Evidence map›Paper›PMID 41983361›Full record

ArticleInternational journal of fertility & sterility2026

Exercise Training Ameliorates The Tramadol-Induced Toxicity on VEGF/VEGFRs/PI3K/AKT Signaling Pathway in Testicular Tissue after Tramadol Withdrawal.

Vahid Saeidifard, Asghar Tofighi, Javad Tolouei Azar, Mazdak Razi

Abstract read
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Article in International journal of fertility & sterility, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Vahid SaeidifardDepartment of Exercise Physiology and Corrective Exercises, Faculty of Sport Sciences, Urmia University, Urmia, Iran.Email: j.toloueiazar@urmia.ac.ir.ORCID 0000-0002-2329-4801
Asghar TofighiDepartment of Exercise Physiology and Corrective Exercises, Faculty of Sport Sciences, Urmia University, Urmia, Iran.
Javad Tolouei AzarDepartment of Exercise Physiology and Corrective Exercises, Faculty of Sport Sciences, Urmia University, Urmia, Iran.ORCID 0000-0002-2724-8474
Mazdak RaziDepartment of Basic Sciences, Faculty of Veterinary Medicine, Urmia University, Urmia, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The study investigated how exercise training protocols (ETPs) with different intensities can ameliorate the tramadol (TRA)-induced toxicity in the testicular tissue by upregulating VEGF/VEGFRs/PI3K/AKT signaling pathway in the post-withdrawal period. Materials and Methods: In this experimental study, thirty-six mature Wistar rats were included in two groups: one being a sedentary control group, and the other receiving TRA treatment (40 mg/kg, daily, ip). After 60 days, six rats from the TRA-received group were excluded (TRA-sole; euthanized after 60 days). The TRA administration was stopped and the rats were further divided into four subgroups: TRA/withdrawal (TRA/W), low (LICT), moderate (MICT), and high (HICT)-intensity continuous exercise training-received groups (n=6/each group). The expression levels of phosphoinositide 3-kinases (PI3K), protein Kinase B (AKT), vascular endothelial growth factor (VEGF), VEGF receptor 1 (VEGF R1) and 2 (VEGF R2) were assessed. Results: The expression levels of PI3K, AKT, VEGF, VEGF R1, and VEGF R2 were decreased in the TRA-sole group. No significant alterations were noted in the PI3K, AKT, VEGF, and VEGF R1 expressions after 60 days of withdrawal compared to the TRA-sole rats. However, this situation was reversed and the expression levels of PI3K, AKT, VEGF, VEGF R1, and VEGF R2 increased in the MICT and HICT-received groups. Conclusion: TRA disrupts the PI3K/AKT interaction, and this disruption is not easily reversed shortly after withdrawal. However, ETPs exert positive effects on PI3K/AKT signaling by promoting the expression of VEGF, VEGFR1, and R2. These results highlight the potential of ETPs to ameliorate the adverse effects of TRA on VEGF/VEGF R1, R2/PI3K/AKT signaling, even a short time after withdrawal.

Indexed as

Exercise trainingSpermatogenesisTramadolvascular endothelial growth factorVascular Endothelial Growth Factor Receptors

Identifiers

PMID41983361
PMCPMC13080709

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