Influence of SGLT2 Inhibitor Treatment on Urine Antioxidant Status in Type 2 Diabetic Patients: A Pilot Study.
Diana Nabrdalik-LeśniakKatarzyna NabrdalikKatarzyna SedlaczekPatryk GłówczyńskiHanna KwiendaczTomasz SawczynWeronika HajzlerKarolina DrożdżMirela HendelKrzysztof IrlikPaweł StelmachZuzanna GamrotAndrzej ParadyszSławomir KasperczykTomasz StompórJanusz GumprechtPublished in: Oxidative medicine and cellular longevity (2021)
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) have been recognized as potent antioxidant agents. Since SGLT2i are nephroprotective drugs, we aimed to examine the urine antioxidant status in patients with type 2 diabetes mellitus (T2DM). One hundred and one subjects participated in this study, including 37 T2DM patients treated with SGLT2i, 31 T2DM patients not using SGLT2i, and 33 healthy individuals serving as a control group. Total antioxidant capacity (TAC), superoxide dismutase (SOD), manganese superoxide dismutase (MnSOD), free thiol groups (R-SH, sulfhydryl groups), and catalase (CAT) activity, as well as glucose concentration, were assessed in the urine of all participants. Urine SOD and MnSOD activity were significantly higher among T2DM patients treated with SGLT2i than T2DM patients without SGLT2i treatment (p = 0.009 and p = 0.003, respectively) and to the healthy controls (p = 0.002 and p = 0.001, respectively). TAC was significantly lower in patients with T2DM treated with SGLT2i when compared to those not treated and healthy subjects (p = 0.036 and p = 0.019, respectively). It could be hypothesized that the mechanism by which SGLT2i provides nephroprotective effects involves improvement of the SOD antioxidant activity. However, lower TAC might impose higher OS (oxidative stress), and elevation of SOD activity might be a compensatory mechanism.
Keyphrases
- end stage renal disease
- oxidative stress
- newly diagnosed
- ejection fraction
- chronic kidney disease
- peritoneal dialysis
- prognostic factors
- type diabetes
- adipose tissue
- blood pressure
- metabolic syndrome
- anti inflammatory
- amyotrophic lateral sclerosis
- insulin resistance
- dna damage
- blood glucose
- nitric oxide
- combination therapy
- heat shock