CB₁ and LPA₁ Receptors Relationship in the Mouse Central Nervous System.

ABSTRACT: Neurolipids are a class of bioactive lipids that are produced locally through specific biosynthetic pathways in response to extracellular stimuli. Neurolipids are important endogenous regulators of neural cell proliferation, differentiation, oxidative stress, inflammation and apoptosis. Endocannabinoids (eCBs) and lysophosphatidic acid (LPA) are examples of this type of molecule and are involved in neuroprotection. The present study analyzes a possible relationship of the main receptor subtypes for both neurolipid systems that are present in the central nervous system, the CB₁ and LPA₁ receptors, by using brain slices from CB₁ KO mice and LPA₁-null mice. Receptor-mediated G protein activation and glycerophospholipid regulation of potential precursors of their endogenous neurotransmitters were measured by two different in vitro imaging techniques, functional autoradiography and imaging mass spectrometry (IMS), respectively. Possible crosstalk between CB₁ and LPA₁ receptors was identified in specific areas of the brain, such as the amygdala, where LPA₁ receptor activity is upregulated in CB₁ KO mice. More evidence of an interaction between both systems was that the CB₁-mediated activity was clearly increased in the prefrontal cortex and cerebellum of LPA₁-null mice. The eCB system was specifically over-activated in regions where LPA₁ has an important signaling role during embryonic development. The modifications on phospholipids (PLs) observed in these genetically modified mice by using the IMS technique indicated the regulation of some of the PL precursors of both LPA and eCBs in specific brain areas. For example, phosphatidylcholine (PC) (36:1) was detected as a potential LPA precursor, and phosphatidylethanolamine (PE) (40:6) and PE (p18:0/22:6) as potential eCB precursors. The absence of the main cerebral receptors for LPA or eCB systems is able to induce modulation on the other at the levels of both signaling and synthesis of endogenous neurotransmitters, indicating adaptive responses between both systems during prenatal and/or postnatal development.

SUBMITTER: Gonzalez de San Roman E 

PROVIDER: S-EPMC6761275 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature