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Main Authors: Yuri Sakai Ishizaki, Masao Kikuchi, Koichi Kaikita, Shouichi Fujimoto
Format: Artículo Open Access
Published: Wiley 2024
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Online Access:https://physoc.onlinelibrary.wiley.com/doi/10.14814/phy2.70121
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author Yuri Sakai Ishizaki
Masao Kikuchi
Koichi Kaikita
Shouichi Fujimoto
author_facet Yuri Sakai Ishizaki
Masao Kikuchi
Koichi Kaikita
Shouichi Fujimoto
Yuri Sakai Ishizaki
Masao Kikuchi
Koichi Kaikita
Shouichi Fujimoto
collection Wiley Open Access
contents Uninephrectomy and sodium‐glucose cotransporter 2 inhibitor administration delay the onset of hyperglycemia Yuri Sakai Ishizaki Masao Kikuchi Koichi Kaikita Shouichi Fujimoto Physiological Reports AbstractThe kidneys are essential for glucose homeostasis, as they perform gluconeogenesis, utilize glucose, and reabsorb glucose. Reabsorption is performed by SGLT2, which is responsible for about 90%. However, little is known about how renal glucose handling is altered in patients with chronic kidney disease (CKD). SGLT2 inhibitors have demonstrated efficacy in suppressing CKD progression in clinical trials, but their mechanisms are not fully understood. Therefore, this study aimed to evaluate how each uninephrectomy (UNx) and SGLT2 inhibitor affects blood glucose concentrations and SGLTs dynamics in rats with type 2 diabetes mellitus. Male rats were divided into four treatment groups: sham + placebo, sham + dapagliflozin, UNx + placebo, and UNx + dapagliflozin. There were few group differences in food intake or body weight, but blood glucose concentrations continued to rise in the sham + placebo, whereas this rise was delayed for several weeks in the UNx + placebo, and largely suppressed by dapagliflozin. SGLT2 mRNA expression was significantly lower in the UNx group, but SGLT1 mRNA expression did not significantly differ. Dapagliflozin did not alter SGLT1 or SGLT2 mRNA expression. In animal models of diabetes, renal glucose reabsorption appears likely to be a major contributor to the development of hyperglycemia. 10.14814/phy2.70121 http://creativecommons.org/licenses/by/4.0/
doi_str_mv 10.14814/phy2.70121
format Artículo Open Access
id wiley_oa_10_14814_phy2_70121
institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by/4.0/
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle Uninephrectomy and sodium‐glucose cotransporter 2 inhibitor administration delay the onset of hyperglycemia
Yuri Sakai Ishizaki
Masao Kikuchi
Koichi Kaikita
Shouichi Fujimoto
Physiological Reports
Uninephrectomy and sodium‐glucose cotransporter 2 inhibitor administration delay the onset of hyperglycemia Yuri Sakai Ishizaki Masao Kikuchi Koichi Kaikita Shouichi Fujimoto Physiological Reports AbstractThe kidneys are essential for glucose homeostasis, as they perform gluconeogenesis, utilize glucose, and reabsorb glucose. Reabsorption is performed by SGLT2, which is responsible for about 90%. However, little is known about how renal glucose handling is altered in patients with chronic kidney disease (CKD). SGLT2 inhibitors have demonstrated efficacy in suppressing CKD progression in clinical trials, but their mechanisms are not fully understood. Therefore, this study aimed to evaluate how each uninephrectomy (UNx) and SGLT2 inhibitor affects blood glucose concentrations and SGLTs dynamics in rats with type 2 diabetes mellitus. Male rats were divided into four treatment groups: sham + placebo, sham + dapagliflozin, UNx + placebo, and UNx + dapagliflozin. There were few group differences in food intake or body weight, but blood glucose concentrations continued to rise in the sham + placebo, whereas this rise was delayed for several weeks in the UNx + placebo, and largely suppressed by dapagliflozin. SGLT2 mRNA expression was significantly lower in the UNx group, but SGLT1 mRNA expression did not significantly differ. Dapagliflozin did not alter SGLT1 or SGLT2 mRNA expression. In animal models of diabetes, renal glucose reabsorption appears likely to be a major contributor to the development of hyperglycemia. 10.14814/phy2.70121 http://creativecommons.org/licenses/by/4.0/
title Uninephrectomy and sodium‐glucose cotransporter 2 inhibitor administration delay the onset of hyperglycemia
topic Physiological Reports
url https://physoc.onlinelibrary.wiley.com/doi/10.14814/phy2.70121