Acute ultrastructural response of hypoxic hypoxia with relative ischemia in the isolated brain
- PMID: 2816306
- DOI: 10.1007/BF00691291
Acute ultrastructural response of hypoxic hypoxia with relative ischemia in the isolated brain
Abstract
The acute cortical response to surgical brain isolation and subsequent extracorporal normoxic or 30 min hypoxic (PaO2 = 20 mm Hg) perfusions (hypoxic hypoxia with relative ischemia) was evaluated. Cerebral blood flow, arterial pH and CO2 were maintained constant during both perfusions; only the arterial oxygen content was changed. The isolated brain model used in this and previous investigations produces no qualitative ultrastructural changes in the neocortex following brain isolation and normoxic perfusion. However, the acute cortical structural response to 30 min of hypoxic hypoxia with relative ischemia demonstrated a number of important observations. Hypoxic hypoxia produced ultrastructural responses common to cerebral ischemia such as nuclear chromatin clumping, nucleolar condensation and cytoskeletal breakdown. Although neuronal abnormalities seen after 30 min of hypoxic hypoxia were similar to those acute neuronal changes observed following complete cerebral ischemia without recirculation, they differed three ways: (a) mitochondrial swelling and microvacuolation were observed in many cortical pyramidal neurons. (b) Glycogen particles within astroglial processes were observed even after a 30-min period of hypoxic hypoxia. (c) Perivascular astroglial swelling was minimal despite considerable perineuronal swelling. In contrast, incomplete cerebral ischemia produces mitochondrial changes similar to those in hypoxic hypoxia but also causes the depletion of tissue glycogen and perivascular glial swelling. Thus, hypoxic hypoxia with relative ischemia produces a unique acute ultrastructural response compared to either complete or incomplete cerebral ischemia.
Similar articles
-
Subcellular distribution of calcium and ultrastructural changes after cerebral hypoxia-ischemia in immature rats.Brain Res Dev Brain Res. 2000 Dec 29;125(1-2):31-41. doi: 10.1016/s0165-3806(00)00110-3. Brain Res Dev Brain Res. 2000. PMID: 11154758
-
Hypoxia, hyperoxia, ischemia, and brain necrosis.Neurology. 2000 Jan 25;54(2):362-71. doi: 10.1212/wnl.54.2.362. Neurology. 2000. PMID: 10668697
-
Neuroprotective effects of propofol in models of cerebral ischemia: inhibition of mitochondrial swelling as a possible mechanism.Anesthesiology. 2006 Jan;104(1):80-9. doi: 10.1097/00000542-200601000-00014. Anesthesiology. 2006. PMID: 16394694
-
Influence of systemic factors on experimental epileptic brain injury. Structural changes accompanying bicuculline-induced seizures in rats following manipulations of tissue oxygenation or alpha-tocopherol levels.Acta Neuropathol. 1983;60(1-2):81-91. doi: 10.1007/BF00685351. Acta Neuropathol. 1983. PMID: 6880625
-
Current concepts of hypoxic-ischemic cerebral injury in the term newborn.Pediatr Neurol. 1991 Sep-Oct;7(5):317-25. doi: 10.1016/0887-8994(91)90060-x. Pediatr Neurol. 1991. PMID: 1764132 Review.
Cited by
-
Histological changes of neuronal damage in vegetative dogs induced by 18 minutes of complete global brain ischemia: two-phase damage of Purkinje cells and hippocampal CA1 pyramidal cells.Acta Neuropathol. 1990;80(5):527-34. doi: 10.1007/BF00294614. Acta Neuropathol. 1990. PMID: 2251910