Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture.
BACKGROUND AND PURPOSE:Diabetes mellitus (DM) is the most common metabolic disorder that is characterized by hyperglycemia, it can be categorized by T1DM and T2DM. T1DM is also reported to cause bone loss. However, most reports regarding this aspect of T1DM have only investigated a single site; a co...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2018-01-01
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| Series: | PLoS ONE |
| Online Access: | http://europepmc.org/articles/PMC6197850?pdf=render |
| _version_ | 1818027190526148608 |
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| author | Yunwei Hua Ruiye Bi Yue Zhang Luchen Xu Jiaoyang Guo Yunfeng Li |
| author_facet | Yunwei Hua Ruiye Bi Yue Zhang Luchen Xu Jiaoyang Guo Yunfeng Li |
| author_sort | Yunwei Hua |
| collection | DOAJ |
| description | BACKGROUND AND PURPOSE:Diabetes mellitus (DM) is the most common metabolic disorder that is characterized by hyperglycemia, it can be categorized by T1DM and T2DM. T1DM is also reported to cause bone loss. However, most reports regarding this aspect of T1DM have only investigated a single site; a comparison of bone loss from different areas of the body is still lacking. METHODS:Thirty-five 12-week-old Sprague Dawley® (SD) rats were separated to seven groups. Five rats were euthanized without any surgery at 0 weeks for histological examination and determination of baseline characteristics. In 15 of the rats, DM was induced via Streptozotocin (STZ)-injection, and they were separated to 3 groups (4 weeks, 8 weeks and 12 weeks after STZ-injection). The remaining 15 rats were used as the control group (4 weeks, 8 weeks and 12 weeks after saline-injection). We tested bone-mass loss at four skeletal sites, the tibia, the femur greater trochanter, the spine, and the mandibular bones using micro-computed tomography (CT) and histological tests. RESULTS:Tibia was influenced the most obvious(BV/TV decreased by 27.3%, 52.5%, and 81.2% at 4 weeks, 8 weeks, and 12 weeks, respectively. p<0.05). In contrast, the other three sites were influenced to a lesser extent and bone loss became prominent at a later time point according to the histological and micro-CT tests(Femur: BV/TV did not decrease significantly at the first month or second month. However, and decreased by 49.4% at the third month, P<0.05. Mandible: the BV/TV only decreased by 6.5% at 1 month after STZ-injection. There was still a significant difference between the second and third months. The BV/TV decreased by 47.0% and 68.1% at 2 months and 3 months, respectively, (p<0.05) Spine: the BV/TV only decreased by 6.7%. However, significant change was observed in the spine at the second month and third month after STZ injection. The BV/TV decreased by 45.4% and 64.3%, respectively, p<0.05). CONCLUSION:The results indicate that T1DM can severely influence the bone structure of the 4 skeletal sites. Further, areas with dense trabecular bones were influenced less and at a later time point in comparison to the tibial region. CLINICAL RELEVANCE:Our research can serve as a guide to help increase the success rate of implant treatment, and help decrease the fracture risk in different bone types with greater accuracy. |
| first_indexed | 2024-12-10T04:43:58Z |
| format | Article |
| id | doaj.art-2c4f91a48df64a23b1e1e0ece2626552 |
| institution | Directory Open Access Journal |
| issn | 1932-6203 |
| language | English |
| last_indexed | 2024-12-10T04:43:58Z |
| publishDate | 2018-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS ONE |
| spelling | doaj.art-2c4f91a48df64a23b1e1e0ece26265522022-12-22T02:01:47ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-011310e020550310.1371/journal.pone.0205503Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture.Yunwei HuaRuiye BiYue ZhangLuchen XuJiaoyang GuoYunfeng LiBACKGROUND AND PURPOSE:Diabetes mellitus (DM) is the most common metabolic disorder that is characterized by hyperglycemia, it can be categorized by T1DM and T2DM. T1DM is also reported to cause bone loss. However, most reports regarding this aspect of T1DM have only investigated a single site; a comparison of bone loss from different areas of the body is still lacking. METHODS:Thirty-five 12-week-old Sprague Dawley® (SD) rats were separated to seven groups. Five rats were euthanized without any surgery at 0 weeks for histological examination and determination of baseline characteristics. In 15 of the rats, DM was induced via Streptozotocin (STZ)-injection, and they were separated to 3 groups (4 weeks, 8 weeks and 12 weeks after STZ-injection). The remaining 15 rats were used as the control group (4 weeks, 8 weeks and 12 weeks after saline-injection). We tested bone-mass loss at four skeletal sites, the tibia, the femur greater trochanter, the spine, and the mandibular bones using micro-computed tomography (CT) and histological tests. RESULTS:Tibia was influenced the most obvious(BV/TV decreased by 27.3%, 52.5%, and 81.2% at 4 weeks, 8 weeks, and 12 weeks, respectively. p<0.05). In contrast, the other three sites were influenced to a lesser extent and bone loss became prominent at a later time point according to the histological and micro-CT tests(Femur: BV/TV did not decrease significantly at the first month or second month. However, and decreased by 49.4% at the third month, P<0.05. Mandible: the BV/TV only decreased by 6.5% at 1 month after STZ-injection. There was still a significant difference between the second and third months. The BV/TV decreased by 47.0% and 68.1% at 2 months and 3 months, respectively, (p<0.05) Spine: the BV/TV only decreased by 6.7%. However, significant change was observed in the spine at the second month and third month after STZ injection. The BV/TV decreased by 45.4% and 64.3%, respectively, p<0.05). CONCLUSION:The results indicate that T1DM can severely influence the bone structure of the 4 skeletal sites. Further, areas with dense trabecular bones were influenced less and at a later time point in comparison to the tibial region. CLINICAL RELEVANCE:Our research can serve as a guide to help increase the success rate of implant treatment, and help decrease the fracture risk in different bone types with greater accuracy.http://europepmc.org/articles/PMC6197850?pdf=render |
| spellingShingle | Yunwei Hua Ruiye Bi Yue Zhang Luchen Xu Jiaoyang Guo Yunfeng Li Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture. PLoS ONE |
| title | Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture. |
| title_full | Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture. |
| title_fullStr | Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture. |
| title_full_unstemmed | Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture. |
| title_short | Different bone sites-specific response to diabetes rat models: Bone density, histology and microarchitecture. |
| title_sort | different bone sites specific response to diabetes rat models bone density histology and microarchitecture |
| url | http://europepmc.org/articles/PMC6197850?pdf=render |
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