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©The Author(s) 2020.
World J Gastroenterol. Jun 21, 2020; 26(23): 3225-3235
Published online Jun 21, 2020. doi: 10.3748/wjg.v26.i23.3225
Published online Jun 21, 2020. doi: 10.3748/wjg.v26.i23.3225
Figure 3 The diabetic retinopathy pathogenic metabolite, succinate, is downregulated with sodium glucose co-transporter 2 inhibition in Akimba mice.
A: Serum succinate levels in Akimba mice treated with dapapagliflozin; B: Serum succinate levels in Akimba mice treated with empagliflozin; C: Serum levels of the beneficial short chain fatty acid, butyric acid, are elevated in diabetic Akita mice with sodium glucose co-transporter 2 inhibition. n = 3-7 mice/group for all groups except for control Akimba (Figure 3B) where n = 2; aP < 0.03; Data represented as mean ± SE.
- Citation: Herat LY, Ward NC, Magno AL, Rakoczy EP, Kiuchi MG, Schlaich MP, Matthews VB. Sodium glucose co-transporter 2 inhibition reduces succinate levels in diabetic mice. World J Gastroenterol 2020; 26(23): 3225-3235
- URL: https://www.wjgnet.com/1007-9327/full/v26/i23/3225.htm
- DOI: https://dx.doi.org/10.3748/wjg.v26.i23.3225