Evidence map›Paper›PMID 42666179›Full record

ArticleFrontiers in endocrinology2026

Effect of atrazine and curcumin on mouse I-10 Leydig cells: steroidogenesis and beyond.

Hoda Elkady, Pengli Bu

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

2 authors.

Hoda ElkadyDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, United States.
Pengli BuDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Chronic exposure to pesticides is increasingly becoming a concern in the modern world. Atrazine (ATZ), a widely used pesticide in the U.S., is known to interfere with the male reproductive system. In the present study, we examined the effects of ATZ on viability, cell cycle progression, steroid production, and steroidogenic gene expression profile of testicular Leydig cells using the mouse Leydig cell line I-10 as an Methods: I-10 cells were treated for 6 days with either ATZ (3.3, 10, 33, 100 µM), Cur (3, 10, 30 µM), or a co-treatment of Cur (3 µM) + ATZ (33 or 100 µM). Cell viability, cell cycle progression, production of progesterone (P4) and testosterone (T), and expression of key steroidogenic genes were assessed on Days 2, 4, and 6. Additionally, AutoDock Vina v1.2.7 was used to predict the binding affinities of Cur and ATZ to key mouse and human steroidogenic proteins in comparison to their endogenous substrates. Results: ATZ decreased I-10 cell viability while increasing T levels in a concentration-dependent manner. Cur transiently stimulated I-10 cell proliferation and increased P4 but showed mixed effects on T levels. Co-treatment decreased viability, as supported by changes in cell cycle distributions. Co-treatment also significantly increased both P4 and T production, with induction of expression of the steroidogenic genes StAR, Cyp11a1, Hsd3β6, and Hsd17β3 at specific time points. Furthermore, Cur exhibited strong predicted binding to both mouse and human steroidogenic proteins, comparable to that of their endogenous substrates. Conclusion: Our findings suggest a potential interaction between Cur and ATZ, which was more prominent at ATZ 100 μM, stimulating steroidogenesis in I-10 Leydig cells at the expense of decreased viability.

Indexed as

AtrazineCurcuminHerbicidesLeydig CellsSteroidsAnimalsCell CycleCell LineCell ProliferationCell SurvivalHumansMaleMiceMolecular Docking SimulationProgesteroneTestosteroneAtrazineCurcuminHerbicidesProgesteroneSteroidsTestosteroneatrazinecurcuminLeydig cellsteroidogenesistestosterone

Identifiers

PMID42666179
PMCPMC13521775

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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.