Characterization of ultrapotent chemogenetic ligands for research applications in non-human primates

Raper, J.; Eldridge, M. A. G.; Sternson, S.; Shim, J. Y.; Fomani, G. P.; Richmond, B. J.; Wichmann, T.; Galvan, A.

doi:10.1101/2022.01.06.475241

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bioRxiv · 10.1101/2022.01.06.475241

Characterization of ultrapotent chemogenetic ligands for research applications in non-human primates

Raper, J.·Eldridge, M. A. G.·Sternson, S.·Shim, J. Y.·Fomani, G. P.·Richmond, B. J.·Wichmann, T.·Galvan, A.

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Abstract

Chemogenetics is a technique for obtaining selective pharmacological control over a cell population by expressing an engineered receptor that is selectively activated by an exogenously administered ligand. A promising approach for neuronal modulation involves the use of "Pharmacologically Selective Actuator Modules" (PSAMs); these chemogenetic receptors are selectively activated by ultrapotent "Pharmacologically Selective Effector Molecules" (uPSEMs). To extend the use of PSAM/PSEMs to studies in nonhuman primates it is necessary to thoroughly characterize the efficacy and safety of these tools. We describe the time course and brain penetrance in rhesus monkeys of two compounds with promising binding specificity and efficacy profiles in in vitro studies, uPSEM792 and uPSEM817, after systemic administration. Rhesus macaques received subcutaneous (s.c.) or intravenous (i.v.) administration of uPSEM817(0.064 mg/kg) or uPSEM792 (0.87 mg/kg) and plasma and CSF samples were collected over the course of 48 hours. Both compounds exhibited good brain penetrance, relatively slow washout and negligible conversion to potential metabolites - varenicline or hydroxyvarenicline. In addition, we found that neither of these uPSEMs significantly altered heart rate or sleep. Our results indicate that both compounds are suitable candidates for neuroscience studies using PSAMs in nonhuman primates.

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Raper, J., Eldridge, M. A. G., Sternson, S., Shim, J. Y., Fomani, G. P., Richmond, B. J., Wichmann, T., Galvan, A.. 2022-01-07. Characterization of ultrapotent chemogenetic ligands for research applications in non-human primates. https://doi.org/10.1101/2022.01.06.475241

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