İçeriğe geç
akaturk Akademik ölçüm

Makale detayı · 2020

Antenatal pentoxifylline therapy to prevent endotoxin induced fetal injury in the preterm goat model

Turkish Journal of Obstetrics and Gynecology

YÖKSİS OpenAlex Açık erişim · diamond SJR Q3 TR Index Atıf 3 Yüzdelik 59.5% FWCI 0.28
Yıl
2020
ISSN
2149-9322
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

OBJECTIVE: Pentoxifylline (PTX) has immunomodulatory properties and is known to reduce sepsis-associated infant mortality. We aimed to evaluate maternal oral and intra-amniotic administration of PTX for the prevention of fetal inflammation and injury in a caprine model. MATERIALS AND METHODS: Inflammation-mediated fetal injury was induced with maternal granulocyte-colony stimulating factor and intra-amniotic endotoxin at 0.76 of gestation in date-mated pregnant goats. Eight groups were formed (n=4 each): Control, fetal injury, oral 30 mg/kg/day and 60 mg/kg/day PTX for 15 days + fetal injury, intra-amniotic 400 mg/kg and 800 mg/kg estimated fetal weight single-dose PTX with and without fetal injury. Preterm delivery by hysterotomy was performed at 0.80 of gestation to evaluate the fetal and placental effects. Immunochemistry for various markers including interleukins, caspases, cyclooxygenases, vimentin, myelin basic protein, and surfactant proteins were carried out in the fetal lungs, fetal brain, and placenta. Fetal plasma and amniotic fluid interleukins were also evaluated. Kruskal-Wallis H test and Mann-Whitney U test were used for comparisons. RESULTS: High-dose (60 mg/kg/day) maternal prophylactic oral treatment attenuated endotoxin-related histological injury and was related to low inflammatory marker expressions comparable to the controls (p>0.05 except cyclooxygenase 2). Following maternal oral administration, fetal plasma and amniotic fluid levels of the studied interleukins were also lower than the untreated endotoxin-exposed animals (p<0.05 for all comparisons). Intra-amniotic PTX was associated with inconsistent results and increased inflammatory markers in some fetuses. CONCLUSION: Oral PTX before preterm birth mitigates intrauterine inflammation with neuroprotective effects in the fetus. PTX can be considered as a candidate drug for fetal brain injury prevention in the preterm period.

Konular

  • Preterm Birth and Chorioamnionitis
  • Immune Response and Inflammation
  • Reproductive System and Pregnancy

Birincil konu Preterm Birth and Chorioamnionitis

Yazarlar

  1. MEKİN SEZİK SÜLEYMAN DEMİREL ÜNİVERSİTESİ
  2. AFŞİN KÖKER
  3. ÖZLEM ÖZMEN
  4. MEHMET HALIGÜR ÇUKUROVA ÜNİVERSİTESİ
  5. DUYGU KAŞIKCI ISPARTA UYGULAMALI BİLİMLER ÜNİVERSİTESİ
  6. AHMET AYDOĞAN ÇUKUROVA ÜNİVERSİTESİ
  7. ORHAN ÖZATİK KÜTAHYA SAĞLIK BİLİMLERİ ÜNİVERSİTESİ