ArticleBiological trace element research2026
Protective Effects of Mesembryanthemum Crystallinum Extract Against Cadmium-Induced Reproductive Oxidative Stress: Experimental and Docking Evidence for a Sustainable Therapeutic Strategy.
Article in Biological trace element research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Mesembryanthemum crystallinum -guided green synthesis of ZnO nanoparticles with selective anticancer activity via ROS-mediated mitochondrial dysfunction.Bioresources and bioprocessing · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
One hazardous heavy metal that causes oxidative stress is cadmium (Cd) and harms male reproductive function. Although various antioxidants have been explored for protection, the potential of Mesembryanthemum crystallinum (M. crystallinum) – a flavonoid and phenolic-rich halophyte- remains understudied in this context. According to the United Nations Sustainable Development Goals (SDGs), specifically SDG 3 on Good Health and Well-Being and SDG 12 Responsible Consumption and Production this novel research evaluated the protective potential of M. crystallinum aqueous extract (MAE) to mitigate cadmium chloride (CdCl2)-induced testicular dysfunction. After acclimatization, Eight groups (n = 5) of forty male rats were allocated into groups: (1) control; (2) CdCl₂ (2 mg/kg); (3) MAE 200 mg/kg; (4) MAE 400 mg/kg; (5) CdCl₂ + MAE 200 mg/kg; (6) CdCl₂ + MAE 400 mg/kg; (7) MAE (200 mg/kg) pre-treatment + CdCl₂; (8) MAE (400 mg/kg) pre-treatment + CdCl₂. For 14 days, oral treatments were administered. HPLC profiling revealed eight major phenolic compounds in M. crystallinum like quercetin and ellagic acid. CdCl2 exposure impaired sperm indices, reduced serum LH and testosterone and induced oxidative and histological damage with elevated caspase-3 and TNF-α expression. MAE treatment especially at 400 mg/kg restored hormonal levels, improved sperm quality, normalized antioxidant defense, and preserved testicular architecture. Molecular docking confirmed binding of hesperidin, rutin, and ellagic acid to apoptotic and inflammatory proteins. MAE may exhibit potent anti-inflammatory, antioxidant, and anti-apoptotic activity, protecting against CdCl₂-induced reproductive injury. M. crystallinum represents a sustainable, plant based therapeutic candidate aligned with SDG-driven strategies for combating environmental toxicity-related infertility.
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Registered trials
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 Socratic graph.