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Study · Animal study (in vivo) · mouse · 2001

10 results

Human parathyroid hormone 1-34 reverses bone loss in ovariectomized mice.

Alexander JM, Bab I, Fish S, Müller R, Uchiyama T, Gronowicz G, Nahounou M, Zhao Q, White DW, Chorev M, Gazit D, Rosenblatt M

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research1 Sept 2001Cited by 127 (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 study10

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH recovered approximately 35% of trabecular bone loss versus vehicle.

    In plain wordsIn mice, PTH partly restored trabecular bone volume compared with vehicle.

    Outcome
    IncreaseTrabecular bone volume recovery
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Source sentences

    Summary
    PTH induced a approximately 35% recovery of this loss and a approximately 40% reversal of the associated decreases in trabecular number (Tb.N) and connectivity.
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH reversed approximately 40% of the decrease in trabecular number versus vehicle.

    In plain wordsIn mice, PTH partly restored trabecular number compared with vehicle.

    Outcome
    IncreaseTrabecular number
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Source sentences

    Summary
    PTH induced a approximately 35% recovery of this loss and a approximately 40% reversal of the associated decreases in trabecular number (Tb.N) and connectivity.
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH reversed approximately 40% of the decrease in trabecular connectivity versus vehicle.

    In plain wordsIn mice, PTH partly restored trabecular connectivity compared with vehicle.

    Outcome
    IncreaseTrabecular connectivity
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Source sentences

    Summary
    PTH induced a approximately 35% recovery of this loss and a approximately 40% reversal of the associated decreases in trabecular number (Tb.N) and connectivity.
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH shifted trabecular surfaces from single to double calcein labeling versus vehicle.

    In plain wordsIn mice, PTH increased double-labeled trabecular surfaces compared with vehicle.

    Outcome
    IncreaseCalcein-labeled surfaces
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Source sentences

    Summary
    PTH also caused a shift from single to double calcein-labeled trabecular surfaces, a significant enhancement in the mineralizing perimeter and a respective 2- and 3-fold stimulation of the mineral appositional rate (MAR) and bone formation rate (BFR).
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH significantly increased the mineralizing perimeter versus vehicle.

    In plain wordsIn mice, PTH increased the mineralizing perimeter compared with vehicle.

    Outcome
    IncreaseMineralizing perimeter
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Source sentences

    Summary
    PTH also caused a shift from single to double calcein-labeled trabecular surfaces, a significant enhancement in the mineralizing perimeter and a respective 2- and 3-fold stimulation of the mineral appositional rate (MAR) and bone formation rate (BFR).
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  6. 06AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH stimulated trabecular mineral appositional rate versus vehicle.

    In plain wordsIn mice, PTH increased trabecular mineral apposition compared with vehicle.

    Outcome
    IncreaseTrabecular mineral appositional rate
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Measurements

    MAR stimulation
    2 fold
    PTH

    Source sentences

    Summary
    PTH also caused a shift from single to double calcein-labeled trabecular surfaces, a significant enhancement in the mineralizing perimeter and a respective 2- and 3-fold stimulation of the mineral appositional rate (MAR) and bone formation rate (BFR).
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  7. 07AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH stimulated trabecular bone formation rate versus vehicle.

    In plain wordsIn mice, PTH increased trabecular bone formation compared with vehicle.

    Outcome
    IncreaseTrabecular bone formation rate
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Measurements

    BFR stimulation
    3 fold
    PTH

    Source sentences

    Summary
    PTH also caused a shift from single to double calcein-labeled trabecular surfaces, a significant enhancement in the mineralizing perimeter and a respective 2- and 3-fold stimulation of the mineral appositional rate (MAR) and bone formation rate (BFR).
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  8. 08AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH increased diaphyseal endosteal cortical mineral appositional rate versus vehicle.

    In plain wordsIn mice, PTH increased endosteal cortical mineral apposition compared with vehicle.

    Outcome
    IncreaseEndosteal cortical mineral appositional rate
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Source sentences

    Summary
    Diaphyseal endosteal cortical MAR and thickness also were increased with a high correlation between these parameters.
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.
  9. 09AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized mice, PTH increased diaphyseal cortical thickness versus vehicle.

    In plain wordsIn mice, PTH increased cortical thickness compared with vehicle.

    Outcome
    IncreaseCortical thickness
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Comparator
    Vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    Dose not stated · 4 weeksAs given in this study (mouse).

    Source sentences

    Summary
    Diaphyseal endosteal cortical MAR and thickness also were increased with a high correlation between these parameters.
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.

Studies that did not test the peptide alone1

In this study, Teriparatide (PTH 1-34) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Teriparatide (PTH 1-34).

  1. 10AnimalNot a test of Teriparatide (PTH 1-34) aloneAnimal study (in vivo)Mechanism

    In ovariectomized mice, diaphyseal endosteal cortical mineral appositional rate correlated highly with cortical thickness.

    In plain wordsIn mice, cortical mineral apposition correlated with cortical thickness.

    Outcome
    Not applicableCortical apposition-thickness correlation
    Study

    mousen: not reported in source

    Ovariectomized Swiss-Webster mice
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    Diaphyseal endosteal cortical MAR and thickness also were increased with a high correlation between these parameters.
    1 context sentence
    Summary · context
    Adult Swiss-Webster mice were OVX, and after the fifth postoperative week were treated intermittently with human PTH(1-34) [hPTH(1-34)] or vehicle for 4 weeks.

    In this study, Teriparatide (PTH 1-34) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Teriparatide (PTH 1-34).

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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