AI Article Synopsis

  • The study investigates the effects of Kraussianone-2 (Kr2) on fetal and physiological outcomes in pregnant rats treated with L-NAME, simulating pre-eclampsia.
  • The researchers divided 24 pregnant Sprague-Dawley rats into three groups: a control group, one with induced pre-eclampsia symptoms, and one treated with Kr2 during pre-eclampsia.
  • Results showed that Kr2 administration led to lower fetal mortality, increased birth and placental weights, reduced blood pressure, and lower levels of certain antiangiogenic factors, suggesting that Kr2 may improve fetal health by enhancing blood flow in the uterus.

Article Abstract

This study aimed to investigate the effects of Kraussianone-2 (Kr2), a pyrano-isoflavone isolated from the roots of Eriosema kraussianum N. E. Br. (Fabaceae) on various fetal and physiological parameters in pregnant, L-NAME treated Sprague-Dawley rats. Twenty-four pregnant Sprague-Dawley dams were divided into three groups (n = 8), i.e. the control group (CON), the experimental control group (PRE), where the pre-eclampsia-like symptoms were induced using L-NAME, and the experimental group (EK2), where the pre-eclampsia-like symptoms were once again induced using L-NAME, however, these animals were treated with Kr2. On gestation day 20 the animals were sacrificed, at which time a laparotomy was performed and the number of live pups were counted and their corresponding birth and placental weights were recorded. Blood was also collected in heparin-coated tubes and the plasma samples were then analysed for specific variables using commercially available kits for rats. Kraussianone-2 administration decreased fetal mortality and demonstrated a trend toward increasing birth and placental weights in this model. Furthermore, Kr2 administration also reduced blood pressure amplification and decreased the plasma concentrations of two antiangiogenic factors, soluble fms-like tyrosine kinase1 (sFlt-1) and soluble endoglin (sEng). We speculate that Kr2, by improving uterine artery blood flow, results in improved fetal outcomes and decreased antiangiogenic factors in pregnant, L-NAME treated, Sprague-Dawley rats.

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Source
http://dx.doi.org/10.1002/ptr.3697DOI Listing

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