Autor: |
Ju‐Hyun An, Han‐Sol Choi, Ji‐Soo Choi, Hyun‐Woo Lim, Wan Huh, Ye‐In Oh, Joon Seok Park, Jumi Han, Soo Lim, Chae‐Young Lim, Tae‐Hee Kim, Jae‐Bong Moon, Hwa‐Young Youn |
Jazyk: |
angličtina |
Rok vydání: |
2024 |
Předmět: |
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Zdroj: |
Veterinary Medicine and Science, Vol 10, Iss 3, Pp n/a-n/a (2024) |
Druh dokumentu: |
article |
ISSN: |
2053-1095 |
DOI: |
10.1002/vms3.1454 |
Popis: |
Abstract Background Sodium‐glucose cotransporter‐2 (SGLT2) inhibitors are a novel class of anti‐hyperglycaemic agents. Objective This study aimed to evaluate the safety and the adjuvant glycaemic control effect of an SGLT2 inhibitor, DWP16001, in diabetic dogs receiving insulin treatment. Methods Nineteen diabetic dogs receiving insulin treatment (NPH, porcine lente and glargine insulin) were divided into two groups according to dosing frequency: DWP TOD group (n = 10) and DWP SID group (n = 9). In the DWP TOD group, 0.025 mg/kg of DWP16001 was administered once every 3 days, whereas, in the DWP SID group, 0.025 mg/kg of DWP16001 was administered once a day. Food intake was maintained during the trial period. Hypoglycaemia, ketoacidosis or unexpected life‐threatening reactions were assessed as adverse effects before and after DWP16001 administration. We compared insulin requirement reduction and blood glucose level control between two groups. Results No specific adverse effects were observed during the clinical trial, and haematological parameter remained unchanged. Moreover, the fasting glucose levels and daily insulin dose in the DWP TOD group were lower than the pre‐administration values, but not significantly different for 8 weeks. Systolic blood pressure, fructosamine and insulin dose decreased significantly in the DWP SID group compared to the DWP TOD group at 8 weeks (p |
Databáze: |
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