Laboratory of Veterinary Public Health, Faculty of Veterinary Medicine, Universitas Brawijaya, Malang, Indonesia.
Department of Anatomy, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Open Vet J. 2024 Aug;14(8):1761-1770. doi: 10.5455/OVJ.2024.v14.i8.3. Epub 2024 Aug 31.
Diabetes is a degenerative disease associated with metabolic disorders. The majority of people have type 2 diabetes mellitus (DM) insulin resistance due to an unhealthy lifestyle. The development of DM treatment is also growing, one of which is using conditioned medium.
This study aims to determine the effect of Bovine umbilical mesenchymal stem cell-conditioned medium (BUMSC-CM) on nicotinamide (NA) and streptozotocin (STZ) induced rats as an animal model of DM.
The study began with the docking of Cholecalciferol with aldolase reductase and glucokinase. In the study, animal models were divided into five groups: group A (negative control), group B (diabetic rats), group C (NA+STZ+Metformin), group D (NA+STZ+ BUMSC-CM 0.2 ml/kg BW), and group E (NA+STZ+ BUMSC-CM 0.5 ml/kg BW). Blood sugar levels were checked, and BUMSC-CM was administered by intramuscular injection at four-day intervals for a duration of 16 days. Blood sugar levels were also sampled, and GLUT4 histochemical and immunohistochemical staining was performed.
The results showed that Cholecalciferol can bind to aldolase reductase ASP43 and TYR48 and bind to glucokinase at TYR214 with hydrogen bonds. BUMSC-CM administration was able to reduce blood sugar well. In addition, BUMSC-CM also helped repair the tissue structure of the pancreas damaged by inflammation from STZ administration.
This study can be concluded that the administration of BUMSC-CM can be an alternative cell-free therapy for patients with DM.
糖尿病是一种与代谢紊乱相关的退行性疾病。大多数人因不健康的生活方式而患有 2 型糖尿病(DM)胰岛素抵抗。DM 治疗的发展也在不断增长,其中之一是使用条件培养基。
本研究旨在确定牛脐带间充质干细胞条件培养基(BUMSC-CM)对烟酰胺(NA)和链脲佐菌素(STZ)诱导的大鼠的影响,作为 DM 的动物模型。
该研究首先进行了胆钙化醇与醛缩酶还原酶和葡萄糖激酶的对接。在研究中,动物模型分为五组:A 组(阴性对照)、B 组(糖尿病大鼠)、C 组(NA+STZ+二甲双胍)、D 组(NA+STZ+BUMSC-CM 0.2 ml/kg BW)和 E 组(NA+STZ+BUMSC-CM 0.5 ml/kg BW)。检查血糖水平,并每隔四天通过肌肉注射给予 BUMSC-CM,持续 16 天。还采集了血糖样本,并进行了 GLUT4 组织化学和免疫组织化学染色。
结果表明,胆钙化醇可以与醛缩酶还原酶 ASP43 和 TYR48 结合,并与葡萄糖激酶在 TYR214 处通过氢键结合。BUMSC-CM 的给药能够很好地降低血糖。此外,BUMSC-CM 还有助于修复 STZ 给药引起的炎症对胰腺组织结构的损伤。
本研究可以得出结论,BUMSC-CM 的给药可以作为 DM 患者的一种无细胞治疗的替代方法。