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Metformin attenuates renal medullary hypoxia in diabetic nephropathy through inhibition uncoupling protein-2

Christensen, Michael (author)
Aarhus Univ, Dept Clin Med, Aarhus, Denmark
Schiffer, Tomas A. (author)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Uppsala Univ, Sweden
Gustafsson, Håkan (author)
Linköpings universitet,Avdelningen för radiologiska vetenskaper,Medicinska fakulteten,Region Östergötland, Röntgenkliniken i Norrköping
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Krag, Sören Palmelund (author)
Aarhus Univ Hosp, Dept Pathol, Aarhus, Denmark
Nörregaard, Rikke (author)
Aarhus Univ, Dept Clin Med, Aarhus, Denmark
Palm, Fredrik, 1973- (author)
Uppsala universitet,Institutionen för medicinsk cellbiologi,Uppsala Univ, Sweden
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 (creator_code:org_t)
2018-11-08
2019
English.
In: Diabetes/Metabolism Research Reviews. - : WILEY. - 1520-7552 .- 1520-7560. ; 35:2
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: The purpose of the study is to examine the effect of metformin on oxygen metabolism and mitochondrial function in the kidney of an animal model of insulinopenic diabetes in order to isolate any renoprotective effect from any concomitant effect on blood glucose homeostasis.Methods: Sprague-Dawley rats were injected with streptozotocin (STZ) (50 mg kg(-1)) and when stable started on metformin treatment (250 mg kg(-1)) in the drinking water. Rats were prepared for in vivo measurements 25 to 30 days after STZ injection, where renal function, including glomerular filtration rate and sodium transport, was estimated in anesthetized rats. Intrarenal oxygen tension was measured using oxygen sensors. Furthermore, mitochondrial function was assessed in mitochondria isolated from kidney cortex and medulla analysed by high-resolution respirometry, and superoxide production was evaluated using electron paramagnetic resonance.Results: Insulinopenic rats chronically treated with metformin for 4 weeks displayed improved medullary tissue oxygen tension despite of no effect of metformin on blood glucose homeostasis. Metformin reduced UCP2-dependent LEAK and differentially affected medullary mitochondrial superoxide radical production in control and diabetic rats.Conclusions: Metformin attenuates diabetes-induced renal medullary tissue hypoxia in an animal model of insulinopenic type 1 diabetes. The results suggest that the mechanistic pathway to attenuate the diabetes-induced medullary hypoxia is independent of blood glucose homeostasis and includes reduced UCP2-mediated mitochondrial proton LEAK.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Physiology (hsv//eng)

Keyword

diabetic kidney disease
metformin
hypoxia

Publication and Content Type

ref (subject category)
art (subject category)

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