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• W2018643566 abstract "Heme oxygenase-1 (HO-1) has been described as a protein capable of cytoprotection via radical scavenging and apoptosis prevention. The aim of this study was to analyze whether HO-1 overexpression in freshly isolated murine transgenic islets resulted in cell protection and improved in vivo functional performance after transplantation. We produced transgenic mice in which the human HO-1 transgene driven by chicken beta-actin promoter was expressed in the heart, liver, spleen, lung, kidney, muscle, intestine, and pancreas in Balb/c mice. One hundred fifty islets isolated from HO-1 transgenic and control Balb/c mice were syngeneically transplanted under the left kidney capsule of the streptozotocin-diabetic Balb/c mice. The recipients who underwent transplantation with HO-1 transgenic islets showed higher blood glucose than those with control islets at 4 weeks (320 ± 25 vs 189 ± 43 mg/dL; P < .05). Body weight was not significantly different between the 2 groups. Our data indicate transgenic islets with high HO-1 expression did not improve transplantation outcome." @default.
• W2018643566 created "2016-06-24" @default.
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• W2018643566 date "2005-10-01" @default.
• W2018643566 modified "2023-10-18" @default.
• W2018643566 title "Effects of Heme Oxygenase-1 Transgenic Islets on Transplantation" @default.
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• W2018643566 doi "https://doi.org/10.1016/j.transproceed.2005.09.022" @default.
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