The endocannabinoid anandamide inhibits the function of α4β2 nicotinic acetylcholine receptors

Charles E. Spivak, Carl R. Lupica, Murat Oz

Research output: Contribution to journalArticlepeer-review

51 Citations (Scopus)

Abstract

The effects of the endocannabinoid anandamide (arachidonylethanolamide, AEA) on the function of α4β2 nicotinic acetylcholine receptors (nAChR) stably expressed in SH-EP1 cells were investigated using the whole-cell patch-clamp technique. In the concentration range of 200 nM to 2 μM, AEA significantly reduced the maximal amplitudes and increased the desensitization of acetylcholine (ACh)-induced currents. The effects of AEA could be neither replicated by the exogenous cannabinoid Δ9-tetrahydrocannabinol (1 μM) nor reversed by the selective CB1 receptor antagonist 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-N-(piperidin-1-yl) -1H-pyrazole-3-carboxamide (SR-141716A) (1 μM). The actions of AEA were apparent when applied extracellularly but not during intracellular dialysis. Furthermore, the effects of AEA ACh currents were not altered by the calcium chelator 1,2-bis(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid. The onset and washout of the AEA effects required several minutes (10-30 min), but the latter was significantly decreased in the presence of lipid-free bovine serum albumin (BSA). Moreover, BSA alone increased peak ACh current amplitudes and diminished desensitization rates in naive cells, suggesting a tonic modulation of α4β2 nAChR function by an endogenous AEA-like lipid. Further analysis of AEA effects on α4β2 nAChR-mediated currents, using a two-stage desensitization model, indicated that the first forward rate constant leading to desensitization, k1, increased nearly 30-fold as a linear function of the AEA concentration. In contrast, the observation that the other three rate constants were unaltered by AEA suggested that AEA raised the energy of the activated state. These results indicate that AEA directly inhibits the function of α4β2 nAChRs in a CB1 receptor-independent manner.

Original languageEnglish
Pages (from-to)1024-1032
Number of pages9
JournalMolecular Pharmacology
Volume72
Issue number4
DOIs
Publication statusPublished - Oct 2007
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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