Evidence map›Paper›PMID 31496648›Full record

ArticleDrug design, development and therapy2019

Systemic taurine treatment provides neuroprotection against retinal photoreceptor degeneration and visual function impairments.

Ye Tao, Miao He, Qinghua Yang, Zhao Ma, Yingxin Qu, Wen Chen, Guanghua Peng, Dengke Teng

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  3. Rekindling Vision: Innovative Strategies for Treating Retinal Degeneration.International journal of molecular sciences · 2025
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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

8 authors at 3 institutions in 1 country.

Ye Tao *Department of Physiology, Basic Medical College, Zhengzhou University, Zhengzhou 450001, People's Republic of China.
Miao He *Department of Neurosurgery, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430014, People's Republic of China.
Qinghua YangDepartment of Physiology, Basic Medical College, Zhengzhou University, Zhengzhou 450001, People's Republic of China.
Zhao MaDepartment of Neurosurgery, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430014, People's Republic of China.
Yingxin QuDepartment of Physiology, Basic Medical College, Zhengzhou University, Zhengzhou 450001, People's Republic of China.
Wen ChenDepartment of Neurosurgery, Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430014, People's Republic of China.
Guanghua PengDepartment of Physiology, Basic Medical College, Zhengzhou University, Zhengzhou 450001, People's Republic of China.
Dengke TengDepartment of Ultrasound, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
Zhengzhou University · CNHuazhong University of Science and Technology · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveRetinitis pigmentosa causes progressive photoreceptor degeneration in the subjects while no clinical therapy exists. The present study sought to evaluate the potential protective effects of taurine on a pharmacologically induced RP animal model.

methodsPhotoreceptor degeneration in mice was induced by an intraperitoneal injection of N-methyl-N-nitrosourea (MNU). The MNU-administrated mouse received taurine treatment and then they were examined by electroretinography, spectral-domain optical coherence tomography, optokinetic test, and histological and immunohistochemistry assay.

resultsProminent taurine deficiency was found in the retinas of MNU-administered mice. Intravenous taurine treatment increased significantly the retinal taurine level. Morphological studies showed that taurine could alleviate the retinal disorganizations in the MNU-induced mice. Taurine also ameliorated the visual impairments in the MNU-induced mice as evidenced by functional examinations. Immunostaining experiments demonstrated that both the M-cone and S-cone populations in the degenerative retinas are rescued by taurine. In particular, the M-cone photoreceptors in superior-temporal quadrant and the S-cone photoreceptors in inferior-nasal quadrant were preferentially rescued. Mechanism study showed that the photoreceptor apoptosis and oxidative stress in the degenerative retina were effectively alleviated by taurine treatment.

conclusionTaurine is protective against the MNU-induced photoreceptor degeneration. Systemic taurine administration may act as a promising therapeutic potion for retinopathies with chronic cycle.

Indexed as

AnimalsApoptosisDisease Models, AnimalFemaleInjections, IntraperitonealInjections, IntravenousMaleMethylnitrosoureaMiceMice, Inbred C57BLNeuroprotective AgentsPhotoreceptor Cells, VertebrateRetinal DegenerationTaurineTomography, Optical CoherenceVision DisordersMethylnitrosoureaNeuroprotective AgentsTaurineneural degenerationretinatherapeutics

Identifiers

PMID31496648
PMCPMC6689665
OpenAlexW2965504938

What OpenQuestion holds

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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.