4.7 Article

Berberine improves insulin-induced diabetic retinopathy through exclusively suppressing Akt/mTOR-mediated HIF-1α/VEGF activation in retina endothelial cells

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES
Volume 17, Issue 15, Pages 4316-4326

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/ijbs.62868

Keywords

Berberine; Insulin; Diabetic Retinopathy; VEGF; HIF-1 alpha; Akt/mTOR

Funding

  1. Research Grant Council, HKSAR [RGC GRF 17152116, 17121419]
  2. Health and Medical Research Fund [15162961, 16172751, 17181101]
  3. Gaia Family Trust of New Zealand [200007008, 200006276]

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The study demonstrated that berberine can decelerate the progression of diabetic retinopathy by inhibiting insulin-induced neovascularization of retinal endothelial cells. In both experimental type I and type II diabetic mice, berberine effectively suppressed the expression of HIF-1 alpha and VEGF, improving diabetic retinopathy under insulin treatment.
Background: Insulin therapy is the major treatment of glycaemic control in type I diabetes mellitus (DM) and advanced type II DM patients who fail to respond to oral hypoglycemic agents. Nonetheless, insulin therapy is deemed unsuccessful in controlling the incidence of diabetic retinopathy (DR) and is likely a risk factor. Berberine, an isoquinoline alkaloid, has caught great attention towards its anti-diabetic mechanisms. This study aims to investigate the effect of berberine in decelerating DR progression in insulin-treated DM. Methods: To better understand the therapeutic potential of berberine in the presence of insulin, we elaborated the action of mechanism whether berberine inhibited retinal expression of HIF-1 alpha and VEGF through regulating AKT/mTOR pathway. Suppression of insulin-induced neovasculature of retina endothelial cells by berberine was also studied. Lastly, the in vivo efficacy and safety of berberine as adjuvant therapy for the treatment of DR were systemically investigated in experimental type I and type II DM mice with insulin treatment. Results: Among various types of retinal cells, the activity of HIF-1 alpha and VEGF in retinal endothelial cells could be particularly and exclusively stimulated by insulin intervention, which could be inhibited by berberine treatment in a dose- and time-dependent manner. Berberine suppressed Akt/mTOR activity in these cells, and restoration of Akt/mTOR signalling attenuated berberine's inhibition on HIF-1 alpha and VEGF expression. Berberine suppressed the progression of DR in experimental type I and type II diabetic mice receiving insulin therapy. Conclusion: Berberine improves insulin-induced diabetic retinopathy in type I and II diabetes through inhibiting insulin-induced activation of retinal endotheliocytes via Akt/mTOR/ HIF-1 alpha/VEGF pathway.

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