Oxygen transport by a modified haemoglobin solution (PPSFH) in a dog model of acute anaemia following hypovolaemia

1990 ◽  
Vol 16 (4) ◽  
pp. 237-241 ◽  
Author(s):  
D. Gilroy ◽  
W. Odling-Smee
2000 ◽  
Vol 42 (9) ◽  
pp. 195-201 ◽  
Author(s):  
P. Andreasen ◽  
P. B. Mortensen ◽  
A. Stubsgaard ◽  
B. Langdahl

The stabilisation of a sludge-mineral soil mixture and a method to evaluate the state of stabilisation were investigated. The organic matter and nitrogen content are reduced up to 50% during a stabilisation process of three months under Danish climatic conditions. The stabilisation was shown to be an aerobic process limited by oxygen transport within the mixture. The degree of stabilisation was evaluated by oxygen consumption in a water suspension and the results showed that a stable product was achieved when oxygen consumption was stable and in the level of natural occurring aerobic soils (0.1 mgO2/(g DS*hr). The study thereby demonstrates that a stability of a growth media can be controlled by the oxygen consumption method tested.


1972 ◽  
Vol 247 (18) ◽  
pp. 5959-5963
Author(s):  
Gerald L. Klippenstein ◽  
Dee A. Van Riper ◽  
Elizabeth A. Oosterom

1986 ◽  
Vol 71 (6) ◽  
pp. 749-753 ◽  
Author(s):  
J. E. Maddison ◽  
D. Yau ◽  
P. Stewart ◽  
G. C. Farrell

1. Cerebrospinal fluid (CSF) γ-aminobutyric acid (GABA) levels were measured in a dog model of spontaneous chronic portosystemic encephalopathy. 2. Dogs with congenital portacaval shunts (intra- or extra-hepatic) develop neurological features of abnormal psychomotor behaviour and depressed consciousness that are consistent with the symptoms of chronic portosystemic encephalopathy in humans. In the five dogs studied, plasma ammonia was elevated, as was CSF tryptophan, both usual biochemical abnormalities in portosystemic encephalopathy. 3. CSF levels of GABA in five dogs with portosystemic encephalopathy (100 ± 13 pmol/ml) were not significantly different from those in five control dogs (96 ± 14 pmol/ml). CSF levels of GABA were not altered after ammonia infusion. 4. If enhanced GABA-ergic neurotransmission, due to influx of gut-derived GABA into the brain, is responsible for the pathophysiology of chronic portosystemic encephalopathy in this model, it is not reflected by increased levels of GABA in CSF.


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