Modern glucose-lowering treatment effect on bone remodeling in experimental diabetes mellitus and surgical menopause

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM Diabetes Mellitus Pub Date : 2023-05-15 DOI:10.14341/dm12967
© Н.В. Тимкина, Н.Ю. Семенова, А.В. Симаненкова, В.А. Цинзерлинг, Т.Д. Власов, А.А. Байрамов, А.К. Хальзова, А.А. Шимшилашвили, В.А. Тимофеева, Т. Л. Каронова, Natalya V. Тimkina, N.Yu. Semenova, A. Simanenkova, V. Zinserling, Timur D. Vlasov, A. Bairamov, Aleksandra Khalzova, A. Shimshilashvili, Valeria А. Тimofeeva, T. Karonova
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Abstract

BACKGROUND: Diabetes mellitus (DM) is an independent risk factor for low-traumatic fractures. On the other hand, hypoglycemic drugs can have both positive and negative effects on bone remodeling.THE AIM: Тo investigate bone metabolism parameters during surgical menopause and experimental DM under the treatment with glucagon-like peptide receptor agonist type 1 (arGLP-1) liraglutide (LIRA) and sodium-glucose cotransporter type 2 inhibitor (iSGLT-2) canagliflozin (CANA).MATERIALS AND METHODS: Female Wistar rats have been subjected to bilateral ovariectomy at the beginning of the experiment. Diabetes mellitus (DM) was modelled using a high-fat diet and streptozotocin+nicotinamide. Four weeks after the following groups were formed: “OE+DM” (females after ovariectomy with DM and without any therapy, n=4) «OE+DM+CANA» (females after ovariectomy with DM under treatment with CANA, n=4), «OE+DM+LIRA» (females after ovariectomy with DM under treatment LIRA, n=5). The treatment or observation period were continuing for 8 weeks. Calcium, phosphorus and bone turnover markers (fibroblast growth factor-23 (FGF-23), osteocalcin, sclerostin, osteoprotegerin (OPG), nuclear factor-kappa-B receptor activator ligand (RANKL), were measured in the end of experiment. Bone histomorphometry was performed after euthanasia.RESULTS: Treatment with both CANA and LIRA did not significantly affect the phosphorus-calcium metabolism, sclerostin and osteocalcin concentrations. At the same time, the level of OPG was the highest in «OE+DM ‘’ group (9.1 [7.81; 10.045] pmol/l). The differences were significant compared with «OE+DM+CANA’’ (2, 33 [1.84; 5.84] pmol/l, p = 0.003) and «OE+DM+LIRA» (1.7 [1; 2] pmol/l, p = 0.003) groups. There were no differences in OPG levels between animals treated with different drugs. Similarly, the OPG/RANKL ratio was similarly reduced with both types of treatment. In “OE+DM+CANA’’ group the bone trabeculae number of   the femur epiphysis (p=0.042) were decreased in comparison to «OE+DM» group. LIRA did not change the histoarchitectonic parameters.CONCLUSION: Bone metabolism markers did not differ when using as canagliflozin as liraglutide. Besides, canagliflosin can lead to the activation of bone resorption, which is expressed in the femur epiphyseal trabeculae number decreasing.
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现代降糖治疗对实验性糖尿病及手术绝经期骨重塑的影响
背景:糖尿病(DM)是低创伤性骨折的独立危险因素。另一方面,降糖药物对骨重塑既有积极的影响,也有消极的影响。目的:Тo研究胰高血糖素样肽受体激动剂1型(arGLP-1)利拉脲肽(LIRA)和钠-葡萄糖共转运蛋白2型抑制剂(iSGLT-2)卡格列净(canagliflozin, CANA)治疗下手术绝经和实验性糖尿病期间的骨代谢参数。材料与方法:雌性Wistar大鼠在实验开始时进行双侧卵巢切除术。采用高脂肪饮食和链脲佐菌素+烟酰胺建立糖尿病模型。四周后分为以下组:“OE+DM”(卵巢切除合并DM且未接受任何治疗的女性,n=4)“OE+DM +CANA”(卵巢切除合并DM且接受CANA治疗的女性,n=4),“OE+DM +LIRA”(卵巢切除合并DM且接受LIRA治疗的女性,n=5)。治疗或观察期均为8周。实验结束时测定钙、磷和骨转换标志物(成纤维细胞生长因子-23 (FGF-23)、骨钙素、硬化蛋白、骨保护素(OPG)、核因子- κ b受体激活剂配体(RANKL))。安乐死后进行骨组织形态学测定。结果:CANA和LIRA治疗对磷钙代谢、硬化蛋白和骨钙素浓度均无显著影响。同时,“OE+DM”组OPG水平最高,为9.1 [7.81;10.045] pmol / l)。与“OE+DM+CANA”相比,差异有统计学意义(2,33)[1.84;5.84] pmol/l, p = 0.003)和«OE+DM+LIRA»(1.7 [1;2] pmol/l, p = 0.003)组。不同药物治疗动物的OPG水平没有差异。同样,两种治疗方式的OPG/RANKL比值也同样降低。“OE+DM+CANA”组股骨骨骺骨小梁数较“OE+DM”组减少(p=0.042)。LIRA未改变组织结构参数。结论:卡格列净与利拉鲁肽使用时,骨代谢指标无显著差异。此外,卡格列素可导致骨吸收活化,表现为股骨骨骺小梁数量减少。
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来源期刊
Diabetes Mellitus
Diabetes Mellitus ENDOCRINOLOGY & METABOLISM-
CiteScore
1.90
自引率
40.00%
发文量
61
审稿时长
7 weeks
期刊最新文献
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