CO2 venous blood
СО2 release is indissolubly related to the oxygen consumption and СО2
generation in organism. СО2 is generated in organism as a result of biochemical
transformations of glucose, amino acids, fats in the liver and blood under the
influence of enzymes. Since glucose is one of the main oxygen source for a
cell, its level is connected with СО2 generation and release in organism. Under
the influence of glucose oxydase, glucose is oxidized by air oxygen to gluconic
acid, and hydrogen peroxide in equimolecular quantities is formed. In this
relation, СО2 generation rate must be lower than СО2 release rate, and total
venous blood CO2 must be higher than total arterial blood CO2.
Too much CO2 in the blood can be a sign of many
conditions, including:
Too little CO2 in the blood may be a sign of:
The carbon dioxide journey (FIGURE 1a) begins in the mitochondrion of
tissue cells where it is produced. Due to the prevailing concentration gradient
carbon dioxide diffuses from mitochondria (where pCO2 is highest) across the
cytoplasm, out of the cell and into the capillary network.
FIGURE 1a: CO2 in tissues
A little of the CO2 arriving in blood from tissue cells remains
physically dissolved in blood plasma (see above) and an even smaller proportion
binds to NH2 (amino) terminal groups of plasma proteins, forming so called
carbamino compounds. Most however, diffuses down a concentration gradient into
red cells.
A little of this remains dissolved in the cytoplasm of the red cell and
some is loosely bound to amino terminal groups of reduced hemoglobin forming
carbamino-Hb. However most of the carbon dioxide arriving in red cells is
rapidly hydrated to carbonic acid by the red cell isoform of the enzyme
carbonic anhydrase. At physiological pH almost all (≈ 96 %) of this carbonic
acid dissociates to bicarbonate and hydrogen ions:
Equation 1:
The hydrogen ions are buffered by reduced hemoglobin and most of the
bicarbonate ions pass from the red cell to plasma in exchange for chloride ions
(this so called ‘chloride shift’ maintains electrochemical neutrality). It is
clear from the above that most carbon dioxide is transported as bicarbonate
(predominantly in blood plasma), but there are in total four modes of CO2
transport [1,2]:
90 % is transported as bicarbonate in plasma (65 %) and red cells (25 %)
5 % is transported physically dissolved in plasma and red cell cytoplasm
5 % is transported loosely bound to hemoglobin in red cells and < 1 %
to proteins in plasma - so called carbamino compounds
< 0.1 % is transported as carbonic acid
Total carbon dioxide blood content is the sum of these four components.
Within the microvasculature of the lungs (FIGURE 1b) the partial
pressure gradient across the alveolar membrane determines that dissolved CO2
passes from blood to alveoli. This loss of carbon dioxide from blood favors
reversal of the red cell reactions described above.
Thus bicarbonate passes from plasma to red cell, buffering hydrogen ions
released from hemoglobin, as it is oxygenated. Reversal of the carbonic
anhydrase reaction, results in production of CO2 that diffuses from red cells
to plasma and onwards to alveoli.
Mixed venous blood arriving at the lungs has a total CO2 content of
approximately 23.5 mmol/L (or 52 mL/dL) whereas arterial blood leaving the
lungs has a total CO2 content of 21.5 mmol/L (48 mL/dL).
This arterio-venous difference (2 mmol/L or 4 mL/dL) represents the
amount of CO2 added to blood from tissue cells and lost from blood as it passes
through the pulmonary microvasculature, to be eventually excreted from the body
in expired air.
FIGURE 1b: CO2 in lungs
https://medlineplus.gov/lab-tests/carbon-dioxide-co2-in-blood/
https://www.nps.org.au/assets/AP/pdf/The-interpretation-of-arterial-blood-gases.pdf
https://acutecaretesting.org/en/articles/parameters-that-reflect-the-carbon-dioxide-content-of-blood
Published on 6 May 2024