# Protective Effects of Eugenol Against Monosodium Glutamate-Induced Reproductive Toxicity in Male Wistar Rats

**Authors:** Kouthulgama Veekshith Reddy, Majid Shafi, Abhinav Madari, Sharath Chandra Goud, Shayaib Ahmad Kamil, Akeel Bashir, Masood Saleem Mir, Mir Nadeem Hassan, Mudasir Ali Rather, Zahoor Ahmad Wani, Showkeen Muzamil Bashir, Atif Khurshid Wani, Showkat Ahmad Shah

PMC · DOI: 10.3390/jox16010033 · Journal of Xenobiotics · 2026-02-13

## TL;DR

This study shows that eugenol can protect male rats from reproductive damage caused by monosodium glutamate, likely due to its antioxidant properties.

## Contribution

The study demonstrates eugenol's protective effects against MSG-induced reproductive toxicity in male rats for the first time.

## Key findings

- Eugenol significantly reversed MSG-induced reductions in testosterone and antioxidant levels.
- Higher eugenol doses restored testicular structure and spermatogenesis in rats.
- Eugenol showed no adverse effects when administered alone.

## Abstract

Monosodium glutamate (MSG), a widely used flavor enhancer, has been implicated in oxidative stress-mediated systemic and reproductive toxicity, particularly affecting the male gonadal system. This study evaluated the ameliorative potential of eugenol, a phenolic compound with potent antioxidant properties, against MSG-induced reproductive toxicity in male Wistar rats. Thirty rats were randomly divided into five groups: group 1 (control), group 2 (MSG 2.5 g/kg), group 3 (eugenol 200 mg/kg), group 4 (MSG + eugenol 100 mg/kg), and group 5 (MSG + eugenol 200 mg/kg). Treatments were administered orally for 28 days. Hematological, biochemical, hormonal, antioxidant, gross, and histopathological assessments were conducted after sacrifice on Day 29. MSG exposure significantly reduced testicular weight, testosterone levels, TEC, Hb, PCV, serum proteins, and testicular GSH and SOD, while markedly elevating TLC, AST, ALT, BUN, creatinine, and TBARS. Severe testicular degeneration, vascular congestion, germ-cell loss, and disrupted seminiferous tubules were observed histologically. Co-administration of eugenol resulted in significant and dose-dependent amelioration of MSG-induced alterations, restoring hematological and biochemical parameters, improving antioxidant status, and elevating testosterone levels. Gross pathology and histopathology demonstrated progressive structural recovery, with the higher eugenol dose showing near-normal testicular architecture and active spermatogenesis. Eugenol alone produced no adverse effects and remained comparable to the control group across all parameters. The findings indicate that eugenol confers strong protective effects against MSG-induced reproductive toxicity, primarily through its antioxidant and cytoprotective actions. Eugenol may serve as a promising natural therapeutic agent for mitigating chemically induced male reproductive impairments.

## Linked entities

- **Chemicals:** Eugenol (PubChem CID 3314), Monosodium Glutamate (PubChem CID 23672308), testosterone (PubChem CID 6013), GSH (PubChem CID 124886), ALT (PubChem CID 10219674), BUN (PubChem CID 91971254), creatinine (PubChem CID 588)

## Full-text entities

- **Genes:** Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}, Epo (erythropoietin) [NCBI Gene 24335], Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Alb (albumin) [NCBI Gene 24186] {aka Alb1, Albza}
- **Diseases:** dislocation (MESH:D004204), muscle tightness (MESH:C536920), metabolic disorders (MESH:D008659), Reproductive Toxicity (MESH:D060737), MG (MESH:D009157), tissue injury (MESH:D017695), obesity (MESH:D009765), hemorrhage (MESH:D006470), systemic organ damage (MESH:D020261), oligozoospermia (MESH:D009845), weight gain (MESH:D015430), liver and kidney damage (MESH:D056486), weakness (MESH:D018908), fertility (MESH:D007246), tubular (MESH:D000230), neurotoxicity (MESH:D020258), congestion (MESH:D002311), edema (MESH:D004487), insulin resistance (MESH:D007333), atrophy (MESH:D001284), Toxicity (MESH:D064420), testicular damage (MESH:D013733), flushing (MESH:D005483), injury to (MESH:D014947), anemia (MESH:D000740), Inflammation (MESH:D007249), headache (MESH:D006261), impaired spermatogenesis (MESH:C536875), mitochondrial dysfunction (MESH:D028361), hypothalamic damage (MESH:D007027)
- **Chemicals:** TBARS (MESH:D017392), copper (MESH:D003300), HCl (MESH:D006851), glutamate (MESH:D018698), eosin (MESH:D004801), ROS (MESH:D017382), calcium (MESH:D002118), creatinine (MESH:D003404), formalin (MESH:D005557), MG (MESH:D008274), 4-allyl-2-methoxyphenol (MESH:D005054), flavonoids (MESH:D005419), GSH (MESH:D005978), water (MESH:D014867), thio-barbituric acid (MESH:C029684), essential oil (MESH:D009822), terpenes (MESH:D013729), iron (MESH:D007501), Testosterone (MESH:D013739), urea nitrogen (MESH:C530477), lipid (MESH:D008055), K3 (MESH:C058433), EDTA (MESH:D004492), MSG (MESH:D012970), MDA (MESH:D008315), carbohydrate (MESH:D002241), corn starch (MESH:D013213), T (MESH:D014316), H&amp;E (MESH:D006371), metal (MESH:D008670), Chemicals (-), oxygen (MESH:D010100), hematoxylin (MESH:D006416), polyunsaturated fatty acids (MESH:D005231), Isoeugenol (MESH:C036643)
- **Species:** Zingiber officinale (ginger, species) [taxon 94328], Cinnamomum verum (Ceylon cinnamon, species) [taxon 128608], Curcuma longa (turmeric, species) [taxon 136217], Rattus norvegicus (brown rat, species) [taxon 10116], Syzygium aromaticum (clove, species) [taxon 219868], Homo sapiens (human, species) [taxon 9606], Corynebacterium glutamicum (species) [taxon 1718]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12921986/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921986/full.md

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Source: https://tomesphere.com/paper/PMC12921986