Hypoxia-Induced Developmental Delays of Inhibitory Interneurons Are Reversed by Environmental Enrichment in the Postnatal Mouse Forebrain

Effects of hypoxic rearing and environmental enrichment on PV-expressing interneurons. A, B, PV immunohistochemistry in the neocortex of normoxic (NX) and hypoxic (HX)-reared mice at P15 (A) and P47 (B); P47 groups of NX and HX mice were reared in standard, nonenriched (NE) or enriched (EN) environments from P21 until analysis. Stereological quantification of PV⁺ cells in P15 (C), P35 (D), and P47 (E) cortex (Ctx) for all four experimental groups. Rearing mice in HX decreased PV interneuron numbers in neocortex and subsequent EN normalized PV⁺ cell numbers (P35: main effect of hypoxia, p < 0.05; P47: main effect of hypoxia and enrichment, both p < 0.001). F–I, Hippocampal (Hp) PV immunolabeling (F) and stereological quantification of PV⁺ cells at P15 (G), 35 (H), and 47 (I). Rearing mice in HX decreased PV⁺ interneurons in the hippocampus at P15 but PV⁺ cells recovered spontaneously. Scale bars: 20 μm. Asterisks denote significant differences from all other groups at p < 0.05.

Effects of hypoxic and enriched environment on SST, RLN, and VIP-immunopositive interneurons in neocortex. A, Immunolabeling with EGFP, RLN, and SST antibodies in P47 cortex from GAD67-EGFP mice, illustrating the presence of different subpopulations of interneurons: EGFP⁺/SST⁺/RLN⁻ (small closed arrows), EGFP⁺/SST/⁺/RLN⁺ (arrowheads), and EGFP⁺/RLN⁺/SST⁻ (open arrow). Asterisk indicates an EGFP⁻/RLN⁺/SST⁻ cell. B, C, Stereological quantification of EGFP⁺ cells coexpressing SST and/or RLN at P15 (B) and at P47 (C). Both SST⁺/RLN⁻ and SST⁺/RLN⁺ interneurons were decreased in hypoxic-reared mice, but while the first recovered to control levels with subsequent enrichment, SST⁺/RLN⁺ interneurons did not recover with subsequent enrichment. In contrast, RLN⁺/SST⁻ interneurons increased after hypoxia and were also normalized with enriched environment at P47. D, Decreased number VIP⁺ interneurons in P15 hypoxic cortex (Ctx) shown by immunostaining with VIP antibodies; stereological quantification shown in F. E, Higher magnification image of supragranular Ctx demonstrating that all VIP⁺ cells coexpress GAD67-EGFP at P15. G, Stereological quantification of VIP⁺ cells in neocortex at P47 showing that VIP⁺ cells recovered spontaneously and there was no further effect of enriched environment. NX NE, normoxic nonenriched; NX EN, normoxic enriched; HX NE, hypoxic nonenriched; HX EN, hypoxic enriched. Scale bars: 20 μm. Asterisks denote significant differences from all other groups at p < 0.05.

Intensity and distribution of expression of interneuron marker expression in upper (L1–L4) and lower (L5–L6) layers of primary motor or primary somatosensory cortex (hindlimb) of normoxic and hypoxic mice at P47. Quantification of average expression and numbers of cells with distinct expression levels, respectively, with regards to PV (A, B), SST (C, D), and RLN (E, F). Asterisks denote significant differences (p < 0.05) as determined by factorial ANOVA conducted for each marker. Images depict representative examples of single cells expressing low or high levels of a given marker. The numbers signify the background corrected intensity of cell fluorescence for each cell and marker. NX, normoxia; HX, hypoxia; M, motor cortex; SS, somatosensory cortex; L1–4, cortical layers 1–4; L5–6, cortical layers 5 and 6; ctx, cortex.

Analysis of interneuron lineage cells in the neocortex. A, Costaining of PV (red) and GAD67-EGFP reporter (green) in P15 cortex (Ctx). B, C, Stereological quantification of GAD67 EGFP⁺ cells in the cortex (Ctx) at P15 (B) and P47 (C). EGFP⁺ cell numbers do not change across conditions, whereas PV⁺ cells counted in the same sections are decreased by hypoxia (HX) and increased by enriched environment (EN). D–F, P12–P15 neocortex from HX-reared mice labeled with antibodies to activated caspase-3 (red) and GAD67-EGFP (green; D), Dlx-2 (red), and Olig2 (blue; E), and activated caspase-3 (green) and Dlx-2 (red; F). Interneurons do not undergo noticeable increases in cell death in response to rearing in HX. G, H, Stereological quantification of Dlx-2⁺ cells in P15 (G) and P47 (H) neocortex. There are no significant changes in Dlx-2⁺ cell numbers in response to HX or EN. I, The numbers of all GABA⁺ cells and GABA⁺Dlx-2⁺ colabeled cells in P15 cortex were decreased in HX-reared mice. J, HPLC measurement of GABA content in different brain regions showed that HX rearing significantly decreased GABA in frontal cortex. Scale bars: A, E, 20 μm; D, 10 μm. Asterisks denote significant differences from normoxic controls at p < 0.05. NX NE, normoxic nonenriched; NX EN, normoxic enriched; HX NE, hypoxic nonenriched; HX EN, hypoxic enriched; Fr, frontal; Par, parietal; Occ, occipital, Hipp, hippocampus; Str, striatum.