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Study · Animal study (in vivo) · rat · 2015

6 results

PTH(1-34) Treatment Increases Bisphosphonate Turnover in Fracture Repair in Rats.

Murphy CM, Schindeler A, Cantrill LC, Mikulec K, Peacock L, Little DG

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research1 Jun 2015Cited by 22 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study6

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

  1. 01AnimalAnimal study (in vivo)Mechanism

    In Wistar rats, PTH(1-34) reduced long-bone bisphosphonate fluorescence versus control, consistent with increased remobilization.

    In plain wordsIn rats, PTH(1-34) reduced fluorescent bisphosphonate signals in long bones versus control.

    Outcome
    DecreaseLong-bone bisphosphonate fluorescence
    Study

    ratn: not reported in source

    Wistar normal growth and closed fracture repair
    Comparator
    Saline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 μg/kg/dAs given in this study (rat).

    Source sentences

    Summary
    Consistent with increased BP remobilization with PTH(1-34) , there was a significant decrease in fluorescence in both the long bones and in the fracture callus in treated animals compared with controls.
    2 context sentences
    Summary · context
    These traceable BPs were dosed to Wistar rats in models of normal growth and closed fracture repair.
    Summary · context
    Rats were cotreated with saline or 25 μg/kg/d PTH(1-34) , and the effects on BP liberation and bone healing were examined by X-ray, micro-CT, autoradiography, and fluorescent confocal microscopy.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In Wistar rats, PTH(1-34) reduced bisphosphonate fluorescence in fracture callus versus control.

    In plain wordsIn rats, PTH(1-34) reduced fluorescent bisphosphonate signals at fracture repair sites versus control.

    Outcome
    DecreaseFracture callus bisphosphonate fluorescence
    Study

    ratn: not reported in source

    Wistar normal growth and closed fracture repair
    Comparator
    Saline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 μg/kg/dAs given in this study (rat).

    Source sentences

    Summary
    Consistent with increased BP remobilization with PTH(1-34) , there was a significant decrease in fluorescence in both the long bones and in the fracture callus in treated animals compared with controls.
    2 context sentences
    Summary · context
    These traceable BPs were dosed to Wistar rats in models of normal growth and closed fracture repair.
    Summary · context
    Rats were cotreated with saline or 25 μg/kg/d PTH(1-34) , and the effects on BP liberation and bone healing were examined by X-ray, micro-CT, autoradiography, and fluorescent confocal microscopy.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In Wistar rats, autoradiography confirmed increased bisphosphonate remobilization with PTH(1-34) versus control.

    In plain wordsIn rats, radioactive imaging confirmed that PTH(1-34) increased bisphosphonate remobilization versus control.

    Outcome
    IncreaseRadiolabeled zoledronic acid remobilization
    Study

    ratn: not reported in source

    Wistar normal growth and closed fracture repair
    Comparator
    Saline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 μg/kg/dAs given in this study (rat).

    Source sentences

    Summary
    Consistent with increased BP remobilization with PTH(1-34) , there was a significant decrease in fluorescence in both the long bones and in the fracture callus in treated animals compared with controls. This was further confirmed by autoradiography for (14) C-ZA.
    2 context sentences
    Summary · context
    These traceable BPs were dosed to Wistar rats in models of normal growth and closed fracture repair.
    Summary · context
    Rats were cotreated with saline or 25 μg/kg/d PTH(1-34) , and the effects on BP liberation and bone healing were examined by X-ray, micro-CT, autoradiography, and fluorescent confocal microscopy.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In rats receiving acute bisphosphonate treatment, PTH(1-34) did not alter callus bone volume despite reducing callus-bound bisphosphonate.

    In plain wordsIn rats receiving bisphosphonates, PTH(1-34) did not change repair-site bone volume versus control.

    Outcome
    No significant changeCallus bone volume
    Study

    ratn: not reported in source

    Wistar normal growth and closed fracture repair
    Comparator
    Saline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 μg/kg/dAs given in this study (rat).

    Source sentences

    Summary
    In this model of acute BP treatment, callus bone volume (BV) was significantly increased in fractured limbs, and although we noted significant decreases in callus-bound BP with PTH(1-34) , these were not sufficient to alter this BV.
    2 context sentences
    Summary · context
    These traceable BPs were dosed to Wistar rats in models of normal growth and closed fracture repair.
    Summary · context
    Rats were cotreated with saline or 25 μg/kg/d PTH(1-34) , and the effects on BP liberation and bone healing were examined by X-ray, micro-CT, autoradiography, and fluorescent confocal microscopy.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In rats receiving acute bisphosphonate treatment, PTH(1-34) significantly reduced callus-bound bisphosphonate versus control.

    In plain wordsIn rats receiving bisphosphonates, PTH(1-34) reduced bisphosphonate bound at fracture repair sites versus control.

    Outcome
    DecreaseCallus-bound bisphosphonate
    Study

    ratn: not reported in source

    Wistar normal growth and closed fracture repair
    Comparator
    Saline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 μg/kg/dAs given in this study (rat).

    Source sentences

    Summary
    In this model of acute BP treatment, callus bone volume (BV) was significantly increased in fractured limbs, and although we noted significant decreases in callus-bound BP with PTH(1-34) , these were not sufficient to alter this BV.
    2 context sentences
    Summary · context
    These traceable BPs were dosed to Wistar rats in models of normal growth and closed fracture repair.
    Summary · context
    Rats were cotreated with saline or 25 μg/kg/d PTH(1-34) , and the effects on BP liberation and bone healing were examined by X-ray, micro-CT, autoradiography, and fluorescent confocal microscopy.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In Wistar rats, PTH(1-34) increased intracellular bisphosphonate in resorbing osteoclasts.

    In plain wordsIn rats, PTH(1-34) increased bisphosphonate inside bone-resorbing cells versus control.

    Outcome
    IncreaseIntracellular bisphosphonate in osteoclasts
    Study

    ratn: not reported in source

    Wistar normal growth and closed fracture repair
    Comparator
    Saline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 μg/kg/dAs given in this study (rat).

    Source sentences

    Summary
    However, increased intracellular BP was noted in resorbing osteoclasts, confirming that, in principle, PTH(1-34) increases bone turnover as well as BP turnover.
    2 context sentences
    Summary · context
    These traceable BPs were dosed to Wistar rats in models of normal growth and closed fracture repair.
    Summary · context
    Rats were cotreated with saline or 25 μg/kg/d PTH(1-34) , and the effects on BP liberation and bone healing were examined by X-ray, micro-CT, autoradiography, and fluorescent confocal microscopy.

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, 02:26 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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