1967
DOI: 10.2337/diab.16.2.83
|View full text |Cite
|
Sign up to set email alerts
|

Effect of Alloxan on the Mouse Pancreas during and after Recovery from Diabetes

Abstract: Temporary diabetes was produced in mice by the intravenous injection of alloxan, 75 mg. per kilogram of body weight. The beta cells were degranulated within 6 hrs., but changes in microcirculation did not occur until 24 hrs., and did not appear to play arole in initiating damage to the beta cells. The total number of islets was decreased markedly within one week, but cellular proliferation of ducts and islets began as early as two weeks as indicated by in vivo study and radioautography. Improvement in the diab… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
8
0
1

Year Published

1969
1969
2012
2012

Publication Types

Select...
7
3

Relationship

0
10

Authors

Journals

citations
Cited by 34 publications
(10 citation statements)
references
References 10 publications
0
8
0
1
Order By: Relevance
“…Replication of residual p-cells has been noted in a variety of experimental animal models in which p-cell mass has been depleted by the (3-cell toxins streptozotocin (STZ) or alloxan (28)(29)(30)(31)(32), or following sustained hyperglycemia induced by steroid (33). Data demonstrating islet neogenesis from ductal progenitors is, however, sparse in nontransgenic adult animals (28), but extensive in transgenic adult mice and STZadministered neonatal rats (34).…”
Section: Discussionmentioning
confidence: 99%
“…Replication of residual p-cells has been noted in a variety of experimental animal models in which p-cell mass has been depleted by the (3-cell toxins streptozotocin (STZ) or alloxan (28)(29)(30)(31)(32), or following sustained hyperglycemia induced by steroid (33). Data demonstrating islet neogenesis from ductal progenitors is, however, sparse in nontransgenic adult animals (28), but extensive in transgenic adult mice and STZadministered neonatal rats (34).…”
Section: Discussionmentioning
confidence: 99%
“…3) As has been shown by Bunnag, Warner and Bunnag (1967) and Rerup (1968) alloxan diabetic mice often recover from their diabetic condition after some time. The improvement in the diabetic state coinci-des with restoration of the islets; indeed 3 months after alloxan injection the number of islets had increased to more than 50% of the control level (Bunnag, Warner and Bunnag 1967). For this rea30n the alloxan diabetic mice in the present study were allowed to recover for about 8 weeks in order to ob-tain a colony of diabetic and subdiabetic animals with a significant number of functioning ß-cells.…”
Section: Discussionmentioning
confidence: 81%
“…Pancreatic endocrine cells are regenerated by transformation of acinar or ductular epithelial cells in alloxan-treated rats and mice (Bunnang et al 1967). In alloxan treated mice clamping of superior mesenteric artery causes selective damage and neogenesis of B-cells (Waguri et al 1997).…”
Section: Discussionmentioning
confidence: 99%