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The loss of platelets greatly increases the chance of fatal hemorrhage, while the lack of white blood cells causes infections; the fall in red blood cells is minimal, and only causes mild anemia. [10] The exposure to 4.5 Gray of penetrating gamma rays has many effects that occur at different times: In 24 hours: [10] vomiting; diarrhea
The brain also uses glucose during starvation, but most of the body's glucose is allocated to the skeletal muscles and red blood cells. The cost of the brain using too much glucose is muscle loss. If the brain and muscles relied entirely on glucose, the body would lose 50% of its nitrogen content in 8–10 days. [13]
Patients with brain injuries acquired in explosions often develop sudden, unexpected brain swelling and cerebral vasospasm despite continuous monitoring. However, the first symptoms of blast-induced neurotrauma (BINT) may occur months or even years after the initial event, and are therefore categorized as secondary brain injuries. [12]
Brain oedema formation is due to the breakdown of red blood cells, where haemoglobin and other contents of red blood cells are released. The release of these red blood cells contents causes toxic effect on the brain and causes brain oedema. Besides, the breaking down of blood-brain barrier also contributes to the odema formation. [13]
Brain ischemia has been linked to a variety of diseases or abnormalities. Individuals with sickle cell anemia, compressed blood vessels, ventricular tachycardia, plaque buildup in the arteries, blood clots, extremely low blood pressure as a result of heart attack, and congenital heart defects have a higher predisposition to brain ischemia in comparison to the average population.
Affected cells then proceed to blebbing, and this is followed by pyknosis, in which nuclear shrinkage transpires. [21] In the final step of this pathway cell nuclei are dissolved into the cytoplasm, which is referred to as karyolysis. [21] The second pathway is a secondary form of necrosis that is shown to occur after apoptosis and budding. [21]
In rats, it has been shown that neurons often die a full 24 hours after blood flow returns. Some theorize that this delayed reaction derives from the various inflammatory immune responses that occur during reperfusion. [11] These inflammatory responses cause intracranial pressure, pressure which leads to cell injury and in some situations cell ...
Brain damage can occur both during and after oxygen deprivation. During oxygen deprivation, cells die due to an increasing acidity in the brain tissue . Additionally, during the period of oxygen deprivation, materials that can easily create free radicals build up. When oxygen enters the tissue these materials interact with oxygen to create high ...