Histochemical Investigation of Influence of Diabetogenic Zinc Binding Chemicals In Vitro on Human Pancreatic Β-Cells and its Prevention

Authors

  • Gabit G. Meyramov Department of Biology, Buketov Karaganda University, 100028, Karaganda, Ka-zakhstan https://orcid.org/0000-0003-3281-9152
  • Vladimir I. Korchin Department of Pathology Hanty-Mansyisk State Medical Academy, Hanty-Mansyisk, Russia
  • Fatima S. Abikenova Department of Pathology, Non-Profit Joint – Stock Company “Karaganda Medical University”, 1000008, Karaganda, Kazakhstan https://orcid.org/0000-0001-6871-303X
  • Altynay S. Shaybek Department of Biology, Buketov Karaganda University, 100028, Karaganda, Kazakhstan
  • Aizhan G. Meyramova Department of Pharmacy, Bolashak Academy, 1000008, Karaganda, Kazakhstan
  • Gulnaz T. Kartbayeva Department of Biology, Buketov Karaganda University, 100028, Karaganda, Kazakhstan
  • Gulmira O. Zhuzbaeva Department of Biology, Buketov Karaganda University, 100028, Karaganda, Kazakhstan
  • Olga L. Kovalenko Department of Biology, Buketov Karaganda University, 100028, Karaganda, Kazakhstan

DOI:

https://doi.org/10.3889/oamjms.2022.8197

Keywords:

Pancreas, ß-cells, Zinc, Insulin, Diabetogenic chelators, Human fetal pancreas, Pancreatic is - lets

Abstract

BACKGROUND: Amount of zinc-ions is correspond to insulin content in cytoplasm of β-cells. Diabetogenic zinc binding chemicals (DZC) formed with zinc in β-cells chelat complex that result destruction and death of β-cells within 10–15 min in animals.

AIM: The aim of the study was to investigate using of specific histochemical methods the content of zinc and insulin in β-cells of pancreatic islets of human intact fetal pancreas tissue and under action of diabetogenic and non-diabetogenic zinc-binding substances diabetogenic zinc diethyldithiocarbamate (DZ and DDC).

METHODS: Pancreas from 8-week-old human embryos and adult rabbits were used. Fixed or frozen islets were used in vitro effect. Histochemical methods for insulin and zinc in β-cells were used.

RESULTS: Results showed that zinc in human β-cells is clearly revealed using of histochemical methods. In embryo pancreas, not integral islets were found as clusters of cells or even individual β-cells. Insulin content in ß-cells is for 7–20% lower and Zn2+ by 16–18% in compared with rabbits; Zinc in human ß-cells formed chelat complexes with 8PTSQ and DZ as Zn2+ –8PTSQ and Zn2+–DZ. Sodium DDC, a non-diabetogenic Zn2+ chelator, formed not toxic complexes with Zn2+ in fetal β-cells that protect cells of destruction caused by DZC as in animal’s pancreas.

CONCLUSION: (1) Intracellular reactive zinc contained in human fetal pancreatic ß-cells clearly revealed using of histochemical methods and also (2) demonstrated that DZC in human ß-cells result formation with zinc of chelat complexes. (3) As in animals, non-toxic chemical as DDC is able to block zinc in ß-cells that result prevention of its destruction caused by DZC.

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Published

2022-08-10

How to Cite

1.
Meyramov GG, Korchin VI, Abikenova FS, Shaybek AS, Meyramova AG, Kartbayeva GT, Zhuzbaeva GO, Kovalenko OL. Histochemical Investigation of Influence of Diabetogenic Zinc Binding Chemicals In Vitro on Human Pancreatic Β-Cells and its Prevention. Open Access Maced J Med Sci [Internet]. 2022 Aug. 10 [cited 2024 Nov. 21];10(A):1392-6. Available from: https://oamjms.eu/index.php/mjms/article/view/8197

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