Unconjugated Bilirubin Mediates Heme Oxygenase-1-Induced Vascular Benefits in Diabetic Mice
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AbstractHeme oxygenase-1 (HO-1) exerts vasoprotective effects. Such benefit in diabetic vasculopathy, however, remains unclear. We hypothesize that bilirubin mediates HO-1-induced vascular benefits in diabetes. Diabetic db/db mice were treated with hemin (HO-1 inducer) for 2 weeks, and aortas were isolated for functional and molecular assays. Nitric oxide (NO) production was measured in cultured endothelial cells. Hemin treatment augmented endothelium-dependent relaxations (EDRs) and elevated Akt and endothelial NO synthase (eNOS) phosphorylation in db/db mouse aortas, which were reversed by the HO-1 inhibitor SnMP or HO-1 silencing virus. Hemin treatment increased serum bilirubin, and ex vivo bilirubin treatment improved relaxations in diabetic mouse aortas, which was reversed by the Akt inhibitor. Biliverdin reductase silencing virus attenuated the effect of hemin. Chronic bilirubin treatment improved EDRs in db/db mouse aortas. Hemin and bilirubin reversed high glucose-induced reductions in Akt and eNOS phosphorylation and NO production. The effect of hemin but not bilirubin was inhibited by biliverdin reductase silencing virus. Furthermore, bilirubin augmented EDRs in renal arteries from diabetic patients. In summary, HO-1-induced restoration of endothelial function in diabetic mice is most likely mediated by bilirubin, which preserves NO bioavailability through the Akt/eNOS/NO cascade, suggesting bilirubin as a potential therapeutic target for clinical intervention of diabetic vasculopathy.
All Author(s) ListLiu J, Wang L, Tian XY, Liu LM, Wong WT, Zhang Y, Han QB, Ho HM, Wang NP, Wong SL, Chen ZY, Yu J, Ng CF, Yao XQ, Huang Y
Journal nameDiabetes
Year2015
Month5
Day1
Volume Number64
Issue Number5
PublisherAMER DIABETES ASSOC
Pages1564 - 1575
ISSN0012-1797
eISSN1939-327X
LanguagesEnglish-United Kingdom
Web of Science Subject CategoriesEndocrinology & Metabolism

Last updated on 2020-29-11 at 00:58