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Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling
Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling
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Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling
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Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling
Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling

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Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling
Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling
Journal Article

Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling

2025
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Overview
Manganese, an essential nutrient for male reproductive health, exerts dose-dependent effects, with excessive exposure—particularly to manganese dioxide nanoparticles ( MnO 2 -NPs ) from environmental or industrial sources inducing gonadal damage via oxidative stress, hormonal disruption, and impaired steroidogenesis. This study evaluated rosemary essential oil ( REO ) against MnO 2 -NP -induced reproductive dysfunction in male rats. Seventy-two Sprague–Dawley rats (130 ± 10 g) were divided into six groups ( n  = 12): Group I (deionized water), Group II (saline), Group III ( MnO 2 -NP , 100 mg/kg bw/day), Group IV ( REO , 250 mg/kg/day), Protective Group V ( REO pre-treatment +  MnO 2 -NPs ), and Therapeutic Group VI ( MnO 2 -NPs + REO co-treatment) for 56 days. MnO 2 -NP exposure caused testicular injury, marked by elevated lipid peroxidation (↑malondialdehyde, ↑nitric oxide), suppressed antioxidants (↓total antioxidant capacity, ↓catalase, ↓glutathione), impaired sperm parameters (motility, count, morphology), and altered serum hormone levels (follicle-stimulating hormone, luteinizing hormone, testosterone). These effects correlated with downregulated steroidogenesis genes ( StAR , HSD-3β , CYP11A1 ). Both Protective and Therapeutic REO treatment mitigated MnO 2 -NPs oxidative stress, restored hormonal balance, and normalized gene expression. Histopathology revealed reduced seminiferous tubule degeneration and enhanced spermatogenesis in REO groups. Findings demonstrate REO’s efficacy in alleviating MnO 2 -NPs induced reproductive toxicity via antioxidant and steroidogenic modulation, positioning REO as a promising therapeutic against nanomaterial-induced gonadotoxicity.