A1M/α1-Microglobulin Protects from Heme-Induced Placental and Renal Damage in a Pregnant Sheep Model of Preeclampsia.

Lena Wester Rosenlöf, Vera Casslén, Josefin Axelsson, Anneli Edström, Magnus Gram, Madlene Holmqvist, Martin Johansson, Irene Larsson, David Ley, Karel Marsal, Matthias Mörgelin, Bengt Rippe, Sigurbjörg Rutardottir, Behnaz Shohani, Bo Åkerström, Stefan Hansson

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskriftPeer review

43 Citeringar (SciVal)
234 Nedladdningar (Pure)

Sammanfattning

Preeclampsia (PE) is a serious pregnancy complication that manifests as hypertension and proteinuria after the 20(th) gestation week. Previously, fetal hemoglobin (HbF) has been identified as a plausible causative factor. Cell-free Hb and its degradation products are known to cause oxidative stress and tissue damage, typical of the PE placenta. A1M (α1-microglobulin) is an endogenous scavenger of radicals and heme. Here, the usefulness of A1M as a treatment for PE is investigated in the pregnant ewe PE model, in which starvation induces PE symptoms via hemolysis. Eleven ewes, in late pregnancy, were starved for 36 hours and then treated with A1M (n = 5) or placebo (n = 6) injections. After injections, the ewes were re-fed and observed for additional 72 hours. They were monitored for blood pressure, proteinuria, blood cell distribution and clinical and inflammation markers in plasma. Before termination, the utero-placental circulation was analyzed with Doppler velocimetry and the kidney glomerular function was analyzed by Ficoll sieving. At termination, blood, kidney and placenta samples were collected and analyzed for changes in gene expression and tissue structure. The starvation resulted in increased amounts of the hemolysis marker bilirubin in the blood, structural damages to the placenta and kidneys and an increased glomerular sieving coefficient indicating a defect filtration barrier. Treatment with A1M ameliorated these changes without signs of side-effects. In conclusion, A1M displayed positive therapeutic effects in the ewe starvation PE model, and was well tolerated. Therefore, we suggest A1M as a plausible treatment for PE in humans.
Originalspråkengelska
Artikelnummere86353
TidskriftPLoS ONE
Volym9
Utgåva1
DOI
StatusPublished - 2014

Bibliografisk information

The information about affiliations in this record was updated in December 2015.
The record was previously connected to the following departments: Medical Inflammation Research (013212019), Paediatrics (Lund) (013002000), Department of Obstetrics and Gynaecology (Lund) (013018000), Pathology (Malmö) (013031000), Department of Nephrology (013230024), Division of Infection Medicine (BMC) (013024020)

Ämnesklassifikation (UKÄ)

  • Reproduktionsmedicin och gynekologi
  • Urologi och njurmedicin

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