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Am J Obstet Gynecol ; 212(3): 383.e1-7, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25263733

ABSTRACT

OBJECTIVE: To reduce the harmful effect of bowel exposure to amniotic fluid in gastroschisis, we used the nitric oxide (NO) donor S-nitrosoglutathione (GSNO) in an animal model of gastroschisis and assessed the ideal concentration for treatment of changes in bowel. STUDY DESIGN: Gastroschisis was surgically induced in rat fetuses on day 18.5 of gestation. The fetuses were divided into 5 groups (n = 12 animals/group): control (C), gastroschisis (G), gastroschisis + GSNO 5 µmol/L (GNO1), gastroschisis + GSNO 0.5 µmol/L (GNO2), and gastroschisis + GSNO 0.05 µmol/L (GNO3). On day 21.5 of gestation, fetuses were collected by cesarean delivery. Body and intestinal weight were measured and the bowels were either fixed for histometric and immunohistochemical study or frozen for Western blotting. We analyzed bowel morphometry on histological sections and expression of the NO synthase (NOS) enzymes by Western blotting and immunohistochemistry. Data were analyzed by analysis of variance or Kruskal-Wallis test when appropriate. RESULTS: Morphological and histometric measurements of weight, diameter, and thickness of the layers of the intestinal wall decreased with GSNO treatment, especially in the GNO3 group, when compared with the G group (P < .05). The expression of neuronal NOS, endothelial NOS, and inducible NOS decreased mainly in GNO3 group compared to the G group (P < .05), with no difference compared to C group (P > .05). CONCLUSION: Fetal treatment with 0.05 µmol/L GSNO resulted in significant improvement of bowel morphology in gastroschisis.


Subject(s)
Fetal Therapies/methods , Gastroschisis/drug therapy , Nitric Oxide Donors/therapeutic use , S-Nitrosoglutathione/therapeutic use , Animals , Biomarkers/metabolism , Blotting, Western , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Gastroschisis/enzymology , Gastroschisis/pathology , Immunohistochemistry , Intestines/enzymology , Intestines/pathology , Nitric Oxide Synthase/metabolism , Pregnancy , Rats , Rats, Sprague-Dawley , Treatment Outcome
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