Ghrelin's second life - World Journal of Gastroenterology
Ghrelin's second life - World Journal of Gastroenterology
Ghrelin's second life - World Journal of Gastroenterology
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CCl4/YGJ CCl4 Control Wang XL et al . YGJ decoction protects against hepatic injury<br />
A 8 wk 9 wk 10 wk 13 wk<br />
B<br />
α-SMA staining (fold change)<br />
1600<br />
1400<br />
1200<br />
1000<br />
800<br />
600<br />
400<br />
200<br />
0<br />
b<br />
CCl4<br />
CCl4 + YGJ<br />
0 7 8 9 10 13<br />
t /wk<br />
Figure 3 Immunostaining and Western blot analysis <strong>of</strong> α-smooth muscle actin in liver tissues. A: α-smooth muscle actin (α-SMA) immunostaining, × 200; B:<br />
Semi-quantification <strong>of</strong> α-SMA positive area, with the level in the week 0 control group set as the basal level; C: Western blotting <strong>of</strong> α-SMA; D: Semi-quantification <strong>of</strong><br />
the α-SMA Western blot results, with the week 0 control group level set as the basal level. b P < 0.01 vs week 0 control group; d P < 0.01 vs the same time-point CCl4<br />
group. Results are mean ± SD. CCl4: Carbone tetrachloride; YGJ: Yiguanjian; GAPDH: Glyceraldehydes-3-phosphate dehydrogenase.<br />
constitution. In YGJtreated mice, the number <strong>of</strong> EGFP +<br />
cells decreased markedly as compared with the CCl4injected<br />
mice at the same time point. Moreover, unlike the<br />
distribution <strong>of</strong> EGFP + cells which were mainly found in<br />
the fibrotic area in CCl4injected mice, the EGFP + cells<br />
were distributed not only in mesenchymal but also in parenchymal<br />
areas in YGJtreated mice (Figures 46).<br />
YGJ decoction-mediated bone marrow-derived cell<br />
differentiation in chronically injured liver<br />
In accordance with the results <strong>of</strong> the dynamic CCl4 injec-<br />
WJG|www.wjgnet.com<br />
b<br />
b<br />
b<br />
b d<br />
d<br />
d d<br />
C D<br />
α-SMA<br />
GAPDH<br />
CCl4<br />
YGJ<br />
- + + + + + + + + +<br />
- - - + - + - + - +<br />
7 wk 8 wk 9 wk 10 wk 13 wk<br />
α-SMA content (fold change)<br />
2.0<br />
1.5<br />
1.0<br />
0.5<br />
0<br />
CCl4<br />
CCl4 + YGJ<br />
0 7 8 9 10 13<br />
t /wk<br />
tion model without BM transplantation, both the number<br />
and distribution <strong>of</strong> αSMA + cells increased constantly<br />
over the course <strong>of</strong> liver injury in mice with bone marrow<br />
reconstitution. Treatment with YGJ reduced the number<br />
<strong>of</strong> αSMA + cells in fibrotic livers. The results <strong>of</strong> EGFP/<br />
αSMA double staining showed that there were almost no<br />
double positive cells in the vehicle control mice. In contrast,<br />
the number <strong>of</strong> the EGFP + /αSMA + cells increased<br />
over time in all mice after receiving CCl4 injections for 7<br />
wk (P < 0.01) and remained high to the final timepoint (P<br />
< 0.01); moreover, the EGFP + /αSMA + cells were mainly<br />
3240 July 7, 2012|Volume 18|Issue 25|<br />
b<br />
b<br />
d<br />
b<br />
d<br />
b<br />
d