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10.4196/kjpp.2015.19.4.327

http://scihub22266oqcxt.onion/10.4196/kjpp.2015.19.4.327
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C4499644!4499644!26170736
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suck abstract from ncbi


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pmid26170736      Korean+J+Physiol+Pharmacol 2015 ; 19 (4): 327-34
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  • Involvement of Heme Oxygenase-1 in Orexin-A-induced Angiogenesis in Vascular Endothelial Cells #MMPMID26170736
  • Kim MK; Park HJ; Kim SR; Choi YK; Bae SK; Bae MK
  • Korean J Physiol Pharmacol 2015[Jul]; 19 (4): 327-34 PMID26170736show ga
  • The cytoprotective enzyme heme oxygenase-1 (HO-1) influences endothelial cell survival, proliferation, inflammatory response, and angiogenesis in response to various angiogenic stimuli. In this study, we investigate the involvement of HO-1 in the angiogenic activity of orexin-A. We showed that orexin-A stimulates expression and activity of HO-1 in human umbilical vein endothelial cells (HUVECs). Furthermore, we showed that inhibition of HO-1 by tin (Sn) protoporphryin-IX (SnPP) reduced orexin-A-induced angiogenesis in vivo and ex vivo. Orexin-A-stimulated endothelial tube formation and chemotactic activity were also blocked in SnPP-treated vascular endothelial cells. Orexin-A treatment increased the expression of nuclear factor erythroid-derived 2 related factor 2 (Nrf2), and antioxidant response element (ARE) luciferase activity, leading to induction of HO-1. Collectively, these findings indicate that HO-1 plays a role as an important mediator of orexin-A-induced angiogenesis, and provide new possibilities for therapeutic approaches in pathophysiological conditions associated with angiogenesis.
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