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Blood was drawn before (0 min) and after the intraperitoneal administration of glucose (2.0 g/kg body weight) at intervals of 2, 6, 10, 30, 60, and 120 min ( n = 34 per time point)

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This study was performed at Masaryk University as part of the project Preclinical and clinical research at the Institute of Pharmacology: Pharmacokinetics, behavioral neuropsychopharmacology, and personalized pharmacotherapy number MUNI/A/1819/2025 with the support of the Specific University Research Grant, as provided by the Ministry of Education, Youth and Sports of the Czech Republic in the year 2026

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