrogen species; nitric oxide; nitrosative stress; cannabinoid receptor; NITRIC-OXIDE SYNTHASE; DEPENDENT PROTEIN-KINASE; INDUCED INSULIN-RESISTANCE; CANNABINOID RECEPTOR ACTIVATION; RAT MICROGLIAL CELLS; ACID AMIDE HYDROLASE; DIET-INDUCED OBESITY; CB1; RECEPTOR; S-NITROSYLATION; MITOCHONDRIAL BIOGENESIS;
D O I
10.1093/jmcb/mjx008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The endocannabinoid system (ECS) is a key cellular signalling system that has been implicated in the regulation of diverse cellular functions. Importantly, growing evidence suggests that the biological actions of the ECS may, in part, be mediated through its ability to regulate the production and/or release of nitric oxide, a ubiquitous bioactive molecule, which functions as a versatile signalling intermediate. Herein, we review and discuss evidence pertaining to ECS-mediated regulation of nitric oxide production, as well as the involvement of reactive nitrogen species in regulating ECS-induced signal transduction by highlighting emerging work supporting nitrergic modulation of ECS function. Importantly, the studies outlined reveal that interactions between the ECS and nitrergic signalling systems can be both stimulatory and inhibitory in nature, depending on cellular context. Moreover, such crosstalk may act to maintain proper cell function, whereas abnormalities in either system can undermine cellular homoeostasis and contribute to various pathologies associated with their dysregulation. Consequently, future studies targeting these signalling systems may provide new insights into the potential role of the ECS-nitric oxide signalling axis in disease development and/or lead to the identification of novel therapeutic targets for the treatment of nitrosative stress-related neurological, cardiovascular, and metabolic disorders.
引用
收藏
页码:91 / 103
页数:13
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共 141 条
[1]  
ABUSOUD HM, 1994, J BIOL CHEM, V269, P32047
[2]   WIN 55,212-2, Agonist of Cannabinoid Receptors, Prevents Amyloid β1-42 Effects on Astrocytes in Primary Culture [J].
Aguirre-Rueda, Diana ;
Guerra-Ojeda, Sol ;
Aldasoro, Martin ;
Iradi, Antonio ;
Obrador, Elena ;
Mauricio, Maria D. ;
Vila, Jose Ma ;
Marchio, Patricia ;
Valles, Soraya L. .
PLOS ONE, 2015, 10 (04)
[3]   Nitric oxide synthases: structure, function and inhibition [J].
Alderton, WK ;
Cooper, CE ;
Knowles, RG .
BIOCHEMICAL JOURNAL, 2001, 357 (03) :593-615
[4]   Supply and demand for endocannabinoids [J].
Alger, Bradley E. ;
Kim, Jimok .
TRENDS IN NEUROSCIENCES, 2011, 34 (06) :304-315
[5]   Anandamide and decidual remodelling: COX-2 oxidative metabolism as a key regulator [J].
Almada, M. ;
Piscitelli, F. ;
Fonseca, B. M. ;
Di Marzo, V. ;
Correia-da-Silva, G. ;
Teixeira, N. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2015, 1851 (11) :1473-1481
[6]   Cannabinoid Receptor 2 Participates in Amyloid-β Processing in a Mouse Model of Alzheimer's Disease but Plays a Minor Role in the Therapeutic Properties of a Cannabis-Based Medicine [J].
Aso, Ester ;
Andres-Benito, Pol ;
Carmona, Margarita ;
Maldonado, Rafael ;
Ferrer, Isidre .
JOURNAL OF ALZHEIMERS DISEASE, 2016, 51 (02) :489-500
[7]   Cannabinoid receptor agonists are mitochondrial inhibitors: A unified hypothesis of how cannabinoids modulate mitochondrial function and induce cell death [J].
Athanasiou, Andriam ;
Clarke, Anna B. ;
Turner, Amy E. ;
Kumaran, Nethia M. ;
Vakilpour, Sara ;
Smith, Paul A. ;
Bagiokou, Dimitra ;
Bradshaw, Tracey D. ;
Westwell, Andrew D. ;
Fang, Lin ;
Lobo, Dileep N. ;
Constantinescu, Cris S. ;
Calabrese, Vittorio ;
Loesch, Andrzej ;
Alexander, Stephen P. H. ;
Clothier, Richard H. ;
Kendall, David A. ;
Bates, Timothy E. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 364 (01) :131-137
[8]   Loss of Endothelial Nitric Oxide Synthase Promotes p25 Generation and Tau Phosphorylation in a Murine Model of Alzheimer's Disease [J].
Austin, Susan A. ;
Katusic, Zvonimir S. .
CIRCULATION RESEARCH, 2016, 119 (10) :1128-1134
[9]   S-nitrosylation of Bcl-2 inhibits its ubiquitin-proteasomal degradation -: A novel antiapoptotic mechanism that suppresses apoptosis [J].
Azad, Neelam ;
Vallyathan, Val ;
Wang, Liying ;
Tantishaiyakul, Vimon ;
Stehlik, Christian ;
Leonard, Stephen S. ;
Rojanasakul, Yon .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (45) :34124-34134
[10]   Neuropharmacology of the endocannabinoid signaling system-molecular mechanisms, biological actions and synaptic plasticity [J].
Basavarajappa, Balapal S. .
CURRENT NEUROPHARMACOLOGY, 2007, 5 (02) :81-97