Intrinsic factor secretion in the gastric juice in diabetes mellitus

1973 ◽  
Vol 18 (2) ◽  
pp. 85-91 ◽  
Author(s):  
T. Kanaghinis ◽  
N. Iatromanolakis ◽  
D. Ikkos ◽  
P. Gatsou ◽  
C. Gardikas
Blood ◽  
1967 ◽  
Vol 30 (6) ◽  
pp. 777-784 ◽  
Author(s):  
SHULAMITH BAR-SHANY ◽  
VICTOR HERBERT

Abstract A newborn infant was found to have circulating maternal intrinsic factor antibody in the same titer as his 41 year old mother, who had had known pernicious anemia since age 33. At 11 days of age, no intrinsic factor was demonstrable in the infant’s gastric juice; whether this was related to the presence of serum IF antibody or was a variant of normal is not certain. At three months of age, the infant had B12 deficiency, manifested by a low serum B12 level and hypersegmentation of the nuclei of the neutrophilic leukocytes, but the gastric biopsy was normal, as was the intrinsic factor secretion. Maternal antibody to intrinsic factor was no longer present. These findings support the concepts that: (1) Intrinsic factor antibody may accelerate the development of B12 deficiency; (2) The antibody may not, of itself, produce any permanent gastric damage.


1977 ◽  
Vol 64 (11) ◽  
pp. 795-797 ◽  
Author(s):  
D. D. Meikle ◽  
J. Bull ◽  
S. T. Callender ◽  
S. C. Truelove

Blood ◽  
1965 ◽  
Vol 25 (6) ◽  
pp. 875-884 ◽  
Author(s):  
CHESTER GOTTLIEB ◽  
KAM-SENG LAU ◽  
LOUIS R. WASSERMAN ◽  
VICTOR HERBERT

Abstract The principle of the dialysis assays for intrinsic factor (IF) and antibody to IF was integrated with the demonstration that protein-coated charcoal adsorbs only free and not bound B12, in a single rapid method for 4 separate assays: (1) assay of IF, (2) assay of gastric juice unsaturated B12 binding capacity, (3) assay of serum antibodies to IF and (4) assay of serum unsaturated B12 binding capacity. The method is sensitive, accurate, reproducible, and can easily be completed within an hour. The simplicity and ready availability of reagents and equipment lends itself to ready adoption in any clinical laboratory using radioisotopes. The charcoal particle is considered as a solid microsponge, and its coat of albumin, other protein, carbohydrate, or other large molecule as a molecular sieve surrounding the sponge. The whole constitutes a system of "instant dialysis," with a wide range of applications in the separation of large from small molecules.


Blood ◽  
1951 ◽  
Vol 6 (12) ◽  
pp. 1234-1239 ◽  
Author(s):  
SHEILA T. CALLENDER ◽  
L. G. LAJTHA

Abstract 1. Normal gastric juice (intrinsic factor) and vitamin B12 together form a thermolabile hemopoietic factor which ripens megaloblasts in vitro, both gastric juice and B12 alone being inactive. 2. The hemopoietic factor in normal serum which ripens megaloblasts in vitro also appears to be thermolabile, heating to 56 C. for 2 hours destroying some of its activity. 3. The relationship of these factors is discussed and an extra-gastric as well as a gastric source of intrinsic factor is postulated.


1982 ◽  
Vol 28 (8) ◽  
pp. 1794-1796 ◽  
Author(s):  
G Marcoullis ◽  
S P Rothenberg

Abstract The traditional radioimmunoassay for gastric intrinsic factor, in which this protein is measured on the basis of immunoreactivity rather than function, is of no value for identifying intrinsic factor that binds cobalamin but does not bind to the ileal receptor site, or for detecting animal intrinsic factor, which does not cross react with human intrinsic factor. Accordingly, we have applied a radioassay for the intrinsic factor receptor protein to measure the functional activity of intrinsic factor in gastric juice. The receptor protein reagent was partly purified from guniea pig ilea and its interaction with intrinsic factor--CN[57Co]-cobalamin was determined by precipitation with sodium sulfate at a final concentration of 150 g/L. Results of this assay were comparable with results obtained for intrinsic factor by radioimmunoassay. The receptor protein did not bind immunoreactive intrinsic factor that was functionally abnormal. This functional radioassay for intrinsic factor is not species specific and will be of value when specific antiserum to intrinsic factor is not available and when cobalamin malabsorption is to be evaluated in patients who are secreting normal amounts of immunoreactive intrinsic factor.


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