Physiology of the Endocannabinoid System During Development
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Abstract
The endocannabinoid (eCB) system comprises endogenously produced cannabinoids (CBs), enzymes of their production and degradation, and CB-sensing receptors and transporters. The eCB system plays a critical role in virtually all stages of animal development. Studies on eCB system components and their physiological role have gained increasing attention with the rising legalization and medical use of marijuana products. The latter represent exogenous interventions that target the eCB system. This chapter summarizes knowledge in the field of CB contribution to gametogenesis, fertilization, embryo implantation, fetal development, birth, and adolescence-equivalent periods of ontogenesis. The material is complemented by the overview of data from our laboratory documenting the functional presence of the eCB system within cerebral arteries of baboons at different stages of development.
Keywords
Cannabis Cannabinoid Baboon Nonhuman primate Fetal artery Cerebral arteryAbbreviations
- ABHD4
α/β-hydrolase domain 4
- AEA
anandamide
- CB
cannabinoid
- COX-2
cyclooxygenase-2
- CP55,940
(-)-cis-3-[2-hydroxy-4-(1,1-dimethylheptyl)phenyl]-trans-4-(3-hydroxypropyl)cyclohexanol
- DAGL
diacylglycerol lipase
- eCB
endocannabinoid (system)
- ERK
extracellular-signal-regulated kinase
- FAAH
fatty acid amide hydrolase
- GABA
gamma aminobutyric acid
- LTP
long-term potentiation
- MAPK
mitogen-activated protein kinase
- MAGL
monoacylglycerol lipase
- NAE
N-acylethanolamine
- NAPE
N-acylphosphatidylethanolamine
- NAPE-PLD
N-acylphosphatidylethanolamine-specific phospholipase D
- PCR
polymerase chain reaction
- THC
Δ9-tetrahydrocannabinol
- TRP
transient receptor potential (protein, channel)
- VGAT
vesicular GABA transporter
- 2-AG
2-arachidonoylglycerol.
Notes
Acknowledgements
The author is thankful to Dr. Dejian Ma and Dr. Wei Li (Dept. Pharmaceutical Sciences, University of Tennessee Health Science Center) for mass spectroscopy quantifications of cannabinoid levels in baboon blood and tissue samples. The author also extends gratitude to Dr. Syed Ali (US Food and Drug Administration) for critical reading of the manuscript and Dr. Richard Redfearn (Office of Scientific Writing, Office of Research, University of Tennessee Health Science Center) for editorial assistance. This work was supported by the National Institutes of Health grant number R21 AA022433 [ANB].
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