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Study · Ex vivo tissue · rat · 2016

6 results

Mechanisms of vasodilation to PTH 1-84, PTH 1-34, and PTHrP 1-34 in rat bone resistance arteries.

Benson T, Menezes T, Campbell J, Bice A, Hood B, Prisby R

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA5 Jan 2016Cited by 21 (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

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

  1. 01LabEx vivo tissueMechanism

    In rat bone arteries, vasodilation was lowest with PTH 1‑34 among the three analogs.

    In plain wordsIn lab tests, PTH 1‑34 produced less artery dilation than the other analogs.

    Outcome
    DecreaseVasodilation relative to other analogs
    Study

    ratn: not reported in source

    Femoral principal nutrient arteries
    Comparator
    PTH 1-84 and PTHrP 1-34
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    10(-13)-10(-8) MAs given in this study (rat).

    Source sentences

    Summary
    Vasodilation was lowest to PTH 1-34, and maximal dilation was highest to PTHrP 1-34.
    2 context sentences
    Summary · context
    Femoral principal nutrient arteries (PNAs) were given cumulative doses (10(-13)-10(-8) M) of PTH 1-84, PTH 1-34, and PTHrP 1-34 with and without signaling pathway blockade.
    Summary · context
    Vasodilation was also determined following endothelial cell removal (i.e., denudation), PTH 1 receptor (PTH1R) inhibition and to sodium nitroprusside (SNP; a nitric oxide [NO] donor).

Studies that did not test the peptide alone5

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. 02LabNot a test of Teriparatide (PTH 1-34) aloneEx vivo tissueMechanism

    In rat bone arteries, eNOS inhibition reduced PTH 1‑34-induced vasodilation by 66%.

    In plain wordsIn lab tests, eNOS inhibition reduced artery dilation induced by PTH 1‑34.

    Outcome
    DecreaseeNOS-dependent vasodilation
    Study

    ratn: not reported in source

    Femoral principal nutrient arteries
    Outcome group
    Receptor activity and mechanism · Cardiovascular

    Source sentences

    Summary
    Inhibition of eNOS reduced vasodilation to PTH 1-84 (-80 %), PTH 1-34 (-66 %), and PTHrP 1-34 (-48 %), evidencing the contribution of NO.
    2 context sentences
    Summary · context
    Femoral principal nutrient arteries (PNAs) were given cumulative doses (10(-13)-10(-8) M) of PTH 1-84, PTH 1-34, and PTHrP 1-34 with and without signaling pathway blockade.
    Summary · context
    Vasodilation was also determined following endothelial cell removal (i.e., denudation), PTH 1 receptor (PTH1R) inhibition and to sodium nitroprusside (SNP; a nitric oxide [NO] donor).

    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).

  2. 03LabNot a test of Teriparatide (PTH 1-34) aloneEx vivo tissueMechanism

    In rat bone arteries, endothelial removal impaired PTH 1‑34 vasodilation to 17% of maximum.

    In plain wordsIn lab tests, removal of the artery lining reduced dilation induced by PTH 1‑34.

    Outcome
    DecreaseEndothelium-dependent vasodilation
    Study

    ratn: not reported in source

    Femoral principal nutrient arteries
    Outcome group
    Receptor activity and mechanism · Cardiovascular

    Source sentences

    Summary
    Vasodilation following denudation was eliminated (PTH 1-84 and PTHrP 1-34) and impaired (PTH 1-34, 17 % of maximum), highlighting the importance of endothelial cells for PTH signaling.
    2 context sentences
    Summary · context
    Femoral principal nutrient arteries (PNAs) were given cumulative doses (10(-13)-10(-8) M) of PTH 1-84, PTH 1-34, and PTHrP 1-34 with and without signaling pathway blockade.
    Summary · context
    Vasodilation was also determined following endothelial cell removal (i.e., denudation), PTH 1 receptor (PTH1R) inhibition and to sodium nitroprusside (SNP; a nitric oxide [NO] donor).

    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).

  3. 04LabNot a test of Teriparatide (PTH 1-34) aloneEx vivo tissueMechanism

    In rat bone arteries, PKA inhibition diminished vasodilation induced by PTH 1‑34 and the other analogs.

    In plain wordsIn lab tests, PKA inhibition reduced artery dilation induced by PTH 1‑34 and the other analogs.

    Outcome
    DecreasePKA-dependent vasodilation
    Study

    ratn: not reported in source

    Femoral principal nutrient arteries
    Outcome group
    Receptor activity and mechanism · Cardiovascular

    Source sentences

    Summary
    Both PKA and PKC inhibition diminished vasodilation in all three analogs to varying degrees.
    2 context sentences
    Summary · context
    Femoral principal nutrient arteries (PNAs) were given cumulative doses (10(-13)-10(-8) M) of PTH 1-84, PTH 1-34, and PTHrP 1-34 with and without signaling pathway blockade.
    Summary · context
    Vasodilation was also determined following endothelial cell removal (i.e., denudation), PTH 1 receptor (PTH1R) inhibition and to sodium nitroprusside (SNP; a nitric oxide [NO] donor).

    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).

  4. 05LabNot a test of Teriparatide (PTH 1-34) aloneEx vivo tissueMechanism

    In rat bone arteries, PKC inhibition diminished vasodilation induced by PTH 1‑34 and the other analogs.

    In plain wordsIn lab tests, PKC inhibition reduced artery dilation induced by PTH 1‑34 and the other analogs.

    Outcome
    DecreasePKC-dependent vasodilation
    Study

    ratn: not reported in source

    Femoral principal nutrient arteries
    Outcome group
    Receptor activity and mechanism · Cardiovascular

    Source sentences

    Summary
    Both PKA and PKC inhibition diminished vasodilation in all three analogs to varying degrees.
    2 context sentences
    Summary · context
    Femoral principal nutrient arteries (PNAs) were given cumulative doses (10(-13)-10(-8) M) of PTH 1-84, PTH 1-34, and PTHrP 1-34 with and without signaling pathway blockade.
    Summary · context
    Vasodilation was also determined following endothelial cell removal (i.e., denudation), PTH 1 receptor (PTH1R) inhibition and to sodium nitroprusside (SNP; a nitric oxide [NO] donor).

    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).

  5. 06LabNot a test of Teriparatide (PTH 1-34) aloneEx vivo tissueMechanism

    In rat bone arteries, PTH1R blockade reduced PTH 1‑34-induced vasodilation to 12%.

    In plain wordsIn lab tests, receptor blockade reduced artery dilation induced by PTH 1‑34.

    Outcome
    DecreasePTH1R-dependent vasodilation
    Study

    ratn: not reported in source

    Femoral principal nutrient arteries
    Outcome group
    Receptor activity and mechanism · Cardiovascular

    Source sentences

    Summary
    PTH1R blockade reduced vasodilation to 1, 12, and 12 % to PTH 1-84, PTH 1-34, and PTHrP 1-34, respectively.
    2 context sentences
    Summary · context
    Femoral principal nutrient arteries (PNAs) were given cumulative doses (10(-13)-10(-8) M) of PTH 1-84, PTH 1-34, and PTHrP 1-34 with and without signaling pathway blockade.
    Summary · context
    Vasodilation was also determined following endothelial cell removal (i.e., denudation), PTH 1 receptor (PTH1R) inhibition and to sodium nitroprusside (SNP; a nitric oxide [NO] donor).

    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 3Current

    27 Oct 2026, 16:37 UTC

    Study data updated · source update from Europe PMC

  2. Version 2

    22 Oct 2026, 02:26 UTC

    Study results updated

  3. 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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