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Krzysztof Jozwiak

4 papers in the library · 50 citations · publishing 2008-2011

Papers

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Structure-activity relationship of ibogaine analogs interacting with nicotinic acetylcholine receptors in different conformational states.

The international journal of biochemistry & cell biology September 1, 2011 Hugo R Arias, Dominik Feuerbach, Katarzyna M Targowska-Duda et al. 10 citations

The interaction of ibogaine analogs with nicotinic acetylcholine receptors (AChRs) in different conformational states was studied by functional and structural approaches. The results established that ibogaine analogs: (a) inhibit (±)-epibatidine-induced Ca²⁺ influx in human embryonic muscle AChRs with the following potency sequence (IC(50) in μM): (±)-18-methylaminocoronaridine...

Interaction of ibogaine with human alpha3beta4-nicotinic acetylcholine receptors in different conformational states.

The international journal of biochemistry & cell biology September 1, 2010 Hugo R Arias, Avraham Rosenberg, Katarzyna M Targowska-Duda et al. 29 citations

The interaction of ibogaine and phencyclidine (PCP) with human (h) alpha3beta4-nicotinic acetylcholine receptors (AChRs) in different conformational states was determined by functional and structural approaches including, radioligand binding assays, Ca2+ influx detections, and thermodynamic and kinetics measurements. The results established that (a) ibogaine inhibits (+/-)-epibatidine-induced...

Catharanthine alkaloids are noncompetitive antagonists of muscle-type nicotinic acetylcholine receptors.

Neurochemistry International September 1, 2010 Hugo R Arias, Dominik Feuerbach, Katarzyna M Targowska-Duda et al. 9 citations

We compared the interaction of several catharanthine alkaloids including, ibogaine, vincristine, and vinblastine, with that for the noncompetitive antagonist phencyclidine (PCP) at muscle nicotinic acetylcholine receptors (AChRs) in different conformational states. The results established that catharanthine alkaloids: (a) inhibit, in a noncompetitive manner, (+/-)-epibatidine-induced Ca(2+)...

Interaction of ibogaine analogs with the nicotinic acetylcholine receptor

The FASEB Journal April 1, 2008 Krzysztof Jozwiak, Ruin Moaddel, Irving W. Wainer et al. 2 citations

PURPOSE: Characterization of the binding sites for ibogaine analogs on the nicotinic acetylcholine receptor (AChR) in the resting and desensitized states. METHODS: [ 3 H]18‐methoxycoronaridine ([ 3 H]18‐MC) Scatchard‐plots using Torpedo AChR membranes, [ 3 H]TCP (a well characterized noncompetitive antagonist) competition binding experiments and Schild‐type analysis, analog‐induced binding...