The mechanism of periventricular leukomalacia onset

  • ARAKI Tsutomu
    Principal Investigator
    NIPPON MEDICAL SCHOOL,OBSTETRICS AND GYNECOLOGY,Professor
  • ASAKURA Hirobumi
    Co-Investigator
    NIPPON MEDICAL SCHOOL,OBSTETRICS AND GYNECOLOGY,Associate Professor
  • SHIN Sumio
    Co-Investigator
    NIPPON MEDICAL SCHOOL,OBSTETRICS AND GYNECOLOGY,Associate Professor
  • SAWA Rintaro
    Co-Investigator
    NIPPON MEDICAL SCHOOL,OBSTETRICS AND GYNECOLOGY,Instructor
  • YONEYAMA Yoshio
    Co-Investigator
    NIPPON MEDICAL SCHOOL,OBSTETRICS AND GYNECOLOGY,Lecturer

About This Project

Japan Grant Number
JP06454480 (JGN)
Funding Program
Grants-in-Aid for Scientific Research
Funding Organization
Japan Society for the Promotion of Science

Kakenhi Information

Project/Area Number
06454480
Research Category
Grant-in-Aid for Scientific Research (B)
Allocation Type
  • Single-year Grants
Review Section / Research Field
  • Medicine > 外科 > Obstetrics and gynecology
Research Institution
  • NIPPON MEDICAL SCHOOL
Project Period (FY)
1994 〜 1996
Project Status
Completed
Budget Amount*help
3,100,000 Yen (Direct Cost: 3,100,000 Yen)

Research Abstract

Some brain damages in the newborn has been induced not by perinatal asphyxia but by some perinatal complications, such as preterm delivery and infection. However, the exact mechnism that induces brain damages, expecially periventricular leukomalacia in the newborn has not been clarified. Adenosine, one of purine metabolites, is a potent vasodilator and has strong brain protective action. The physiological roles and metabolism of adenosine in the human fetuses has not been well investigated. In this research, we measured fetal plasma adenosine concentration in various pathophysical conditions that sometimes induced brain damage in complicated pregnancies, such as IUGR and preeclampsia. We then evaluated the relationship between plasma adenosine concentration and fetal PO_2, pCO_2, pH,breathing movements, fetoplacental circulation. Plasma adenosine concentraion was elevated significantly in IUGR fetuses, and which inversely correlated with fetal PO_2 and pH.An elevation of plasma adenosine concentration was related to the decrease of fetal breathing movements. Moreover, the production of adenosine in fetoplacental circulation was enhanced during uteroplacental ischemia. Our results suggest that adenosine may play an important role in prevention of brain damage in fetuses.

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