Evidence map›Paper›PMID 36484981›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2023

Taurine Improves Sperm Mitochondrial Indices, Blunts Oxidative Stress Parameters, and Enhances Steroidogenesis and Kinematics of Sperm in Lead-Exposed Mice.

Mohammad Mehdi Ommati, Samira Sabouri, Socorro Retana-Marquez, Hassan Nategh Ahmadi, Abdollah Arjmand, Sepideh Alidaee, Sahra Mazloomi, Alireza Akhlagh, Narges Abdoli, Hossein Niknahad and 5 more

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In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Taurine in canine physiology and metabolic regulation.Frontiers in veterinary science · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
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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

15 authors at 6 institutions in 3 countries.

Mohammad Mehdi Ommati *College of Veterinary Medicine, Shanxi Agricultural University, Taigu, 030801, Shanxi, China. mehdi_ommati@outlook.com.ORCID 0000-0003-0514-2414
Samira Sabouri *College of Veterinary Medicine, Shanxi Agricultural University, Taigu, 030801, Shanxi, China.
Socorro Retana-MarquezDepartment of Biology of Reproduction, Autonomous Metropolitan University-Iztapalapa, Mexico City, Mexico.
Hassan Nategh AhmadiCollege of Veterinary Medicine, Shanxi Agricultural University, Taigu, 030801, Shanxi, China.
Abdollah ArjmandDepartment of Toxicology and Pharmacology, Faculty of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Sepideh AlidaeePharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Sahra MazloomiPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Alireza AkhlaghPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Narges AbdoliIran Food and Drug Administration, Ministry of Health, Tehran, Iran.
Hossein NiknahadPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Akram JamshidzadehPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Yanqin MaCollege of Life Sciences, Shanxi Agricultural University, Taigu, 030801, Shanxi, China.
Negar AzarpiraTransplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Yaser AsefiDepartment of Genetics, Ahar Branch, Islamic Azad University, Ahar, Iran.
Reza HeidariPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. rezaheidari@hotmail.com.ORCID 0000-0002-7038-9838
Shiraz University of Medical Sciences · IRShanxi Agricultural University · CNIslamic Azad University of Ahar · IRMinistry of Health and Medical Education · IRShahid Beheshti University of Medical Sciences · IRUniversidad Autónoma Metropolitana · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lead (Pb) is a highly toxic heavy metal. Pb exposure could adversely affect many organs, including the male reproductive system. Oxidative stress and mitochondrial impairment play a fundamental role in the pathogenesis of Pb-induced male reproductive system injury. Taurine (TAU) is abundantly found in mammalian bodies. The positive effects of TAU on oxidative stress biomarkers and mitochondrial function have been reported. The current study evaluated the effects of TAU on Pb-induced reproductive toxicity. Mice received Pb (20 mg/kg/day; gavage, 35 consecutive days). Then, sperm indices (quality and quantity) together with sperm kinetics, sperm mitochondrial parameters, testicular and sperm oxidative stress biomarkers, testis and plasma testosterone levels, and the expression of genes involved in the steroidogenesis process have been evaluated. Pb caused significant histopathological alterations and oxidative stress in male mice's reproductive system and sperm. Moreover, significant mitochondrial function impairment was evident in sperm isolated from Pb-treated mice. Pb exposure also suppressed the expression of StAR, 17β-HSD, CYP11A, and 3β-HSD genes in the male gonad. It was found that TAU (500 and 1000 mg/kg) significantly improved oxidative stress biomarkers in both male gonads and gametes of Pb-treated mice. TAU also significantly restored sperm mitochondrial function and kinetics. The expression of genes involved in steroidogenesis was also higher in TAU-treated animals. These data suggest TAU as an effective agent against Pb-induced reproductive toxicity. The effects of TAU on oxidative stress markers, mitochondrial function, and the steroidogenesis process seem to play a fundamental role in its protective properties. Further studies are warranted to detect the precise protective effects of this amino acid in the reproductive system. Lead (Pb) is a toxic element that adversely affects the male reproductive system. Mitochondrial impairment and oxidative stress have a crucial role in the Pb-induced reproductive toxicity. Taurine (TAU) could considerably improve the reproductive toxicity induced by Pb via enhancing mitochondrial function and mitigating oxidative stress indices. ΔΨ, mitochondrial membrane potential; ATP, adenosine triphosphate.

Indexed as

LeadTaurineAnimalsBiomarkersBiomechanical PhenomenaMaleMammalsMiceMitochondriaOxidative StressSemenSpermatozoaTestisTestosteroneBiomarkersLeadTaurineTestosteroneHeavy metalsMitochondrial impairmentOxidative stressReproductive toxicitySpermatozoa

Identifiers

PMID36484981
OpenAlexW4310943231

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.