Discovery of Procognitive Antipsychotics by Combining Muscarinic M 1 Receptor Structure-Activity Relationship with Systems Response Profiles in Zebrafish Larvae

Current antipsychotic drugs are notably ineffective at addressing the cognitive deficits associated with schizophrenia. -Desmethylclozapine (NDMC), the major metabolite of clozapine, displays muscarinic M receptor (M ) agonism, an activity associated with improvement in cognitive functioning. Precli...

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Veröffentlicht in:ACS chemical neuroscience 2020-01, Vol.11 (2), p.173-183
Hauptverfasser: Hellman, Karin, Ohlsson, Jörgen, Malo, Marcus, Olsson, Roger, Ek, Fredrik
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Sprache:eng
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Zusammenfassung:Current antipsychotic drugs are notably ineffective at addressing the cognitive deficits associated with schizophrenia. -Desmethylclozapine (NDMC), the major metabolite of clozapine, displays muscarinic M receptor (M ) agonism, an activity associated with improvement in cognitive functioning. Preclinical and clinical data support that M agonism may be a desired activity in antipsychotic drugs. However, NDMC failed clinical phase II studies in acute psychotic patients. NDMC analogues were synthesized to establish a structure-activity relationship (SAR) at the M receptor as an indication of potential procognitive properties. In vitro evaluation revealed a narrow SAR in which M agonist activity was established by functionalization in the 4- and 8-positions in the tricyclic core. In vivo behavioral response profiles were used to evaluate antipsychotic efficacy and exposure in zebrafish larvae and peripheral side effect related M activity in adult zebrafish. The NDMC analogue demonstrated antipsychotic activity similar to clozapine including M agonist activity. Cotreatment with trospium chloride, an M1 peripheral acting antagonist, counteracted peripheral side effects. Thus, the NDMC analogue , in combination with a peripherally acting anticholinergic compound, could be suitable for further development as an antipsychotic compound with potential procognitive activity.
ISSN:1948-7193
1948-7193
DOI:10.1021/acschemneuro.9b00524