Recently there has been growing interest in magnesium deficiency and its correlation with coronary artery disease, chronic complications of diabetes mellitus and antioxidant enzyme activity. Hypomagnesemia is a common association of diabetes mellitus, and the blood glutathione (GSH) level is signifi
Potential antiosteoporosis effect of biodegradable magnesium implanted in STZ-induced diabetic rats
✍ Scribed by Weili Yang; Yu Zhang; Jianhong Yang; Lili Tan; Ke Yang
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 541 KB
- Volume
- 99A
- Category
- Article
- ISSN
- 1549-3296
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Pure magnesium (Mg) was implanted intramedullary into the femur of streptozotocin (STZ)‐induced diabetic rats to investigate its effect on bone growth after 6 weeks degradation. The experimental results showed that the femoral BMD in diabetic rats was significantly lower than that in controls (p < 0.01) but restored notably by Mg implantation. The contents of calcium (Ca), phosphorus (P), Mg, zinc (Zn), potassium (K), strontium (Sr), and sulfur (S) in bone of diabetic group were significantly lower than those in controls but remarkably increased with implantation of Mg. The residual weight calculation showed that 29.41% of Mg was degraded in vivo. The energy dispersive X‐ray spectroscopy (EDS) analysis showed that the reaction layer on the surface of the Mg implant mainly consisted of C, Ca, O, P, and Mg. Besides, serum Mg level was significantly decreased in diabetic group compared with the control group but increased by Mg treatment. Also, there were no significant differences in body weight and blood glucose, as well as blood glycosylated hemoglobin (HbAIc%), serum Ca, alanine aminitransperase (ALT), aspartate aminotransferase (AST), uric acid (UA), nonesterified fatty acid (NEFA), cholinesterase (CHE), and creatinine (CR) levels between diabetic and Mg‐implanted rats. The study indicated that Mg implant had no obvious toxicity in STZ‐induced diabetic rats and may act as a potential agent to treat osteoporosis. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part A:, 2011.
📜 SIMILAR VOLUMES
A study of anionic sites in the glomerular basement membrane (GBM) of streptozotocin (ST2)-induced diabetic rats with or without treatment by an antiplatelet drug, dilazep dihydrochloride, is described. Expression of glomerular extracellular matrix (ECM) components was examined by immunofluorescence
## Abstract Insulin‐dependent diabetes mellitus (IDDM) is an autoimmune disease that is characterized by selective destruction of insulin secreting pancreatic islets β‐cells. The formation of cytokines (IL‐1β, IL‐6, TNF‐α, etc.) leads to extensive morphological damage of β‐cells, DNA fragmentation,