Chronic hypoperfusion alters the content and structure of proteins and lipids of rat brain homogenates: a Fourier transform infrared spectroscopy study

Toyran N., Zorlu F., Donmez G., Oge K., Severcan F.

EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, cilt.33, sa.6, ss.549-554, 2004 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 33 Sayı: 6
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1007/s00249-004-0396-1
  • Dergi Adı: EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.549-554
  • Anahtar Kelimeler: brain, hypoperfusion, macromolecules, secondary structure, Fourier transform infrared spectroscopy, CEREBRAL HYPOPERFUSION, BREAST-TUMORS, MODEL, LIVER, MEMBRANES, CHANNELS, TISSUES, HYPOXIA
  • Orta Doğu Teknik Üniversitesi Adresli: Hayır

Özet

Arteriovenous malformations (AVMs), masses of abnormal blood vessels which grow in the brain, produce high flow shunts that steal blood from surrounding brain tissue, which is chronically hypoperfused. Hypoperfusion is a condition of inadequate tissue perfusion and oxygenation, resulting in abnormal tissue metabolism. Fourier transform infrared (FTIR) spectroscopy is used in this study to investigate the effect of hypoperfusion on homogenized rat brain samples at the molecular level. The results suggest that the lipid content increases, the protein content decreases, the lipid-to-protein ratio increases, and the state of order of the lipids increases in the hypoperfused brain samples. FTIR results also revealed that, owing to hypoperfusion, not only the protein synthesis but also the protein secondary structure profile is altered in favor of beta-sheets and random coils. These findings clearly demonstrate that, FTIR spectroscopy can be used to extract valuable information at the molecular level so as to have a better understanding of the effect of hypoperfusion on rat brain.