The position of the double bond in monounsaturated free fatty acids is essential for the inhibition of the nicotinic acetylcholine receptor

• Published in: Biochimica et biophysica acta Vol. 1818; no. 11; pp. 2511 - 2520
• Main Authors: Perillo, Vanesa L., Fernández-Nievas, Gaspar A., Vallés, Ana S., Barrantes, Francisco J., Antollini, Silvia S.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-11-2012
• Subjects: Allosteric Regulation; Animals; Electrophysiology; Fatty Acids, Nonesterified - chemistry; Fluorescence Resonance Energy Transfer; Fluorescence spectroscopy; Free fatty acid; Lipid Bilayers; Lipid–protein interaction; Nicotinic acetylcholine receptor; Nicotinic Antagonists - pharmacology; Receptors, Nicotinic - drug effects; Torpedo; Fluorescence spectroscopy; Chol; ACh; CrV; cis-FFAs; Electrophysiology; GP; Free fatty acid; NCA; trans-FFAs; sFFAS; Carb; AChR; FFAs; POPA; POPC; Nicotinic acetylcholine receptor; N-PyrM; TM; FRET; Lipid–protein interaction; DPH; 5-SLFA
• ISSN: 0005-2736; 0006-3002; 1879-2642
• DOI: 10.1016/j.bbamem.2012.06.001

Free fatty acids (FFAs) are non-competitive antagonists of the nicotinic acetylcholine receptor (AChR). Their site of action is supposedly located at the lipid-AChR interface. To elucidate the mechanism involved in this antagonism, we studied the effect that FFAs with a single double-bond at different positions (ω6, ω9, ω11 and ω13 cis-18:1) have on different AChR properties. Electrophysiological studies showed that only two FFAs (ω6 and ω9) reduced the duration of the channel open-state. The briefest component of the closed-time distribution remained unaltered, suggesting that ω6 and ω9 behave as allosteric blockers. Fluorescence resonance energy transfer studies indicated that all FFAs locate at the lipid-AChR interface, ω6 being restricted to annular sites and all others occupying non-annular sites. The perturbation of the native membrane order by FFAs was evaluated by DPH (1,6-diphenyl-1,3,5-hexatriene) and Laurdan fluorescence polarization studies, with the greatest decrease observed for ω9 and ω11. AChR conformational changes produced by FFAs present at the lipid bilayer were evaluated by fluorescence quenching studies of pyrene-labeled AChR and also using the AChR conformational-sensitive probe crystal violet. All cis-FFAs produced AChR conformational changes at the transmembrane level, but only ω9, ω11 and ω13 perturbed the resting state. Thus, the position and isomerism of the torsion angle of unsaturated FFAs are probably a key factor in terms of AChR blockage, suggesting that FFAs with a unique cis double bond at a superficial position inside the membrane directly inhibit AChR function by perturbing a potential conserved core structure for AChR gating at that level.
► We studied AChR function inhibition by monounsaturated free fatty acids (FFA). ► Fluorescence spectroscopy and patch-clamp techniques were used. ► AChR function was inhibited by only two of the FFAs studied. ► Double bond position in FFAs was directly related to AChR inhibition.