Constriction of Human Umbilical Vein Under Aerobic and Anaerobic Conditions

1972 ◽  
Vol 50 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Xina Nair ◽  
Donald C. Dyer

In the presence of metabolic inhibitors, the responses to serotonin of helically cut strips of human umbilical vein in Krebs–Henseleit solution at 37 °C were recorded isotonically. The tissues contracted to serotonin in a 95% nitrogen – 5% carbon dioxide atmosphere and in the presence of sodium cyanide (NaCN, 10−3M) and 2,4-dinitrophenol (DNP, 10−3M). The results indicate that human umbilical vein is capable of responding quite well to serotonin at very low oxygen levels and in the presence of sodium cyanide. The average maximum contractions to serotonin in the presence of NaCN and in the 95% nitrogen – 5% carbon dioxide atmosphere were, respectively, 91% and 88% of control. The contractile responses to serotonin were quite inhibited in the presence of 2,4-dinitrophenol. The combination of NaCN plus DNP did not inhibit the contractions to serotonin over that inhibited by DNP alone.

1946 ◽  
Vol 24f (1) ◽  
pp. 1-11 ◽  
Author(s):  
G. A. Adams

Aeration by mechanical agitation of 15% wheat mash fermented by Aerobacillus polymyxa inhibited the formation of 2,3-butanediol and particularly of ethanol. Aeration of similar mashes by passage of finely dispersed air or oxygen at the rate of 333 ml. per minute per litre of mash increased the rate of formation and yield of 2,3-butanediol but inhibited ethanol formation. However, the over-all time required for the completion of fermentation was not shortened from the usual 72 to 96 hr. required for unaerated mashes. There was no evidence of a shift from fermentative to oxidative dissimilation. Under aerobic conditions, the final butanediol–ethanol ratio was approximately 3:1. Anaerobic conditions, as produced by the passage of nitrogen or hydrogen through the mash, increased the rate of formation of both butanediol and ethanol and shortened the fermentation time to about 48 hr. Under these conditions, the butanediol–ethanol ratio was reduced to about 1.3:1.0. Carbon dioxide gave a butanediol–ethanol ratio resembling that of anaerobic fermentation but did not reduce fermentation time.


Transfusion ◽  
2009 ◽  
Vol 49 (8) ◽  
pp. 1738-1746 ◽  
Author(s):  
Michel Jeanne ◽  
Milica Kovacevic-Filipovic ◽  
Milène Szyporta ◽  
Marija Vlaski ◽  
Francis Hermitte ◽  
...  

1969 ◽  
Vol 22 (4) ◽  
pp. 1061
Author(s):  
NG Nair ◽  
NH White ◽  
DM Griffin ◽  
Suzanne Blair§

The number of mitochondria apparently vary with the energy requirements of the cell (see Rouiller 1960). Although swelling and multiplication of mitochondria have been observed to occur in cells, a quantitative analysis of these changes has not been recorded. Matile and Bahr (1968) have recently provided electron micro-scopic evidence of the heterogeneity of density, mass, and volume of the mitochon-drial population in respiring baker's yeast. There are reports in the literature of the complete absence of mitochondria in yeast cells growing under anaerobic conditions (see Marchant and Smith 1968). Griffin and Nair (1968) demonstrated that the growth of Sclerotium rolfsii was inhibited by concentrations of oxygen below 4% and by concentrations of carbon dioxide above 0�03 %. It was, therefore, thought worthwhile to study the changes in mitochondria of this fungus when the cells are subjected to external stresses of low oxygen and high carbon dioxide levels.


1950 ◽  
Vol 27 (1) ◽  
pp. 73-95
Author(s):  
BARBARA M. WALSHE

1. The behaviour of final-instar larvae of Chironomus plumosus housed in U-shaped glass tubes was observed at various concentrations of dissolved oxygen and carbon dioxide. 2. Respiratory behaviour, consisting of intermittent irrigation of the tube, alternates with periods of filter-feeding or complete immobility. In well-aerated water about 50% of the time is occupied by respiratory behaviour, 35% by filter-feeding and the remainder by periods of rest. As the oxygen concentration in the water drops, progressively less time is occupied by filter-feeding and immobility and more by respiratory irrigation. Below 10% air saturation of the water larvae no longer feed. When placed in completely anaerobic conditions larvae at first irrigate intermittently but subsequently relapse into immobility. 3. During respiratory behaviour the amount of irrigation and the length of pauses between periods of irrigation change at different oxygen and carbon dioxide contents of the water in such a way as to suggest that the respiratory irrigation is controlled by internal pH changes in the larvae. 4. A spectroscopic examination of the haemoglobin in living larvae showed that the blood pigment holds an approximately 9-min. store of oxygen for the resting animal. In addition to this it acts in the transport of oxygen from the tube water to the larval tissues when the larva pauses between periods of irrigation. It thus decreases the amount of anaerobiosis to be endured during short periods of inactivity. Nevertheless, larvae without a functional haemoglobin (i.e. with carboxyhaemoglobin) still continue to pause during their respiratory behaviour, and the pauses are not strikingly curtailed in length. 5. At very low oxygen concentrations (7.5-9.0% air saturation), when the larva irrigates the tube almost unceasingly, the haemoglobin remains in a state of partial oxygenation, during which time it is functioning continuously in oxygen transport. At these oxygen concentrations larvae with carboxyhaemoglobin do not show respiratory activity but assume the immobility characteristic of anaerobic conditions. 6. Larvae with carboxyhaemoglobin tend to be less active than normal animals, except in well-aerated water, the decreased activity being largely due to a reduction in the amount of filter-feeding. Such larvae have not been observed to filter-feed at oxygen concentrations below 26% air saturation, whereas the limiting concentration for normal larvae is 10%. 7. After a prolonged period of anaerobiosis larvae show evidence of the repayment of an oxygen debt by prolonged irrigation of the tube when oxygen is once more available. A return to a normal irrigation rate is rapid and is usually followed by a period of filter-feeding The rate of recovery is proportional to the oxygen content of the incoming water, but normal larvae can recover even in water only 7 % air saturated. Larvae with carboxyhaemoglobin, on the other hand, show a considerably retarded rate of recovery from anaerobic conditions, and cannot recover in water less than 15% air saturated. 8. The main significance of haemoglobin in the life of a full-grown Chironomus larva would thus seem to be threefold: (a) haemoglobin enables the larva to maintain the active process of filter-feeding when relatively little oxygen is present; (b) it acts in oxygen transport at very low oxygen concentrations, thereby enabling continued respiratory irrigation; and (c) it greatly increases the rate of recovery from periods of oxygen lack, making such recovery possible even under adverse respiratory conditions.


1976 ◽  
Vol 54 (8) ◽  
pp. 724-733 ◽  
Author(s):  
E. Nieboer ◽  
K. J. Puckett ◽  
B. Grace

The uptake of nickel by U. muhlenbergii (Ach.)Tuck. has been investigated. The data suggest that the uptake is physicochemical in nature. Metabolic inhibitors caused no significant decrease in nickel uptake. Dead thalli accumulated the metal to a slightly greater extent than live thalli. Nickel uptake was similar under aerobic and anaerobic conditions. Uptake was pH dependent and increased with temperature. The development of a model for nickel uptake by U. muhlenbergii based on thermodynamically rigorous expressions is described in this paper.


1969 ◽  
Vol 22 (2) ◽  
pp. 279 ◽  
Author(s):  
LAT Ballard ◽  
AE Grant Lipp

When imbibed dormant subterranean clover seeds were exposed to low concentrations of oxygen for up to 6 days, and then transferred to either air or 100% oxygen atmospheres, germination was markedly increased above that of seeds held only in air. Stimulation of germination was similar whether the atmosphere of the second phase was air or 100% oxygen; it was maximal when that of the first phase contained no oxygen, and became insignificant above concentrations in the region of 5% oxygen. The additional germination was roughly proportional to the duration of exposure to low oxygen concentrations, and the effects of two separated exposures to low oxygen were additive. These effects could be produced only in those dormant samples whose seeds or embryos could also be made germinable by exposure to 2�5% carbon dioxide. At higher temperatures, anaerobic conditions were less effective in breaking dormancy, paralleling the reduced efficacy of carbon dioxide at these temperatures.


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