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    Structured Review

    MedChemExpress aea
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    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
    aea - by Bioz Stars, 2026-11
    94/100 stars

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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

    (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.
    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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    Functional Assay:

    Article Title: Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior
    Article Snippet: For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.. Valine (Sigma-Aldrich, cat. no. V0513), leucine (Sigma-Aldrich, cat. no. L8912), isoleucine (Sigma-Aldrich, cat. no. I2752), CHPG (MedChemExpress, cat. no. HY-101364), MPEP (MedChemExpress, cat. no. HY-14609A), MCPG (MedChemExpress, cat. no. HY-100371), AEA (MedChemExpress, cat. no. HY-10863) and the corresponding vehicle solutions were infused 30 min before behavioral testing unless otherwise indicated in the relevant figure legends.. CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.

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    Article Title: Differential neuromodulatory role of endocannabinoids in the rodent trigeminal sensory ganglion and cerebral cortex relevant to pain processing.
    Article Snippet: Abstract: Endocannabinoids are suggested to control pain, even though their clinical use is not fully validated and the underlying mechanisms are incompletely understood.. To clarify the targets of endocannabinoid actions, we studied how activation of the endocannabinoid CB1 receptor (CB1R) affects neuronal responses in two in vitro preparations of rodents, namely the trigeminal sensory ganglion (TG) in culture and a coronal slice of the cerebral cortex.. On TG small-medium size neurons, we tested whether submicromolar concentrations of the endogenous CB1R agonist anandamide (AEA) modulated inhibitory GABAA receptors and excitatory ATP-gated P2X3 receptors.

    RNAscope:

    Article Title: Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior
    Article Snippet: For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.. Valine (Sigma-Aldrich, cat. no. V0513), leucine (Sigma-Aldrich, cat. no. L8912), isoleucine (Sigma-Aldrich, cat. no. I2752), CHPG (MedChemExpress, cat. no. HY-101364), MPEP (MedChemExpress, cat. no. HY-14609A), MCPG (MedChemExpress, cat. no. HY-100371), AEA (MedChemExpress, cat. no. HY-10863) and the corresponding vehicle solutions were infused 30 min before behavioral testing unless otherwise indicated in the relevant figure legends.. CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.

    Article Title: FAAH initiates a positive feedback loop to promote lung adenocarcinoma progression through inhibition of ferroptosis.
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    Article Title: Differential neuromodulatory role of endocannabinoids in the rodent trigeminal sensory ganglion and cerebral cortex relevant to pain processing.
    Article Snippet: Abstract: Endocannabinoids are suggested to control pain, even though their clinical use is not fully validated and the underlying mechanisms are incompletely understood.. To clarify the targets of endocannabinoid actions, we studied how activation of the endocannabinoid CB1 receptor (CB1R) affects neuronal responses in two in vitro preparations of rodents, namely the trigeminal sensory ganglion (TG) in culture and a coronal slice of the cerebral cortex.. On TG small-medium size neurons, we tested whether submicromolar concentrations of the endogenous CB1R agonist anandamide (AEA) modulated inhibitory GABAA receptors and excitatory ATP-gated P2X3 receptors.

    Analysis:

    Article Title: Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior
    Article Snippet: For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.. Valine (Sigma-Aldrich, cat. no. V0513), leucine (Sigma-Aldrich, cat. no. L8912), isoleucine (Sigma-Aldrich, cat. no. I2752), CHPG (MedChemExpress, cat. no. HY-101364), MPEP (MedChemExpress, cat. no. HY-14609A), MCPG (MedChemExpress, cat. no. HY-100371), AEA (MedChemExpress, cat. no. HY-10863) and the corresponding vehicle solutions were infused 30 min before behavioral testing unless otherwise indicated in the relevant figure legends.. CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.

    Article Title: FAAH initiates a positive feedback loop to promote lung adenocarcinoma progression through inhibition of ferroptosis.
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    Article Title: Differential neuromodulatory role of endocannabinoids in the rodent trigeminal sensory ganglion and cerebral cortex relevant to pain processing.
    Article Snippet: Abstract: Endocannabinoids are suggested to control pain, even though their clinical use is not fully validated and the underlying mechanisms are incompletely understood.. To clarify the targets of endocannabinoid actions, we studied how activation of the endocannabinoid CB1 receptor (CB1R) affects neuronal responses in two in vitro preparations of rodents, namely the trigeminal sensory ganglion (TG) in culture and a coronal slice of the cerebral cortex.. On TG small-medium size neurons, we tested whether submicromolar concentrations of the endogenous CB1R agonist anandamide (AEA) modulated inhibitory GABAA receptors and excitatory ATP-gated P2X3 receptors.

    Control:

    Article Title: Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior
    Article Snippet: For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.. Valine (Sigma-Aldrich, cat. no. V0513), leucine (Sigma-Aldrich, cat. no. L8912), isoleucine (Sigma-Aldrich, cat. no. I2752), CHPG (MedChemExpress, cat. no. HY-101364), MPEP (MedChemExpress, cat. no. HY-14609A), MCPG (MedChemExpress, cat. no. HY-100371), AEA (MedChemExpress, cat. no. HY-10863) and the corresponding vehicle solutions were infused 30 min before behavioral testing unless otherwise indicated in the relevant figure legends.. CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.

    Article Title: FAAH initiates a positive feedback loop to promote lung adenocarcinoma progression through inhibition of ferroptosis.
    Article Snippet: The following antibodies and reagents were used in this study: β-actin (1:20000, 66009, proteintech), LaminB1 (1:5000, 12987, proteintech), FAAH (1:1000, ab128917, Abcam), GPX4 (1:1000, CY6959, Abways), STAT3 (1:1000, 9139, CST), p-STAT3 (1:1000, 9145, CST), ACSL4 (1:10000, ab155282, Abcam), SLC7A11 (1:1000, ab307601, Abcam), FTH1 (1:2000, 11682, proteintech), 4-HNE (1:1000, ab48506, Abcam), anti-DYKDDDDK tag (1:20000, 20543, proteintech), CCK-8(40203ES, YEASEN), JC-1(C2005, Beyotime), PA (HY-N0830, MCE), AA (HY-109590, MCE), PEA (544310, MERCK), AEA (HY-10863, MCE), 2-BP (E0120, Selleck), HJC0152 (S8561, Selleck), PF-3845 (S2666, Selleck), URB597 (S2631, Selleck), BODIPY 493/503 (C2053S, Beyotime), C11 BODIPY 581/591 (D3861, Invitrogen), NSA (S8251, Selleck), Fer-1 (S7243, Selleck), Z-VAD (S7023, Selleck), Liproxstatin-1 (S7699, Selleck).. Palmitic acid (PA) was dissolved in anhydrous ethanol to prepare a 10mM stock solution.Palmitic acid (PA) was dissolved in..

    Article Title: Differential neuromodulatory role of endocannabinoids in the rodent trigeminal sensory ganglion and cerebral cortex relevant to pain processing.
    Article Snippet: Abstract: Endocannabinoids are suggested to control pain, even though their clinical use is not fully validated and the underlying mechanisms are incompletely understood.. To clarify the targets of endocannabinoid actions, we studied how activation of the endocannabinoid CB1 receptor (CB1R) affects neuronal responses in two in vitro preparations of rodents, namely the trigeminal sensory ganglion (TG) in culture and a coronal slice of the cerebral cortex.. On TG small-medium size neurons, we tested whether submicromolar concentrations of the endogenous CB1R agonist anandamide (AEA) modulated inhibitory GABAA receptors and excitatory ATP-gated P2X3 receptors.

    In Situ Hybridization:

    Article Title: Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior
    Article Snippet: For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.For local pharmacological manipulations, compounds were delivered bilaterally into mPFC through guide cannulae.. Valine (Sigma-Aldrich, cat. no. V0513), leucine (Sigma-Aldrich, cat. no. L8912), isoleucine (Sigma-Aldrich, cat. no. I2752), CHPG (MedChemExpress, cat. no. HY-101364), MPEP (MedChemExpress, cat. no. HY-14609A), MCPG (MedChemExpress, cat. no. HY-100371), AEA (MedChemExpress, cat. no. HY-10863) and the corresponding vehicle solutions were infused 30 min before behavioral testing unless otherwise indicated in the relevant figure legends.. CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.CNO (Braincase, cat. no. CNO-25mg) was administered before testing in hM3Dq experiments as indicated in the main text and figure legends.

    Article Title: FAAH initiates a positive feedback loop to promote lung adenocarcinoma progression through inhibition of ferroptosis.
    Article Snippet: The following antibodies and reagents were used in this study: β-actin (1:20000, 66009, proteintech), LaminB1 (1:5000, 12987, proteintech), FAAH (1:1000, ab128917, Abcam), GPX4 (1:1000, CY6959, Abways), STAT3 (1:1000, 9139, CST), p-STAT3 (1:1000, 9145, CST), ACSL4 (1:10000, ab155282, Abcam), SLC7A11 (1:1000, ab307601, Abcam), FTH1 (1:2000, 11682, proteintech), 4-HNE (1:1000, ab48506, Abcam), anti-DYKDDDDK tag (1:20000, 20543, proteintech), CCK-8(40203ES, YEASEN), JC-1(C2005, Beyotime), PA (HY-N0830, MCE), AA (HY-109590, MCE), PEA (544310, MERCK), AEA (HY-10863, MCE), 2-BP (E0120, Selleck), HJC0152 (S8561, Selleck), PF-3845 (S2666, Selleck), URB597 (S2631, Selleck), BODIPY 493/503 (C2053S, Beyotime), C11 BODIPY 581/591 (D3861, Invitrogen), NSA (S8251, Selleck), Fer-1 (S7243, Selleck), Z-VAD (S7023, Selleck), Liproxstatin-1 (S7699, Selleck).. Palmitic acid (PA) was dissolved in anhydrous ethanol to prepare a 10mM stock solution.Palmitic acid (PA) was dissolved in..

    Article Title: Differential neuromodulatory role of endocannabinoids in the rodent trigeminal sensory ganglion and cerebral cortex relevant to pain processing.
    Article Snippet: Abstract: Endocannabinoids are suggested to control pain, even though their clinical use is not fully validated and the underlying mechanisms are incompletely understood.. To clarify the targets of endocannabinoid actions, we studied how activation of the endocannabinoid CB1 receptor (CB1R) affects neuronal responses in two in vitro preparations of rodents, namely the trigeminal sensory ganglion (TG) in culture and a coronal slice of the cerebral cortex.. On TG small-medium size neurons, we tested whether submicromolar concentrations of the endogenous CB1R agonist anandamide (AEA) modulated inhibitory GABAA receptors and excitatory ATP-gated P2X3 receptors.



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    MedChemExpress aea
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    Aea, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 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 1 article reviews
    aea - by Bioz Stars, 2026-11
    94/100 stars
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    86
    Kamada aea
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    Aea, supplied by Kamada, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Tocris aea anandamide
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    Aea Anandamide, supplied by Tocris, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Biosynth Carbosynth aea concentrations
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    Aea Concentrations, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cayman Chemical 2h]8-aea
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    2h]8 Aea, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Tocris unlabeled aea
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    Unlabeled Aea, supplied by Tocris, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cayman Chemical d8-arachidonoylethanolamide (d8-aea)
    (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 <t>anandamide</t> <t>(AEA)</t> (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.
    D8 Arachidonoylethanolamide (D8 Aea), supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cayman Chemical deuterated standards [ 2 h] 8 -aea
    Effect of PGA on the endogenous levels of <t>AEA,</t> 2-AG <t>and</t> <t>PEA</t> in HaCaT cells. A-C Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. *** P < 0.001 and **** P < 0.0001: Vehicle vs. PGA. D-F Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with PGA (10 µM), or Vehicle for 6 h. Student’s t test was used for analysis. * P < 0.05 and ** P < 0.01: Vehicle vs. PGA.
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    Image Search Results


    (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.

    Journal: bioRxiv

    Article Title: Valine Engages a Prefrontal mGluR5 Allosteric Site to Preserve Social Behavior

    doi: 10.64898/2026.10.14.759089

    Figure Lengend 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.

    Article Snippet: Valine (Sigma-Aldrich, cat. no. V0513), leucine (Sigma-Aldrich, cat. no. L8912), isoleucine (Sigma-Aldrich, cat. no. I2752), CHPG (MedChemExpress, cat. no. HY-101364), MPEP (MedChemExpress, cat. no. HY-14609A), MCPG (MedChemExpress, cat. no. HY-100371), AEA (MedChemExpress, cat. no. HY-10863) and the corresponding vehicle solutions were infused 30 min before behavioral testing unless otherwise indicated in the relevant figure legends.

    Techniques: Functional Assay, RNAscope, Analysis, Control

    Effect of PGA on the endogenous levels of AEA, 2-AG and PEA in HaCaT cells. A-C Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. *** P < 0.001 and **** P < 0.0001: Vehicle vs. PGA. D-F Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with PGA (10 µM), or Vehicle for 6 h. Student’s t test was used for analysis. * P < 0.05 and ** P < 0.01: Vehicle vs. PGA.

    Journal: Scientific Reports

    Article Title: Deciphering the interaction between N -palmitoyl-D-glucosamine and the endocannabinoidome

    doi: 10.1038/s41598-025-07103-5

    Figure Lengend Snippet: Effect of PGA on the endogenous levels of AEA, 2-AG and PEA in HaCaT cells. A-C Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. *** P < 0.001 and **** P < 0.0001: Vehicle vs. PGA. D-F Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with PGA (10 µM), or Vehicle for 6 h. Student’s t test was used for analysis. * P < 0.05 and ** P < 0.01: Vehicle vs. PGA.

    Article Snippet: Deuterated standards—[ 2 H] 8 -AEA, [ 2 H] 5 −2-AG and [ 2 H] 4 -PEA—were purchased from Cayman Chemical (Cabru, Arcore, Italy).

    Techniques:

    Effect of PGA on the endogenous levels of AEA, 2-AG and PEA in SH-SY5Y and RBL-2H3 cells. A-C Concentrations of AEA, 2-AG and PEA in SH-SY5Y cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. * P < 0.05 and ** P < 0.01: Vehicle vs. PGA. D-F Concentrations of AEA, 2-AG and PEA in RBL-2H3 cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. * P < 0.05: Vehicle vs. PGA.

    Journal: Scientific Reports

    Article Title: Deciphering the interaction between N -palmitoyl-D-glucosamine and the endocannabinoidome

    doi: 10.1038/s41598-025-07103-5

    Figure Lengend Snippet: Effect of PGA on the endogenous levels of AEA, 2-AG and PEA in SH-SY5Y and RBL-2H3 cells. A-C Concentrations of AEA, 2-AG and PEA in SH-SY5Y cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. * P < 0.05 and ** P < 0.01: Vehicle vs. PGA. D-F Concentrations of AEA, 2-AG and PEA in RBL-2H3 cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. * P < 0.05: Vehicle vs. PGA.

    Article Snippet: Deuterated standards—[ 2 H] 8 -AEA, [ 2 H] 5 −2-AG and [ 2 H] 4 -PEA—were purchased from Cayman Chemical (Cabru, Arcore, Italy).

    Techniques:

    Effect of Glucosamine on the endogenous levels of AEA, 2-AG and PEA in HaCaT cells. A-C Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with Glucosamine (10 µM), or Vehicle for 40 min. D-F Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with Glucosamine (10 µM), or Vehicle for 6 h. Student’s t test was used for analysis.

    Journal: Scientific Reports

    Article Title: Deciphering the interaction between N -palmitoyl-D-glucosamine and the endocannabinoidome

    doi: 10.1038/s41598-025-07103-5

    Figure Lengend Snippet: Effect of Glucosamine on the endogenous levels of AEA, 2-AG and PEA in HaCaT cells. A-C Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with Glucosamine (10 µM), or Vehicle for 40 min. D-F Concentrations of AEA, 2-AG and PEA in HaCaT cells treated with Glucosamine (10 µM), or Vehicle for 6 h. Student’s t test was used for analysis.

    Article Snippet: Deuterated standards—[ 2 H] 8 -AEA, [ 2 H] 5 −2-AG and [ 2 H] 4 -PEA—were purchased from Cayman Chemical (Cabru, Arcore, Italy).

    Techniques:

    Effect of MAFP (10 µM) on the endogenous levels of AEA, 2-AG and PEA in PGA-treated HaCaT cells. A-C Concentrations of AEA, 2-AG and PEA in HaCaT cells co-treated with PGA (10 µM) and MAFP (10 µM), or Vehicle for 40 min. One-way ANOVA followed by Tukey’s multiple comparison test was used for analysis. ** P < 0.01 and **** P < 0.0001: Vehicle vs. PGA; ** P < 0.01 and **** P < 0.0001: Vehicle mix vs. PGA + MAFP.

    Journal: Scientific Reports

    Article Title: Deciphering the interaction between N -palmitoyl-D-glucosamine and the endocannabinoidome

    doi: 10.1038/s41598-025-07103-5

    Figure Lengend Snippet: Effect of MAFP (10 µM) on the endogenous levels of AEA, 2-AG and PEA in PGA-treated HaCaT cells. A-C Concentrations of AEA, 2-AG and PEA in HaCaT cells co-treated with PGA (10 µM) and MAFP (10 µM), or Vehicle for 40 min. One-way ANOVA followed by Tukey’s multiple comparison test was used for analysis. ** P < 0.01 and **** P < 0.0001: Vehicle vs. PGA; ** P < 0.01 and **** P < 0.0001: Vehicle mix vs. PGA + MAFP.

    Article Snippet: Deuterated standards—[ 2 H] 8 -AEA, [ 2 H] 5 −2-AG and [ 2 H] 4 -PEA—were purchased from Cayman Chemical (Cabru, Arcore, Italy).

    Techniques: Comparison

    Effect of PGA on the endogenous levels of AEA, 2-AG and PEA in ABHD4-silenced HaCaT cells. A Bar chart with individual points showing the mRNA expression levels of ABHD4 in control HaCaT cells (scramble) and siRNA ABHD4 transfected HaCaT cells. Student’s t test was used for analysis. **** P < 0.0001: scramble vs. siRNA. B-D Concentrations of AEA, 2-AG and PEA in ABHD4-silenced HaCaT cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. * P < 0.05 and *** P < 0.001: Vehicle vs. PGA.

    Journal: Scientific Reports

    Article Title: Deciphering the interaction between N -palmitoyl-D-glucosamine and the endocannabinoidome

    doi: 10.1038/s41598-025-07103-5

    Figure Lengend Snippet: Effect of PGA on the endogenous levels of AEA, 2-AG and PEA in ABHD4-silenced HaCaT cells. A Bar chart with individual points showing the mRNA expression levels of ABHD4 in control HaCaT cells (scramble) and siRNA ABHD4 transfected HaCaT cells. Student’s t test was used for analysis. **** P < 0.0001: scramble vs. siRNA. B-D Concentrations of AEA, 2-AG and PEA in ABHD4-silenced HaCaT cells treated with PGA (10 µM), or Vehicle for 40 min. Student’s t test was used for analysis. * P < 0.05 and *** P < 0.001: Vehicle vs. PGA.

    Article Snippet: Deuterated standards—[ 2 H] 8 -AEA, [ 2 H] 5 −2-AG and [ 2 H] 4 -PEA—were purchased from Cayman Chemical (Cabru, Arcore, Italy).

    Techniques: Expressing, Control, Transfection