Milanos S, Künzel K, Gilbert D, Janzen D, Sasi M, Büttner A, Frimurer TM, Villmann C (2018)
Publication Language: English
Publication Type: Journal article, Original article
Publication year: 2018
	GABAA receptors are ligand-gated anion channels
	that form pentameric arrangements of various subunits.
	Positive allosteric modulators of GABAA receptors
	have been reported as being isolated either from plants
	or synthesized analogs of known GABAA receptor targeting
	drugs. Recently, we identified monoterpenes, e.g.
	myrtenol as a positive allosteric modulator at α1β2 GABAA
	receptors. Here, along with pharmacophore-based virtual
	screening studies, we demonstrate that scaffold modifications
	of myrtenol resulted in the loss of modulatory activity.
	Two independent approaches, fluorescence-based
	compound analysis and electrophysiological recordings
	in whole-cell configurations were used for analysis
	of transfected cells. C-atoms 1 and 2 of the myrtenol
	backbone were identified as crucial to preserve positive
	allosteric potential. A modification at C-atom 2 and lack
	of the hydroxyl group at C-atom 1 exhibited significantly
	reduced GABAergic currents at α1β2, α1β2γ, α2β3, α2β3γ
	and α4β3δ receptors. This effect was independent of
	the γ2 subunit. A sub-screen with side chain length and
	volume differences at the C-atom 1 identified two compounds
	that inhibited GABAergic responses but without
	receptor subtype specificity. Our combined approach of
	pharmacophore-based virtual screening and functional
	readouts reveals that side chain modifications of the
	bridged six-membered ring structure of myrtenol are
	crucial for its modulatory potential at GABAA receptors.
APA:
Milanos, S., Künzel, K., Gilbert, D., Janzen, D., Sasi, M., Büttner, A.,... Villmann, C. (2018). Structural changes at the myrtenol backbone reverse its positive allosteric potential into inhibitory GABAA receptor modulation. Biological Chemistry. https://doi.org/10.1515/hsz-2017-0262
MLA:
Milanos, Sinem, et al. "Structural changes at the myrtenol backbone reverse its positive allosteric potential into inhibitory GABAA receptor modulation." Biological Chemistry (2018).
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