<?xml version="1.0"?>
<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Cannabinoid ligand-mediated glycogen depletion in astrocytes is associated with increased intracellular calcium, energy metabolism, and membrane dynamics</dc:title><dc:creator>Fink,	Katja	(Avtor)
	</dc:creator><dc:creator>Zorec,	Robert	(Avtor)
	</dc:creator><dc:creator>Kreft,	Marko	(Avtor)
	</dc:creator><dc:subject>astrocytes</dc:subject><dc:subject>calcium signaling</dc:subject><dc:subject>cannabinoid receptors</dc:subject><dc:subject>exocytosis</dc:subject><dc:subject>glucose metabolism</dc:subject><dc:subject>lactate</dc:subject><dc:description>Astrocytes orchestrate brain energy metabolism and respond to endocannabinoids via cannabinoid receptor type 1 (CB1R), whereas the contribution of CB2R remains uncertain. We combined live-cell Förster resonance energy transfer sensors for D-glucose and L-lactate, intracellular Ca$^{2+}$ imaging, glycogen assays, and whole-cell patch-clamp capacitance measurements to define how cannabinoid ligands shape astrocyte physiology in primary rat cultures. The CB1-selective agonist ACEA triggered rapid, transient elevations in [Ca$^{2+}$]ᵢ and metabolic readouts, whereas the CB2-biased ligands AM1241 and Gp1a produced sustained metabolic effects, including prolonged increases in intracellular D-glucose and L-lactate. AM1241 additionally evoked glycogen depletion. Ligand applications also increased membrane capacitance, consistent with enhanced exocytotic activity and altered membrane dynamics. CB1 immunoreactivity predominated over a weak CB2-like signal, and RT-qPCR detected Cnr1 but not Cnr2 transcripts under our conditions. Accordingly, we interpret AM1241/Gp1a actions as ligand-evoked effects that are predominantly CB1-linked (and/or off-target at the concentrations used). Together, these results show that cannabinoid ligands robustly remodel astrocytic energy metabolism and membrane behavior chiefly through CB1-associated pathways, highlighting a functional axis between cannabinoid signaling, Ca$^{2+}$ mobilization, glycogen remodeling, and exocytosis in astrocytes.</dc:description><dc:date>2025</dc:date><dc:date>2026-01-19 08:47:03</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>178100</dc:identifier><dc:identifier>UDK: 616.8</dc:identifier><dc:identifier>ISSN pri članku: 1471-4159</dc:identifier><dc:identifier>DOI: 10.1111/jnc.70332</dc:identifier><dc:identifier>COBISS_ID: 265140227</dc:identifier><dc:language>sl</dc:language></metadata>
