aea (MedChemExpress)
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Aea, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/aea/Anandamide/bio_rxiv__64898__2026__10__14__759089-274-30-31
Average 94 stars, based on 6 article reviews
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1) Product Images from "Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior"
Article Title: Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior
Journal: bioRxiv
doi: 10.64898/2026.10.14.759089
Figure Legend Snippet: (A) Working model. Valine allosterically enhances glutamate-dependent mGluR5 signaling to promote endocannabinoid release, which acts retrogradely on presynaptic CB1 receptors to suppress transmitter release. Enrichment of CB1 on inhibitory terminals biases this feedback towards functional disinhibition. (B) RNAscope/ISH analysis of Cnr1 (CB1 receptor; red) co-localized with inhibitory ( Slc32a1/Vgat , green; top) or excitatory ( Slc17a7/Vglut1 , green; bottom) markers in mPFC. Pie charts report the fraction of Cnr1 + cells that are Vgat + or Vglut1 + , and conversely the fraction of Vgat + or Vglut1 + cells that are Cnr1 + . Scale bars, 10 μm. n = 3 mice per group, with 3 sections analysed per mouse. (C) Cell-type-restricted monitoring of endocannabinoid dynamics in inhibitory neurons using the genetically encoded sensor eCB2.0. Representative ΔF/F traces are shown for control and Bckdk ΔmPFC mice; red-shaded periods indicate social investigation. (D) Heat maps of z-scored eCB2.0 signals aligned to the onset of social investigation (t = 0; dashed line) for inhibitory-neuron recordings. (E) Quantification of inhibitory-neuron eCB2.0 responses as AUC over the analysis window shown in (D). Each dot represents one social investigation bout; 18 bouts pooled from 6 mice per group. (F) Parallel strategy and representative traces for eCB2.0 monitoring in excitatory neurons. (G) Heat maps of z-scored eCB2.0 signals aligned to social onset for excitatory-neuron recordings. (H) Quantification of excitatory-neuron eCB2.0 responses as AUC. Each dot represents one social investigation bout; 18 bouts pooled from 6 mice per group. (I) Chemical structure of the CB1 agonist anandamide (AEA) (left) and experimental design for intra-mPFC AEA or vehicle administration before sociability testing in Bckdk ΔmPFC mice (right). (J) Three-chamber performance after intra-mPFC vehicle or AEA in Bckdk ΔmPFC mice. Left, time spent in S1 versus EM; right, social preference index. n = 10 mice per group. Data are mean ± s.e.m. In (E) and (H), groups were compared using two-sided unpaired Student’s t test. In (J), EM versus S1 was compared within each group by two-sided paired tests and preference index was compared between conditions by two-sided unpaired tests, as indicated. * P < 0.05, ** P < 0.01; N.S., not significant.
Techniques Used: Functional Assay, RNAscope, Analysis, Control
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