Evidence map›Paper›PMID 38480649›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2024

Effect of Advanced Glycation end Products (AGEs) on Sperm Parameters and Function in C57Bl/6 Mice.

Zahra Darmishonnejad, Vahideh Hassan Zadeh, Marziyeh Tavalaee, Farzad Kobarfard, Mahsa Hassani, Parviz Gharagozloo, Joël R Drevet, Mohammad Hossein Nasr-Esfahani

Abstract read
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In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2024. 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
5.3field-weighted citation impact, top 4% 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, 14 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

8 authors at 5 institutions in 3 countries.

Zahra DarmishonnejadDepartment of Biology, Kish International Campus, University of Tehran, Tehran, Iran.ORCID 0000-0001-8568-367X
Vahideh Hassan ZadehDepartment of Cell and Molecular Biology, Faculty of Biology, College of Science, University of Tehran, Tehran, Iran. vhassanzadeh@ut.ac.ir.ORCID 0000-0002-3632-298X
Marziyeh TavalaeeDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.ORCID 0000-0001-9954-964X
Farzad KobarfardDepartment of Medical Chemistry, Shahid Beheshti School of Pharmacy, Tehran, Iran.ORCID 0000-0001-6679-3275
Mahsa HassaniDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.ORCID 0009-0005-4483-6664
Parviz GharagozlooCellOxess LLC, 15 Roszel Road, Princeton, NJ, 08540, USA.ORCID 0000-0003-3955-3297
Joël R DrevetGReD Institute, Faculté de Médecine, CRBC, Université Clermont Auvergne, 63000, Clermont-Ferrand, France.ORCID 0000-0003-3077-6558
Mohammad Hossein Nasr-EsfahaniDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran. mh.nasr-esfahani@royaninstitute.org.ORCID 0000-0003-1983-3435
Royan Institute · IRCellOxess (United States) · USShahid Beheshti University of Medical Sciences · IRUniversité Clermont Auvergne · FRUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated the deleterious impact of advanced glycation end products (AGEs), commonly present in metabolic disorders like diabetes, obesity, and infertility-related conditions, on sperm structure and function using a mouse model where AGE generation was heightened through dietary intervention. Five-week-old C57BL/6 mice were divided into two groups, one on a regular diet (control) and the other on an AGE-rich diet. After 13 weeks, various parameters were examined, including fasting blood glucose, body weight, food consumption, sperm parameters and function, testicular superoxide dismutase levels, malondialdehyde content, total antioxidant capacity, Johnson score, AGE receptor (RAGE) content, and carboxymethyl lysine (CML) content. The results showed that mice in the AGE group exhibited increased body weight and elevated fasting blood glucose levels. Furthermore, the AGE group displayed adverse effects on sperm, including reduced sperm counts, motility, increased morphological abnormalities, residual histone, protamine deficiency, sperm DNA fragmentation, reduced testicular antioxidant capacity, and higher levels of RAGE and CML proteins. These findings underscore the negative impact of AGEs on male reproductive health, particularly within the context of metabolic disorders, emphasizing the crucial role of the AGE/RAGE axis in male infertility, especially in the context of Western dietary patterns.

Indexed as

Glycation End Products, AdvancedMice, Inbred C57BLReceptor for Advanced Glycation End ProductsSpermatozoaSperm MotilityAnimalsBlood GlucoseDNA FragmentationLysineMaleMiceOxidative StressSperm CountTestisBlood GlucoseGlycation End Products, AdvancedLysineN(6)-carboxymethyllysineReceptor for Advanced Glycation End ProductsAdvanced glycation end productsCarboxymethyl lysineDiabetes mellitusReceptor of advanced glycation end productsSperm functionSperm parameters

Identifiers

PMID38480649
OpenAlexW4392744618

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.