Cited by 102Pancreatic function and diabetesDiabetes and associated disordersTransplantation: Methods and Outcomes

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IN VIVO EFFECT OF FK506 ON HUMAN PANCREATIC ISLETS

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Abstract

The purpose of this study was to evaluate the in vivo effect of FK506 on human pancreatic islets. Twenty-five nude mice were made diabetic by one intravenous injection of streptozotocin. Approximately 600 islets were administered in the renal subcapsular space 3-5 days following streptozotocin administration. One week after transplantation, the mice were divided in four groups. In group 1, the animals received 1 injection of 0.5 ml of diluent i.p. daily for one week. In groups 2, 3, and 4 the treatments were daily i.p. injection of 0.3, 1, and 3 mg/kg FK506, respectively. After treatment, the functional integrity of the transplanted human islets was tested by measuring the plasma glucose and human C-peptide response to intraperitoneal glucose injection in groups 1 and 4. IPGTT alone was assessed in groups 2 and 3. The results indicate that i.p. administration of FK506 for one week at a dose 0.3 mg/kg/day did not result in any significant alteration of glucose disappearance and C-peptide response to IPGTT. Higher doses of FK506 produced a significant delay in glucose disappearance in groups 3 and 4, and a significant inhibition of glucose-mediated C-peptide response in group 4.

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Crossref · 10.1097/00007890-199109000-00026

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  • Human islets transplanted into diabetic mice control plasma glucose at the normal non-fasting glucose concentration of humans, suggesting intrinsic β-cell differences.

    “It probably reflects differences in intrinsic β-cell properties as when human islets are transplanted into diabetic mice they control plasma glucose at the normal non-fasting glucose concentration of humans (551).”

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Metadata

Authors
RICORDI, C., ZENG, Y., ALEJANDRO, R., TZAKIS, A., VENKATARAMANAN, R., FUNG, J., BEREITER, D., MINTZ, D. H., & STARZL, T. E.
Affiliations
  • University of Pittsburgh (US)
  • University of Miami (US)
Venue
Transplantation
Published
1991-09
Volume
52
Issue
3
Pages
519-521
ISSN
0041-1337 (ISSN-L)
OpenAlex
W2151777294
Cited by
102
References
0
Citations by year
2021: 1 · 2020: 2 · 2019: 1 · 2018: 1 · 2017: 2 · 2016: 2 · 2015: 2 · 2014: 2 · 2012: 6
FWCI
6.06
Type
journal article
Language
en
Open access
Locations
  • Transplantation (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • D-Scholarship@Pitt (University of Pittsburgh) (acceptedVersion)
Funders
  • U.S. Public Health Service (29961)
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01DK029961)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
  • Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
Keywords
FK506, tacrolimus, human pancreatic islets, islet transplantation, immunosuppression, C-peptide response, glucose tolerance, streptozotocin-induced diabetes, islet graft function, dose-dependent effects
MeSH terms
Insulin Secretion, Anti-Bacterial Agents, Blood Glucose, C-Peptide, Humans, Immunosuppressive Agents, Insulin, Islets of Langerhans, Species Specificity, Tacrolimus

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