Researchers map how street benzodiazepines hijack brain chemistry differently
A new study tested 42 illicit designer benzodiazepines against 11 prescription versions, revealing that many street drugs alter brain receptors in unpredictable ways—some even opposite to their pharmaceutical cousins. The findings could reshape how emergency responders treat overdoses and inform drug policy decisions as these compounds proliferate globally.
Originaltitel: In vitro γ-aminobutyric acid A (GABA<sub>A</sub>) receptor activity and binding interactions at the α<sup>+</sup>/γ<sub>2</sub><sup>–</sup> interface of 53 prescription and designer benzodiazepines
<p>Although widely prescribed globally, benzodiazepines (BZDs) are commonly misused and involved in a high rate of drug-related deaths worldwide. Novel chemically similar compounds, designer BZDs (DBZDs), have emerged on the recreational market with little information available on their pharmacodynamic effects. An in vitro alpha 1 beta 2 gamma 2 GABAA assay was used to determine the activity and explore structure-activity relationships of 42 DBZDs plus 11 prescription BZDs. Their interaction with the BZD alpha+/gamma 2- interface was explored using the BZD antagonist flumazenil. Most of the D/BZDs were positive allosteric modulators, but 4'-chlorodiazepam and 4'-fluorodiazepam were negative allosteric modulators, although the activity was not antagonized by flumazenil. All metabolites tested were active. This data informs the interpretation of intoxications, harm reduction measures, and drugs legislation for DBZDs; demonstrates the importance of testing new drugs as they emerge on the recreational market; and offers insights into how BZD chemical modifications alter GABAA pharmacodynamics.</p>