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Cited by 30Diabetes Treatment and ManagementPancreatic function and diabetesNatural Antidiabetic Agents Studies

The DOI matches its Crossref record; 37 of the 38 references it cites were found in a registry or an index.

Effects of miglitol, an α-glucosidase inhibitor, on glycaemic status and histopathological changes in islets in non-obese, non-insulin-dependent diabetic Goto-Kakizaki rats

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Abstract

Miglitol, a 1-deoxynojirimycin derivative, is an α-glucosidase inhibitor. In the present study, the effects of acute (single-dose) and chronic (8-week) oral administration of miglitol in Goto-Kakizaki (GK) rats, an animal model of type 2 diabetes, were investigated. Dose-dependent decreases in incremental blood glucose concentrations integrated over a period of 2 h (ΔAUC 0–2 h) for values of blood glucose after sucrose-loading in miglitol-treated GK rats were observed following an acute oral administration of miglitol (1, 3 or 10 mg/kg body weight). At 10 mg/kg, the ΔAUC 0–2 h of blood glucose was decreased by 45 % compared with the control group. Following the oral administration of miglitol in a dietary mixture (10 mg, 20 mg or 40 mg miglitol/100 g control diet) for 8 weeks, the ratio of HbA 1c at 8 weeks compared with 0 weeks in GK rats treated with 40 mg miglitol/100 g control diet miglitol was significantly decreased compared with control GK rats without changes in body weight. In oral glucose tolerance testing, miglitol caused a slight decrease in the ΔAUC 0–2 h of plasma glucose concentration. In addition, miglitol treatment slightly inhibited the reduction in β-cell mass, and lessened the irregular contours and fibrosis of the islets in GK rats. These results indicate that miglitol ameliorates the hyperglycaemic state of GK rats and the impaired function of the pancreatic islets, as well as preventing the degeneration of islets in GK rats.

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Citations

Cites

Research works printed but not linked: 4

  1. Tsukamoto, 2001, Pharmacological properties of miglitol, an alpha-glucosidase inhibitor, in rats, Jpn Pharmacol Ther, 29, 623
  2. Odaka, 1994, Effect of AO-128 alone or in combination with sulfonylurea on fasting blood glucose and postprandial hyperglycemia in normal and diabetic rats, Jpn Pharmacol Ther, 22, 2665
  3. Horii, 1993, Valiolamine and its N-substituted derivatives, alpha-D-glucosidase inhibitors: from validamycins to voglibose (AO-128), an antidiabetic agent, J Takeda Res Lab, 52, 1
  4. 10.1002/(sici)1520-7560(199909/10)15:5<332::aid-dmrr55>3.0.co;2-l · DOI

Cited by

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Metadata

Authors
Goda, T., Suruga, K., Komori, A., Kuranuki, S., Mochizuki, K., Makita, Y., & Kumazawa, T.
Affiliations
  • Shizuoka University (JP)
  • Sanwa Kagaku Kenkyusho Co., Ltd. (Japan) (JP)
Corresponding author
Goda, Toshinao
Venue
British Journal of Nutrition
Published
2007-05-31
Volume
98
Issue
4
Pages
702-710
ISSN
  • 0007-1145 (ISSN-L)
  • 1475-2662
OpenAlex
W2020098163
Cited by
30
References
38
Citations by year
2025: 1 · 2024: 2 · 2022: 1 · 2021: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 3 · 2012: 2
FWCI
2.44
Type
journal article
Language
en
Open access
Locations
  • British Journal Of Nutrition (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pancreatic function and diabetes
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Natural Antidiabetic Agents Studies
Keywords
miglitol, alpha-glucosidase inhibitors, type 2 diabetes, Goto-Kakizaki rats, blood glucose, HbA1c, pancreatic islets, beta-cell mass, islet fibrosis, oral glucose tolerance, hyperglycemia, 1-deoxynojirimycin
MeSH terms
Animals, Blood Glucose, Diabetes Mellitus, Hypoglycemic Agents, Islets of Langerhans, Male, Random Allocation, Treatment Outcome, Rats, Wistar, 1-Deoxynojirimycin, Imino Pyranoses, Rats

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