<P>Abstract</P><P><B><I>Background/Aims:</I></B> Lymphedema is a clinically incurable disease that occurs commonly after lymph node dissection and/or irradiation. Several studies have recently demonstrated tha...
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https://www.riss.kr/link?id=A107678337
2013
-
SCOPUS,SCIE
학술저널
124-133(10쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P>Abstract</P><P><B><I>Background/Aims:</I></B> Lymphedema is a clinically incurable disease that occurs commonly after lymph node dissection and/or irradiation. Several studies have recently demonstrated tha...
<P>Abstract</P><P><B><I>Background/Aims:</I></B> Lymphedema is a clinically incurable disease that occurs commonly after lymph node dissection and/or irradiation. Several studies have recently demonstrated that extracorporeal shock wave therapy (ESWT) could promote lymphangiogenesis associated with expression of vascular endothelial growth factor (VEGF)-C. This research concerned primarily the synergistic effect of ESWT combined with VEGF-C incorporated hydrogel (VEGF-C hydrogel) combination therapy for promoting lymphangiogenesis and ultimately alleviating lymphedema. <B><I>Methods:</I></B> The VEGF-C hydrogel was applied to the injury site in a mouse model of lymphedema and then regularly underwent ESWT (0.05 mJ/mm<SUP>2</SUP>, 500 shots) every 3 days for 4 weeks. <B><I>Results:</I></B> Four weeks after the treatment, mice treated with VEGF-C hydrogel and ESWT showed signs of the greatest decrease in edema/collagenous deposits when compared with the other experimental group. LYVE-1-positive vessels also revealed that the VEGF-C/ESWT group had significantly induced the growth of new lymphatic vessels compared to the other groups. Western blot analysis showed that expression of VEGF-C (1.24-fold) and VEGF receptor-3 (1.41-fold) was significantly increased in the VEGF-C/ESWT group compared to the normal group. <B><I>Conclusion:</I></B> These results suggested that VEGF-C and ESWT had a synergistic effect and were very effective in alleviating the symptoms of lymphedema and promoting lymphangiogenesis.</P><P>Copyright © 2012 S. Karger AG, Basel</P>