Impact of gradual blood flow increase on ischaemia-reperfusion injury in the rat cremaster microcirculation model


Ozmen S., AYHAN M. S., Demir Y., Siemionow M., Atabay K.

JOURNAL OF PLASTIC RECONSTRUCTIVE AND AESTHETIC SURGERY, cilt.61, sa.8, ss.939-947, 2008 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 61 Sayı: 8
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1016/j.bjps.2007.05.017
  • Dergi Adı: JOURNAL OF PLASTIC RECONSTRUCTIVE AND AESTHETIC SURGERY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.939-947
  • Anahtar Kelimeler: gradual, ischaemia, reperfusion, microcirculation, NO-REFLOW PHENOMENON, REDUCES INFARCT SIZE, ISCHEMIA/REPERFUSION INJURY, NITRIC-OXIDE, NEUTROPHIL ACCUMULATION, MYOCARDIAL-ISCHEMIA, ENDOTHELIAL INJURY, CEREBRAL-ISCHEMIA, ANESTHETIZED RATS, LIVER ISCHEMIA
  • Gazi Üniversitesi Adresli: Evet

Özet

Introduction: We aimed to evaluate the impact of gradual blood reperfusion on ischaemia-reperfusion injury and to explain the pathophysiology of reperfusion injury in a rat cremaster muscle microcirculation model. Materials and Methods: Twenty-four Sprague-Dawley rats weighing 150-200 g were evaluated in three groups. Cremaster muscles were prepared for microcirculatory observations. Group I (n = 8, control): no ischemia was induced. Group II (n = 8, acute reperfusion): microclamps were applied to the right external iliac vessels for 150 min, then venous and arterial clamps were released at once. Group III (n = 8, gradual reperfusion): microclamps were applied to the right external iliac vessels for 150 min, and then the first venous clamp was released; the arterial clamp was opened gradually by a specially designed microclamp holder (Sheey ossicle holding clamp). In all groups, following a wait of 150 min blood flow velocity was measured for 15 min and then the animals were reperfused freely for 1 h. Next, red blood cell velocity, vessel diameters, functional capillary perfusion and endothelial oedema index were analysed, and rotting, migrating and adhesing leukocytes and lymphocytes were counted. At( observations were videotaped for slow-motion replay. Muscle damage was evaluated histotogically.