MOESM1 of Associations between serum uric acid and the incidence of hypertension: a Chinese senior dynamic cohort study

Additional file 1. Supplement Tables S1 and S2

Additional file 1 of Histone deacetylase inhibitors VPA and WT161 ameliorate the pathological features and cognitive impairments of the APP/PS1 Alzheimer’s disease mouse model by regulating the expression of APP secretases

Additional file 1: Fig. S1. CCK-8 detects drug toxicity in N2a-APPswe. a Cytotoxic effect of VPA on N2a-APPswe. b Cytotoxic effects of WT161 on N2a-APPswe. Fig. S2. Effect of VPA and WT161 on the expression of histone deacetylases. a Western blot detection of HDAC2, SIRT1 and SIRT2 expression in N2a-APPswe treated with different concentrations of VPA for 72 h. d Western blot detection of HDAC2, SIRT1 and SIRT2 expression in N2a-APPswe treated with different concentrations of WT161 for 72 h. b-c e-f The results of grayscale scan analysis ( $$\overline{x }$$ x ¯ ±s, n=3), in which N2a-APPswe treated with VPA and WT161 in group 0 were used as the baseline, and one-way ANOVA was used to compare the differences with other treatment groups, * P < 0.05, ** P < 0.01. Fig. S3. Effect of vitamin C on the expression of HDACs and APP metabolism-related proteins. a Western blot detection of HDAC1, APP, ADAM10, BACE1 and PS-1 expression in N2a-APPswe-shHDAC1 cells after 48 h of treatment with different concentration gradients of vitamin C. b-f The results of grayscale scan analysis ( $$\overline{x }$$ x ¯ ±s, n=3) for N2a-APPswe-shHDAC1 vitamin C treatment group 0 were used as the baseline. g Western blot detection of HDAC1, APP, ADAM10, BACE1 and PS-1 expression in N2a-APPswe-shHDAC6 cells treated with different concentrations of vitamin C for 48 h. h-l The results of grayscale scan analysis ( $$\overline{x }$$ x ¯ ±s, n=3), in which N2a-APPswe-shHDAC6 vitamin C treatment group 0 was used as the baseline to compare the differences with other treatment groups using one-way ANOVA, *P < 0.05 and **P < 0.01. Fig. S4. Effect of the JNK pathway inhibitor SP600125 on APP-related protein expression. a Western blot detection of p-JNK, JNK3, ADAM10, BACE1 and PS-1 expression in N2a-APPswe after 24 h of treatment with SP600125 at concentrations of 5, 10, 20, 40 and 80 μM. b–f The results of grayscale scan analysis ( $$\overline{x }$$ x ¯ ±s, n=3), in which the N2a- APPswe cell group was the baseline, and the differences with other treatment groups were compared using one-way ANOVA, *P < 0.05 and **P < 0.01. Fig. S5. Effect of knockdown of HDAC1 or HDAC6 on the JNK/c-Jun pathway. a Western blot detection of p-JNK, JNK3 and c-Jun expression in N2a-APPswe after stable transfection with shHDAC1 and shHDAC6. b-d The results of grayscale scan analysis ( $$\overline{x }$$ x ¯ ±s, n=3), in which the N2a-APPswe cell group was used as the baseline for comparison using one-way ANOVA differences with other treatment groups, *P < 0.05, **P < 0.01. Fig. S6. Ingestion and weight changes in APP/PS1 mice after VPA and WT161 treatment. a APP/PS1 double transgenic AD mice were treated with VPA and WT161 (n=18). b Body weight changes in APP/PS1 double transgenic AD mice after VPA and WT161 treatment using two-way repeated-measures ANOVA to compare the effects of different treatments and times on the feeding and body weight of AD mice. Fig. S7. Effect of VPA and WT161 treatment on the organ coefficients of APP/PS1 mice. a-f The organ coefficients of the brain, heart, liver, spleen, lung and kidney in the WT group, APP/PS1 group, VPA group and WT161 group mice (n=9). The APP/PS1 group was used as the baseline, and the differences with other treatment groups were compared using one-way ANOVA, *P < 0.05, **P < 0.01. Fig. S8. Effects of VPA and WT161 treatment on APP expression. qPCR detection of APP mRNA expression in the cerebral cortex of each group of mice ( $$\overline{x }$$ x ¯ ±s, n=4), in which the APP/PS1 group was the baseline, and compared with other treatment groups using one-way ANOVA, ***P < 0.0001. Fig. S9. Effects of treatments on the expression of HDACs in the hippocampus and cortex. a Western blot detection of SIRT1, SIRT2 and HDAC2 expression in the cortex of each group of mice. e Western blot detection of SIRT1, SIRT2 and HDAC2 expression in the hippocampus of each group of mice. b-d f-h The results of grayscale scan analysis ( $$\overline{x }$$ x ¯ ±s, n=3), in which the APP/PS1 group was used as the baseline and one-way ANOVA was used to compare the differences with other treatment groups, *P < 0.05, **P < 0.01. Immunohistochemical detection of VPA and WT161 on brain Aβ amyloid deposition in AD mice. i Immunohistochemistry was performed using mouse-derived 6E10 antibody (1:500) to detect Aβ amyloid deposition in the cortex, hippocampus and internal olfactory cortex of each group of mice (200×, coronal cut). j-k The area ratio of Aβ amyloid plaques in the cortex and hippocampus of each group of mice ( $$\overline{x }$$ x ¯ ±s, n=6). l-m The number of Aβ amyloid plaques in the cortex and hippocampus of each group of mice ( $$\overline{x }$$ x ¯ ±s, n=6), all of which were based on the APP/PS1 group. The differences with other treatment groups were compared using one-way ANOVA, *P < 0.05 and **P < 0.01. Tab. S1. Serum biochemical indexes of VPA- and WT161-treated APP/PS1 double transgenic AD mice