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Study · Animal study (in vivo) · rat · 2024

8 results

Abaloparatide promotes bone repair of vertebral defects in ovariectomized rats by increasing bone formation.

Makino A, Hasegawa T, Yamamoto T, Takagi H, Takahashi Y, Miyakoshi N, Amizuka N

Bone23 Feb 2024Cited by 7 (Europe PMC)

Summary

Osteoporotic vertebral fracture (OVF) is the most common type of osteoporotic fracture and is associated with immobility and mortality. Bone anabolic agents, such as abaloparatide (ABL), are usually administered to patients with OVF to prevent subsequent fractures. Although several studies have shown that bone anabolic agents promote healing of long bone fractures, there is little evidence of their healing effect on vertebral bone fractures. In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF. Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery. We found that ABL significantly increased bone mineral content and improved trabecular structural parameters at the vertebral defect site. Moreover, ABL significantly increased bone strength of the defected vertebrae. Bone histochemical analysis revealed formation of thick trabecular bone networks at the defect site after ABL administration, consistent with an improvement in trabecular structural parameters by ABL. ABL increased ALPase- and PHOSPHO1-positive osteoblastic cells and ALPase/PCNA double-positive cells, indicating enhanced preosteoblast proliferation as well as bone formation at the defect site. On the other hand, ABL did not affect the number of cathepsin K-positive osteoclasts per bone surface, suggesting that ABL did not promote excessive bone resorption. Our findings suggest that ABL is useful not only for preventing secondary vertebral fractures but also for promoting bone healing in OVF.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study8

8 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats with vertebral defects, abaloparatide increased bone mineral content at the defect site.

    In plain wordsIn rats with vertebral defects, abaloparatide increased bone mineral content at the injury.

    Outcome
    IncreaseBone mineral content
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    We found that ABL significantly increased bone mineral content and improved trabecular structural parameters at the vertebral defect site.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats with vertebral defects, abaloparatide improved trabecular structural parameters at the defect site.

    In plain wordsIn rats with vertebral defects, abaloparatide improved the structure of spongy bone at the injury.

    Outcome
    MixedTrabecular structural parameters
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    We found that ABL significantly increased bone mineral content and improved trabecular structural parameters at the vertebral defect site.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats with vertebral defects, abaloparatide increased strength of the damaged vertebrae.

    In plain wordsIn rats with vertebral defects, abaloparatide increased the strength of damaged vertebrae.

    Outcome
    IncreaseVertebral bone strength
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    Moreover, ABL significantly increased bone strength of the defected vertebrae.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, thick trabecular bone networks formed at vertebral defect sites after abaloparatide administration.

    In plain wordsIn rats, thick networks of spongy bone formed at vertebral defects after abaloparatide treatment.

    Outcome
    IncreaseTrabecular bone network formation
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    Bone histochemical analysis revealed formation of thick trabecular bone networks at the defect site after ABL administration, consistent with an improvement in trabecular structural parameters by ABL.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In ovariectomized rats with vertebral defects, abaloparatide increased ALPase-positive osteoblastic cells.

    In plain wordsIn rats with vertebral defects, abaloparatide increased bone-forming cells positive for ALPase.

    Outcome
    IncreaseALPase-positive osteoblasts
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    ABL increased ALPase- and PHOSPHO1-positive osteoblastic cells and ALPase/PCNA double-positive cells, indicating enhanced preosteoblast proliferation as well as bone formation at the defect site.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In ovariectomized rats with vertebral defects, abaloparatide increased PHOSPHO1-positive osteoblastic cells.

    In plain wordsIn rats with vertebral defects, abaloparatide increased bone-forming cells positive for PHOSPHO1.

    Outcome
    IncreasePHOSPHO1-positive osteoblasts
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    ABL increased ALPase- and PHOSPHO1-positive osteoblastic cells and ALPase/PCNA double-positive cells, indicating enhanced preosteoblast proliferation as well as bone formation at the defect site.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.
  7. 07AnimalAnimal study (in vivo)Mechanism

    In ovariectomized rats with vertebral defects, abaloparatide increased ALPase/PCNA double-positive cells.

    In plain wordsIn rats with vertebral defects, abaloparatide increased cells positive for both ALPase and PCNA.

    Outcome
    IncreaseALPase/PCNA double-positive cells
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    ABL increased ALPase- and PHOSPHO1-positive osteoblastic cells and ALPase/PCNA double-positive cells, indicating enhanced preosteoblast proliferation as well as bone formation at the defect site.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.
  8. 08AnimalAnimal study (in vivo)Mechanism

    In ovariectomized rats with vertebral defects, abaloparatide did not change cathepsin K-positive osteoclast numbers per bone surface.

    In plain wordsIn rats with vertebral defects, abaloparatide did not change cathepsin K-positive bone-resorbing cell numbers per bone surface.

    Outcome
    No significant changeCathepsin K-positive osteoclasts
    Study

    ratn: not reported in source

    Ovariectomized female Sprague-Dawley rats with vertebral drill-hole defects
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    30 μg/kg once daily · subcutaneous · up to 6 weeksAs given in this study (rat).

    Source sentences

    Summary
    On the other hand, ABL did not affect the number of cathepsin K-positive osteoclasts per bone surface, suggesting that ABL did not promote excessive bone resorption.
    2 context sentences
    Summary · context
    In the present study, we investigated the effect of ABL on vertebral bone defects using ovariectomized (OVX) rats with vertebral body drill-hole defects, an animal model of OVF.
    Summary · context
    Eight-week-old female Sprague-Dawley rats were subjected to OVX, followed by the 32-36 days of bone depletion period, once-daily subcutaneous ABL was administered to OVX rats at a dose of 30 μg/kg for a maximum of 6 weeks from the day of the vertebral defect surgery.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    22 Oct 2026, 02:25 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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