ArticleCell biochemistry and biophysics2025
Therapeutic Potential of Aloe vera and Aloe vera Fabricated Silver Nanoparticles on Reproductive Function in Male Mice Exposed to Hexavalent Chromium.
Article in Cell biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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
2 citing papers in PubMed.
- Therapeutic effect ofRSC advances · 2025Article
- The green healer: an updated review on the phytochemical profile and therapeutic potential ofFrontiers in nutrition · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hexavalent chromium Cr (VI), an endocrine disruptor, has been a possible risk factor for male-oriented infertility, due to its damaging effect on testes. Thus, we sought to analyze the protective effect of Aloe vera (A. vera) and their mediated silver nanoparticles on testes in mice. Sixty male mice were exposed to Cr (VI) and A. vera extract (AV) and their mediated silver nanoparticles (AV+NP) as protective agents for 60 days. The organ index, hormone analysis, enzyme analysis, metal estimation, computer assisted sperm analysis (CASA), histopathology of testes and micrometric data were assessed using one-way ANOVA. A significant reduction was found in the level of catalase (87.1 ± 7.02 mmol/mL), superoxide dismutase (61.8 ± 2.5 mmol/mL), glutathione (1.51 ± 0.9 µmol/mL), luteinizing hormone (LH) (1.6 ± 0.3 ng/mL), and testosterone (2.3 ± 0.2 ng/mL) in Cr exposed group. However, a significant increase was found in Cr exposed mice in follicle-stimulating hormone (FSH) (159.9 ± 4.98 ng/mL) level. With administration of AV and AV+NP, we found a significant increase in level of catalase (143.4 ± 2.6 mmol/mL; 134.8 ± 9.1 mmol/mL), superoxide dismutase (205.8 ± 13.0 mmol/mL; 187.3 ± 9.9 mmol/mL), glutathione (2.98 ± 0.2 µmol/mL; 3.06 ± 0.2 µmol/mL), luteinizing hormone (LH) (2.9 ± 0.2 ng/mL; 3.1 ± 0.2 ng/mL), and testosterone (3.9 ± 0.1 ng/mL; 4.58 ± 0.2 ng/mL) respectively, whereas, FSH level was decreased (84.7 ± 7.2 ng/mL; 70.4 ± 4 ng/mL). The CASA showed a noticeable decrease in sperm quantity and kinematics after Cr exposure. In AV and AV+NP exposed groups, the sperm kinematics were improved significantly. The histopathological studies showed necrosis of Leydig cells, absence of sperm tails, and destruction in the zone of mitosis and meiosis in Cr-exposed groups. The micro morphometric analysis showed a significant reduction in the size of spermatogonia (38.9 ± 0.7 µm), size of spermatocytes (26.91 ± 1.4 µm), head breadth (5.4 ± 0.7 µm), head length (19.98 ± 1.2 µm), middle piece, and tail length (0.00 ± 0.0 µm; 0.00 ± 0.0 µm) in Cr exposed mice. However, with the AV and AV+NP administration, the testis architecture was improved, exhibiting an improved zone of mitosis and meiosis. A. vera exposure induced a significant decrease in the size of spermatogonia (24.1 ± 2.4 µm), and size of spermatocytes (18.7 ± 1.2 µm), whereas a significant increase in sperm head breadth (15.1 ± 0.8 µm), and head length (34.4 ± 2.8 µm) was found. We found that AV and AV+NP can potentially reduce oxidative damage induced by Cr (VI) in testes and promote fertility.
Indexed as
Identifiers
40563078What OpenQuestion holds
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 OpenQuestion graph.