Morphological changes in the human endocrine pancreas induced by chronic excess of endogenous glucagon

1991 ◽  
Vol 60 (1) ◽  
pp. 199-206 ◽  
Author(s):  
Daniele Bani ◽  
Giancarlo Biliotti ◽  
Tatiana Bani Sacchi
1979 ◽  
Vol 80 (2) ◽  
pp. 175-179 ◽  
Author(s):  
F. A. VAN ASSCHE ◽  
L. AERTS ◽  
W. GEPTS

This present study has demonstrated that during normal pregnancy in the rat the number of β-cells is increased (hyperplasia) and the volume of the individual β-cells is increased (hypertrophy). During experimental diabetes, however, the endocrine pancreas has an impaired capacity to compensate during pregnancy. In the experimental diabetic pregnant rat the β-cells cannot replicate due to the unfavourable metabolic environment. This could reflect the complications caused by diabetes during human pregnancy.


2005 ◽  
Vol 34 (1) ◽  
pp. 42-47 ◽  
Author(s):  
J. Nagasao ◽  
K. Yoshioka ◽  
H. Amasaki ◽  
M. Tsujio ◽  
M. Ogawa ◽  
...  

1976 ◽  
Vol 83 (1) ◽  
pp. 133-150 ◽  
Author(s):  
Jørn Egeberg ◽  
Jørn Nerup ◽  
Ole Ortved Andersen ◽  
Gunnar Bendixen ◽  
Hans Kromann ◽  
...  

ABSTRACT The morphologic and metabolic effect of a single intracutaneous injection of homologous endocrine pancreas in Freund's complete adjuvant (CFA) was studied in 100 mice and compared with control groups which had been (1) immunized with murine insulin in CFA, (2) injected with CFA alone, or had (3) received no treatment. There were no differences between the control groups as regards the morphology of the pancreatic islets, and the glucose tolerance was normal. Mice immunized with islet homogenate exhibited morphological changes in the form of degranulation and cytoplasmic disintegration. These changes involved B-cells as well as A2-cells and were present from 7 to 18 days after the immunization. A significant reduction in glucose tolerance was observed 14 days after the immunization. Another characteristic finding in the islets from the immunized mice was the extravascular presence of mononuclear, agranular cells which on the basis of their morphological criteria appeared to represent lymphocytes.


1977 ◽  
Vol 73 (2) ◽  
pp. 339-NP ◽  
Author(s):  
L. AERTS ◽  
F. A. VAN ASSCHE

SUMMARY The endocrine pancreas of foetuses and newborn rats of experimental diabetic mothers showed morphological and ultrastructural changes. Islet hypertrophy and β cell hyperplasia were constantly present, but the β cells of foetuses of severely diabetic mothers were degranulated. The ultrastructural changes indicated hyperfunction in the β cells of foetuses of experimental diabetic mothers. The morphological changes mentioned were similar to those seen in human diabetic pregnancy.


2020 ◽  
Vol 9 (4) ◽  
pp. 299-308 ◽  
Author(s):  
Julia Modesto Vicente ◽  
Junia Carolina Santos-Silva ◽  
Caio Jordão Teixeira ◽  
Dailson Nogueira de Souza ◽  
Jean Franciesco Vettorazzi ◽  
...  

Purpose Observational studies show that longer breastfeeding periods reduce maternal risk of type 2 diabetes mellitus. However, it is currently unknown if the long-term benefits of breastfeeding for maternal glucose homeostasis are linked to changes in the endocrine pancreas. Methods We presently evaluated functional, morphological and molecular aspects of the endocrine pancreas of mice subjected to two sequential cycles of pregnancy and lactation (L21). Age-matched mice not allowed to breastfeed (L0) and virgin mice were used as controls. Results L21 mice exhibited increased tolerance and increased glucose-stimulated insulin secretion (GSIS) by isolated islets. Pancreatic islets of L21 mice did not present evident morphological changes to justify the increased GSIS. On the other hand, islets of L21 mice exhibited a reduction in Cavb3 and Kir6.2 expression with concordant increased intracellular Ca2+ levels after challenge with glucose. Conclusion Altogether, the present findings show the breastfeeding exerts long-term benefits for maternal endocrine pancreas by increasing intracellular Ca2+ levels and GSIS.


Author(s):  
Jelena Savici ◽  
Diana Brezovan ◽  
Florin Muselin

AbstractHexavalent chromium is known as strong oxidizing agent, enters the cells easily and generates reactive oxygen species. It was demonstrated that Cr VI is toxic for liver, kidney, skin, nervous system, female and male reproductive systems. However, chromium effects on pancreas are less studied.Aronia melanocarpa fruits are rich in phenolic constituents: anthocyanins, procyanidins and phenolic acids, which demonstrated to have anti-oxidative, anti-viral, anti-mutagenic, anti-cancer, anti-inflammatory activities.Considering the aforesaid the present study was carried out in idea to see if Cr VI induces structural changes in pancreas, given it’s property of inducing ROS formation in cells, and if aronia extract can play a protective role.The study was carried out on white Wistar rats divided in 5 groups and exposed as follows: C – control –distilled water, Cr group – potassium dichromate, hexavalent chromium compound, in distilled water, 75 ppm for three months; CrA group - 75 ppm Cr VI + extract of A. melanocarpa for three months; Cr2 group - 75 ppm Cr VI for three months followed by one month of distilled water; CrA2 group 75 ppm Cr VI for three months followed by one month of extract of A. melanocarpa. At the end of exposure period pancreas was collected and prepared for histological analysis.Hexavalent chromium administration induced morphological and functional changes in endocrine pancreas cells. Microscopic examination of histological slides from pancreas revealed the size and number reduction of Langerhans islets and presence of degenerative lesions. Experimental group that received Cr VI combined with aqueous extract of Aronia presented almost normal architecture of endocrine cells, even more vascular changes occurred too, probably responsible for repairing phenomena.


1968 ◽  
Vol 36 (1) ◽  
pp. 33-44 ◽  
Author(s):  
J. Gomez-Acebo ◽  
R. Parrilla ◽  
J. L. R-Candela

The cytological changes observed in the A and D cells of rabbit endocrine pancreas incubated in a medium containing 0.6 mg/ml or 3 mg/ml of glucose are described. These cells showed no changes in their fine structure nor any signs of degranulation. When the A cells were incubated in a medium without glucose, they released A granules and synthesized new hormone. The way in which A granules are eliminated is compared to that following insulinic hypoglycemia in the animal in vivo. In both cases, the mechanism of secretion involves margination, emiocytosis of the entire granule, and formation of microvilli, in contrast to previously reported observations (9). The D cells showed no alteration of their fine structure after incubation with different concentrations of glucose in the medium. Only very rarely could we observe morphological changes which were suggestive of emiocytosis of the entire D granule.


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