CHAPTER XX
THE INFLUENCE OF OXYGEN
ADMINISTRATION ON THE CONCENTRATION OF THE
BLOOD WHICH ACCOMPANIES THE DEVELOPMENT OF LUNG EDEMA a
The
enormous and rapid development of edema of the lungs which results from
severe gassing
of animals with the lung irritants used in warfare offers an unusual
opportunity for studying the
physiological effects accompanying this pathological condition. The
rapidity with which the
edema develops precludes the possibility of infection complicating the
symptoms observed, anti
the condition which may develop after exposure to high concentrations
of poisonous gas is so
severe that the correlated symptoms can hardly be overlooked.
Loss of
water from the blood is one of the most characteristic phenomena
accompanying the
development of edema of the lungs in animals gassed with lung
irritants. A concentration of the
blood becomes evident at about the time when the edema of the lungs can
be first demonstrated.
Thereafter the loss of water from the blood and the increase in
severity of the edema run roughly
parallel. The conclusion was made, therefore, that the two are
interrelated and that the pouring of
water into the lungs is the cause of the concentration of the blood.
Other
considerations, however, make it necessary to proceed with caution
before accepting this
hypothesis. During the acute period after gassing there develops a
deficiency of oxygen carried
by the blood. Probably due to the poor aeration of the blood in the
damaged lung the oxygen
content of arterial and venous blood may drop to levels much below
normal. The transport of
oxygen to the tissues may be still further reduced by the decreased
rate of blood flow, with the
probable result that the oxygenation of the tissues is seriously
interfered with.
Physiologists have shown that muscle tissue imbibes water when supplied
with insufficient
oxygen. Based on this observation, the hypothesis may be presented that
the concentration of the
blood is due not primarily to the development of lung edema but to the
imbibition of water from
the blood by the tissues which are not sufficiently oxygenated. To
throw some light on the
validity of this hypothesis the experiments reported below were carried
out.
Goats
were gassed with lethal concentrations of chloropicrin. As soon as
possible after gassing,
half of the animals were fitted with masks and given oxygen
continuously in known quantities
by means of a Haldane oxygen apparatus.b The other animals were used
as controls.
The
hemoglobin content was used as an index of the concentration of the
blood. Hemoglobin
determinations were made frequently, using blood obtained by pricking
an ear vein. Blood from
the heart punctures was also used. The Haldane method was used for the
hemoglobin
determinations.
a This chapter, which deals
with the experimental observations of Capt. D. W. Wilson, C. W. S.,
and Capt. S. Goldschmidt, C. W. S., made in the physiological
laboratories of the Royal
Engineers Experimental Station, Porton, England, is reprinted in full
from the American Journal
of Physiology. Baltimore, 1919, No. 1, 157-164.
b The Haldane oxygen
apparatus furnishes oxygen to a mask fitted with valves for incoming
and
outgoing air. When the mask is worn by the animal, breathing is easy
and the air in the mask
may be enriched by varying amounts of oxygen.
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When the
concentration of the blood was sufficiently marked in the animals to
which oxygen
was being administered, heart punctures were made and the percentage
saturation of the
hemoglobin of the bloods from the right and left hearts was determined
by means of Barcroft's
differential blood gas apparatus.c Some difficulty was experienced in obtaining blood from
the hearts of animals in which the lungs were large and edematous, but
the sample was
considered satisfactory when it was obtained quickly and with little
struggling on the part of the
animal.
The
following protocols give the results obtained in this series of
experiments:
CHART
c We are indebted to Mr.
Barcroft, Captain Dunn, and Captain Peters for these data.
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CHART
Curves showing the concentration of the blood are
reproduced in Charts XXIX, XXX, XXXI. In
the charts, the percentage variations from the normal are plotted to
make all of the curves
directly comparable.
The
maximum concentrations observed in the control animals varied from 30
percent to 60
percent above normal (average 43 percent), while in the animals
receiving oxygen the variation
was from 28 percent to 75 percent above normal (average 48 percent). It
is apparent that, on the
whole, the blood of animals which received oxygen concentrated as
rapidly and to as great an
extent as that of the control animals.
In
order to demonstrate the efficiency of the oxygen administration,
samples of blood were taken
from both sides of the heart at suitable intervals and analyzed for
oxygen. In most of the
experiments the venous and arterial blood samples were obtained from
the heart without
difficulty and contained hemoglobin which was normally saturated with
oxygen. With the
increased concentration of the hemoglobin the oxygen content of the
blood was even above
normal.
Occasionally
the blood was obtained only after considerable struggling on the part
of the animal,
so that the reduced oxygen content of such bloods was to be expected.
These observations are
reported here merely to make the experimental record complete, as
obviously the low oxygen
content of such bloods is without bearing on the present problem.
These
experiments demonstrated that, by breathing oxygen-rich atmospheres,
oxygen could be
absorbed through the damaged and edematous lungs in quantities
sufficient to maintain a
practically normal level of oxygen in the arterial blood. The high
saturation of the hemoglobin of
venous blood with oxygen
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CHART XXIX- Changes in
hemoglobin of the blood after gassing with chloropicrin 1/8500 for
twenty-five minutes. Solid line: Animals receiving oxygen. Broken line:
Control animals
CHART XXX.- Changes in
hemoglobin of the blood after gaesing with chloropicrin 1/8500 for
thirty minutes. Solid line: Animal receiving extra oxygen. Broken line:
Control animal
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would seem to prove that
the blood flow was sufficiently rapid to normally oxygenate the
tissues. Nevertheless, in spite of the normal oxygenation of the
tissues in the animals receiving
oxygen, the blood concentrated as rapidly and to as great an extent as
in the control animals. The
conclusion therefore seems justifiable that the lack of oxygen in the
tissues and consequent
imbibition of water is not an important factor in causing the
concentration of the blood in
animals developing edema after being gassed with lung irritants.
An
indication of the severity of the lung edema was obtained by comparing
the weight of the
lung to the weight of the heart at autopsy. The high lung to heart
ratios obtained in practically all
of the animals studied show that a severe grade of edema had already
developed. The extent of
the edema as indicated by this method was as great in the animals
receiving oxygen as in the
CHART XXXI.- Changes in
hemoglobin of the blood after gassing with chloropicrin l/S54O for
twenty-five minutes. Solid line: Animals receiving extra oxygen. Broken
line: Control animals
controls. Although the data
are necessarily few, it is apparent that the efficient oxygenation of
the lung tissue in the animals receiving oxygen failed to diminish the
tendency for the
development of the edema of the lungs.
With
the enormous accumulation of fluid in the edematous lungs and the loss
of water from the
blood running roughly parallel, it is a tempting study to estimate even
in a rough way the
possible water interchange. An attempt has been made with data which
are more or less
incomplete and with calculations involving gross errors but the
relations are so striking that
they are presented in Table 94. In this table are recorded data and
calculations from animals in
which the hemoglobin was not determined immediately before death but is
estimated from the
curve obtained from the various determinations. These estimated values
are quite similar to
average values obtained at death on other animals.
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TABLE 94.- Comparison of
calculated amounts of fluid lost from blood and extra fluid in the
lungs of gassed animals
Examining
the last two columns of the table it is evident that in only one
instance the amount of
extra fluid in the lung was less than the calculated loss of fluid from
the blood. In some
instances the extra fluid in the lung was much greater than that lost
by the blood. Little or no
water was drunk by goats in this condition and the volume of urine
excreted was small, so that
the external factors did not confuse the picture. Even with the
relatively large errors of
calculation involved, the conclusion seems justified that the loss of
fluid by the blood could be
accounted for by the excess of liquid in the edematous lung.
The
evidence suggests that the muscles, etc., do not imbibe water and cause
the concentration of
the blood. In fact it would appear that water may be drawn from some
tissues to make up part of
the volume of liquid in the lung. One is thus finally led back to the
original point of view that the
development of the edema of the lungs and the concentration of the
blood are interrelated, and
are the important factors in the pathological condition studied. With
this fact established it is
justifiable to conclude that the development of the edema of the lungs
is the primary factor in the
condition and that the development of the edema causes the
concentration of the blood.
SUMMARY
The
continuous administration of oxygen to goats gassed with chloropicrin
did not inhibit the
concentration of the blood.
The
percentage saturation of the hemoglobin with oxygen was normal even
after a considerable
concentration of the blood had occurred.
The
concentration of the blood is not caused by the imbibition of water by
the tissues as the
result of oxygen want.
The
loss of water from the blood is therefore due to the development of the
edema of the lungs.
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