Smoking induced alteration of APP processing.

<p>The total lysate of the hippocampus of the rats were subjected to Western blotting analysis. The levels of APP, sAPPα and sAPPβ were detected (a); quantitative analysis of the band intensity was shown (b to d). *P<0.05 compared to control. Brain sections were stained with anti-rodent Aβ antibody. Photos of the CA1 and dentate gyrus were presented. Positive staining were increased in the smoking group (h and i) when compared to the control group (e and f), magnification, 400X. Enlarged photos of the dentate gyrus of the control (g) and smoking group (j) were shown. Note that Aβ was accumulated in the cell body (j).</p

Level of drebrin was increased in the smoking group. Brain sections were stained with anti-drebrin antibody.

<p>The CA3 region of the control (a) and smoking (b) group were shown, magnification, 100X. Western blot analysis showed that there was a trend of increase in the band intensity of drebrin but it is not statistically significant (c and d).</p

Levels of the pre-synaptic proteins were decreased in the hippocampus of the smoking group.

<p>Brain sections were stained with anti-synapsin-1 antibody. The CA3 region of (a) control group and (c) smoking group were shown, magnification, 200X; with corresponding enlarged images shown in (b and d), magnification, 400X. Western blot analysis was performed on the total lysate of the whole hippocampus, confirming the decrease of synapsin-1 in the hippocampus of the smoking group (e); quantitative analysis of the band intensity of synapsin-1 was shown in (f). Western blot analysis showed that the levels of synaptophysin in the hippocampus were decreased in the smoking group (f); quantitative analysis of the band intensity of synaptophysin was shown in (g). Western blot analysis showed that the levels of PSD95 in the hippocampus were similar among the two groups (h); quantitative analysis of the band intensity of PSD95 was shown in (i). *P<0.05 compared to control.</p

Smoking induced activation of stress kinases.

<p>The total lysate of the hippocampus of the rats were subjected to Western blotting analysis. The levels of p-ERK1/2, total ERK1/2 (a), p-JNK and total JNK (b), p-GSK3β (Ser9), p-GSK3β (pY216), p-PP2A (pY307) (e) and cleaved caspase-3 (i) were detected. α-Tubulin was used as loading control. Quantitative analysis of the band intensity of the detected kinases was shown in (b, d, f–g, and j). *P<0.05 compared to control.</p

Level of acetylated-tubulin was decreased in the hippocampus of the smoking group.

<p>Brain sections were stained with anti-acetylated-tubulin antibody. The CA1 and CA3 regions of control group (a and b), smoking group (c and d) were shown, magnification, 200X. Western blot analysis confirmed the decrease of acetylated-tubulin in the hippocampus of the smoking group (e); quantitative analysis of the band intensity was shown in (f). *P<0.05 compared to control.</p

Smoking induced phosphorylation of tau.

<p>The total lysate of the hippocampus of the rats were subjected to Western blotting analysis. Phosphorylation of tau was detected by pT231 (reacts with phosphorylated tau at Thr 231), pT205 (reacts with phosphorylated tau at Thr 205), pS396 (reacts with phosphorylated tau at Ser 396) and pS404 (reacts with phosphorylated tau at Ser 404). Total tau was detected with the antibody pan-tau. α-tubulin was used as loading control. *P<0.05 compared to control.</p

Level of 8-OHG was elevated in rat hippocampus exposed to cigarette smoking.

<p>Brain sections were stained with anti-8-OHG antibody to detect the level of oxidative stress. Representative photos were selected from the control group (a and c) and the smoking group (b and d), magnification, 100X. An enlarged photo of the CA3 region of the smoking group was shown in (e), magnification, 400X.</p