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. 2021 Mar 10;11:5552. doi: 10.1038/s41598-021-84943-x

Figure 2.

Figure 2

RXRγ KO mice exhibit impaired group 1 mGluR-activated voltage-sensitive currents. (A) Schematic of voltage-clamp stimulation ramp to elicit voltage-sensitive inward currents. (B) Sample current/voltage relations in a wild type CA1 pyramidal neuron during bath-application of the group I agonist DHPG (30 µM, red trace, subtraction of pre-drug baseline I/V plot from I/V relation after 20 min application of DHPG) compared to washout control (black trace) in the same cell. (C) Sample current/voltage relations in an RXRγ KO CA1 pyramidal neuron during bath-application of DHPG (30 µM, red trace, subtraction of pre-drug baseline I/V plot from I/V relation after 20 min application of DHPG) compared to washout control (black trace) in the same cell. (D) Sample inward currents in a wild type CA1 pyramidal neuron before (black trace), during (red trace), and after (blue trace) bath application of 30 µM DHPG (WT peak control current: 40.8 ± 11.4 pA; peak current in presence of DHPG: 21.7 ± 9.6 pA, N = 7 cells, (paired t-test; t = 2.788, P = 0.0317). (E) Sample inward currents in an RXRγ KO CA1 pyramidal neuron before (black trace), during (red trace), and after (blue trace) bath application of 30 µM DHPG (KO peak control current: 37.3 ± 16.5 pA; peak current in presence of DHPG: 42.5 ± 17.6 pA, N = -6 cells, (paired t-test; t = 0.552, P = 0.6044). (F) DHPG (30 µM, grey bar) reduced voltage-sensitive inward currents, plotted as reduction in membrane input resistance Rm, in wild type control neurons. (G) DHPG (30 µM, grey bar) did not alter voltage-sensitive inward currents in CA1 pyramidal neurons in slices from RXRγ KO mice. Data were plotted using Origin Pro (https://www.originlab.com) and the figure assembled using Affinity Designer (https://affinity.serif.com/en-gb/designer/) software.