Evidence map›Paper›PMID 38514644›Full record

ArticleBone research2024

β-Receptor blocker enhances the anabolic effect of PTH after osteoporotic fracture.

Jie Huang, Tong Wu, Yi-Rong Jiang, Xuan-Qi Zheng, Huan Wang, Hao Liu, Hong Wang, Hui-Jie Leng, Dong-Wei Fan, Wan-Qiong Yuan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Bone research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
7.6field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Association of β-adrenergic receptor blockers use with the risk of fracture in adults: a systematic review and meta-analysis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
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  11. Neural Orchestration of Mandibular Development.International dental journal · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Jie Huang *Department of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Tong Wu *Department of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Yi-Rong JiangDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Xuan-Qi ZhengDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Huan WangDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Hao LiuDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Hong WangDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Hui-Jie LengDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Dong-Wei FanDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Wan-Qiong YuanDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China.
Chun-Li SongDepartment of Orthopedics, Peking University Third Hospital, 100191, Beijing, China. schl@bjmu.edu.cn.
Peking University Third Hospital · CNPeking University · CNPrecision Research (United States) · US

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81874010National Natural Science Foundation of China (National Science Foundation of China) 82330078
6 · The paper itself

Abstract

The autonomic nervous system plays a crucial role in regulating bone metabolism, with sympathetic activation stimulating bone resorption and inhibiting bone formation. We found that fractures lead to increased sympathetic tone, enhanced osteoclast resorption, decreased osteoblast formation, and thus hastened systemic bone loss in ovariectomized (OVX) mice. However, the combined administration of parathyroid hormone (PTH) and the β-receptor blocker propranolol dramatically promoted systemic bone formation and osteoporotic fracture healing in OVX mice. The effect of this treatment is superior to that of treatment with PTH or propranolol alone. In vitro, the sympathetic neurotransmitter norepinephrine (NE) suppressed PTH-induced osteoblast differentiation and mineralization, which was rescued by propranolol. Moreover, NE decreased the PTH-induced expression of Runx2 but enhanced the expression of Rankl and the effect of PTH-stimulated osteoblasts on osteoclastic differentiation, whereas these effects were reversed by propranolol. Furthermore, PTH increased the expression of the circadian clock gene Bmal1, which was inhibited by NE-βAR signaling. Bmal1 knockdown blocked the rescue effect of propranolol on the NE-induced decrease in PTH-stimulated osteoblast differentiation. Taken together, these results suggest that propranolol enhances the anabolic effect of PTH in preventing systemic bone loss following osteoporotic fracture by blocking the negative effects of sympathetic signaling on PTH anabolism.

Indexed as

Anabolic AgentsBone ResorptionOsteoporotic FracturesAdrenergic beta-AntagonistsAnimalsARNTL Transcription FactorsMiceParathyroid HormonePropranololAdrenergic beta-AntagonistsAnabolic AgentsARNTL Transcription FactorsParathyroid HormonePropranolol

Identifiers

PMID38514644
PMCPMC10958005
OpenAlexW4393045310

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.