User:Tkadm30/Notebook/Endocannabinoids: Difference between revisions

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=== Model ===
=== Model ===
# Use omega 3 (DHA) fatty acids as substrate for docosahexaenoylethanolamide (DHEA) hydrolysis
# Use omega 3 (DHA) fatty acids as substrate for docosahexaenoylethanolamide (DHEA) hydrolysis
# Protect the hippocampus and neurons from stress induced damage.
# Protect the hippocampus and neurons from glutamate excitoxicity.
# CB1: A synaptogenic receptor
# CB1: A synaptogenic receptor
=== Documentation ===
=== Documentation ===
Protocol:
Protocol:

Revision as of 06:08, 7 October 2014

Notes

Hypothesis

  1. DHA may potentiate synaptic plasticity (and cognition) via retrograde CB1 signaling.
  2. Synaptic activation of GABA(B) receptor by endocannabinoids promotes synaptic function and learning. (synaptogenesis)

Model

  1. Use omega 3 (DHA) fatty acids as substrate for docosahexaenoylethanolamide (DHEA) hydrolysis
  2. Protect the hippocampus and neurons from glutamate excitoxicity.
  3. CB1: A synaptogenic receptor

Documentation

Protocol:

Cannabinoids and hippocampal neurogenesis:

DHA:

Anandamide signaling:

FAAH (fatty acid amide hydrolase):

Introduction to fatty amides:

Synaptic Plasticity:

Keywords

hippocampus, anandamide, FAAH, fatty acids, THC, neurogenesis, synaptogenesis