User:Tkadm30/Notebook/Endocannabinoids: Difference between revisions
Line 54: | Line 54: | ||
** Δ9-THC/DHEA ligands (synaptamide) affect neural stem/progenitor cells (NS/PC) proliferation in the hippocampus. | ** Δ9-THC/DHEA ligands (synaptamide) affect neural stem/progenitor cells (NS/PC) proliferation in the hippocampus. | ||
== | == Endocannabinoid transport == | ||
DHA is an effective promoter of long-term potentiation and its effects on neuronal plasticity are well documented. Moreover, THC may exert a synergistic effect on DHA uptake, glutamate transport, and synaptic plasticity through retrograde signaling. Thus, the combination of THC with DHA is a potent activator of astrocytic channel transporter and exert the modulation of GABA through astrocytes. In addition, endocannabinoids may [http://www.ncbi.nlm.nih.gov/pubmed/21150911 protect neurons from excitoxicity and neuroinflammation upon exposure to stress]. Finally, endocannabinoids represent a family of lipid signaling molecules with potent anti-inflammatory (neuroprotective) bioactivity and promising therapeutic strategies to treat major neurological disorders (Depression, Alzheimer's disease) efficiently. | DHA is an effective promoter of long-term potentiation and its effects on neuronal plasticity are well documented. Moreover, THC may exert a synergistic effect on DHA uptake, glutamate transport, and synaptic plasticity through retrograde signaling. Thus, the combination of THC with DHA is a potent activator of astrocytic channel transporter and exert the modulation of GABA through astrocytes. In addition, endocannabinoids may [http://www.ncbi.nlm.nih.gov/pubmed/21150911 protect neurons from excitoxicity and neuroinflammation upon exposure to stress]. Finally, endocannabinoids represent a family of lipid signaling molecules with potent anti-inflammatory (neuroprotective) bioactivity and promising therapeutic strategies to treat major neurological disorders (Depression, Alzheimer's disease) efficiently. | ||
Revision as of 19:02, 3 July 2015
Introduction
The neurocognitive effects of the marijuana plant are still subject of provocative debates. Hence, the delivery of cannabinoids drug (THC, CBD) to the brain and central nervous system (CNS) remains poorly understood. Moreover, the role of marijuana (THC) may be a beneficial asset in the treatment of epilepsy, Alzheimer, and depression.
Synopsis
- stimulation of endocannabinoid transport with fatty acids derived phospholipids (DHA, EPA) to target major depressive disorders (MDD) and Alzheimer disease (AD).
- endocannabinoid-dependent activity (LTP, synaptogenesis) in the hippocampus promoting brain-derived neurotrophic factor (BDNF) expression.
- effects of the CB1 receptor on excitatory (glutamatergic) synapses and in particular astrocytes. (ATP)
- novel GPR120-CB1 heteromer (DHEA-THC) with potent anti-inflammatory and neuroprotective properties.
- Antioxidant (cytoprotective) properties of GPR120-CB1 heteromer.
Neuroprotective properties of THC/DHEA ligands
Reversible, competitive acetylcholinesterase (AChE) inhibition mecanism of THC
- THC inhibit AChE-induced beta-amyloid aggregation in Alzheimer's disease: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2562334/
- Anti-inflammatory activity of THC agaisnt organophosphate-induced neuroinflammation:
- Unlike THC, caffeine is a noncompetitive reversible inhibitor of AChE
2-arachidonoylglycerol (2-AG)
- 2-AG is an endogenous cannabinoid ligand synthesized by diacylglycerol lipase (DAGL) and phospholipase C (PLC).
- Neuroprotective (anti-inflammatory) and a potent cytoprotective agent (antioxidant)
- retrograde 2-AG signaling
- modulate glutamatergic LTP/DSE
- http://www.ncbi.nlm.nih.gov/pubmed/23307660
- Anxiolytic
- ionotropic (permeable to calcium) P2X7 receptor control 2-AG production
- monoacylglycerol lipase (MAGL), a selective 2-AG hydrolase: http://www.uniprot.org/uniprot/Q99685
- calcium dependent biosynthesis
- novel gliotransmitter (GPR120-CB1) http://www.ncbi.nlm.nih.gov/pubmed/15371507
- 2-AG activate endogenous phospholipase C-dependent TRPV1 channel in the brain.
- ATP-mediated gliotransmission? http://www.ncbi.nlm.nih.gov/pubmed/17207662
- doi:10.1038/srep04329
anandamide (N-arachidonoylethanolamine)
- biosynthesis of endogenous phosphoanandamide/PLC ligands: http://www.ncbi.nlm.nih.gov/pubmed/16938887
- cannabinoid receptor type 1 (CB1) full agonist
- http://www.ncbi.nlm.nih.gov/pubmed/21719698
- CB1 receptor affinity=78nM: http://en.wikipedia.org/wiki/Cannabinoid_receptor
- See also http://en.wikipedia.org/wiki/Anandamide
- Anandamide signaling is metabotropic (CB1) and limit TRPV1-mediated Ca2+ influx. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1201361/
- Anandamide appears a good target to activate TRPV1 receptor and trigger antiepileptogenesis.
Δ9-tetrahydrocannabinol (Δ9-THC)
- Antidepressant effect of Δ9-tetrahydrocannabinol (Δ9-THC). http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866040/
- Regulation of stress-induced neuroinflammation on selective (working) memory?
- Hippocampal neurogenesis is enhanced. http://www.ncbi.nlm.nih.gov/pubmed/16224541/
- Synaptogenic effect of Δ9-THC/DHEA ligands promote hippocampal development.
- Δ9-THC/DHEA ligands (synaptamide) affect neural stem/progenitor cells (NS/PC) proliferation in the hippocampus.
Endocannabinoid transport
DHA is an effective promoter of long-term potentiation and its effects on neuronal plasticity are well documented. Moreover, THC may exert a synergistic effect on DHA uptake, glutamate transport, and synaptic plasticity through retrograde signaling. Thus, the combination of THC with DHA is a potent activator of astrocytic channel transporter and exert the modulation of GABA through astrocytes. In addition, endocannabinoids may protect neurons from excitoxicity and neuroinflammation upon exposure to stress. Finally, endocannabinoids represent a family of lipid signaling molecules with potent anti-inflammatory (neuroprotective) bioactivity and promising therapeutic strategies to treat major neurological disorders (Depression, Alzheimer's disease) efficiently.
Keywords
endocannabinoids, hippocampus, anandamide, 2-AG, CBD, FAAH, DHA, DHEA, THC, TRPV1, neurogenesis, synaptogenesis, GABA, synaptamide, BDNF, LTP, ATP, purinergic signaling, adenosine, acetylcholine, synaptic plasticity, heterosynaptic plasticity, astrocytes, cytokines, neuroinflammation, Alzheimer
References
- Cao D, Kevala K, Kim J, Moon HS, Jun SB, Lovinger D, and Kim HY. Docosahexaenoic acid promotes hippocampal neuronal development and synaptic function. J Neurochem. 2009 Oct;111(2):510-21. DOI:10.1111/j.1471-4159.2009.06335.x |
Docosahexaenoic acid promotes hippocampal neuronal development and synaptic function.
- Gaiarsa JL and Porcher C. Emerging neurotrophic role of GABAB receptors in neuronal circuit development. Front Cell Neurosci. 2013;7:206. DOI:10.3389/fncel.2013.00206 |
Emerging neurotrophic role of GABAB receptors in neuronal circuit development.
- Kim HY, Spector AA, and Xiong ZM. A synaptogenic amide N-docosahexaenoylethanolamide promotes hippocampal development. Prostaglandins Other Lipid Mediat. 2011 Nov;96(1-4):114-20. DOI:10.1016/j.prostaglandins.2011.07.002 |
A synaptogenic amide N-docosahexaenoylethanolamide promotes hippocampal development.
- Wu A, Ying Z, and Gomez-Pinilla F. Docosahexaenoic acid dietary supplementation enhances the effects of exercise on synaptic plasticity and cognition. Neuroscience. 2008 Aug 26;155(3):751-9. DOI:10.1016/j.neuroscience.2008.05.061 |
Docosahexaenoic acid dietary supplementation enhances the effects of exercise on synaptic plasticity and cognition.
- Düster R, Prickaerts J, and Blokland A. Purinergic signaling and hippocampal long-term potentiation. Curr Neuropharmacol. 2014 Jan;12(1):37-43. DOI:10.2174/1570159X113119990045 |
Purinergic signaling and hippocampal long-term potentiation.
- Kim HY and Spector AA. Synaptamide, endocannabinoid-like derivative of docosahexaenoic acid with cannabinoid-independent function. Prostaglandins Leukot Essent Fatty Acids. 2013 Jan;88(1):121-5. DOI:10.1016/j.plefa.2012.08.002 |
Synaptamide, endocannabinoid-like derivative of docosahexaenoic acid with cannabinoid-independent function.
- Monory K, Massa F, Egertová M, Eder M, Blaudzun H, Westenbroek R, Kelsch W, Jacob W, Marsch R, Ekker M, Long J, Rubenstein JL, Goebbels S, Nave KA, During M, Klugmann M, Wölfel B, Dodt HU, Zieglgänsberger W, Wotjak CT, Mackie K, Elphick MR, Marsicano G, and Lutz B. The endocannabinoid system controls key epileptogenic circuits in the hippocampus. Neuron. 2006 Aug 17;51(4):455-66. DOI:10.1016/j.neuron.2006.07.006 |
The Endocannabinoid System Controls Key Epileptogenic Circuits in the Hippocampus.
- Pertwee RG, Howlett AC, Abood ME, Alexander SP, Di Marzo V, Elphick MR, Greasley PJ, Hansen HS, Kunos G, Mackie K, Mechoulam R, and Ross RA. International Union of Basic and Clinical Pharmacology. LXXIX. Cannabinoid receptors and their ligands: beyond CB₁ and CB₂. Pharmacol Rev. 2010 Dec;62(4):588-631. DOI:10.1124/pr.110.003004 |
International Union of Basic and Clinical Pharmacology. LXXIX. Cannabinoid Receptors and Their Ligands: Beyond CB1 and CB2.
- Zogopoulos P, Vasileiou I, Patsouris E, and Theocharis S. The neuroprotective role of endocannabinoids against chemical-induced injury and other adverse effects. J Appl Toxicol. 2013 Apr;33(4):246-64. DOI:10.1002/jat.2828 |
The neuroprotective role of endocannabinoids against chemical-induced injury and other adverse effects.