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The Impact of Psilocybin on High Glucose/Lipid-Induced Changes in INS-1 Cell Viability and Dedifferentiation

Esmaeel Ghasemi Gojani, Bo Wang, Olga Kovalchuk, Igor Kovalchuk, Dongping Li

Genes January 29, 2024 DOI: 10.3390/genes15020183 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics In vitro study Peer reviewed
Population INS-1 832/13 Rat Insulinoma cell line
Intervention Psilocybin
Topics Psilocybin
Keywords Viability assay Cell biology Hallucinogen
Citations 11
Key points Psilocybin pretreatment mitigates high glucose-high lipid-induced β-cell loss and modulates markers of apoptosis and dedifferentiation in rat insulinoma cells.

Abstract

Serotonin emerges as a pivotal factor influencing the growth and functionality of β-cells. Psilocybin, a natural compound derived from mushrooms of the Psilocybe genus, exerts agonistic effects on the serotonin 5-HT2A and 5-HT2B receptors, thereby mimicking serotonin’s behavior. This study investigates the potential impacts of psilocybin on β-cell viability, dedifferentiation, and function using an in vitro system. The INS-1 832/13 Rat Insulinoma cell line underwent psilocybin pretreatment, followed by exposure to high glucose-high lipid (HG-HL) conditions for specific time periods. After being harvested from treated cells, total transcript and cellular protein were utilized for further investigation. Our findings implied that psilocybin administration effectively mitigates HG-HL-stimulated β-cell loss, potentially mediated through the modulation of apoptotic biomarkers, which is possibly related to the mitigation of TXNIP, STAT-1, and STAT-3 phosphorylation. Furthermore, psilocybin exhibits the capacity to modulate the expression of key genes associated with β-cell dedifferentiation, including Pou5f1 and Nanog, indicating its potential in attenuating β-cell dedifferentiation. This research lays the groundwork for further exploration into the therapeutic potential of psilocybin in Type II diabetes intervention.

Comparable studies

Other preclinical and animal studies on psilocybin, most cited first.

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