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Hello Bio Inc chemical compound, drug ly367385
Effect of TTX (1 µM, brown, n=6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 <t>(LY367385,</t> 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n=10 arterioles from 6 mice) on ( A ) kinetics and ( B ) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shaded traces correspond to the kinetics of arteriolar vasoconstriction in control condition ( – 20 Hz). Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition ( – 20 Hz) with p<0.05 and p<0.001, respectively. Figure 3—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .
Chemical Compound, Drug Ly367385, supplied by Hello Bio Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/chemical compound, drug ly367385/product/Hello Bio Inc
Average 90 stars, based on 1 article reviews
chemical compound, drug ly367385 - by Bioz Stars, 2026-02
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1) Product Images from "Elevated pyramidal cell firing orchestrates arteriolar vasoconstriction through COX-2-derived prostaglandin E2 signaling"

Article Title: Elevated pyramidal cell firing orchestrates arteriolar vasoconstriction through COX-2-derived prostaglandin E2 signaling

Journal: eLife

doi: 10.7554/eLife.102424

Effect of TTX (1 µM, brown, n=6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n=10 arterioles from 6 mice) on ( A ) kinetics and ( B ) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shaded traces correspond to the kinetics of arteriolar vasoconstriction in control condition ( – 20 Hz). Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition ( – 20 Hz) with p<0.05 and p<0.001, respectively. Figure 3—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .
Figure Legend Snippet: Effect of TTX (1 µM, brown, n=6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n=10 arterioles from 6 mice) on ( A ) kinetics and ( B ) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shaded traces correspond to the kinetics of arteriolar vasoconstriction in control condition ( – 20 Hz). Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition ( – 20 Hz) with p<0.05 and p<0.001, respectively. Figure 3—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .

Techniques Used: Control

( A, B ) Kinetics of diameter changes (left panels) and comparison of the mean luminal diameter between the 5-min control period and after 15 or 20 min of treatment (right panels) with ( A ) TTX (1 µM, brown, n=4 arterioles from 2 mice) or ( B ) a cocktail of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) glutamate receptor antagonists (gray, n=10 arterioles from 6 mice). n.s. not statistically significant. Figure 3—figure supplement 1—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .
Figure Legend Snippet: ( A, B ) Kinetics of diameter changes (left panels) and comparison of the mean luminal diameter between the 5-min control period and after 15 or 20 min of treatment (right panels) with ( A ) TTX (1 µM, brown, n=4 arterioles from 2 mice) or ( B ) a cocktail of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) glutamate receptor antagonists (gray, n=10 arterioles from 6 mice). n.s. not statistically significant. Figure 3—figure supplement 1—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .

Techniques Used: Comparison, Control


Figure Legend Snippet:

Techniques Used: Sequencing, Reverse Transcription, Software, Microscopy



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Effect of TTX (1 µM, brown, n=6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 <t>(LY367385,</t> 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n=10 arterioles from 6 mice) on ( A ) kinetics and ( B ) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shaded traces correspond to the kinetics of arteriolar vasoconstriction in control condition ( – 20 Hz). Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition ( – 20 Hz) with p<0.05 and p<0.001, respectively. Figure 3—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .
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Effect of TTX (1 µM, brown, n= 6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 <t>(LY367385,</t> 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n= 10 arterioles from 6 mice) on (a) kinetics and (b) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shadow traces correspond to the kinetics of arteriolar vasoconstriction in control condition. Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition with p<0.05 and p<0.001, respectively.
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eCB release is triggered by 5-HT and CCK receptors but not metabotropic glutamate receptors in developing VN neurons (A 1 ) With the bath addition of MDL11939 (a 5-HT receptor antagonist) to P5-8 brain slices, the percentage of P5–8 MVN neurons showing LTD GABA decreased to 30% (green triangles, p = 0.003), contrasting 79% in controls. (A 2 ) With the bath addition of CI988 (a CCKBR antagonist) the percentage of P5–8 MVN neurons showing LTD GABA decrease slightly to 50% (CI988, blue triangles), but was not statistically significant ( p = 0.096). (A 3 ) With the bath addition of LY367385 (a mGLuR1 receptor antagonist, black circles) or MPEP (a mGluR5 antagonist, pink triangles), the percentage of P5–8 MVN neurons showing LTD GABA was similar to the control ( LY367385 : 73%, p = 1; MPEP: 62%, p = 0.347). (A 4 ) Bar charts summarizing the individual PSC GABA (top) and the percentages (bottom) of P5-8 MVN neurons showing each type of response (LTD, light gray; LTP, white; no change, dark gray) in each treatment group after TBS. (B 1 ) In P9–11 brain slices, no LTD or LTP was observed in the averaged response of recorded MVN cells (green circles). This was in agreement with the majority (61%) of cells showing no change after TBS (see B 4 ). With the bath addition of α-m-5-HT (a 5-HT receptor agonist), the percentage of MVN neurons showing LTD GABA after an initial TBS increased to 78% (yellow triangles, p < 0.001). These LTD GABA -expressing cells could not respond to a second TBS with further LTD GABA with the addition of Orlistat to the bath. (B 2 ) With the bath addition of CCK (a CCKBR agonist), 57% of the P9–11 MVN neurons showed LTD GABA (purple triangles, p = 0.011), contrasting control rats in which only 11% of sampled MVN neurons showed LTD GABA . (B 3 ) With the bath addition of DHPG (a mGluR1 agonist), the percentage of MVN neurons showing LTD GABA after TBS did not change significantly (27%, blue circles, p = 0.484). (B 4 ) Bar charts summarizing the individual PSC GABA (top) and the percentages (bottom) of P9–11 MVN neurons in each treatment group after TBS. Mean ± SEM are shown. Fisher’s exact test with Bonferroni’s correction for multiple measurements was used to evaluate change in responses to TBS in (A 4 ) and (B 4 ).

Journal: iScience

Article Title: Cannabinoid overrides triggers of GABAergic plasticity in vestibular circuits and distorts the development of navigation

doi: 10.1016/j.isci.2025.112566

Figure Lengend Snippet: eCB release is triggered by 5-HT and CCK receptors but not metabotropic glutamate receptors in developing VN neurons (A 1 ) With the bath addition of MDL11939 (a 5-HT receptor antagonist) to P5-8 brain slices, the percentage of P5–8 MVN neurons showing LTD GABA decreased to 30% (green triangles, p = 0.003), contrasting 79% in controls. (A 2 ) With the bath addition of CI988 (a CCKBR antagonist) the percentage of P5–8 MVN neurons showing LTD GABA decrease slightly to 50% (CI988, blue triangles), but was not statistically significant ( p = 0.096). (A 3 ) With the bath addition of LY367385 (a mGLuR1 receptor antagonist, black circles) or MPEP (a mGluR5 antagonist, pink triangles), the percentage of P5–8 MVN neurons showing LTD GABA was similar to the control ( LY367385 : 73%, p = 1; MPEP: 62%, p = 0.347). (A 4 ) Bar charts summarizing the individual PSC GABA (top) and the percentages (bottom) of P5-8 MVN neurons showing each type of response (LTD, light gray; LTP, white; no change, dark gray) in each treatment group after TBS. (B 1 ) In P9–11 brain slices, no LTD or LTP was observed in the averaged response of recorded MVN cells (green circles). This was in agreement with the majority (61%) of cells showing no change after TBS (see B 4 ). With the bath addition of α-m-5-HT (a 5-HT receptor agonist), the percentage of MVN neurons showing LTD GABA after an initial TBS increased to 78% (yellow triangles, p < 0.001). These LTD GABA -expressing cells could not respond to a second TBS with further LTD GABA with the addition of Orlistat to the bath. (B 2 ) With the bath addition of CCK (a CCKBR agonist), 57% of the P9–11 MVN neurons showed LTD GABA (purple triangles, p = 0.011), contrasting control rats in which only 11% of sampled MVN neurons showed LTD GABA . (B 3 ) With the bath addition of DHPG (a mGluR1 agonist), the percentage of MVN neurons showing LTD GABA after TBS did not change significantly (27%, blue circles, p = 0.484). (B 4 ) Bar charts summarizing the individual PSC GABA (top) and the percentages (bottom) of P9–11 MVN neurons in each treatment group after TBS. Mean ± SEM are shown. Fisher’s exact test with Bonferroni’s correction for multiple measurements was used to evaluate change in responses to TBS in (A 4 ) and (B 4 ).

Article Snippet: LY367385 ((S)-(+)-α-Amino-4-carboxy-2-methylbenzeneacetic acid), DHPG (RS)-3,5-dihydroxyphenylglycine , Tocris Bioscience 1237/10 , .

Techniques: Control, Expressing

Effect of TTX (1 µM, brown, n=6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n=10 arterioles from 6 mice) on ( A ) kinetics and ( B ) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shaded traces correspond to the kinetics of arteriolar vasoconstriction in control condition ( – 20 Hz). Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition ( – 20 Hz) with p<0.05 and p<0.001, respectively. Figure 3—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .

Journal: eLife

Article Title: Elevated pyramidal cell firing orchestrates arteriolar vasoconstriction through COX-2-derived prostaglandin E2 signaling

doi: 10.7554/eLife.102424

Figure Lengend Snippet: Effect of TTX (1 µM, brown, n=6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n=10 arterioles from 6 mice) on ( A ) kinetics and ( B ) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shaded traces correspond to the kinetics of arteriolar vasoconstriction in control condition ( – 20 Hz). Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition ( – 20 Hz) with p<0.05 and p<0.001, respectively. Figure 3—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .

Article Snippet: Chemical compound, drug , LY367385 , Hello Bio , HB0398 , .

Techniques: Control

( A, B ) Kinetics of diameter changes (left panels) and comparison of the mean luminal diameter between the 5-min control period and after 15 or 20 min of treatment (right panels) with ( A ) TTX (1 µM, brown, n=4 arterioles from 2 mice) or ( B ) a cocktail of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) glutamate receptor antagonists (gray, n=10 arterioles from 6 mice). n.s. not statistically significant. Figure 3—figure supplement 1—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .

Journal: eLife

Article Title: Elevated pyramidal cell firing orchestrates arteriolar vasoconstriction through COX-2-derived prostaglandin E2 signaling

doi: 10.7554/eLife.102424

Figure Lengend Snippet: ( A, B ) Kinetics of diameter changes (left panels) and comparison of the mean luminal diameter between the 5-min control period and after 15 or 20 min of treatment (right panels) with ( A ) TTX (1 µM, brown, n=4 arterioles from 2 mice) or ( B ) a cocktail of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) glutamate receptor antagonists (gray, n=10 arterioles from 6 mice). n.s. not statistically significant. Figure 3—figure supplement 1—source data 1. Diameter measurements (µm) of individual arterioles used to determine diameter changes in .

Article Snippet: Chemical compound, drug , LY367385 , Hello Bio , HB0398 , .

Techniques: Comparison, Control

Journal: eLife

Article Title: Elevated pyramidal cell firing orchestrates arteriolar vasoconstriction through COX-2-derived prostaglandin E2 signaling

doi: 10.7554/eLife.102424

Figure Lengend Snippet:

Article Snippet: Chemical compound, drug , LY367385 , Hello Bio , HB0398 , .

Techniques: Sequencing, Reverse Transcription, Software, Microscopy

Effect of TTX (1 µM, brown, n= 6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n= 10 arterioles from 6 mice) on (a) kinetics and (b) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shadow traces correspond to the kinetics of arteriolar vasoconstriction in control condition. Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition with p<0.05 and p<0.001, respectively.

Journal: bioRxiv

Article Title: Elevated pyramidal cell firing orchestrates arteriolar vasoconstriction through COX-2-derived prostaglandin E2 signaling

doi: 10.1101/2024.03.27.586974

Figure Lengend Snippet: Effect of TTX (1 µM, brown, n= 6 arterioles from 5 mice) and cocktail antagonists of AMPA/kainate (DNQX, 10 µM), NMDA (D-AP5, 50 µM), mGluR1 (LY367385, 100 µM) and mGluR5 (MPEP, 50 µM) receptors (gray, n= 10 arterioles from 6 mice) on (a) kinetics and (b) magnitude of arteriolar vasoconstriction induced by 20 Hz photostimulation (cyan bar). The SEMs envelope the mean traces. Dashed lines represent the initial diameter. The shadow traces correspond to the kinetics of arteriolar vasoconstriction in control condition. Data are presented as the individual values and mean ± SEM. * and *** statistically different from control condition with p<0.05 and p<0.001, respectively.

Article Snippet: The following drugs were dissolved in water: D-(-)-2-amino-5-phosphonopentanoic acid (D-AP5, 50 µM, Hellobio, HB0225), 6,7- dinitroquinoxaline-2,3-dione (DNQX, 10µM, Hellobio, HB0262), LY367385 (100µM, Hellobio, HB0398) and BIBP3226 (1 µM, Tocris, 2707).

Techniques: