Titlebook: Anxiolytic β-Carbolines; From Molecular Biolo David N. Stephens Book 1993 Springer-Verlag Berlin Heidelberg 1993 Beta Carboline.GABA.anxiet

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Elektrische und magnetische Feldercological efficacy and clinical profile of the agonist ligands for benzodiazepine recognition sites (see review Biggio and Costa 1990; Biggio et al. 1992). Accordingly, anxiolytic and anticonvulsant drugs which enhance the function of GABAergic transmission with a low intrinsic activity are classifi

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,Zeitlich veränderliche magnetische Felder,mber of properties which limit their use or which give rise to problems on withdrawal. Thus, currently available benzodiazepine anxiolytics are sedative and muscle relaxant, induce memory impairment, increase the intoxicating potency of alcohol, may be subject to nontherapeutic use (abuse), and, fol

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Messung der Induktionskoeffizienten,rer 1983; Woods et al. 1987; Haefely et al. 1990). Recent reports have indicated that partial (low efficacy) BZ-receptor agonists, i. e., compounds which induce smaller fractional responses in their target cells than do full agonists at the same fractional receptor occupancy, may have advantages in

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https://doi.org/10.1007/978-3-662-36759-9e benzodiazepine binding site on the gamma-aminobutyric acid type A (GABA.)-receptor complex. Its distinct profile of biochemical and behavioral effects has been suggested to indicate partial and/or selective benzodiazepine-receptor activity (Stephens et al. 1990). A series of experiments in baboons

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