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The Effect of Glibenclamide on the Functional Activity of КATP Channels of Cerebral Arteries in Rats with Streptozotocin Diabetes Mellitus

https://doi.org/10.14341/DM13103

Abstract

BACKGROUND: In the treatment of diabetes mellitus (DM) for a persistent reduction in blood glucose levels it was widely used glibenclamide — a KATP channels blocker. However, its effects on cerebral circulation have been studied very little. A decrease in the functional activity of KATP channels due to their blocking by glibenclamide against the background of developed endothelial dysfunction may lead to impaired cerebral circulation (especially at the microcirculatory level) and promote remodeling of the vascular network.

AIM: To evaluate the effect of glibenclamide on the reactivity of cerebral arteries in rats with streptozotocin-induced diabetes mellitus (STZ-T2DM).

TASKS: 1. To study changes in the functional state of KATP channels of pial arteries in STZ-T2DM. 2. To evaluate the effect of glibenclamide on the participation of KATP channels in the formation of basal tone and endothelium-dependent dilatation of pial arteries.

MATERIALS AND METHODS: The study was performed on 54 male Sprague Dawley rats. Streptozotocin-induced diabetes mellitus (STZ-T2DM) was modeled by keeping animals on a high-fat diet and administering streptozocin (35 mg/kg). Using an installation for intravital study of pial vessels reactivity, 3 months from the beginning of the experiment, the diameter of the arteries was measured when the brain surface was irrigated with Krebs-Henseleit solution, acetylcholine, glibenclamide, pinacidil and acetylcholine against the background of the action of glibenclamide or pinacidil.

RESULTS: With modeling STZ-T2DM, rats developed glucose tolerance and insulin resistance. Compared to control animals, body weight was 1,3 times higher, the percentage of visceral fat was 3 times higher, and the blood glucose level was 3,2 times higher. It was shown that in STZ-T2DM the number of pial artery constrictions under the action of glibenclamide decreased by 1,3 — 1,9 times compared to intact rats. Glibenclamide did not block endothelium-dependent dilation.

CONCLUSION: In rats with streptozotocin diabetes, KATP channels take part in the formation of the basal tone of the pial arteries, but the contribution of these channels is reduced on average by 1.5 times compared to healthy rats.

The use of glibenclamide in STZ-T2DM does not affect endothelium-dependent dilatation of cerebral arteries.

About the Authors

I. B. Sokolova
Pavlov Institute of Physiology, Russian Academy of Sciences
Russian Federation

Irina B. Sokolova - PhD in Biology.

36 Bykova str., 188680 Pavlovo village, Leningrad Region


Competing Interests:

none



G. I. Lobov
Pavlov Institute of Physiology, Russian Academy of Sciences
Russian Federation

Gennadii I. Lobov - MD, PhD, Professor.

St. Petersburg


Competing Interests:

none



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Supplementary files

1. Figure 1. Dynamics of weight change in experimental rats and blood glucose levels.
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2. Figure 2. Graphs of experimental rats tested for glucose tolerance using an oral glucose tolerance test (OGTT) and for insulin resistance using an insulin tolerance test (ITT).
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3. Figure 3. Original images of the pial microvascular network of the cerebral cortex in experimental animals.
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4. Figure 4. Comparison of the number of pial arteries that responded with dilation to acetylcholine stimulation and acetylcholine stimulation with glibenclamide blockade in pial arteries with a diameter of 40–60 µm and less than 20 µm.
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5. Figure 5. Comparison of the number of pial arteries that responded with dilation to pinacidil stimulation and acetylcholine stimulation with pinacidil activation in pial arteries with a diameter of 40–60 µm and less than 20 µm.
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Type Исследовательские инструменты
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Review

For citations:


Sokolova I.B., Lobov G.I. The Effect of Glibenclamide on the Functional Activity of КATP Channels of Cerebral Arteries in Rats with Streptozotocin Diabetes Mellitus. Diabetes mellitus. 2024;27(4):304-312. (In Russ.) https://doi.org/10.14341/DM13103

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ISSN 2072-0351 (Print)
ISSN 2072-0378 (Online)