Evidence map›Paper›PMID 27553527›Full record

ArticleScientific reports2016

Induction of renal senescence marker protein-30 (SMP30) expression by testosterone and its contribution to urinary calcium absorption in male rats.

Po-Han Lin, Cai-Yun Jian, Jou-Chun Chou, Chien-Wei Chen, Chih-Chieh Chen, Christina Soong, Sindy Hu, Fu-Kong Lieu, Paulus S Wang, Shyi-Wu Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 15 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

10 authors at 5 institutions in 1 country.

Po-Han LinInstitute and Department of Physiology, School of Medicine, National Yang-Ming University, Taipei 11221, Taiwan, Republic of China.
Cai-Yun JianInstitute and Department of Physiology, School of Medicine, National Yang-Ming University, Taipei 11221, Taiwan, Republic of China.
Jou-Chun ChouMedical Center of Aging Research, China Medical University Hospital, Taichung 40402, Taiwan, Republic of China.
Chien-Wei ChenInstitute and Department of Physiology, School of Medicine, National Yang-Ming University, Taipei 11221, Taiwan, Republic of China.
Chih-Chieh ChenInstitute and Department of Physiology, School of Medicine, National Yang-Ming University, Taipei 11221, Taiwan, Republic of China.
Christina SoongDepartment of Rehabilitation, Cheng Hsin General Hospital, Taipei 11212, Taiwan, Republic of China.
Sindy HuAesthetic Medical Center, Department of Dermatology, Chang Gung Memorial Hospital, Taoyuan 33378, Taiwan, Republic of China.
Fu-Kong LieuDepartment of Rehabilitation, Cheng Hsin General Hospital, Taipei 11212, Taiwan, Republic of China.
Paulus S WangInstitute and Department of Physiology, School of Medicine, National Yang-Ming University, Taipei 11221, Taiwan, Republic of China.
Shyi-Wu WangAesthetic Medical Center, Department of Dermatology, Chang Gung Memorial Hospital, Taoyuan 33378, Taiwan, Republic of China.
National Yang Ming Chiao Tung University · TWChang Gung Memorial Hospital · TWCheng Hsin General Hospital · TWAsia University · TWChina Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the involvement of androgen, mainly testosterone, in the expression of renal senescence marker protein-30 (SMP30) in male rats. We found that the renal SMP30 expression was up-regulated by endogenous testosterone stimulation during puberty. Interestingly, androgen-deficient orchidectomized (ORX) rats exhibited lower SMP30 mRNA and protein expression in the kidney, and that was restored by testosterone propionate (TP) replacement. Abrogation of androgen receptor (AR) activity by co-treatment with flutamide abolished testosterone-induced SMP30 expression in the kidney as well as in the NRK52E cells. However, SMP30 expression was unaltered in the liver of ORX rats. We also showed a positive correlation between renal SMP30 expression and plasma testosterone level during the aging process. TP-induced SMP30 expression in ovariectomized (OVX) rats was observed and was an evidence to explain the gender difference of SMP30 levels. Immunofluorescence assay showed that renal SMP30 was specifically expressed in the proximal tubular segments of the kidney. The urinary Ca(2+) level was increased in both ORX and male aging rats. Taken together, our results indicate a novel role of testosterone in regulating SMP30 expression specifically in the kidney to contribute to urinary calcium absorption.

Indexed as

AgingAnimalsCalciumCalcium-Binding ProteinsCalcium-Transporting ATPasesCarboxylic Ester HydrolasesFemaleIntracellular Signaling Peptides and ProteinsKidneyLiverMaleOrchiectomyOvariectomyPubertyRats, Sprague-DawleyReceptors, AndrogenCalciumCalcium-Binding ProteinsCalcium-Transporting ATPasesCarboxylic Ester HydrolasesIntracellular Signaling Peptides and ProteinsReceptors, AndrogenRgn protein, ratTestosteroneTestosterone Propionate

Identifiers

PMID27553527
PMCPMC4995462
OpenAlexW2509353400

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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.