Role of leukocytes in uterine hypoperfusion and fetal growth retardation induced by ischemia-reperfusion

Kei Miyakoshi, Hitoshi Ishimoto, Osamu Nishimura, Shinji Tanigaki, Mamoru Tanaka, Toyohiko Miyazaki, Michiya Natori, Yasunori Yoshimura

研究成果: Article査読

12 被引用数 (Scopus)

抄録

We investigated leukocyte involvement in uterine hypoperfusion and intrauterine fetal growth retardation (IUGR) induced by ischemia-reperfusion (I/R) in Sprague-Dawley rats. On day 17 of gestation, leukocyte accumulation in the uterus and placenta subjected to 30 min of ischemia, followed by reperfusion, was assessed by measuring myeloperoxidase (MPO) activity. Uterine MPO activity was significantly higher after 1 h of reperfusion than it was before ischemia (P < 0.05), without any increase in placental MPO activity. Immunohistochemical staining showed leukocyte accumulation in the uterus subjected to I/R. The effects of treatment with monoclonal antibodies against CD11a (WT1) and CD18 (WT3) at a dose of 0.8 mg/kg on uterine blood flow and IUGR were investigated. Laser-Doppler flowmetry demonstrated that uterine hypoperfusion at 2 h after ischemia (blood flow, -51.7 ± 1.2%; P < 0.01) was inhibited by WT1 and WT3 treatment. I/R-induced IUGR at full term (P < 0.05 vs. nonischemic horn) was prevented by WT1 and WT3 treatment on day 17. These results indicate that leukocyte accumulation may play an important role in the pathogenesis of uterine hypoperfusion and IUGR induced by I/R in pregnant rats.

本文言語English
ページ(範囲)H1215-H1221
ジャーナルAmerican Journal of Physiology - Heart and Circulatory Physiology
280
3 49-3
DOI
出版ステータスPublished - 2001

ASJC Scopus subject areas

  • 生理学
  • 循環器および心血管医学
  • 生理学(医学)

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