Abstract:The ability to eliminate any form of oxygen debt by transporting oxygen to organs and tissues, by dissolving it in body fluids, brings hyperbaric oxygenation to a new level of application in transplantology. The review discusses the pathophysiological aspects of hyperbaric oxygenation during ischemia and reinfusion, especially when used in transplantology, and also investigations on the use of hyperbaric oxygenation in model experiments and in clinical practice. Analysis of the efficacy of hyperbaric oxygenati… Show more
“…In a large number of studies, it was shown that oxygen persufflation has the ability to increase storage time of donor organs [14][15][16]. Hyperoxia facilitates the diffusion of oxygen into the cell, activates oxidative phosphorylation, increases the synthesis of high-energy compound and reduces lactose levels in cells [17]. The combined use of CO and O 2 has proven to be highly effective in prolonging the storage time of warm-blooded animal organs by four to six times when compared to traditional hypothermal preservation techniques using specialized solutions [18][19][20][21].…”
The maximum hypothermic storage time of amphibian oocytes is several hours, which is due to the peculiarities of the structure of the cell envelope. The authors of this paper have already demonstrated the possibility of increasing the storage period of unfertilized oocytes of the common frog (Rana temporaria) up to 5–7 days. The aim of the current study was to determine the possibility of using a 6.5 atm gaseous mixture of carbon monoxide and oxygen, for prolonged hypothermic preservation of unfertilized oocytes for 4 to 12 days. After four days, oocytes stored under CO+O2 conditions exhibited fertilization and hatching rates that were 1.6 and 2.2-fold higher than control, respectively. While no oocytes in the control group survived to day twelve, oocytes held under CO +O2 gas exhibited a 39±14% (38 out of 99 oocytes in total) fertilization rate, however only 1±2% (1/99) of those hatched. This approach is promising for the storage of genetic material from female amphibians, particularly in respect to managing and restoring endangered species, but may also be applicable to oocytes of other classes of vertebrates.
“…In a large number of studies, it was shown that oxygen persufflation has the ability to increase storage time of donor organs [14][15][16]. Hyperoxia facilitates the diffusion of oxygen into the cell, activates oxidative phosphorylation, increases the synthesis of high-energy compound and reduces lactose levels in cells [17]. The combined use of CO and O 2 has proven to be highly effective in prolonging the storage time of warm-blooded animal organs by four to six times when compared to traditional hypothermal preservation techniques using specialized solutions [18][19][20][21].…”
The maximum hypothermic storage time of amphibian oocytes is several hours, which is due to the peculiarities of the structure of the cell envelope. The authors of this paper have already demonstrated the possibility of increasing the storage period of unfertilized oocytes of the common frog (Rana temporaria) up to 5–7 days. The aim of the current study was to determine the possibility of using a 6.5 atm gaseous mixture of carbon monoxide and oxygen, for prolonged hypothermic preservation of unfertilized oocytes for 4 to 12 days. After four days, oocytes stored under CO+O2 conditions exhibited fertilization and hatching rates that were 1.6 and 2.2-fold higher than control, respectively. While no oocytes in the control group survived to day twelve, oocytes held under CO +O2 gas exhibited a 39±14% (38 out of 99 oocytes in total) fertilization rate, however only 1±2% (1/99) of those hatched. This approach is promising for the storage of genetic material from female amphibians, particularly in respect to managing and restoring endangered species, but may also be applicable to oocytes of other classes of vertebrates.
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