INTRACEREBRAL ALLOTRANSPLANTATION OF PURIFIED PANCREATIC ENDOCRINE CELLS AND PANCREATIC ISLETS IN DIABETIC RATS

1984 ◽  
Vol 38 (2) ◽  
pp. 107-110 ◽  
Author(s):  
WAH JUN TZE ◽  
JOSEPH TAI
2007 ◽  
Vol 67 (4) ◽  
pp. 735-740 ◽  
Author(s):  
AA Nascimento ◽  
A Sales ◽  
TRD Cardoso ◽  
NL Pinheiro ◽  
RMM Mendes

In the present study, we investigated types of pancreatic endocrine cells and its respective peptides in the Brazilian sparrow species using immunocytochemistry. The use of polyclonal specific antisera for somatostatin, glucagon, avian pancreatic polypeptide (APP), YY polypeptide (PYY) and insulin, revealed a diversified distribution in the pancreas. All these types of immunoreactive cells were observed in the pancreas with different amounts. Insulin- Immunoreactive cells to (B cells) were most numerous, preferably occupying the central place in the pancreatic islets. Somatostatin, PPA, PYY and glucagon immunoreactive cells occurred in a lower frequency in the periphery of pancreatic islets.


2020 ◽  
Vol 4 (6) ◽  
pp. 329-333
Author(s):  
T.P. Tuchina ◽  
◽  
K.P. Skotnikova ◽  
A.A. Vtorushina ◽  
O.V. Rogoza ◽  
...  

Aim: to study the morphology of pancreatic islet cells in rats aged more than 1 year with experimental type 2 diabetes (T2D) that receive sulphonylureas for a long time.Patients and Methods: albino laboratory rats aged more than 1 year (equal to 40 years in humans) were enrolled in this experimental study. Streptozotocin and nicotinamide were administered to induce T2D (streptozotocin-nicotinamide-induced diabetic rats). The animals were divided into four groups, i.e., healthy controls, T2D with no treatment, T2D treated with glibenclamide, and T2D treated with gliclazide. After the experimental study, immunohistochemistry with the antibodies against insulin, glucagon, and Ki-67 was performed. Morphometric analysis was performed using microphotographs. Insulin-, glucagon- and Ki-67-positive cells in islets were calculated.Results: by the 24th week of the study, the ratio of the total volume of α-cells to islet area in rats receiving glibenclamide was similar compared to diabetic rats receiving no treatment (p=0.75). Meanwhile, the significant reduction in the number of α-cells was reported in rats receiving gliclazide compared to diabetic rats receiving no treatment (p=0.000004). Moreover, the number of α-cells was equal to healthy controls. The total volume of β-cells remained unchanged in rats receiving glibenclamide or gliclazide as compared with diabetic rats with no treatment.Conclusion: our findings demonstrate that older animals (>1 year of age) are characterized by the changes in the ratio of α- and β-cells that are similar to the adults with T2D, i.e., the reduction in the percentage of β-cells and the increase in the percentage of α-cells. Long-term treatment with sulphonylureas does not result in the additional changes in the number and total volume of β-cells (rats receiving sulphonylureas for 24 weeks are similar to T2D rats with no treatment in terms of the volume of β-cells). However, 24-week treatment with gliclazide results in the normalization of the total volume of α-cells, and their number is comparable to healthy controls.KEYWORDS: sulphonylureas, α-cells, β-cells, pancreas, type 2 diabetes. FOR CITATION: Tuchina T.P., Skotnikova K.P., Vtorushina A.A. et al. Morphology of pancreatic endocrine cells in rats with type 2 diabetes after the long-term treatment with sulphonylureas. Russian Medical Inquiry. 2020;4(6):329–333. DOI: 10.32364/2587-6821-2020-4-6-329-333.


1996 ◽  
Vol 31 (1-3) ◽  
pp. 57-62 ◽  
Author(s):  
Qiang Fu ◽  
Masashi Honda ◽  
Hisako Ohgawara ◽  
Noriko Igarashi ◽  
Chisato Toyada ◽  
...  

1997 ◽  
Vol 153 (1) ◽  
pp. 73-80 ◽  
Author(s):  
M Bendayan ◽  
I-S Park

Abstract The existence of extrapancreatic islets in the duodenal mucosa of the adult rat has been established by morphological studies and the development of these islets has been followed from the early embryonic stage to neonatal and adult life. Like the pancreatic islets, glucagon cells were the first to appear at day 12 of gestation. However, in contrast to the pancreatic islets, insulin was not detected in the extrapancreatic islets until birth. At this stage, the different endocrine cells assume their classical topography, insulin cells being surrounded by non-insulin endocrine cells. In addition, the behaviour of these extrapancreatic islets in diabetic conditions was evaluated on streptozotocin-induced diabetic rats as well as on spontaneous BB Wistar diabetic rats. In both conditions, the extrapancreatic islets were found in the duodenal mucosa but were mainly composed of glucagon cells, the insulin cells having disappeared. These results demonstrate that the extrapancreatic islets are a common normal feature of the rat duodenal mucosa. They appear during fetal development, are present in different strains of rats and behave similarly to the pancreatic islets under spontaneous or chemically induced diabetic conditions. Although their exact role remains to be established, they probably react to local hyperglycaemic environment due to intestinal absorption. Journal of Endocrinology (1997) 153, 73–80


1986 ◽  
Vol 41 (4) ◽  
pp. 531-533 ◽  
Author(s):  
PAUL F. GORES ◽  
JAIME MAYORAL ◽  
M. JANE FIELD ◽  
DAVID R. R. SUTHERLAND

Diabetes ◽  
1994 ◽  
Vol 43 (11) ◽  
pp. 1345-1352 ◽  
Author(s):  
A. Gardemann ◽  
K. Jungermann ◽  
V. Grosse ◽  
L. Cossel ◽  
F. Wohlrab ◽  
...  

Development ◽  
1984 ◽  
Vol 82 (1) ◽  
pp. 131-145
Author(s):  
B. B. Rawdon ◽  
Beverley Kramer ◽  
Ann Andrew

The aim of this experiment was to find out whether or not, at early stages of development, progenitors of the various types of gut endocrine cells are localized to one or more specific regions of the gastrointestinal tract. Transverse strips of blastoderm two to four somites in length were excised between the levels of somites 5 and 27 in chick embryos at 5- to 24-somite stages and were cultured as chorioallantoic grafts. The distribution of endocrine cells in the grafts revealed confined localization of progenitor cells only in the case of insulinimmunoreactive cells. Theprogenitors of cells with somatostatin-, pancreatic polypeptide-, glucagon-, secretin-, gastrin/CCK-, motilin-, neurotensin- and serotonin-like immunoreactivity were distributed along the length of the presumptive gut at the time of explantation; indeed, in many cases they were more widespread than are their differentiated progeny in normal gut of the same age. This finding indicates that conditions in grafts must differ from those that operate in the intact embryo. Also it may explain the occurrence of ectopic gut or pancreatic endocrine cells in tumours of the digestive tract.


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