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

• Published in: Turkish journal of obstetrics and gynecology Vol. 17; no. 4; pp. 259 - 269
• Main Authors: Sezik,Mekin, Köker,Afşin, Özmen,Özlem, Halıgür,Mehmet, Kaşıkçı,Duygu, Aydoğan,Ahmet, Özatik,Orhan
• Format: Journal Article
• Language: English
• Published: Türk Jinekoloji ve Obstetrik Derneği 2020
• Subjects: Kadın Hastalıkları; Tıp; Ankara; Türkiye; preterm birth; Animal model; endotoksinler; Hayvan modeli; nörokorunma; endotoxins; neuroprotection; pentoksifilin; fetal brain injury; fetal beyin hasarı; pentoxifylline; preterm doğum
• ISSN: 2149-9322; 2149-9330
• DOI: 10.4274/tjod.galenos.2020.19794

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.