Cerebrospinal fluid and serum nitric oxide levels in asphyxiated newborns

Ergenekon E., Gucuyener K., Erbas D., Ezgu F. S., Atalay Y.

BIOLOGY OF THE NEONATE, cilt.76, sa.4, ss.200-206, 1999 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 76 Sayı: 4
  • Basım Tarihi: 1999
  • Doi Numarası: 10.1159/000014159
  • Dergi Adı: BIOLOGY OF THE NEONATE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.200-206
  • Anahtar Kelimeler: newborn, hypoxic-ischemic encephalopathy, cerebrospinal fluid, nitric oxide levels, ISCHEMIC BRAIN INJURY, SYNTHASE, SEPSIS
  • Gazi Üniversitesi Adresli: Evet

Özet

Hypoxic-ischemic encephalopathy (HIE) is the result of a chain of events caused mainly by cytokines and nitric oxide (NO) release, which is later on followed by free oxygen radical injury. To investigate NO involvement in asphyxiated newborns, serum and cerebrospinal fluid (CSF) values of NO levels in 17 neonates with HIE were detected. Infants at or above 37 weeks of gestation were classified to have mild, moderate and severe HIE due to Sarnat and Sarnat. Samples obtained between 24 and 72 h of life were immediately frozen at -70 degrees C till the time of measurement by Sievers NOA. Five patients had mild, 6 patients had moderate and 6 patients had severe HIE, 4 in the severe HIE group also had multisystem involvement. The CSF NO levels were significantly higher in moderate and severe HIE groups compared to the mild HIE group (p = 0.028 and p = 0.018 respectively). Our results show that NO level increases in CSF with the severity of HIE between 24 and 72 h following asphyxia. According to the animal work, this is the time period where inducible NO synthase gets activated and could cause neurotoxicity, which might perhaps be prevented by interventions.