Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0038002 (
splenomegaly
)
9,873
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The time course of metabolic and physiological adjustment to moderate iron deficiency anemia (
MIDA
, 8 g Hb/dl) and to severe iron deficiency anemia (SIDA, 4 g Hb/dl) was studied in adult, male Sprague-Dawley rats at 3, 7, 14, 30, 60, 90, 150, and 360 days, respectively. Our previous studies using the same rats used in the present study indicated that bone marrow iron was absent and plasma iron was significantly lower (p less than 0.001) in
MIDA
and SIDA relative to control. The following results with
MIDA
and SIDA rats are all expressed relative to control values. Red cell 2,3-diphosphoglycerate ranged from 45 to 146% greater in
MIDA
over the 360-day period and was 130% greater in SIDA at 30 days. Exhaustive run time consistently averaged 64 +/- 3% (SEM) less in
MIDA
over the time course and was further lowered to 18% in SIDA at 30 days. Heart rates of
MIDA
were elevated (p less than 0.05) at 180 days but lower (p less than 0.001) at 360 days in response to exercise. Resting heart rates of
MIDA
were the same at 180 and 360 days. Heart rates of SIDA were elevated (p less than 0.05) at rest and during exercise at 30 days. Organ weight/body weight changes indicated cardiomegaly in
MIDA
from 90 to 150 days which reverted to normal at 360 days;
splenomegaly
in
MIDA
from 90 to 360 days; and kidney atrophy in
MIDA
at 60 and 90 days which reverted to normal thereafter; in SIDA cardiomegaly and
splenomegaly
were present at 30 days. These results indicate that the onset and magnitude of physiological and metabolic adjustments occur in proportion to the severity of the anemia, and despite compensatory adjustments in parameters related to work performance, a new stable, lowered level of work tolerance is reached.
...
PMID:Changes in work tolerance associated with metabolic and physiological adjustment to moderate and severe iron deficiency anemia. 629 71