dba 2j gpnmb1 mice (Jackson Laboratory)
Structured Review
![Intraocular pressure and glaucoma pathology <t>in</t> <t>DBA/2J</t> mice (A) Peak IOP measurements from individual eyes in the current study show significantly increased intraocular pressure in D2 mice compared to D2-controls [∗∗∗∗p << 0.0001 with Mann Whitney test; n = 71 mice, 142 eyes (D2-control) and n = 66 mice, 132 eyes (D2)]. Individual data points represent the measurement from an individual eye. (B) Cross section images of optic nerves from 12-month-old D2 and D2-control animals. Scale bars represent 200 μm. (C) Glial scarring as a percentage of cross-sectional optic nerve area was quantified in D2 and D2-controls (∗∗ p = 0.0071 with t test; N = 12 nerves from seven mice [D2-control] and N = 9 nerves from six mice [D2]). Bars and error show mean ± SEM. (D) Individual (gray and light red) and average (black, dark red) pattern electroretinogram (pERG) waveforms from D2-control (black) and D2 (red) mice. n = 16 eyes from eight mice (D2-control) and n = 14 eyes from seven mice. (E) P1 and N2 pERG amplitudes measured from pre-stimulus baseline in D2-control (black) and D2 (red) mice. P1 and N2 amplitude measurements were significantly decreased in D2 mice compared to D2-controls (∗∗∗∗ p = 0.000056 [P1] and ∗∗∗ p = 0.00033 [N2]; n = 16 eyes from eight mice [D2-control] and n = 14 eyes from seven mice [D2]). Bars and error show mean ± SEM. (F) Linear regression of P1 pERG amplitude with maximum IOP, showing a significant correlation. Best fit line and 95% confidence intervals are shown. (G) Linear regression of P1 pERG amplitude with glial scarring, showing a weak but significant correlation. Best fit line and 95% confidence intervals are shown.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_5702/pmc12995702/pmc12995702__gr1.jpg)
Dba 2j Gpnmb1 Mice, supplied by Jackson Laboratory, 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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1) Product Images from "Compensatory responses to glaucoma pathology in the dorsolateral geniculate nucleus"
Article Title: Compensatory responses to glaucoma pathology in the dorsolateral geniculate nucleus
Journal: iScience
doi: 10.1016/j.isci.2026.115176
Figure Legend Snippet: Intraocular pressure and glaucoma pathology in DBA/2J mice (A) Peak IOP measurements from individual eyes in the current study show significantly increased intraocular pressure in D2 mice compared to D2-controls [∗∗∗∗p << 0.0001 with Mann Whitney test; n = 71 mice, 142 eyes (D2-control) and n = 66 mice, 132 eyes (D2)]. Individual data points represent the measurement from an individual eye. (B) Cross section images of optic nerves from 12-month-old D2 and D2-control animals. Scale bars represent 200 μm. (C) Glial scarring as a percentage of cross-sectional optic nerve area was quantified in D2 and D2-controls (∗∗ p = 0.0071 with t test; N = 12 nerves from seven mice [D2-control] and N = 9 nerves from six mice [D2]). Bars and error show mean ± SEM. (D) Individual (gray and light red) and average (black, dark red) pattern electroretinogram (pERG) waveforms from D2-control (black) and D2 (red) mice. n = 16 eyes from eight mice (D2-control) and n = 14 eyes from seven mice. (E) P1 and N2 pERG amplitudes measured from pre-stimulus baseline in D2-control (black) and D2 (red) mice. P1 and N2 amplitude measurements were significantly decreased in D2 mice compared to D2-controls (∗∗∗∗ p = 0.000056 [P1] and ∗∗∗ p = 0.00033 [N2]; n = 16 eyes from eight mice [D2-control] and n = 14 eyes from seven mice [D2]). Bars and error show mean ± SEM. (F) Linear regression of P1 pERG amplitude with maximum IOP, showing a significant correlation. Best fit line and 95% confidence intervals are shown. (G) Linear regression of P1 pERG amplitude with glial scarring, showing a weak but significant correlation. Best fit line and 95% confidence intervals are shown.
Techniques Used: MANN-WHITNEY, Control
Figure Legend Snippet: Pharmacology of inhibition indicates decreased activation of extrasynaptic GABA A receptors in DBA/2J TC neurons (A) Example peak-normalized IPSCs from TC neurons from D2 and D2-control mice evoked by stimulation with an aCSF-filled patch pipette positioned approximately 25 microns from the recorded TC neuron in the presence of CNQX (20 μM) and D-AP5 (50 μM). Traces show before (gray) and after (black) bath application of 10 μM DS2. (B) Relative effect of DS2 application on peak response of the IPSC (n.s., p = 0.16 via nested t test) and area (∗∗∗ p = 0.0010 via nested t test) of D2 (red) and D2-control (black) mice ( n = 8 cells, four mice [D2-control] and n = 16 cells, six mice [D2]). Bar graphs and error bars show mean ± SEM. (C) Example peak-normalized traces of IPSCs from D2 and D2-control mice before (gray) and after (black) application of SNAP5114 (60 μM). IPSCs were evoked as in A. (D) Relative effect of SNAP5114 application on peak response (n.s., p = 0.70 via nested t test) and area (n.s., p = 0.91 via nested t test) of D2 (red) and D2-control (black) mice ( n = 16 cells, six mice [D2] and n = 14 cells, five mice [D2-control]). Bar graphs and error bars show mean ± SEM.
Techniques Used: Inhibition, Activation Assay, Control, Transferring

