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A Multimodal, In Vivo Approach for Assessing Structurally and Phenotypically Related Neuroactive Molecules.
- Source :
-
ACS chemical neuroscience [ACS Chem Neurosci] 2024 Nov 20; Vol. 15 (22), pp. 4171-4184. Date of Electronic Publication: 2024 Sep 17. - Publication Year :
- 2024
-
Abstract
- A recently reported behavioral screen in larval zebrafish for phenocopiers of known anesthetics and associated drugs yielded an isoflavone. Related isoflavones have also been reported as GABA <subscript>A</subscript> potentiators. From this, we synthesized a small library of isoflavones and incorporated an in vivo phenotypic approach to perform structure-behavior relationship studies of the screening hit and related analogs via behavioral profiling, patch-clamp experiments, and whole brain imaging. This revealed that analogs effect a range of behavioral responses, including sedation with and without enhancing the acoustic startle response. Interestingly, a subset of compounds effect sedation and enhancement of motor responses to both acoustic and light stimuli. Patch clamp recordings of cells with a human GABA <subscript>A</subscript> receptor confirmed that behavior-modulating isoflavones modify the GABA signaling. To better understand these molecules' nuanced effects on behavior, we performed whole brain imaging to reveal that analogs differentially effect neuronal activity. These studies demonstrate a multimodal approach to assessing activities of neuroactives.
- Subjects :
- Animals
Receptors, GABA-A metabolism
Receptors, GABA-A drug effects
Humans
Reflex, Startle drug effects
Reflex, Startle physiology
Behavior, Animal drug effects
Patch-Clamp Techniques
Structure-Activity Relationship
Phenotype
Neurons drug effects
Neurons metabolism
Zebrafish
Isoflavones pharmacology
Brain drug effects
Brain metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1948-7193
- Volume :
- 15
- Issue :
- 22
- Database :
- MEDLINE
- Journal :
- ACS chemical neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 39287508
- Full Text :
- https://doi.org/10.1021/acschemneuro.4c00426