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Study · Animal study (in vivo) · rat · 2017

15 results

One year of abaloparatide, a selective peptide activator of the PTH1 receptor, increased bone mass and strength in ovariectomized rats.

Varela A, Chouinard L, Lesage E, Guldberg R, Smith SY, Kostenuik PJ, Hattersley G

Bone25 Nov 2016Cited by 36 (Europe PMC)

Summary

Abaloparatide is a novel 34 amino acid peptide selected to be a potent and selective activator of the parathyroid hormone receptor 1 (PTHR1) signaling pathway. The effects of 12months of abaloparatide treatment on bone mass, bone strength and bone quality was assessed in osteopenic ovariectomized (OVX) rats. SD rats were subjected to OVX or sham surgery at 6months of age and left untreated for 3months to allow OVX-induced bone loss. Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months. Sham controls (n=18) received vehicle daily. Bone changes were assessed by DXA and pQCT after 0, 3, 6 or 12months of treatment, and destructive biomechanical testing was conducted at month 12 to assess bone strength and bone quality. Abaloparatide dose-dependently increased bone mass at the lumbar spine and at the proximal and diaphyseal regions of the tibia and femur. pQCT revealed that increased cortical bone volume at the tibia was a result of periosteal expansion and endocortical bone apposition. Abaloparatide dose-dependently increased structural strength of L4-L5 vertebral bodies, the femur diaphysis, and the femur neck. Increments in peak load for lumbar spine and the femur diaphysis of abaloparatide-treated rats persisted even after adjusting for treatment-related increments in BMC, and estimated material properties were maintained or increased at the femur diaphysis with abaloparatide. The abaloparatide groups also exhibited significant and positive correlations between bone mass and bone strength at these sites. These data indicate that gains in cortical and trabecular bone mass with abaloparatide are accompanied by and correlated with improvements in bone strength, resulting in maintenance or improvement in bone quality. Thus, this study demonstrated that long-term daily administration of abaloparatide to osteopenic OVX rats led to dose-dependent improvements in bone mass, geometry and strength.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study15

15 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, abaloparatide dose-dependently increased lumbar spine bone mass.

    In plain wordsIn rats, abaloparatide increased lumbar spine bone mass with increasing dose compared with vehicle.

    Outcome
    IncreaseLumbar spine bone mass
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased bone mass at the lumbar spine and at the proximal and diaphyseal regions of the tibia and femur.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide dose-dependently increased proximal tibial bone mass.

    In plain wordsIn rats, abaloparatide increased proximal tibial bone mass with increasing dose compared with vehicle.

    Outcome
    IncreaseProximal tibial bone mass
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased bone mass at the lumbar spine and at the proximal and diaphyseal regions of the tibia and femur.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide dose-dependently increased tibial diaphysis bone mass.

    In plain wordsIn rats, abaloparatide increased tibial shaft bone mass with increasing dose compared with vehicle.

    Outcome
    IncreaseTibial diaphysis bone mass
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased bone mass at the lumbar spine and at the proximal and diaphyseal regions of the tibia and femur.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide dose-dependently increased proximal femoral bone mass.

    In plain wordsIn rats, abaloparatide increased proximal femoral bone mass with increasing dose compared with vehicle.

    Outcome
    IncreaseProximal femoral bone mass
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased bone mass at the lumbar spine and at the proximal and diaphyseal regions of the tibia and femur.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  5. 05AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide dose-dependently increased femoral diaphysis bone mass.

    In plain wordsIn rats, abaloparatide increased femoral shaft bone mass with increasing dose compared with vehicle.

    Outcome
    IncreaseFemoral diaphysis bone mass
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased bone mass at the lumbar spine and at the proximal and diaphyseal regions of the tibia and femur.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  6. 06AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide increased tibial cortical bone volume.

    In plain wordsIn rats, abaloparatide increased tibial cortical bone volume compared with vehicle.

    Outcome
    IncreaseTibial cortical bone volume
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    pQCT revealed that increased cortical bone volume at the tibia was a result of periosteal expansion and endocortical bone apposition.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  7. 07AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide dose-dependently increased vertebral body structural strength.

    In plain wordsIn rats, abaloparatide increased vertebral strength with increasing dose compared with vehicle.

    Outcome
    IncreaseVertebral structural strength
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased structural strength of L4-L5 vertebral bodies, the femur diaphysis, and the femur neck.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  8. 08AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide dose-dependently increased femoral diaphysis structural strength.

    In plain wordsIn rats, abaloparatide increased femoral shaft strength with increasing dose compared with vehicle.

    Outcome
    IncreaseFemoral diaphysis structural strength
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased structural strength of L4-L5 vertebral bodies, the femur diaphysis, and the femur neck.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  9. 09AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide dose-dependently increased femoral neck structural strength.

    In plain wordsIn rats, abaloparatide increased femoral neck strength with increasing dose compared with vehicle.

    Outcome
    IncreaseFemoral neck structural strength
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Abaloparatide dose-dependently increased structural strength of L4-L5 vertebral bodies, the femur diaphysis, and the femur neck.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  10. 10AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, lumbar spine peak-load increases with abaloparatide persisted after adjustment for bone mineral content increases.

    In plain wordsIn rats, lumbar spine load capacity increased with abaloparatide even after adjustment for bone mineral content compared with vehicle.

    Outcome
    IncreaseBMC-adjusted lumbar peak load
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Increments in peak load for lumbar spine and the femur diaphysis of abaloparatide-treated rats persisted even after adjusting for treatment-related increments in BMC,
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  11. 11AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, femoral diaphysis peak-load increases with abaloparatide persisted after adjustment for bone mineral content increases.

    In plain wordsIn rats, femoral shaft load capacity increased with abaloparatide even after adjustment for bone mineral content compared with vehicle.

    Outcome
    IncreaseBMC-adjusted femoral diaphysis peak load
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    Increments in peak load for lumbar spine and the femur diaphysis of abaloparatide-treated rats persisted even after adjusting for treatment-related increments in BMC,
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  12. 12AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, estimated femoral diaphysis material properties were maintained or increased with abaloparatide.

    In plain wordsIn rats, abaloparatide maintained or increased estimated femoral shaft material properties compared with vehicle.

    Outcome
    MixedFemoral diaphysis material properties
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    and estimated material properties were maintained or increased at the femur diaphysis with abaloparatide.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  13. 13AnimalAnimal study (in vivo)Other

    In abaloparatide-treated ovariectomized rats, bone mass correlated positively and significantly with bone strength at the measured sites.

    In plain wordsIn rats receiving abaloparatide, greater bone mass was linked to greater bone strength.

    Outcome
    IncreaseBone mass-strength correlation
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    The abaloparatide groups also exhibited significant and positive correlations between bone mass and bone strength at these sites.
    2 context sentences
    Summary · context
    Abaloparatide dose-dependently increased structural strength of L4-L5 vertebral bodies, the femur diaphysis, and the femur neck.
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  14. 14AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide-associated increases in tibial cortical bone volume resulted partly from periosteal expansion.

    In plain wordsIn rats, outer tibial surface expansion contributed to increased cortical volume with abaloparatide compared with vehicle.

    Outcome
    IncreaseTibial periosteal expansion
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    pQCT revealed that increased cortical bone volume at the tibia was a result of periosteal expansion and endocortical bone apposition.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.
  15. 15AnimalAnimal study (in vivo)Efficacy outcome

    In ovariectomized rats, abaloparatide-associated increases in tibial cortical bone volume resulted partly from endocortical bone apposition.

    In plain wordsIn rats, inner tibial surface bone deposition contributed to increased cortical volume with abaloparatide compared with vehicle.

    Outcome
    IncreaseTibial endocortical bone apposition
    Study

    ratn: not reported in source

    osteopenic ovariectomized SD rats
    Comparator
    vehicle
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    1, 5 or 25μg/kg/d · subcutaneous · 12 monthsAs given in this study (rat).

    Source sentences

    Summary
    pQCT revealed that increased cortical bone volume at the tibia was a result of periosteal expansion and endocortical bone apposition.
    1 context sentence
    Summary · context
    Eighteen OVX rats were sacrificed after this bone depletion period, and the remaining OVX rats received daily s.c. injections of vehicle (n=18) or abaloparatide at 1, 5 or 25μg/kg/d (n=18/dose level) for 12months.

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

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