• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

运动改善了多食 OLETF 大鼠股骨整体和组织水平的生物力学性能。

Exercise improves femoral whole-bone and tissue-level biomechanical properties in hyperphagic OLETF rats.

机构信息

a Department of Nutrition and Exercise Physiology, University of Missouri-Columbia, 204 Gwynn Hall, Columbia, MO 65211, USA.

b Research Service-Harry S. Truman Memorial Veterans Medical Center, Columbia, MO, USA.

出版信息

Appl Physiol Nutr Metab. 2017 Aug;42(8):884-892. doi: 10.1139/apnm-2017-0077. Epub 2017 May 1.

DOI:10.1139/apnm-2017-0077
PMID:28460190
Abstract

An often-overlooked comorbidity of type 2 diabetes (T2D) is increased fracture risk. Since traditional T2D therapies focus solely on glucose homeostasis, there is an increased need for effective treatment strategies that improve both metabolic and bone health. The current study evaluated if previously reported protective effects of exercise (EX) on cortical bone geometry and biomechanical properties are due to the prevention of obesity compared with obese Otsuka Long-Evans Tokushima Fatty (OLETF) rats or the unique skeletal effects of exercise. Four-week-old male OLETF rats were randomly assigned to 1 of 3 groups, each fed a standard rodent chow diet until 40 weeks of age: ad libitum-fed sedentary (O-SED), ad libitum-fed EX (O-EX), or a control group body-weight-matched to the O-EX group by caloric restriction (O-CR). Ad libitum-fed sedentary Long-Evans Tokushima Otsuka (L-SED) rats were used as a lean control. EX or CR prevented the excess body mass accumulation and elevated HbA1c observed in O-SED. Total-body bone mineral density was greater in O-EX than O-CR, but similar to L-SED and O-SED. O-EX and O-CR had lower osteocalcin and TRAP5b than O-SED and L-SED. EX or CR prevented the ∼3-fold increase in CTx in O-SED versus L-SED. EX increased femoral cortical mass accumulation and expansion at the mid-diaphysis compared with O-CR. EX or CR significantly increased tissue-level stiffness and strength compared with O-SED and L-SED, but O-EX had greater whole-bone stiffness than all other groups. In summary, EX has distinct advantages over CR for improving bone biomechanical properties in hyperphagic OLETF rats.

摘要

2 型糖尿病(T2D)常伴有骨折风险增加,这一并发症常被忽视。由于传统的 T2D 治疗方法仅专注于血糖稳态,因此需要新的有效治疗策略来改善代谢和骨骼健康。本研究评估了之前报道的运动(EX)对皮质骨几何形状和生物力学特性的保护作用是否是通过预防肥胖与肥胖 Otsuka Long-Evans Tokushima Fatty(OLETF)大鼠相比,或者是运动的独特骨骼作用。4 周龄雄性 OLETF 大鼠随机分为 3 组,每组均喂食标准啮齿动物饲料,直至 40 周龄:自由进食久坐(O-SED)、自由进食 EX(O-EX)或通过热量限制与 O-EX 组体重匹配的对照组(O-CR)。自由进食久坐 Long-Evans Tokushima Otsuka(L-SED)大鼠作为瘦对照。EX 或 CR 可防止 O-SED 中观察到的体重过度增加和 HbA1c 升高。与 O-CR 相比,O-EX 的全身骨矿物质密度更高,但与 L-SED 和 O-SED 相似。与 O-SED 和 L-SED 相比,O-EX 和 O-CR 的骨钙素和 TRAP5b 水平较低。EX 或 CR 可防止 O-SED 与 L-SED 相比 CTx 增加约 3 倍。与 O-CR 相比,EX 增加了股骨皮质的质量积累和骨干中段的扩张。与 O-SED 和 L-SED 相比,EX 或 CR 显著增加了组织水平的刚度和强度,但 O-EX 的整体骨骼刚度大于其他所有组。总之,EX 对改善多食性 OLETF 大鼠的骨骼生物力学特性具有明显优于 CR 的优势。

相似文献

1
Exercise improves femoral whole-bone and tissue-level biomechanical properties in hyperphagic OLETF rats.运动改善了多食 OLETF 大鼠股骨整体和组织水平的生物力学性能。
Appl Physiol Nutr Metab. 2017 Aug;42(8):884-892. doi: 10.1139/apnm-2017-0077. Epub 2017 May 1.
2
Exercise initiated after the onset of insulin resistance improves trabecular microarchitecture and cortical bone biomechanics of the tibia in hyperphagic Otsuka Long Evans Tokushima Fatty rats.胰岛素抵抗发生后开始运动可改善肥胖 Otsuka Long Evans Tokushima Fatty 大鼠胫骨的小梁微结构和皮质骨生物力学。
Bone. 2017 Oct;103:188-199. doi: 10.1016/j.bone.2017.07.010. Epub 2017 Jul 12.
3
Obesity-related changes in bone structural and material properties in hyperphagic OLETF rats and protection by voluntary wheel running.肥胖相关的高食量OLETF大鼠骨骼结构和材料特性的变化以及自愿轮转运动的保护作用。
Metabolism. 2015 Aug;64(8):905-16. doi: 10.1016/j.metabol.2015.04.004. Epub 2015 May 1.
4
Modulating fibroblast growth factor 21 in hyperphagic OLETF rats with daily exercise and caloric restriction.通过日常运动和热量限制调节多食性 OLETF 大鼠中的成纤维细胞生长因子 21。
Appl Physiol Nutr Metab. 2012 Dec;37(6):1054-62. doi: 10.1139/h2012-091. Epub 2012 Aug 15.
5
Daily exercise vs. caloric restriction for prevention of nonalcoholic fatty liver disease in the OLETF rat model.每日运动与热量限制预防 OLETF 大鼠模型非酒精性脂肪肝的比较。
Am J Physiol Gastrointest Liver Physiol. 2011 May;300(5):G874-83. doi: 10.1152/ajpgi.00510.2010. Epub 2011 Feb 24.
6
Obesity and type 2 diabetes, not a diet high in fat, sucrose, and cholesterol, negatively impacts bone outcomes in the hyperphagic Otsuka Long Evans Tokushima Fatty rat.肥胖和 2 型糖尿病,而不是高脂肪、高蔗糖和高胆固醇的饮食,会对过度进食的 Otsuka Long Evans Tokushima Fatty 大鼠的骨骼产生负面影响。
Bone. 2017 Dec;105:200-211. doi: 10.1016/j.bone.2017.09.003. Epub 2017 Sep 9.
7
Effects of voluntary running exercise on bone histology in type 2 diabetic rats.2 型糖尿病大鼠自愿跑步运动对骨组织学的影响。
PLoS One. 2018 Feb 15;13(2):e0193068. doi: 10.1371/journal.pone.0193068. eCollection 2018.
8
Daily physical activity enhances reactivity to insulin in skeletal muscle arterioles of hyperphagic Otsuka Long-Evans Tokushima Fatty rats.日常身体活动增强了多食 Otsuka Long-Evans Tokushima Fatty 大鼠骨骼肌小动脉对胰岛素的反应性。
J Appl Physiol (1985). 2010 Oct;109(4):1203-10. doi: 10.1152/japplphysiol.00064.2010. Epub 2010 Jul 15.
9
Insulin-Stimulated Bone Blood Flow and Bone Biomechanical Properties Are Compromised in Obese, Type 2 Diabetic OLETF Rats.胰岛素刺激的骨血流量和骨生物力学特性在肥胖的2型糖尿病OLETF大鼠中受损。
JBMR Plus. 2017 Jun 12;1(2):116-126. doi: 10.1002/jbm4.10007. eCollection 2017 Oct.
10
Aerobic exercise training in the treatment of non-alcoholic fatty liver disease related fibrosis.有氧运动训练用于治疗非酒精性脂肪性肝病相关纤维化
J Physiol. 2016 Sep 15;594(18):5271-84. doi: 10.1113/JP272235. Epub 2016 May 27.

引用本文的文献

1
Bioactive Agent Discovery from the Natural Compounds for the Treatment of Type 2 Diabetes Rat Model.从天然化合物中发现用于治疗 2 型糖尿病大鼠模型的生物活性药物。
Molecules. 2020 Dec 3;25(23):5713. doi: 10.3390/molecules25235713.