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. 2022 Oct 12;130(10):107002. doi: 10.1289/EHP10255

Figure 7.

Figure 7A is a stained tissue with four columns, namely, control, 0.5 micrometer (1,000 micrograms per liter), 4 micrometers (1,000 micrograms per liter), and 10 micrometers (1,000 micrograms per liter). Figure 7B is a bar graph, plotting spine density (spines per 10 micrometers of dendrite), ranging from 0 to 15 in increments of 5 (y-axis) across control, 0.5 micrometer, 4 micrometers, and 10 micrometers (x-axis). Figure 7C is a set of clustered bar graphs, plotting protein levels (relative unit), ranging from 0.0 to 1.5 in increments of 0.5 (y-axis) across synapsin 1, synaptophysin, and P S D 95 (x-axis) for control, 0.5 micrometer (100 micrograms per liter), 0.5 micrometer (1,000 micrograms per liter), 4 micrometers (100 micrograms per liter), 4 micrometers (1,000 micrograms per liter), 10 micrometers (100 micrograms per liter), and 10 micrometers (1,000 micrograms per liter). Figures 7D and 7E are bar graphs titled brain-derived neurotrophic factor and synaptotagmin-1, plotting Messenger Ribonucleic acid levels (relative unit), ranging from 0.0 to 1.5 in increments of 0.5 (y-axis) across control, 0.5 micrometer with 100 and 1,000, 4 micrometers with 100 and 1,000, and 10 micrometers with 100 and 1,000 (x-axis), respectively.

The density of dendritic spines and expression of proteins related to synaptogenesis in the hippocampus of polystyrene microplastics (PS-MPs)–treated mice. (A) Golgi–Cox staining examined the effect of PS-MPs on the density of dendritic spines in the hippocampus. (B) The number of spines were counted. The mean and SD summary data for quantification are shown in Table S3. p-Values for all comparisons are reported in Table S4. (C) The expression of synapsin 1, synaptophysin, and PSD 95 protein in the hippocampus was measured via western blotting. The western blotting results are shown in Figure S10. Quantification of western blotting evaluating synapsin 1, synaptophysin, and PSD95 protein in the hippocampus of PS-MPs treated mice. The expression levels were quantified with ImageJ36 (n=3). Data are presented as the means±SDs. The mean and SD summary data for quantification are shown in Table S3. p-Values for all comparisons are reported in Table S4. *, p<0.05; **, p<0.01 compared with the control group, as determined by one-way ANOVA with Dunnett’s multiple comparison test. (D,E) The mRNA levels of Bdnf and syt 1 in the hippocampus were tested with qRT-PCR by normalizing to Gapdh. The results are expressed as means±SDs (n=3, N=3 mice/group). The mean and SD summary data for quantification are shown in Table S3. p-Values for all comparisons are reported in Table S4. *p<0.05; **p<0.01 compared with the control group, as determined by one-way ANOVA followed by Dunnett’s multiple comparison tests. Note: ANOVA, analysis of variance; Bdnf, brain-derived neurotrophic factor; Gapdh, glyceraldehyde 3-phosphate dehydrogenase; qRT-PCT, quantitative real-time polymerase chain reaction; SD, standard deviation; syt1, synaptotagmin-1.