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Study · Animal study (in vivo) · mouse · 2026

5 results

Abaloparatide-Zoledronate combination protects against 4-vinylcyclohexene diepoxide-induced postmenopausal osteoporosis in mice: an osteoanabolic-antiresorptive approach.

Ara T, Iqbal Z, Jain S, Sheikh AA, Vohora D

Naunyn-Schmiedeberg's archives of pharmacology24 Jan 2026

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 study5

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

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In mice, abaloparatide alone partially reversed VCD-induced changes in bone microarchitecture.

    In plain wordsIn mice, abaloparatide alone partially reversed bone structure changes caused by VCD.

    Outcome
    Direction not reportedBone microarchitecture with abaloparatide alone
    Study

    mousen: not reported in source

    VCD-induced postmenopausal osteoporosis in female Swiss albino mice
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    20 µg/kg/d · subcutaneous · 30 daysAs given in this study (mouse).

    Source sentences

    Summary
    Treatment with abaloparatide and zoledronate combination for 30 days reversed VCD-induced alterations of BV/TV, BMD, Tb.N, and Tb.Sp, while the individual treatments were only partially effective.
    2 context sentences
    Summary · context
    This study aimed to investigate the impact of abaloparatide (20 µg/kg/d; s.c.), an osteoanabolic drug with an antiresorptive drug zoledronate (125 µg/kg i.v.) twice weekly for a month against 4-vinylcyclohexene diepoxide (VCD)-induced postmenopausal osteoporosis in mice.
    Summary · context
    Female Swiss albino mice were made ovotoxic by treatment with VCD (160 mg/kg/d) for 15 days to mimic a postmenopausal state, confirmed by primordial follicle destruction in histopathological assessment.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In mice, abaloparatide alone reversed VCD-induced alterations in P1NP, CTX-1, and RANKL.

    In plain wordsIn mice, abaloparatide alone reversed changes in three bone markers caused by VCD.

    Outcome
    Direction not reportedBone turnover markers with abaloparatide alone
    Study

    mousen: not reported in source

    VCD-induced postmenopausal osteoporosis in female Swiss albino mice
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    20 µg/kg/d · subcutaneousAs given in this study (mouse).

    Source sentences

    Summary
    The abaloparatide individually and in combination reversed the VCD-induced alterations in P1NP, CTX-1, and RANKL.
    2 context sentences
    Summary · context
    This study aimed to investigate the impact of abaloparatide (20 µg/kg/d; s.c.), an osteoanabolic drug with an antiresorptive drug zoledronate (125 µg/kg i.v.) twice weekly for a month against 4-vinylcyclohexene diepoxide (VCD)-induced postmenopausal osteoporosis in mice.
    Summary · context
    Female Swiss albino mice were made ovotoxic by treatment with VCD (160 mg/kg/d) for 15 days to mimic a postmenopausal state, confirmed by primordial follicle destruction in histopathological assessment.

Studies that did not test the peptide alone3

In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  1. 03AnimalNot a test of Abaloparatide (Tymlos) aloneAnimal study (in vivo)Efficacy outcome

    In mice, abaloparatide plus zoledronate reversed VCD-induced changes in BV/TV, BMD, Tb.N, and Tb.Sp, while individual treatments were partially effective.

    In plain wordsIn mice, abaloparatide plus zoledronate reversed bone structure changes, while each drug alone had partial effects.

    Outcome
    Direction not reportedBone microarchitecture with combination
    Study

    mousen: not reported in source

    VCD-induced postmenopausal osteoporosis in female Swiss albino mice
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    Treatment with abaloparatide and zoledronate combination for 30 days reversed VCD-induced alterations of BV/TV, BMD, Tb.N, and Tb.Sp, while the individual treatments were only partially effective.
    2 context sentences
    Summary · context
    This study aimed to investigate the impact of abaloparatide (20 µg/kg/d; s.c.), an osteoanabolic drug with an antiresorptive drug zoledronate (125 µg/kg i.v.) twice weekly for a month against 4-vinylcyclohexene diepoxide (VCD)-induced postmenopausal osteoporosis in mice.
    Summary · context
    Female Swiss albino mice were made ovotoxic by treatment with VCD (160 mg/kg/d) for 15 days to mimic a postmenopausal state, confirmed by primordial follicle destruction in histopathological assessment.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  2. 04AnimalNot a test of Abaloparatide (Tymlos) aloneAnimal study (in vivo)Efficacy outcome

    In mice, abaloparatide plus zoledronate reversed VCD-induced alterations in P1NP, CTX-1, and RANKL.

    In plain wordsIn mice, abaloparatide plus zoledronate reversed changes in three bone markers caused by VCD.

    Outcome
    Direction not reportedBone turnover markers with combination
    Study

    mousen: not reported in source

    VCD-induced postmenopausal osteoporosis in female Swiss albino mice
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    The abaloparatide individually and in combination reversed the VCD-induced alterations in P1NP, CTX-1, and RANKL.
    2 context sentences
    Summary · context
    This study aimed to investigate the impact of abaloparatide (20 µg/kg/d; s.c.), an osteoanabolic drug with an antiresorptive drug zoledronate (125 µg/kg i.v.) twice weekly for a month against 4-vinylcyclohexene diepoxide (VCD)-induced postmenopausal osteoporosis in mice.
    Summary · context
    Female Swiss albino mice were made ovotoxic by treatment with VCD (160 mg/kg/d) for 15 days to mimic a postmenopausal state, confirmed by primordial follicle destruction in histopathological assessment.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

  3. 05AnimalNot a test of Abaloparatide (Tymlos) aloneAnimal study (in vivo)Efficacy outcome

    In mice, abaloparatide plus zoledronate lowered the RANKL/OPG ratio.

    In plain wordsIn mice, abaloparatide plus zoledronate lowered the ratio of two bone regulation markers.

    Outcome
    DecreaseRANKL/OPG ratio with combination
    Study

    mousen: not reported in source

    VCD-induced postmenopausal osteoporosis in female Swiss albino mice
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    The combination therapy also lowered the RANKL/OPG ratio.
    2 context sentences
    Summary · context
    This study aimed to investigate the impact of abaloparatide (20 µg/kg/d; s.c.), an osteoanabolic drug with an antiresorptive drug zoledronate (125 µg/kg i.v.) twice weekly for a month against 4-vinylcyclohexene diepoxide (VCD)-induced postmenopausal osteoporosis in mice.
    Summary · context
    Female Swiss albino mice were made ovotoxic by treatment with VCD (160 mg/kg/d) for 15 days to mimic a postmenopausal state, confirmed by primordial follicle destruction in histopathological assessment.

    In this study, Abaloparatide (Tymlos) 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 Abaloparatide (Tymlos).

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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