There are a number of methods to measure hypoxia in tissues; all have advantages and disadvantages. Three key methods that are relevant to the discussions in this paper are below (for reviews see Refs 142,143,144,145,146,147).
Hypoxia marker drugs
These drugs are 2-nitroimidazoles; after entering cells they undergo 1-2 electron reduction in cells and the reduced drug is a highly reactive free radical that binds to macromolecules, including proteins148. However, when oxygen is present, the drug is oxidized and reverts back to its original state, allowing it to diffuse out of the cell and eventually into the circulation. The rate of protein binding of the reduced drug increases exponentially with a decrease in partial pressure of O2, particularly below 10 mmHg144, 149. The presence of drug-protein adducts can be detected immunohistochemically using antibodies specific for the drug protein adduct. 18F-labelled versions of these drugs are also being developed for positron-emission tomography imaging150, 151.
Hypoxia marker proteins
As HIF1 upregulates the synthesis of many proteins, it has been proposed that identification of such proteins in tissues could be markers of hypoxia. Literally dozens of such proteins have been studied at the preclinical level and in clinical trials152. Some of the more promising endogenous markers include carbonic anhydrase IX (CA9), plasminogen activator inhibitor 1 (PAI1, also known as SERPINE), osteopontin and lysyl oxidase. Combinations of markers might prove to be better predictors of clinical outcome than any single marker153.
Oxygen electrodes and optical probes
Oxygen can be measured in any aqueous media using polarography. In principle, two electrodes are placed into the medium and a polarizing voltage of - 0.7 volts is applied across them. This voltage corresponds to the binding energy of outer shell electrons of oxygen. The electrons are captured by the cathode and the current generated is linearly proportional to oxygen concentration. In practice, the cathode is embedded into a needle that can be introduced into tissues and the anode is placed on the body surface. This technique has been used extensively in preclinical and clinical studies; the presence of hypoxia is an independent predictive factor for poor prognosis in many different tumour types154. Optical probes have also been developed: these are implanted into tissues and contain a fluorochrome that emits fluorescent light with a certain decay rate when illuminated. The rate of fluorescent light decay is proportional to the oxygen concentration in the region of measurement. These probes yield data similar to that of the oxygen electrode6.
Humans have no organs that detect oxygen deficiency. That is why people pass out and die if they get into an oxygen deficient atmosphere without warning equipment and help available from outside.
a machine used by clinics that they put on your fingers to tell what the blood to oxygen ratio is
No.
hypoxia. I believe
B I U S x x 123
Effector organ is a part of the body that responds to a stimulus and a stimulus is a change in the environment that is detected by a receptor. And is a receptor is a nerve cell that detects a stimulus.
The lungs absorbs oxygen into the blood
sense organ
Sense Organs
The nervous system.
Heat pit
the liver
Patients with granulocytopenia (deficiency of white blood cells) are particularly at risk for deep organ candidiasis.
No.
Hypoperfusion!
The lungs are the organ that gets oxygen into the blood.
ear is the organ that detects sounds. eyes is organ that allowed you to see thing.
Lack of oxygen is called Hypoxia
A lack of the ability of the body to carry oxygen may be due to a deficiency in