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Abstract
Sufficient numbers of pancreatic islets transplanted into the splenic pulp of streptozotocin-induced
diabetic rats can result in complete reversal of hyperglycemia, glycosuria, and polyuria
while promoting weight gain. These changes are constant for at least 3 months. Animals
transplanted in this way, however, fail to exhibit a normal biphasic insulin response
during an intravenous glucose tolerance test. This lack of biphasic response is in
marked contrast to that observed in portal-vein-transplanted animals. Basal serum
insulin in intrasplenic-transplanted animals is twice that observed in normal animals
and portal-vein-transplanted animals which have received the same number of islet
isografts. Direct injection of islets into the splenic pulp does not insure that subsequently
all islets will remain in the splenic pulp, and, in fact, subsequent splenectomy suggests
that in some cases a majority of transplanted tissue lodges in other organs—most likely,
the liver.
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References
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Article info
Footnotes
☆Supported by grants from the Kroc Foundation and the National Institutes of Health (5R01-17188 and AM-18235).
☆☆Presented at the Thirty-fourth Annual Meeting of the Central Surgical Association, Buffalo, N. Y., March 3–5 1977.
Identification
Copyright
© 1977 Published by Elsevier Inc.