scholarly journals The Circulatory Response to Acute Hypoxia in Octopus

1983 ◽  
Vol 104 (1) ◽  
pp. 59-71 ◽  
Author(s):  
M.J. WELLS ◽  
J. WELLS

Octopus vulgaris can regulate its oxygen uptake in a closed respirometer down to a Poo2 of less than 70 mmHg. As the tankwater Poo2 falls the hearts slow down. Pulse amplitudes and mean pressures fall in the afferent branchial vessels and in the dorsal aorta. Despite behavioural changes - expansion of the interbrachial web and extension of the arms - that might imply this, the proportion of the total oxygen uptake attributable to cutaneous respiration (less than 13%) does not alter as the external Poo2 falls. The response of the hearts to a low Poo2 is not affected by severing the nerve supply from the central nervous system, or by removal of the heart ganglia. It is evidently determined by oxygen lack and not by the accumulation of CO2 or other metabolites, since the same effects are achieved by placing the animals in water where the Poo2 has been reduced by boiling. The conclusion that regulation does not depend upon circulatory responses to hypoxia is considered in the light of recent work on the changes in blood oxygen affinity associated with acute hypoxia in cephalopods.

1982 ◽  
Vol 48 (1) ◽  
pp. 89-105 ◽  
Author(s):  
Lee R.G. Snyder ◽  
Stephen Born ◽  
Andrew J. Lechner

1989 ◽  
Vol 39 (6) ◽  
pp. 833-846 ◽  
Author(s):  
Satoshi SHIMIZU ◽  
Susumu SAKATA ◽  
Yasunori ENOKI ◽  
Yoshimi OHGA ◽  
Izumi OKI ◽  
...  

Blood ◽  
1985 ◽  
Vol 66 (5) ◽  
pp. 1208-1214 ◽  
Author(s):  
JT Prchal ◽  
WM Crist ◽  
E Goldwasser ◽  
G Perrine ◽  
JF Prchal

Two families with polycythemia inherited as an autosomal dominant trait are described. Serial hemoglobin determinations in multiple family members and RBC volume measurements in selected affected subjects documented their polycythemia. Measurements of arterial p02s, p50s, and blood oxygen affinity were normal in all affected individuals from each family who were tested. Erythropoietin (EPO) levels were low in affected individuals from family 1 and normal in affected members of family 2. Stimulation of in vitro CFU-E colony growth by low levels of EPO was significantly increased in subjects from family 1, but normal in those affected from family 2. We conclude that although the inheritance pattern for the polycythemia in both of these families appeared to be the same, the biologic defect leading to the disorder in each of these unique families was different. The precise mechanism of the increased EPO sensitivity noted in affected subjects from family 1 awaits elucidation.


1978 ◽  
Vol 33 (3) ◽  
pp. 263-270 ◽  
Author(s):  
Michael A. Krall ◽  
James D. Bristow ◽  
J. Eugene Welch ◽  
James Metcalfe

1980 ◽  
Vol 238 (1) ◽  
pp. H73-H79 ◽  
Author(s):  
P. A. Mueggler ◽  
G. Jones ◽  
J. S. Peterson ◽  
J. M. Bissonnette ◽  
R. D. Koler ◽  
...  

A rightward shift in the blood oxygen dissociation curve occurs during the 1st mo of canine life. A detailed peptide analysis indicated that dogs do not have a separate fetal hemoglobin. Other erythrocyte components such as ATP, K+, Na+, and H+ were excluded as significant mediators of the postnatal oxygen affinity change. Erythrocyte 2,3-DPG levels essentially zero in fetal dogs, increased rapidly during the 1st mo of canine life. There was a significant correlation between this postnatal 2,3-DPG increase and the postnatal decrease in blood oxygen affinity. Dialyzed hemolysates of fetal or adult canine blood have the same intrinsic oxygen affinity and the same response to normal adult levels of 2,3-DPG. Furthermore, the magnitude and direction of this 2,3-DPG-induced decrease in oxygen affinity in vitro are comparable to the in vivo postnatal change in oxygen affinity.


1996 ◽  
Vol 115 (2) ◽  
pp. 111-115 ◽  
Author(s):  
Fernando Moraga ◽  
Carlos Monge ◽  
Raquel Riquelme ◽  
Aníbal J. Llanos

Blood ◽  
1972 ◽  
Vol 39 (3) ◽  
pp. 398-406 ◽  
Author(s):  
Frank G. de Furia ◽  
Denis R. Miller

Abstract Oxygen affinity studies in a splenectomized patient with sporadically occurring Hb Köln disease revealed high whole blood oxygen affinity (P50 O2 17.6 mm Hg) with increased 2, 3-diphosphoglycerate (DPG), low ATP, and normal RBC ΔpH. Isolated electrophoretically slow migrating Hb Köln had a high oxygen affinity, decreased Hill’s number, and normal DPG reactivity. Functional evidence for hybrid tetramers with normal mobility is presented. Partial deoxygenation may play a role in the denaturation of the Hb Köln molecule and thus account for a higher oxygen affinity (low P50 O2), measured by the mixing technique, than the actual values for P50 that exist in vivo. Increased oxygen affinity and decreased P50 O2 would result in increased erythropoiesis and account for a well-compensated hemolytic process in this patient with a normal red cell mass and normal values of hemoglobin.


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