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Image Search Results
Journal: Cell reports
Article Title: Cerebellar nuclei neurons projecting to the lateral parabrachial nucleus modulate classical fear conditioning.
doi: 10.1016/j.celrep.2023.112291
Figure Lengend Snippet: Figure 1. DCN neurons project to the lPBN (A) Viral injection of AAV-hSyn-EYFP into the DCN. Left: EYFP expression in the DCN. Right: EYFP signals in the lPBN. Scale bars: 500 mm (left) and 200 mm (right). (B) Retrograde tracing from the lPBN to DCN. Left: strategy for labeling lPBN-projecting DCN neurons. Right: representative images of retro bead injection into the lPBN and retrogradely labeled DCN neurons. FN, fastigial nucleus; IpN, interpositus nucleus; DN, dentate nucleus. Scale bars: 1 mm (top) and 500 mm (bottom). (C) Number of labeled cells along the rostro-caudal axis (n = 3 mice). (D) Whole-cell patch-clamp recordings of optogenetically evoked EPSCs (oEPSCs) in the lPBN via stimulation of ChR2-expressing cerebellar axons. Of 49 cells recorded, 37 cells exhibited time-locked synaptic responses to blue laser stimulation. (E) Example recording traces of oEPSCs with pharmacological treatment. (F) oEPSCs recorded in the lPBN treated with TTX, 4-AP, and NBQX (n = 5 slices from 5 mice; ACSF vs. +TTX, two-tailed paired t test, ***p = 0.0002; +TTX vs. +4- AP, two-tailed paired t test, **p = 0.0036; +4-AP vs. +NBQX, two-tailed paired t test, **p = 0.0088). (G) Anterograde labeling from the DCN to lPBN. AAV8-EF1a-mCherry-IRES-WGA-Cre and AAV1-EF1a-DIO-EYFP were injected into the DCN and the lPBN, respectively. The anterograde transneuronal tracer wheat germ agglutinin (WGA) fused to Cre recombinase in the DCN permits EYFP expression in lPBN neurons receiving input from the DCN. (H) Representative images of DCN-connected lPBN projections. BLA, basolateral amygdala; BNST, bed nucleus of the stria terminalis; CeA, central amygdala; LH, lateral hypothalamic area; PAG, periaqueductal gray; PVH, paraventricular nucleus of the hypothalamus; GPi, globus pallidus internus; ZI, zona incerta; 3V, third ventricle. Scale bar: 500 mm. (I) Anterograde labeling from the DCN to lPBN using synaptophysin-mRuby. AAV1-hSyn-Cre and AAV1-hSyn-DIO-synaptophysin-mRuby were injected into the DCN and the lPBN, respectively. (J) Representative images of synaptophysin-mRuby signals of the DCN-connected lPBN projections. Scale bar: 500 mm. Data are presented as mean ± SEM. See also Figures S1 and S2.
Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Rabbit monoclonal anti-c-Fos (9F6) Cell Signaling Technology Cat# 2250; RRID: AB_2247211 Rabbit polyclonal anti-PACAP-38 Peninsula Laboratories Cat# T-4473; RRID: AB_519166 Sheep polyclonal anti-FoxP2 R&D Systems Cat# AF5647; RRID: AB_2107133 Mouse monoclonal anti-CGRP Abcam Cat# ab81887; RRID: AB_1658411 Alexa Fluor 568-conjugated donkey anti-mouse Invitrogen Cat# A10037; RRID: AB_2534013 Alexa Fluor 594-conjugated donkey anti-sheep Abcam Cat# ab150180; RRID: AB_2716768 Alexa Fluor 568-conjugated goat anti-rabbit Invitrogen Cat# A11011; RRID: AB_143157 Alexa Fluor 647-conjugated donkey anti-rabbit Invitrogen Cat# A31573; RRID: AB_2536183 Bacterial and virus strains AAV-EF1ɑ-DIO-EYFP Addgene Cat#
Techniques: Injection, Expressing, Retrograde Tracing, Labeling, Patch Clamp, Two Tailed Test
Journal: Nature Communications
Article Title: Ventral hippocampus neurons encode meal-related memory
doi: 10.1038/s41467-025-59687-1
Figure Lengend Snippet: a Left: Diagram of a coronal section of the nucleus accumbens (ACB), adapted from the Brain Maps 4.0 structure of the rat brain . Middle: Representative photomicrographs of axonal green fluorescent protein (GFP) + expression in the ACB from ventral CA1 neurons active in the Fasted (Fasted GFP )( n = 5) or Fed (Fed GFP )( n = 4) state, relative to the anterior commissure (ac); scale bar 100 μm. Right: Average number of GFP + pixels in the ACB. b Left: Diagram of a coronal section of the lateral septum (LS), adapted from the Brain Maps 4.0 structure of the rat brain . Middle: Representative photomicrographs of axonal GFP + expression in the LS from ventral CA1 neurons active in the Fasted (Fasted GFP )( n = 5) or Fed (Fed GFP )( n = 4) state, relative to the lateral ventricle (lv); scale bar 100 μm. Right: Average number of GFP + pixels in the LS. c Left: Diagram of a coronal section of the lateral hypothalamic area (LHA), adapted from the Brain Maps 4.0 structure of the rat brain . Middle: Representative photomicrographs of axonal GFP + expression in the LHA from ventral CA1 neurons active in the Fasted (Fasted GFP )( n = 5) or Fed (Fed GFP )( n = 4) state, relative to the fornix (fx) and 3rd ventricle (3 v); scale bar 100 μm. Right: Average number of GFP + pixels in the LHA ( p value = 0.0159). d Left: Representative photomicrograph of retrograde GFP viral expression in the LS, relative to the lv; scale bar 200 μm. Right: Representative photomicrograph of retrograde mCherry viral expression in the LHA, relative to the fx; scale bar 200 μm. e Average number of LS (GFP)( n = 4) and LHA (mCherry)( n = 4)-projecting neurons labeled in the CA1v. f Average percentage of CA1v neurons sending axonal projections to both the LS (GFP)( n = 4) and LHA (mCherry)( n = 4). g Average percentage of LS (GFP)( n = 4) and LHA (mCherry)( n = 4)-projecting CA1v neurons expressing cFos in the Fed state ( p value < 0.0001). h Representative photomicrograph of fluorescent in situ hybridization for Fos (cyan) in LS (GFP) and LHA (mCherry)-projecting neurons of the CA1v, relative to the alveus (alv); scale bar 100 μm. Data are presented as mean ± SEM. For a – c and d – g , two-tailed unpaired t-test; * p < 0.05, **** p < 0.0001. No symbol indicates lack of significance.
Article Snippet: The same rats also received a unilateral injection (200nL) of a
Techniques: Expressing, Labeling, In Situ Hybridization, Two Tailed Test
Journal: Nature Communications
Article Title: Ventral hippocampus neurons encode meal-related memory
doi: 10.1038/s41467-025-59687-1
Figure Lengend Snippet: a Diagram of viral approach for expression of GCaMP7s in ventral CA1 neurons projecting to the lateral hypothalamic area and implantation of the optic fiber, adapted from the Brain Maps 4.0 structure of the rat brain . b Representative photomicrograph of GCaMP7s expression for placement validation of viral injections, relative to the alveus (alv); scale bar 100 μm (representative pattern was observed in all animals used in the analyses, n = 3). c Representative trace of a single animal of the increase in calcium-dependent activity during the interbout intervals (purple) in ventral hippocampus neurons projecting to the lateral hypothalamic area. d Average change in z-score for fluorescence over the course of an eating bout versus during an interbout interval ( n = 3 animals)( p value = 0.0165). e Diagram of viral approach for expression of hM4Di receptors in ventral CA1 neurons projecting to the lateral hypothalamic area and administration of vehicle (VEH) or clozapine-N-oxyde (CNO) through a lateral ventricle (LV) cannula, adapted from the Brain Maps 4.0 structure of the rat brain . f Representative photomicrograph of mCherry expression for placement validation of viral injections, relative to the alveus (alv); scale bar 100 μm (representative pattern was observed in all animals used in the analyses, n = 10). g Average number of errors and h latency to find the food during training for the foraging-related spatial memory task in animals assigned to VEH ( n = 6) or CNO ( n = 4) groups. i Performance index during the probe for the foraging-related spatial memory task, 1 h following LV administration of VEH ( n = 6) or CNO ( n = 4)(Group comparison p value = 0.0024; p value for 1-sample t-test = 0.0014 for VEH group). Data are presented as mean ± SEM. For d , two-tailed paired t-test. For g – h , two-way ANOVA. For i , two-tailed unpaired t-test ( n = 4–6/group); * p < 0.05, ** p < 0.01. For i , one-sample t-test, different from chance set at 0.1667; ## p < 0.01. No symbol indicates lack of significance.
Article Snippet: The same rats also received a unilateral injection (200nL) of a
Techniques: Expressing, Biomarker Discovery, Activity Assay, Fluorescence, Comparison, Two Tailed Test