Evidence map›Paper›PMID 35229281›Full record

ArticleHistology and histopathology2022

Asiatic acid improves high-fat-diet-induced osteoporosis in mice via regulating SIRT1/FOXO1 signaling and inhibiting oxidative stress.

Xiaosi Chen, Dengpeng Han, Tianfeng Liu, Chengshuo Huang, Zibing Hu, Xiaoyan Tan, Shaoke Wu

Abstract read
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In one paragraph

Article in Histology and histopathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 8 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Xiaosi ChenInternational and Special Medical Service ward, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, Guangdong Province, China.
Dengpeng HanDepartment of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, Guangdong Province, China.
Tianfeng LiuDepartment of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, Guangdong Province, China.
Chengshuo HuangDepartment of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, Guangdong Province, China.
Zibing HuDepartment of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, Guangdong Province, China.
Xiaoyan TanDepartment of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, Guangdong Province, China.
Shaoke WuDepartment of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, Guangdong Province, China. skwu3226@163.com.
Guangdong Medical College · CN

Funding

Natural Science Foundation of Guangdong Province 2018A030307019
6 · The paper itself

Abstract

Asiatic acid can attenuate osteoporosis through suppressing adipogenic differentiation and osteoclastic differentiation. Oxidative stress enhances osteoclastic differentiation but represses osteogenic differentiation to promote osteoporosis. However, the role and mechanism of asiatic acid in osteoporosis have not been reported. Firstly, mice were fed with high-fat-diet (HFD) with or without asiatic acid for 16 weeks. Data from an automatic biochemical analyzer showed that HFD induced down-regulation of high-density lipoprotein (HDL) and an increase of serum levels of triglyceride (TG), total cholesterol (TC) and low-density lipoprotein (LDL). However, asiatic acid administration attenuated the decrease of HDL and increase of serum TG, TC and LDL in osteoporotic mice. Secondly, HFD induced high levels of malondialdehyde (MDA) and reactive oxygen species (ROS), low levels of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in osteoporotic mice. However, the levels of MDA, ROS, SOD and GSH-Px in osteoporotic mice were reversed by asiatic acid administration. (this section is unclear and requires revision) Asiatic acid administration reduced expression of c-telopeptide of type 1 collagen (CTX-1), enhanced alkaline phosphatase (ALP) and procollagen type 1 N-terminal propeptide (P1NP) in HFD-induced osteoporotic mice. (this section is unclear and requires revision) Thirdly, asiatic acid promoted calcium deposition in bone marrow cells and osteogenic differentiation in osteoporotic mice, but decreased ALP in bone marrow cells. Lastly, asiatic acid enhanced SIRT1 and nuclear FOXO1 (Nu-FOXO1) expression, while it reduced Acetyl FOXO1 (Ac-FOXO1) in osteoporotic mice. In conclusion, asiatic acid might inhibit oxidative stress and promote osteogenic differentiation through activating SIRT1/FOXO1 to attenuate HFD-induced osteoporosis in mice.

Indexed as

OsteoporosisSirtuin 1Alkaline PhosphataseAnimalsCalciumCholesterolCollagen Type IDiet, High-FatForkhead Box Protein O1Glutathione PeroxidaseLipoproteins, HDLLipoproteins, LDLMalondialdehydeMiceOsteogenesisOxidative StressAlkaline Phosphataseasiatic acidCalciumCholesterolCollagen Type IForkhead Box Protein O1Foxo1 protein, mouseGlutathione PeroxidaseLipoproteins, HDLLipoproteins, LDLMalondialdehydePentacyclic TriterpenesProcollagenReactive Oxygen SpeciesSirt1 protein, mouseSirtuin 1Superoxide DismutaseTriglycerides

Identifiers

PMID35229281
OpenAlexW4214698652

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Registered trials

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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 OpenQuestion graph.