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Representative μCT images of (A) trabecular bone microarchitecture and (B) cortical thickness in Mature and Middle-Aged CON, 5dPTH, and 10dPTH mice. The black boxes overlaying the secondary spongiosa (Fig. 1A) and cortical midshaft (Fig. 1B) represent the regions of analyses and correspond with the representative images provided for each group. There were no significant differences.

Representative μCT images of (A) trabecular bone microarchitecture and (B) cortical thickness in Mature and Middle-Aged CON, 5dPTH, and 10dPTH mice. The black boxes overlaying the secondary spongiosa (Fig. 1A) and cortical midshaft (Fig. 1B) represent the regions of analyses and correspond with the representative images provided for each group. There were no significant differences.

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Intermittent parathyroid hormone (PTH) administration augments bone and progressive bone marrow blood vessel (BMBV) ossification occurs with advancing age. Since intermittent PTH administration augments bone, it may also serve to increase BMBV ossification. We assessed the influence of 5- and 10-days of intermittent PTH 1–34 administration on trabe...

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... 5dPTH The black boxes overlaying the secondary spongiosa (Fig. 1A) and cortical midshaft (Fig. 1B) represent the regions of analyses and correspond with the representative images provided for each group. There were no significant ...
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... 5dPTH The black boxes overlaying the secondary spongiosa (Fig. 1A) and cortical midshaft (Fig. 1B) represent the regions of analyses and correspond with the representative images provided for each group. There were no significant ...
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... no gender-related differences were observed ( Supplementary Tables 1-4), female and male data were pooled and analyzed according to group. Body mass did not differ among groups (Mature CON, 31 ± 2 g; Mature 5dPTH, 32 ± 2 g; Mature 10dPTH, 30 ± 1 g; Middle-Aged CON, 30 ± 1 g; Middle-Aged 5dPTH, 31 ± 1 g; and Middle-Aged 10dPTH, 31 ± 1 g). ...
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... any significant interactions observed for the trabecular bone parameters. As antici- pated, trabecular bone microarchitecture (i.e., BV/TV, Tb.N, Tb.Th, Tb.Sp) did not differ with PTH treatment (Table 1). Likewise, no main effects for age or treatment nor any significant interactions were ob- served for Ct.Th at the femoral mid-shaft (Table 1). Fig. 1 illustrates representative 3D μCT reconstructions of trabecular bone micro- architecture in the secondary spongiosa of the distal femoral meta- physis and Ct.Th. The μCT images of the entire femora are provided to illustrate the regions of analyzes for the trabecular and cortical bone parameters. The black boxes overlaying the ...
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... illustrates representative 3D μCT reconstructions of trabecular bone micro- architecture in the secondary spongiosa of the distal femoral meta- physis and Ct.Th. The μCT images of the entire femora are provided to illustrate the regions of analyzes for the trabecular and cortical bone parameters. The black boxes overlaying the secondary spongiosa (Fig. 1A) and cortical midshaft (Fig. 1B) depict the regions of analyses and correspond to the representative μCT images for each group. In regards to CSMI, significant main effects for age and treatment were observed ( Fig. 2A and 2B, respectively), whereby CSMI was 22% higher (p < 0.05) in Middle-Aged vs. Mature and was lower (p < 0.05) in ...
Context 6
... reconstructions of trabecular bone micro- architecture in the secondary spongiosa of the distal femoral meta- physis and Ct.Th. The μCT images of the entire femora are provided to illustrate the regions of analyzes for the trabecular and cortical bone parameters. The black boxes overlaying the secondary spongiosa (Fig. 1A) and cortical midshaft (Fig. 1B) depict the regions of analyses and correspond to the representative μCT images for each group. In regards to CSMI, significant main effects for age and treatment were observed ( Fig. 2A and 2B, respectively), whereby CSMI was 22% higher (p < 0.05) in Middle-Aged vs. Mature and was lower (p < 0.05) in 5dPTH vs. CON and ...

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... [2] Osteoporosis causes chronic pain and reduced quality of life when it is in more severe expressions, [3] leading to increased healthcare-related funds and an important health issue [4] and increased mortality. [5,6] Even though the presence of known unfavorable clinical and experimental findings, [7][8][9] treatment options for osteoporosis in the elderly are available, such as a well-known bone anabolic agent treatment for osteoporosis, intermittent parathyroid hormone (iPTH), [10] and osteoclast activity inhibitor, denosumab. [9] Despite the fact that pharmaceutical methods are beneficial, non-pharmacochemical approaches, including nutrition and exercise, have been highlighted to prevent ageassociated bone loss and osteoporosis. ...
... Trabecular bone microarchitecture parameters in the distal femoral metaphysis were determined as previously described. [8] Briefly, 60 slices were made in the distal femoral metaphysis, beginning 600 µm superior from the growth plate. Trabecular bone microarchitectural parameters including BV/tissue volume ratio (BV/TV, %), trabecular thickness (Tb.Th, µm), trabecular number (Tb.N, /mm 2 ) and trabecular separation (Tb.Sp, µm) were calculated. ...
... [23,24] Moreover, preclinical evidence suggests that aging is associated with a 57% reduction in osteoblast activity and a 40% reduction in bone mineralization, thereby leading to lower bone cell turnover, resulting in ~53% lower BV in the distal femoral trabecular bone microarchitecture. [25] Although the pharmacological treatment options could lead to some side effects, [7,8,26] the development and use of a number of pharmacological therapies have led to the main treatment options to treat multifactorial processes of osteoporosis progression. For example, iPTH administration is a common therapy for treating osteoporosis. ...
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... Interestingly, Lee and Prisby found that treating mice with daily injections of PTH(1-34), an intermittent regimen, causes coalescence of mineral deposits in femoral bone marrow blood vessels. 25 Similarly, we recently reported that intermittent PTH(1-34) regimen altered the microarchitecture of aortic calcification by promoting the coalescence of calcium deposits. 17 The present study has limitations. ...
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... All of these modifications serve to aid in the regulation of bone cellular activity and promote an environment supportive of bone formation. A note of caution, however, as recent evidence suggests a potential exacerbation of bone marrow blood vessel ossification with intermittent PTH administration [178]. Interestingly, 2 weeks of intermittent PTH administration improved the age-related decrements in aortic function in old rats [179]. ...
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