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Scientific Reports volume 15, Article number: 20201 (2025)
2015
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Manganese, an essential nutrient for male reproductive health, exerts dose-dependent effects, with excessive exposure—particularly to manganese dioxide nanoparticles (MnO2-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 MnO2-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 (MnO2-NP, 100 mg/kg bw/day), Group IV (REO, 250 mg/kg/day), Protective Group V (REO pre-treatment + MnO2-NPs), and Therapeutic Group VI (MnO2-NPs + REO co-treatment) for 56 days. MnO2-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 MnO2-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 MnO2-NPsinduced reproductive toxicity via antioxidant and steroidogenic modulation, positioning REO as a promising therapeutic against nanomaterial-induced gonadotoxicity.
The rapid integration of engineered nanoparticles into industrial and biomedical applications has unearthed a paradoxical challenge: their unique physicochemical properties, while enabling technological breakthroughs, also potentiate unforeseen biological hazards1. Among these, Manganese dioxide nanoparticles MnO2-NPs, employed in energy storage, catalysis, and environmental remediation, exemplify this duality, as emerging studies associate their bioaccumulation with male reproductive dysfunction—a pressing concern in industrialized regions2,3. MnO2-NPs instigate testicular injury via oxidative stress, hormonal disruption, and mitochondrial dysfunction, yet targeted interventions remain underdeveloped4. Although manganese serves as an essential enzymatic cofactor5, its nanoparticulate form circumvents physiological barriers, accumulating in gonadal tissues and inducing lipid peroxidation, glutathione depletion, and suppression of steroidogenic acute regulatory protein (StAR), a pivotal regulator of testosterone biosynthesis6. StAR mediates mitochondrial cholesterol transport, the rate-limiting step in steroidogenesis, regulated by luteinizing hormone (LH)-dependent cAMP/PKA signaling7. LH activates G protein-coupled receptors, elevating intracellular cAMPs to induce CREB phosphorylation. Phosphorylated CREB binds cAMP response elements (CREs) on the StAR promoter, synergizing with steroidogenic factor 1 (SF-1) to enhance transcription. Upregulated StAR promotes cholesterol transfer to CYP11A1 (P450scc) in the mitochondrial inner membrane, catalyzing pregnenolone synthesis—the precursor for gonadal steroid hormones. Post-translational phosphorylation further modulates StAR activity, optimizing steroidogenic output8. MnO2-NPs disrupt this pathway, downregulating StAR, CYP11A1, and HSD-3β, thereby impairing spermatogenesis and steroidogenic capacity9.
Rosemary essential oil (REO) (Rosmarinus officinalis L.), a phytochemical complex enriched with carnosic acid, rosmarinic acid, camphor, and polyphenols (e.g., flavonoids, isoflavones), enhances fertility through dual antioxidative and endocrine-modulatory mechanisms10,11. Its phenolic constituents scavenge reactive oxygen species (ROS), attenuating oxidative stress in steroidogenic tissues such as Leydig cells. This action preserves mitochondrial membrane integrity, inhibits lipid peroxidation, and boosts endogenous antioxidant enzyme activity, thereby safeguarding spermatogenic cells and preventing sperm quality deterioration12. Concurrently, REO modulates endocrine pathways by reactivating LH/CREB/StAR signalling, restoring testosterone biosynthesis via upregulation of StAR gene expression in testicular tissues. REO’s phenolic constituents enhance hormonal regulation by inhibiting ROS-mediated suppression of steroidogenic enzymes, thereby restoring testosterone biosynthesis13. The synergistic interplay between polyphenol-mediated anti-inflammatory effects and endocrine pathway modulation enhances reproductive function, notably improving sperm motility and viability14.
This study fills a critical gap in managing nanoparticle-induced testicular damage by introducing rosemary essential oil (REO) as the first natural treatment that simultaneously tackles oxidative stress and hormonal dysfunction. REO uniquely combines ROS neutralization (via α-pinene, carnosic acid) with direct restoration of testosterone production by reactivating LH/StAR signaling and steroidogenic enzymes (HSD-3β, CYP11A1). This dual-action mechanism—unreported in prior studies—offers a transformative solution for holistic recovery of reproductive health, bridging the divide between antioxidant therapies and endocrine restoration.
Seventy-two male Sprague-dawley rats (130 ± 10 g) and aged 10–12 weeks were purchased from Vacsera animal house colony, Cairo, Egypt. All experimental procedures were carried out in accordance with the NIH Guide for the Care and Use of Laboratory Animals, the ARRIVE guidelines for in vivo experiment reporting, and received approval from the Institutional Animal Care and Use Committee (VET.CU. IACUC) at the Faculty of Veterinary Medicine, Cairo University, following the Animal Use Protocol (Vet CU 25122023884). Water was given to rats ad-libitum while ration was given to rats according to National Research Council15. The rats were fed on standard granulated ration (2.5% Crude Fat, 23% Crude Protein, 5.5% Crude Fibers and Metabolizable Energy = 3600 Kcal/Kg). Following a two-week acclimation period, 72 rats were randomly allocated into six experimental groups (n = 12 per group), each housed in three replicate cages (four rats per cage) to minimize crowding-related stress. To account for route-specific administration effects, two vehicle control groups were utilized: an oral saline vehicle and a subcutaneous saline vehicle. The study duration spanned 56 days, encompassing the full spermatogenic cycle of the species to enable systematic assessment of germ cell maturation across all developmental stages.
Oral Control Group (CO): Received 1 mL/kg body weight (bwt) sterile saline via daily oral gavage.
Subcutaneous Control Group (CS): Administered 1 mL/kg bwt sterile saline via daily subcutaneous injection [vehicle for the manganese oxide nanoparticles (MnO2-NPs)]
MnO2-NP Exposure roup (III): Rats received a daily subcutaneous injection of manganese oxide nanoparticles (MnO2-NPs; 100 mg/kg bwt) dissolved in saline, based on prior toxicity studies2.
REO Alone Group (IV): Rats were orally administered rosemary essential oil (REO; 250 mg/kg bwt), a dosage established for bioactive efficacy10.
Protective Group (V): Rats received REO (250 mg/kg bwt, oral) 30 min prior to MnO2-NP (100 mg/kg bwt, subcutaneous) administration.
Therapeutic Group (VI): Rats were administered MnO2-NP (100 mg/kg bwt, subcutaneous) followed by REO (250 mg/kg bwt, oral) after a 30-minute interval.
Manganese oxide nanoparticles (MnO2-NPs) were prepared by the green synthesis method according to16. The preparation and characterization of MnO2-NPs were performed at the central laboratories network, National Research Centre, Cairo, Egypt. A High-Resolution Transmission Electron Microscope (HR-TEM) with an accelerating voltage of 200 kV was used to image the morphology of NPs (Tecnai G2, FEI, Netherlands). A TEM micrograph (Fig. 1a–c) reveals that MnO2-NPs have lattice fringes shape, which points to the development of a good nanocrystalline structure. The particles’ size ranges from 50 to 100 nm. A Nano-zeta sizer (Malvern, ZS Nano, U.K.) was used to assess the particle size using dynamic light scattering (DLS). The findings of the particle size analysis investigation (Fig. 1d) showed that the produced MnO2-NPs have a size range of 50 nm. The findings demonstrate the creation of MnO2 nanomaterials. The phase and structure of the produced NPs were investigated using an X-ray diffractometer (XRD, X’Pert Pro, Malvern Analytical Ltd, Malvern, UK) at 40 kV and 30 mA, the standard ICCD was used to evaluate the data. The corresponding results are shown in (Fig. 1e, f). The sample’s various diffraction peaks correlate to 2θ values of 18.03, 28.71, 37.58, 47.78 and 59.01, which match the presence of MnO2-NPs with lack of impurity phases. Fourier transforms infrared spectroscopy (FTIR) is carried out and these considerations are considered: 16 scans, spectral range 0–4500 cm− 1, spectral resolution 4 cm− 1. The software used to utilize FTIR was Opus (Bruker, Germany), VERTEX 70, RAMII. Multiple absorption bands at 762, 570, and 435 cm− 1 are visible in the FT-IR spectra of MnO2-NPs, as shown in (Fig. 1g). The metal oxide nanoparticles, such as MnO2 NPs, typically exhibit an absorption peak in the fingerprint area below 1000 nm wavelength which is due to inter-atomic vibrations. The Mn–O bond can be identified by the absorption bands at 570 and 530 cm− 1. The peaks at 1690 and 1494 cm− 1 are associated with manganese atoms and -O-H bending vibrations.
The essential oil of Salvia rosmarinus Spenn. (syn. Rosmarinus officinalis L.; family Lamiaceae) was procured from the Essential Oils Extraction Unit, National Research Centre (NRC, Egypt; Lot No. 19-02-2024). Chemical profiling was performed via gas chromatography-mass spectrometry (GC-MS) at the NRC Central Laboratories Network. Constituents were identified by comparing mass spectral fragmentation patterns against the Wiley 11th Edition and NIST 2020 databases, with match similarity indices ≥ 90%. Results are reported in Table 1; Fig. 1h.
Characterization of MnO2-NPs . Including (a–c) High-resolution transmission electron microscope image of MnO2-NPs exhibited irregular shape, with an average size of 50–100 nm. (d) Dynamic light scattering analysis showed particle size 50 nm. (e,f) X-ray powder diffraction patterns of MnO2– NPs. (g) Fourier transforms infrared spectroscopy of MnO2-NPs. Gas chromatography–mass spectrometry analysis (GC-MS) of rosemary essential oil. (h) Shows the fragmentation pattern of its components.
At the end of the experiment, blood samples were collected between 8:00 and 10:00 a.m. to mitigate circadian rhythm in hormones levels. Blood was drawn via retro-orbital sinus puncture under anesthesia induced with isoflurane (30% in propylene glycol (Sigma-Aldrich, St. Louis, MO, USA; Catalog #I4381), following established protocols17. Post-collection, samples were processed without anticoagulant for serum samples, and they were centrifuged for 15 min at 4000 rpm. Sera were stored at -20 °C to be used for further examination.
The animals were sacrificed after anesthesia overdosed by cervical dislocation and testicular tissues and epididymis were collected. Following semen collection via epididymal dissection for comprehensive analysis, testes tissues were surgically excised from all rats. Tissues were rinsed in physiological saline (0.9% NaCl) and partitioned into two cohorts: Snap-frozen cohort: Tissues were immediately snap-frozen in liquid nitrogen and stored at − 80 °C for subsequent RNA/protein extraction, oxidative stress marker, and gene expression profiling. Fixed cohort: Tissues were immersion-fixed in 10% neutral buffered formalin (24–48 h) for histomorphology evaluations, followed by paraffin embedding and hematoxylin-eosin staining.
The final body weight and testicular weight in grams of all rats were recorded at the end of the experiment. Additionally, relative testes weight of rats of all groups were calculated using the following equation as described by18.
Evaluation of epididymal sperm count, motility, viability and morphological abnormalities were done according to methods described by19.
Tissue preparation, tissue samples were homogenized using an Ultra-Turrax T-25 homogenizer in 5–10 ml of cold PBS (phosphate-buffered saline) solution at pH 7.4 per 1 g of tissue. Centrifuge at 4000 rpm for 15 min, then collect the supernatant for further examination20.
Evaluation of redox status, serum total antioxidant capacity (TAC) and testicular antioxidant parameters including catalase (CAT) activity, reduced glutathione (GSH) concentration, malondialdehyde (MDA) concentration and nitric oxide (NOx) were detected spectrophotometrically according to the method described by21,22,23,24,25 respectively.
Serum free testosterone was detected according to the method of26, using commercial kits purchased from Bios Company, USA (CAT. No10007). Serum follicle stimulating hormone (FSH) and luteinizing hormone (LH) were measured according to the method of27 using commercial kits purchased from ELK Company, China, (CATNO. ELK1315 and ELK2367, respectively).
Isolation of Total RNA, total RNA was isolated from the samples using the GeneJET RNA Purification Kit (Thermo Scientific, catalog #K0731/K0732). The extraction protocol included cell lysis, removal of genomic DNA contamination, and column-based RNA purification. RNA quality was evaluated by assessing purity and concentration with a NanoDrop™ One spectrophotometer (Thermo Fisher Scientific, USA), where A260/A280 ratios between 1.8 and 2.0 confirmed acceptable purity. RNA integrity was further validated via 1% agarose gel electrophoresis (100 V, 30 min), which resolved distinct 28 S and 18 S ribosomal RNA bands.
cDNA Synthesis from Total RNA, the Enzynomics cDNA Synthesis Kit (#RT220, RT221) was used to synthesize complementary DNA (cDNA). The reverse transcription reaction was performed in a thermocycler under optimized conditions to ensure accurate and efficient conversion of RNA into cDNA. This process utilized a combination of reverse transcriptase enzyme, primers, and dNTPs to generate high-quality cDNA for downstream applications.
qPCR-based Gene Expression Analysis, the synthesized cDNA was used as a template for quantitative polymerase chain reaction (qPCR). Quantitative PCR amplification was performed using Maxima SYBR Green qPCR Master Mix (Thermo Scientific, Waltham, MA, USA; Cat# K0251) on a Q3 Tower Real-Time PCR System (Analytik Jena, Jena, Germany). Reactions (20 µL) contained 2 µL cDNA template and gene-specific primers (Table 2) for CYP11A1, StAR, and HSD-3β. Primers were designed using Primer3 (v0.4.0; http://bioinfo.ut.ee/primer3-0.4.0/)28. Cycling conditions: 95 °C for 3 min; 40 cycles of 95 °C for 15 s, 60 °C for 30 s. Amplification specificity was confirmed by melting curve analysis (65–95 °C). β-actin served as internal control, with expression stability validated across experimental groups using NormFinder software29.
Gene Expression Relative Quantification (RQ), the ΔΔCt method, as described by30, was applied to determine relative gene expression levels. This approach involved normalizing the cycle threshold (Ct) values of target genes to those of an internal reference gene, followed by comparison with a control group. The fold-change in gene expression was determined using the formula:
Testicular samples from all experimental groups were fixed in 10% neutral buffered formalin (NBF) for 24–48 h. Following fixation, tissues were dehydrated through a graded ethanol series, cleared in xylene, and embedded in paraffin wax using standardized protocols31. Serial sections (4–5 μm thickness) were cut using a rotary microtome (Leica RM2235) and mounted on glass slides then stained with hematoxylin and eosin (H&E) for histopathological examination. Stained sections were examined under an Olympus BX43 light microscope equipped with a DP21 digital camera. Representative images were captured at 100×, and 200× magnifications using CellSens Dimension software (Olympus, version 1.16).
Histopathological evaluation of testicular tissues was performed using standardized criteria to ensure objectivity. Spermatogonia, primary spermatocytes, spermatids, and Leydig cells were quantified in 10 randomly selected seminiferous tubule cross-sections per animal (at 400× magnification) by two blind observers. Cell counts were averaged and expressed as cells per tubule. For spermatogenic staging, we adapted the Johnsen score system32, which assesses tubular integrity and germ cell presence on a scale of 1–10. Leydig cell populations were evaluated based on cytoplasmic volume and nuclear morphology, as described in33.
The data were reported as mean ± standard error (n = 5) and P < 0.05 was designated as the level of statistical significance. Differences between groups were analyzed using one-way ANOVA followed by Tukey’s post hoc test using the statistical analysis system program (SPSS). A *p*-value < 0.05 was considered statistically significant.
As shown in Fig. 2, dietary exposure to MnO2-NPs resulted in a statistically significant reduction in gonadosomatic index (GSI) compared to control groups (*p* < 0.05). However, co-administration of rosemary essential oil (REO) in both therapeutic (MnO2-NPs + REO) and prophylactic (REO + MnO2-NPs) regimens effectively attenuated this decline, restoring GSI values to levels comparable with controls. These findings suggest that REO supplementation mitigates MnO2-NPs-induced gonadal impairment, highlighting its potential protective role in maintaining reproductive organ homeostasis.
Gonado-somatic index of different experimental groups: Effects of MnO2-NPs and REO on (A) Body weight, (B) Testis weight (C) Relative Testis weight. Data represented as means ± SE (n = 5/replicate). Letters a, b denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*). Where control (-ve-1) oral vehicle and control saline (-ve-2) subcutaneous vehicle.
As illustrated in Figs. 3 and 4, MnO2-NP exposure induced significant adverse effects on sperm quality in treated rats. Compared to untreated controls, the MnO2-NP group exhibited marked reductions in sperm motility (↓-56%), viability (↓-36%), and count (↓-31%), alongside a pronounced increase in sperm head and tail morphological abnormalities (*p* < 0.05 for all parameters). Notably, rosemary essential oil (REO) co-administration in both prophylactic (REO prior to MnO2-NPs) and therapeutic (REO post MnO2-NPs) regimens improved sperm motility, viability, and count, though values in therapeutic groups remained 12% below controls, while the incidence of morphological defects was significantly reduced (*p* < 0.05 vs. MnO2-NP group). These results demonstrate that REO supplementation preserves sperm integrity and mitigates MnO2-NPs effects.
Semen analysis: Effects of MnO2-NPs and REO on (a,b) control negative group showing normal sperm. (c) MnO2-NPs group showing bent tail (black arrow) (d) group administered with REO. (e) therapeutic group. (f) prophylactic group (×40). Smears stained with eosin nigrosine. Graphs (G–I) represented Sperm count, motility, viability of different experimental groups respectively. Data represented as means ± SE (n = 5/replicate). Letters a, b, c, d denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*”). Where control -ve 1(oral vehicle) and control saline (-ve 2) subcutaneous vehicle
Graphs (a–i) Sperm abnormalities normal sperm (black arrow), looped tail (yellow arrow), curled tail (black head arrow), detached head (red arrow), bent tail (red arrow-head), curved tail (yellow arrow-head), and broken tail (blue arrow) (15 μm), Graphs (J–M) Effects of MnO2-NPs and REO on (J) Total abnormalities (%), (K) Detached head (%) (L) Bent tail (%) (M) Broken tail (%) of different experimental groups respectively. Data represented as means ± SE (n = 5/replicate). Letters a, b, c, d denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*). Where control (-ve-1) oral vehicle and control saline (-ve-2) subcutaneous vehicle.
As shown in Fig. 5, MnO2-NPs exposure induced pronounced oxidative stress, marked by a significant increase in malondialdehyde (MDA, ↑12.5-fold) and nitric oxide (NOx, ↑40%) levels, coupled with a decrease in catalase (CAT, ↓88%), glutathione (GSH, ↓51%), and total antioxidant capacity (TAC, ↓60%) relative to untreated controls (*p* < 0.05). Critically, Co-administration of REO (therapeutically or prophylactically) with MnO2-NPs attenuated oxidative damage, restoring MDA and NO concentrations to near-baseline levels while rescuing CAT, GSH, and TAC activity (*p* < 0.05 vs. MnO2-NP group). Notably, rosemary essential oil (REO) supplementation alone significantly elevated GSH (↑130%) and TAC (↑125%) levels with significant reduction in NOx (↓34%), and MDA (↓37.5%) compared to controls (*p* < 0.05), suggesting intrinsic antioxidant activity.
Antioxidant status: Effects of MnO2-NPs and REO on (A) Total antioxidant capacity. (B) Nox (C) MDA (E) GSH (D) Catalase levels. Data represented as means ± SE (n = 5/replicate). Letters a, b, c, d, e denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*). Where control (-ve-1) oral vehicle and control saline (-ve-2) subcutaneous vehicle.
As depicted in Fig. 6, MnO2-NPs exposure significantly suppressed serum levels of free testosterone, follicle-stimulating hormone (FSH), and luteinizing hormone (LH) compared to untreated controls (*p* < 0.05). In contrast, rosemary essential oil (REO) supplementation alone significantly elevated free testosterone, FSH, and LH levels relative to negative controls (*p* < 0.05), underscoring its endocrine-modulatory potential. Both prophylactic (REO pre-treatment) and therapeutic (REO post-MnO2-NP exposure) restoring free testosterone, FSH, and LH concentrations to near-baseline values (*p* < 0.05 vs. MnO2-NPs group). These results indicate that REO not only enhances endogenous reproductive hormone synthesis under normal conditions but also counteracts MnO2-NPs-driven endocrine dysfunction.
Reproductive hormones: Effects of MnO2-NPs and REO on (A) free testosterone level. (B) Follicle-stimulating hormone (FSH), Luteinizing Hormone (LH) Levels. Data represented as means ± SE (n = 5/replicate). Letters a, b, c, d denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*). Where control (-ve-1) oral vehicle and control saline (-ve-2) subcutaneous vehicle.
As shown in Fig. 7, MnO2-NPs exposure significantly downregulated testicular transcript levels of StAR (− 79%), HSD-3β (− 58%), and CYP11A1 (− 76%) compared to the negative control groups (*p* < 0.05). In contrast, prophylactic REO co-administration restored expression to near-normal levels (85% of control values for StAR, 82% for HSD-3β, and 78% for CYP11A1), while therapeutic REO intervention partially reversed the suppression (62% recovery for StAR, 57% for HSD-3β, and 53% for CYP11A1). Notably, REO alone (without MnO2-NPs exposure) upregulated basal expression of StAR (+ 44%), HSD-3β (+ 23%), and CYP11A1 (+ 20%) relative to controls (*p* < 0.05), suggesting intrinsic stimulatory effects on steroidogenic pathways.
Gene expression analysis: Effects of MnO2-NPs and REO on (A) StAR, (B) HSD-3β and (C) CYP11A1 Levels. Data represented as means ± SE (n = 5/replicate). Letters a, b, c, d, e denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*). Where control (-ve-1) oral vehicle and control saline (-ve-2) subcutaneous vehicle.
Microscopic evaluation of testicular sections (Fig. 8a–f) revealed distinct histological profiles across experimental groups. In both negative control groups (oral and subcutaneous administration routes), seminiferous tubules exhibited normal architecture, characterized by densely packed spermatogonia, primary spermatocytes, spermatids, Sertoli cells, and abundant luminal spermatozoa, with no evidence of histopathological alterations. Similarly, rosemary essential oil (REO)-supplemented groups demonstrated preserved testicular morphology, comparable to controls, confirming REO’s lack of adverse effects. The therapeutic REO group displayed mild but discernible histopathological changes. Some seminiferous tubules exhibited focal vacuolization of the germinal epithelium, accompanied by interstitial vascular congestion (Fig. 8d). However, > 80% of tubules retained near-normal cellular organization, with intact spermatogenic stages. In contrast, the prophylactic REO group showed markedly attenuated pathology, with 95% of tubules maintaining structural integrity, a well-defined germinal epithelium, and complete spermatogenic cycles (Fig. 8e).
Quantitative morphometric analysis (Fig. 8G-I) corroborated these observations, MnO2-NPs-exposed group exhibited severe germinal epithelial disruption, with significant reductions in spermatogonia (-58%%), primary spermatocytes (-49%), spermatids (-63%), and Leydig cells (-45%) compared to controls (*p* < 0.05). In contrast, therapeutic REO administration attenuated these effects, partially restoring spermatogonia (+ 32%), spermatocytes (+ 28%), spermatids (+ 37%), and Leydig cells (+ 24%) though mild vacuolation and vascular congestion persisted. Prophylactic REO pre-treatment yielded near-normal histology, with minimal vacuolation, intact germinal epithelium, and robust recovery of spermatogonia (+ 51%), spermatocytes (+ 43%), spermatids (+ 59%), and Leydig cells (+ 40%), closely resembling control levels (*p* < 0.05 vs. MnO2-NPs group). These findings collectively demonstrate that REO mitigates MnO2-NPs induced testicular damage, prophylactic REO exposure preserved testicular cytoarchitecture and spermatogenic efficiency more effectively than post-exposure therapeutic intervention.
Photomicrograph of testes tissue sections in different groups of rats stained with H&E stain (200x). (a,b) control groups showing seminiferous tubules (ST) exhibit a typical structure, enclosed by a thin and uniform basement membrane (BM). The lumina of the tubules are filled with spermatozoa (Z), while the narrow interstitial spaces (IT) separate the tubules. The ST contain well-organized spermatogenic cords, which consist of spermatogonia (SP), primary spermatocytes (PSP), spermatids (SPR), and Sertoli cells. (c) MnO2-NPs group showing testicular degeneration with complete absence of germinal cells lining in some seminiferous tubules (arrow) with marked decrease of spermatogenesis, (d) rosemary essential oil group showing the normal histological structure with increased diameters of seminiferous tubules, (e) therapeutic group, (f) protective group showing apparently normal testicular seminiferous tubules with sperm production. Graphs (G–I) represented Effects of MnO2-NPs and REO on numbers of spermatogonia cells, primary spermatocyte cell, spermatid cell and Leydig cells. Data represented as means ± SE (n = 5/replicate). Letters a, b, c, d denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*). Where control (-ve-1) oral vehicle and control saline (-ve-2) subcutaneous vehicle.
Testicular tissues from MnO2-NPsexposed animals exhibited marked histopathological degeneration (Fig. 9). Seminiferous tubules displayed extensive vacuolization, characterized by both microvacuolar and macrovacuolar cytoplasmic lesions within the germinal epithelium (Fig. 9b, c). Germ cell depletion was pronounced, with a reduction in spermatogonia populations compared to controls, and complete absence of spermatids in 30–40% of tubule cross-sections. Disruption of spermatogenic staging was evident, accompanied by frequent exfoliation of immature germ cells into the tubular lumen (Fig. 9d, arrows). Interstitial pathology included severe vascular congestion (increased vascular diameter) and edema, with extracellular fluid accumulation displacing Leydig cell clusters (Fig. 9e). Tubular atrophy quantified by reduced epithelial height. These findings collectively indicate MnO2-NPs-induced disruption of spermatogenesis and compromised testicular microarchitecture.
Photomicrograph of testes tissue sections in MnO2NPs group stained with H&E stain. (200x) showing (a–c) vacuolar degeneration with cellular disruption (blue arrow), (e,f) exfoliation and sloughing of germ cells into the lumen of seminiferous tubules (red arrow), (f) interstitial congestion and fluid accumulation (head arrow), where spermatogonia (SP), primary spermatocytes (PSP), spermatids (SPR) and Leydig cell (L).
Quantitative assessment of testicular morphometry revealed significant alterations in tubular architecture across experimental groups (Fig. 10). Animals exposed to MnO2-NPs exhibited a marked reduction in seminiferous tubular diameter and germinal epithelial height, indicative of tubular atrophy and germ cell loss. In contrast, the REO-supplemented group showed enhanced diameter tubular parameter and epithelial height exceeding baseline control values, suggesting a pro-spermatogenic effect of REO. Both therapeutic and protective regimens attenuated MnO2-NPs-induced morphometric deficits. The prophylactic group demonstrated near-complete restoration of tubular diameter and epithelial height, whereas the therapeutic group showed partial recovery in tubular diameter and epithelial height. These findings align with histopathological observations (Figs. 8 and 9), underscoring REO’s capacity to preserve testicular structure, particularly when administered prophylactically.
Photomicrograph of testes tissue sections in different groups of rats stained with H&E stain (100x): (a,b) control groups, (c) MnO2-NPs group showing decrease in tubular diameter and epithelial height, (d) rosemary essential oil group showing increase in tubular diameter and epithelial height, (e) therapeutic group, (fx( protective group showing an enhancement in tubular diameter and epithelial height, Graphs (G, H) represent the Effects of MnO2-NPs and REO on tubal diameter and epithelial height, Data represented as means ± SE (n = 5/replicate). Letters a, b, c, d, e denote significant differences between groups, ANOVA with Tukey’s post-hoc, p < 0.05*). Where control (-ve-1) oral vehicle and control saline (-ve-2) subcutaneous vehicle.
Manganese plays a dual role in male reproductive health, with essential physiological benefits at optimal levels34 but detrimental effects at elevated concentrations. Excessive manganese exposure, particularly via manganese dioxide nanoparticles MnO2-NPs, disrupts reproductive function by overwhelming antioxidant defenses, leading to reactive oxygen species (ROS) overproduction35. Testicular tissue, characterized by high metabolic activity, polyunsaturated fatty acid (PUFA) content, and rapid cell division, is exceptionally vulnerable to oxidative damage. MnO2-NPs-induced oxidative stress in this study manifested as elevated lipid peroxidation marker, alongside depleted antioxidant enzymes—consistent with prior findings36. This redox imbalance correlated with impaired semen quality (reduced sperm count, motility, viability; increased abnormalities) and diminished gonadosomatic index (GSI), reflecting spermatogenic disruption and germ cell loss37,38.
Mechanistically, MnO2-NPs penetrate the blood-brain barrier, accumulate in the hypothalamus, and disrupt the hypothalamic-pituitary-gonadal (HPG) axis, suppressing gonadotropin-releasing hormone (GnRH) secretion39,40. This GnRH deficiency disrupts pituitary release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), thereby impairing Leydig cell testosterone synthesis—a cascade consistent with the hormonal deficits observed in this study and prior reports40,41. Concurrently, MnO2-NPs directly inhibit testicular steroidogenesis by downregulating steroidogenic acute regulatory protein StAR, HSD-3β, and CYP11A1—genes critical for cholesterol transport and testosterone production8,41,42. Mitochondrial manganese accumulation exacerbates this by impairing StAR-mediated cholesterol shuttling and disrupting LH/FSH signaling. Further molecular disruptions include NF-κB-mediated inflammation, which suppresses StAR via inhibition of Creb phosphorylation, and upregulation of Cox-2/PGE2 pathways, impairing GnRH neuronal activity42,43.
Histopathological analyses revealed MnO2-NPsinduced testicular degeneration, interstitial hyalinization, and suppressed spermatogenesis, aligning with observed hormonal deficits and germ cell apoptosis43. Epididymal dysfunction—marked by weight loss and impaired cell development—underscores systemic reproductive toxicity37. Elevated caspase-3 mRNA levels and reduced vimentin expression in Sertoli cell further indicate disrupted structural support and increased apoptotic signaling44. Collectively, excessive manganese exposure disrupts redox balance, hormonal homeostasis, and cellular integrity via oxidative, inflammatory, and apoptotic pathways, culminating in dose-dependent male infertility. These findings emphasize the necessity of regulating manganese exposure to mitigate its reproductive risks.
Rosemary essential oil (REO) supplementation effectively mitigated manganese dioxide nanoparticle MnO2-NPsinduced testicular injury, primarily through the synergistic antioxidant and anti-inflammatory actions of its bioactive constituents, such as α-pinene, β-myrcene, and 1,8-cineole45,46. These monoterpenes attenuated oxidative damage by neutralizing reactive oxygen species (ROS) via electron donation, inhibiting lipid peroxidation and enhancing endogenous antioxidant enzyme defenses thereby preserving sperm membrane integrity and mitochondrial function47,48. Restoration of the gonadosomatic index (GSI) and seminiferous epithelial architecture in REO-treated groups underscored rosemary’s capacity to promote germ cell survival and regeneration. This protective effect likely stems from modulation of apoptotic pathways (caspase-3 suppression) and stabilization of Sertoli cell vimentin networks, which are critical for structural and functional support during spermatogenesis48,49,50. Furthermore, improvements in sperm motility, count, and viability were attributed to REO’s dual role in scavenging ROS and shielding spermatogenic cells from oxidative DNA damage, thereby maintaining genomic stability and cellular viability51,52,53.
In the present study, REO mitigated manganese nanoparticle (MnO2NP)-induced reproductive toxicity in mature males by attenuating oxidative stress, restoring steroidogenic function, and preserving hypothalamic-pituitary-gonadal (HPG) axis activity. Our results demonstrate that REO treatment significantly reduced testicular oxidative damage alongside restored antioxidant enzymatic activity. This antioxidant efficacy is attributable to REO’s bioactive constituents, including rosmarinic acid, carnosic acid, and α-pinene, which directly scavenged reactive oxygen species (ROS) and inhibited lipid peroxidation. α-Pinene attenuated oxidative stress by activating the Nrf2 pathway, enhancing glutathione synthesis and superoxide dismutase (SOD) activity, as demonstrated in cisplatin-induced reproductive toxicity models54. 1,8-Cineole suppressed NF-κB-mediated inflammation and COX-2/PGE2 production, as shown in cadmium-induced testicular injury55, thereby preserving sperm membrane integrity and mitochondrial function47,51. Furthermore, REO suppressed caspase-3-mediated germ cell apoptosis and stabilized vimentin expression in Sertoli cells, correlating with improved seminiferous tubule architecture and spermatogenic recovery48,56,57.
Notably, REO restored serum testosterone, FSH, and LH levels, indicating HPG axis stabilization. Mechanistically, this hormonal recovery was driven by enhanced StAR protein expression and upregulation of key enzymes (HSD-3β, CYP11A1) in Leydig cells, facilitated by rosemary flavonoids’ activation of the cAMP/PKA/Creb signalling pathway58,59. Concurrently, REO attenuated NF-κB-mediated inflammatory signaling, which correlated with reduced systemic inflammation, normalized gonadotropin secretion, and alleviated GnRH neuronal dysfunction, thereby restoring HPG axis activity60,61,62. Histopathological analysis corroborated these findings, showing reduced seminiferous tubule degeneration and interstitial hyalinization in REO-treated groups49,63.
To our knowledge, this is the first study to demonstrate that the timing of antioxidant intervention critically dictates functional versus structural recovery in nanotoxicity, with prophylactic rosemary essential oil (REO) conferring superior protection against MnO2-NPsinduced testicular damage by bolstering glutathione (GSH) reserves, upregulating StAR-mediated steroidogenesis, and mitigating the initial ROS surge that disrupts mitochondrial and germ cell integrity. Notably, while therapeutic REO partially restored steroidogenic signaling (Creb/StAR) and attenuated NF-κB-driven inflammation but failed to fully reverse structural deficits such as interstitial hyalinization and Sertoli cell vacuolation due to irreversible impact of early oxidative insults on mitotically active germ cells. These insights advocate for integrating prophylactic REO into dietary regimens for populations at risk of occupational or environmental MnO2 NPs exposure.
This study has several limitations. First, the exclusive use of male rodents precludes evaluation of sex-specific effects. Second, the dose of REO (250 mg/kg) was selected based on prior studies14, but dose-response relationships and pharmacokinetics remain uncharacterized. Third, while oxidative stress markers were assessed, additional endpoints (e.g., DNA fragmentation, apoptotic indices) could strengthen mechanistic claims. Fourth, the prophylactic and therapeutic regimens were tested in a controlled experimental setting, which may not fully replicate chronic occupational exposure scenarios. Future studies should investigate long-term outcomes, individual REO constituents, and translational relevance to humans.
REO demonstrates potential in mitigating MnO2-NPs induced testicular injury in rodents, primarily via antioxidant activity and partial restoration of steroidogenic pathways. Prophylactic administration showed greater efficacy, suggesting preventive applications in high-risk settings. However, clinical translation requires further investigation into bioavailability, safety, and efficacy in human-relevant models.
All relevant data, detailed methodologies, and supplementary information necessary to reproduce the study’s results and analyses are fully included within the manuscript.
Catalase
cAMP response elements
Cytochrome P450 family 11
Dynamic light scattering
Follicle-stimulating hormone
Fourier-transform infrared spectroscopy
Gas chromatography–mass spectrometry
Reduced glutathione
3β-hydroxysteroid dehydrogenase
Luteinizing hormone
Malondialdehyde
Manganese oxide nanoparticles
Nitric oxide
Rosemary essential oil
Reactive oxygen species
Steroidogenic acute regulatory protein
Total antioxidant capacity
Transmission electron microscopy
X-ray diffraction
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Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB).
Department of Physiology, Faculty of Veterinary Medicine, Cairo University, P.O. 12211, Giza, Egypt
Hager M. Ramadan, Nadia A. Taha & Asmaa S. Morsi
Packaging Materials Department, National Research Centre, P.O. 12622, Dokki, Giza, Egypt
Ahmed M. Youssef
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N.A.T.: Designed the study, provided critical manuscript review, oversaw the research process, and granted final approval for publication. A.S.M.: Responsible for data collection, methodology development, manuscript drafting, data analysis and interpretation, writing, review and editing, and supervision. H.M.R.: Contributed to the original draft preparation, methodology, data curation and interpretation. A.M.Y.: Managed the preparation and characterization of the nanoparticles.
Correspondence to Asmaa S. Morsi.
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Ramadan, H.M., Taha, N.A., Youssef, A.M. et al. Rosemary essenitial oil counters MnO2 nanoparticle-induced fertility deficits in rats via antioxidant mechanisms and upregulation of StAR signalling. Sci Rep 15, 20201 (2025). https://doi.org/10.1038/s41598-025-06345-7
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