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Modulation of the Endocannabinoid System Following Central Nervous System Injury
- Source :
- International Journal of Molecular Sciences, International Journal of Molecular Sciences, Vol 20, Iss 2, p 388 (2019)
- Publication Year :
- 2019
- Publisher :
- MDPI, 2019.
-
Abstract
- Central nervous system (CNS) injury, such as stroke or trauma, is known to increase susceptibility to various infections that adversely affect patient outcomes (CNS injury-induced immunodepression—CIDS). The endocannabinoid system (ECS) has been shown to have immunoregulatory properties. Therefore, the ECS might represent a druggable target to overcome CIDS. Evidence suggests that cannabinoid type 2 receptor (CB2R) activation can be protective during the early pro-inflammatory phase after CNS injury, as it limits neuro-inflammation and, therefore, attenuates CIDS severity. In the later phase post CNS injury, CB2R inhibition is suggested as a promising pharmacologic strategy to restore immune function in order to prevent infection.
- Subjects :
- 0301 basic medicine
Time Factors
central nervous system injury
Neuroimmunomodulation
medicine.medical_treatment
Central nervous system
Review
Adaptive Immunity
Catalysis
lcsh:Chemistry
Inorganic Chemistry
03 medical and health sciences
0302 clinical medicine
Immune system
Central Nervous System Diseases
Medicine
Animals
Humans
Trauma, Nervous System
Physical and Theoretical Chemistry
endocannabinoid system
Receptor
lcsh:QH301-705.5
Molecular Biology
Stroke
Spectroscopy
business.industry
Organic Chemistry
General Medicine
medicine.disease
Endocannabinoid system
Immunity, Innate
Computer Science Applications
Cns injury
030104 developmental biology
medicine.anatomical_structure
lcsh:Biology (General)
lcsh:QD1-999
Cannabinoid
business
Neuroscience
030217 neurology & neurosurgery
immunodepression
Endocannabinoids
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 14220067
- Volume :
- 20
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- International Journal of Molecular Sciences
- Accession number :
- edsair.doi.dedup.....f506b588827cb0a2b3f2c8fcb32cbff0