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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

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