scholarly journals Protective effects of zinc oxide nanoparticles against doxorubicin induced testicular toxicity and DNA damage in male rats

2019 ◽  
Vol 8 (5) ◽  
pp. 654-662 ◽  
Author(s):  
Zeynab Khamis El-Maddawy ◽  
Walaa Slouma Hamouda Abd El Naby
Keyword(s):  
Zinc Oxide ◽  
Zinc Oxide Nanoparticles ◽  
Histopathological Examination ◽  
Sperm Count ◽  
Treated Group ◽  
Male Rats ◽  
Oxide Nanoparticles ◽  
Testicular Toxicity ◽  
Protective Effects ◽  
Zno Nps

Abstract The present study aims to investigate the protective effects of zinc oxide nanoparticles (ZnO NPs) on doxorubicin-induced testicular injury. Forty mature male rats were randomly allocated into four equal groups: G1 (control), G2 (3 mg per kg BW of zinc oxide nanoparticles was administered), G3 (6 mg per kg BW of doxorubicin was intraperitoneally injected), and G4 (doxorubicin + ZnO NPs). Some fertility parameters, antioxidant status, genotoxicity assay, and a histopathological examination were used for this investigation. The doxorubicin-treated group showed a significant decrease in the index weight of reproductive organs, epididymal sperm count, motility%, and live sperm% and a significant increase in sperm abnormalities. Moreover, GSH and CAT activities were significantly decreased, and MDA content was significantly increased in the doxorubicin-treated group. Interestingly, co-administration of ZnO NPs significantly reduced the doxorubicin-induced changes in the investigated parameters. In addition, ZnO NPs alone did not show any undesirable effects on the sperm parameters, testis or DNA. However, its administration improves the reproductive parameters and significantly increases the testosterone level. We concluded that the administration of ZnO NPs at 3 mg per kg BW ameliorated the testicular toxicity and genotoxicity caused by doxorubicin through its antioxidant and androgenic activity.

Comparative study of zinc oxide nanoparticles and its bulk form on liver function of Wistar rat

2019 ◽  
Vol 35 (10) ◽  
pp. 627-637 ◽  
Author(s):  
Eman Raafat Moatamed ◽  
Aida Ahmed Hussein ◽  
Mohamed Mahmoud El-desoky ◽  
Zakaria EL Khayat
Keyword(s):  
Zinc Oxide ◽  
Liver Function ◽  
Zinc Oxide Nanoparticles ◽  
Liver Enzymes ◽  
Histopathological Examination ◽  
Reduction Process ◽  
Wistar Rat ◽  
Oxide Nanoparticles ◽  
Zno Nps ◽  
Oxidation Reduction

Zinc oxide nanoparticles (ZnO NPs) are produced in high tonnage each year; they are widely used in consumer and industrial products, also now finding applications in bioimaging and drug delivery. In the present study, comparison between ZnO NPs (39 nm) and its bulk/micron form (particle size = 5 µm) on liver function of rats was determined. In our study, liver enzymes biomarkers, serum lipid profile, zinc concentration, and histopathological examination in liver tissues were used to evaluate liver injury. Moreover, lipid peroxidation (malondialdehyde), nitric oxide, and reduced glutathione levels were determined to detect the oxidation–reduction process in liver tissue. The results showed dose-dependent toxicity of ZnO NPs. Three different dose levels (25, 50, and 100 mg/kg bw) were used, and the 100-mg/kg bw ZnO NPs group showed the most significant changes in liver enzymes and histopathological structure, as well as redox state. The dose of 100 mg/kg bw of ZnO bulk group showed no significant effects on liver function. The study concluded that ZnO NPs caused hepatic impairments.

scholarly journals Effect of Green Tea and Zinc oxide Nanoparticles Complex on Histopathology of Spleen of Male Rats Induced by Monosodium Glutamate

2019 ◽  
pp. 04-11
Author(s):  
Fawziah A Al-Salmi ◽  
Reham Z Hamza ◽  
Nahla S El-Shenawy
Keyword(s):  
Zinc Oxide ◽  
Green Tea ◽  
Zinc Oxide Nanoparticles ◽  
Monosodium Glutamate ◽  
Male Rats ◽  
Albino Rats ◽  
Oxide Nanoparticles ◽  
White Pulp ◽  
Zno Nps ◽  
Red Pulp

Background and objective: Synthesis of zinc oxide nanoparticles (ZnO NPs) with green tea extract (GTE) to form a complex is known to be one of the most multiuse nanoparticles with its application in treatment the toxicity of monosodium glutamate (MSG) on liver, kidney, testis, and pancreas. Therefore, the present study was concerned with the pontifical effect of ZnO NPs / GTE complex on the histological structure of spleen exposed to MSG. Materials and Methods: The toxicity of MSG was evaluated in male albino rats using two dosages (low, 6.0 and high, 17.5 mg/kg). The albino rats were taken for the experiment and randomly assigned into six groups; control, ZnO NPs, MSG-LD, MSG-HD, ZnO NPs / GTE + MSG-LD, and ZnO NPs / GTE + MSG-HD. The animals were decapitated after 30 days of exposure and spleens were dissected out and processed for the histological examination by light microscope. Results: The result revealed that MSG causes shrinkage in the white pulp nodule with increasing the area of the white pulp and degeneration of red pulp as compared to the control. The changes were more prominent in the rats treated with the higher dosage of MSG. The finding suggests that MSG may effect on adhesion of splenocytes and degeneration of red pulp in the rat leading to the reduced immunogenic response. Conclusions: The data could be demonstrated the effect of MSG on spleen tissue was a dose-dependent and led to hypertrophy of white pulp of the spleen. The ZnO NPs/GTE complex could provide a protective benefit against MSG-induced splenomegaly through its potent antioxidant properties due to the presence of GTE and reduction of the ZnO. The future study will be a concern on the thymus histology as it acts as the center of lymphoid organ. Keywords: Monosodium glutamate, ZnO nanoparticles, Spleen, Histology, Rats

scholarly journals Zinc Oxide Nanoparticles Prime a Protective Immune Response in Galleria mellonella to Defend Against Candida albicans

2021 ◽  
Vol 12 ◽  
Author(s):  
Mei-nian Xu ◽  
Li Li ◽  
Wen Pan ◽  
Huan-xin Zheng ◽  
Meng-lei Wang ◽  
...  
Keyword(s):  
Immune Response ◽  
Zinc Oxide ◽  
Candida Albicans ◽  
Zinc Oxide Nanoparticles ◽  
Galleria Mellonella ◽  
Oxide Nanoparticles ◽  
Protective Effects ◽  
Zno Nps

Purpose: Zinc oxide nanoparticles (ZnO-NPs) have exerted antimicrobial properties. However, there is insufficient evaluation regarding the in vivo antifungal activity of ZnO-NPs. This study aimed to investigate the efficacy and mechanism of ZnO-NPs in controlling Candida albicans in the invertebrate Galleria mellonella.Methods:Galleria mellonella larvae were injected with different doses of ZnO-NPs to determine their in vivo toxicity. Non-toxic doses of ZnO-NPs were chosen for prophylactic injection in G. mellonella followed by C. albicans infection. Then the direct in vitro antifungal effect of ZnO-NPs against C. albicans was evaluated. In addition, the mode of action of ZnO-NPs was assessed in larvae through different assays: quantification of hemocyte density, morphology observation of hemocytes, characterization of hemocyte aggregation and phagocytosis, and measurement of hemolymph phenoloxidase (PO) activity.Results: Zinc oxide nanoparticles were non-toxic to the larvae at relatively low concentrations (≤20 mg/kg). ZnO-NP pretreatment significantly prolonged the survival of C. albicans-infected larvae and decreased the fungal dissemination and burden in the C. albicans-infected larvae. This observation was more related to the activation of host defense rather than their fungicidal capacities. Specifically, ZnO-NP treatment increased hemocyte density, promoted hemocyte aggregation, enhanced hemocyte phagocytosis, and activated PO activity in larvae.Conclusion: Prophylactic treatment with lower concentrations of ZnO-NPs protects G. mellonella from C. albicans infection. The innate immune response primed by ZnO-NPs may be part of the reason for the protective effects. This study provides new evidence of the capacity of ZnO-NPs in enhancing host immunity and predicts that ZnO-NPs will be attractive for further anti-infection applications.

scholarly journals The Effects of Pentoxifylline on Memory in Male Rats Treated with Zinc Oxide NPs

2021 ◽  
Vol 25 (1) ◽  
pp. 1-10
Author(s):  
Niloufar Darbandi ◽  
◽  
Zeynab Vasheghani Farahani ◽  
Hamidreza Momeni ◽  
◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Zinc Oxide ◽  
Treatment Group ◽  
Blood Serum ◽  
Zinc Oxide Nanoparticles ◽  
Male Rats ◽  
Control Group ◽  
Oxide Nanoparticles ◽  
Zno Nps ◽  
Ca1 Region

Background: Zinc oxide Nanoparticles (NPs) present irreversible effects on the nervous system, memory, and learning. Objective: The current study aimed to investigate the effects of pentoxifylline on memory impairments, CA1 hippocampal pyramidal cells, and blood serum antioxidant enzymes in male rats treated with zinc oxide NPs. Methods: Male Wistar rats were divided into the control, zinc oxide NPs (1.25 mg/kg), pentoxifylline (50 mg/kg), and pentoxifylline with zinc oxide NPs groups. In all study groups, saline, zinc oxide NPs, and pentoxifylline were intraperitoneally injected 30 minutes before training. In the co-treatment group, pentoxifylline was injected one hour before injecting Zno NPs. After performing the behavioral test, the tested animals’ brains were fixed and the number of healthy neurons in the CA1 region of the hippocampus was counted. In all research groups, malondialdehyde levels, total antioxidant power, superoxide dismutase levels, and glutathione peroxidase in blood serum were measured. Results: Zinc oxide nanoparticles decreased memory and the number of healthy neurons in the CA1 region of the hippocampus and increased oxidative stress in blood serum, compared to the controls. In the co-treatment group, using pentoxifylline improved the above-mentioned factors and reached the level of the control group. Pentoxifylline alone presented no significant effect on the aforementioned characteristics, compared to the control group. Conclusion: ZnO NPs may decrease memory retrieval and cause cell death in the pyramidal neurons of the CA1 region of the hippocampus by increasing oxidative stress. Pentoxifylline, as a potent antioxidant, can prevent the harmful effects of ZnO NPs.

scholarly journals Insight Study on the Comparison between Zinc Oxide Nanoparticles and Its Bulk Impact on Reproductive Performance, Antioxidant Levels, Gene Expression, and Histopathology of Testes in Male Rats

Antioxidants ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 41 ◽  
Author(s):  
Amira A. Goma ◽  
Hossam G. Tohamy ◽  
Sara E. El-Kazaz ◽  
Mohamed M. Soliman ◽  
Mustafa Shukry ◽  
...  
Keyword(s):  
Gene Expression ◽  
Zinc Oxide ◽  
Sexual Behavior ◽  
Reproductive Performance ◽  
Zinc Oxide Nanoparticles ◽  
Histopathological Examination ◽  
Male Rats ◽  
Oxide Nanoparticles ◽  
Antioxidants Activity ◽  
Semen Characteristics

Background: Despite the beneficial effects of zinc oxide nanoparticles (ZnONPs) on different biomedical applications, including their antioxidant and anti-inflammatory ones, it might have cytotoxic and genotoxic impacts on the male reproductive system. Objective: The current study compares the effect of zinc oxide nanoparticles and their bulk form, at different doses, on male rats’ reproductive performance, testicular antioxidants, gene expression, and histopathology. Materials and Methods: Thirty male rats were randomly allocated equally in five groups. The control one was injected with Tween 80 (10%). The zinc oxide nanoparticle (ZnONP) groups received ZnONPs < 50 nm, specifically, 5 mg/kg (ZnONP-1) and 10 mg/kg (ZnONP-2). The bulk zinc oxide (BZnO) groups were administered 5 mg/kg (BZnO-1) and 10 mg/kg (BZnO-2), correspondingly. Rats were injected intraperitoneally with the respected materials, twice/week for eight consecutive weeks. Finally, the male rats’ sexual behavior and their pup’s performance were determined in a monogamous mating system. Rats were then anesthetized and sacrificed for semen characteristics evaluation and tissue collection for antioxidant and hormones analysis, gene expression, and histopathological examination. Results: It was shown that ZnONP-1 improved sexual behavior, semen characteristics, and pup’s performance compared to its bulk form. Similarly, the testicular antioxidants activity, glutathione (GSH), and superoxide dismutase (SOD) increased with a decrease in the malonaldehyde (MDA), interleukin 6 (IL-6), and tumor necrosis factor (TNF-α) levels. It also improves the reproductive hormone levels and mRNA expression of different steroidogenesis-associated genes and anti-apoptotic genes. Conclusion: It can be concluded that zinc oxide nanoparticles, administered at 5 mg/kg, had the most beneficial effect on male reproductive performance, while 10 mg/kg could have a detrimental effect.

scholarly journals Zinc oxide nanoparticles improve testicular steroidogenesis machinery dysfunction in benzo[α]pyrene-challenged rats

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Niveen M. Daoud ◽  
Mohamed S. Aly ◽  
Omaima H. Ezzo ◽  
Naglaa A. Ali
Keyword(s):  
Oxidative Stress ◽  
Zinc Oxide ◽  
Zinc Oxide Nanoparticles ◽  
Molecular Mechanisms ◽  
Regulatory Protein ◽  
Male Rats ◽  
Oxide Nanoparticles ◽  
Mrna Levels ◽  
Zno Nps ◽  
Positive Effects

AbstractZinc oxide nanoparticles (ZnO NPs) demonstrate potential positive effects on reproduction. However, their protective role against the reproductive toxicity pollutants has not yet been adequately studied at the molecular level. This study was designed to assess this objective using Benzo[α]pyrene B[a]P as reproductive toxic agent . Forty-eight mature male rats were randomly distributed into six groups: Group1 (negative control); Groups 2 and 3 (positive control I and II, wherein the animals were treated with 10 and 30 mg ZnO NPs/kg BW, respectively); Group 4 (B[a]P group; treated with 150 mg B[a]P/kg BW); and Groups 5 and 6 (subjected to B[a]P treatment co-administered with different concentrations of ZnO NPs). We investigated oxidative stress biomarkers; cholesterol side-chain cleavage enzyme (CYP11A1), steroidogenic acute regulatory protein (StAR), and 3β-hydroxysteroid dehydrogenase (3β-HSD) gene expression; testosterone levels; and histopathology of the liver, kidney, and testicles. The B[a]P-treated group showed significant deterioration in all reproductive parameters and displayed induced oxidative stress. ZnO NPs remarkably reduced oxidative stress, effectively upregulated the mRNA levels of CY11A1, StAR, and 3β-HSD, and improved the histological pictures in the examined organs. At their investigated doses and given their NPs properties, ZnO NPs demonstrated a marked ameliorative effect against the reproductive toxic effects of B[a]P. Further studies are needed to thoroughly investigate the molecular mechanisms of ZnO NPs.

scholarly journals Zinc Oxide Nanoparticles Improve Testicular Steroidogenesis Machinery Dysfunction In Benzo [α] Pyrene Challenged Rats

2021 ◽  
Author(s):  
Niveen M. Daoud ◽  
S Aly Mohamed ◽  
Omaima H. Ezzo ◽  
Naglaa A. Ali
Keyword(s):  
Oxidative Stress ◽  
Zinc Oxide ◽  
Zinc Oxide Nanoparticles ◽  
Male Reproduction ◽  
Male Rats ◽  
Oxide Nanoparticles ◽  
Zno Nps ◽  
Positive Effects ◽  
Defensive Role ◽  
The Impact

Abstract Although Zinc oxide nanoparticles (ZnO NPs) in low doses have potentially positive effects on reproduction by their antioxidant effects, the defensive role of Zinc nanomaterials against environmental pollutants that affect male reproduction has not been adequately studied. We designed our study to assess the impact of ZnO NPs towards reproductive dysfunction induced by Benzo[α]Pyrene (B[a]P). Forty-eight mature male rats were randomly distributed into six equal groups: G1; negative control, G2&3- positive control I &II (either 10 or 30 mg ZnO NPs / kg BW); G4. (150 mg Bap / kg BW), G 5 & 6 (Co- administrated B[a]P with different concentrations of ZnO NPs). Oxidative stress biomarkers, semiquantitative real-time PCR for steroidogenic enzymes (CY11A1, StAR, and 3β- HSD), testosterone levels and histopathology in the liver, kidney, and testicles were examined for this investigation. B[a] P treated group showed significant deterioration in all reproductive parameters and induced oxidative stress. Co-administration ZnO NPs eased oxidative stress and effectively increased the expression of CY11A1, StAR, and 3β- HSD and improved histopathological changes in the examined organs. Our results using the selected doses and with Nano particle properties confirm that ZnO NPs have an obvious ameliorative effect against B[a] P.

scholarly journals Investigation of the Zinc Oxide Nanoparticles Effect on Thyroid and Testosterone Hormones in Male Rats

2020 ◽  
Vol 4 (1) ◽  
pp. 26-31
Author(s):  
Noori M. Luaibi ◽  
Noor A. Zayed
Keyword(s):  
Zinc Oxide ◽  
Zinc Oxide Nanoparticles ◽  
Thyroid Stimulating Hormone ◽  
Male Rats ◽  
Oxide Nanoparticles ◽  
Sprague Dawley ◽  
Zno Nps ◽  
Adult Rats ◽  
Male Adult ◽  
Intraperitoneal Dose

Exposure to zinc oxide nanoparticles (ZnO NPs) has been increasing steadily, causing more attention being paid to their potential toxicity, including cytotoxicity and genotoxicity. Hence, this study aimed to investigate the effect of ZnO NPs on thyroid hormone triiodothyronine (T3), thyroxine (T4), and thyroid-stimulating hormone (TSH) as well as testosterone hormone in male adult rats. A total of 54 Sprague-Dawley albino adult male rats were divided into nine groups each of six rats, daily treated intraperitoneal with ZnO NPs two different doses (30 and 60) mg/kg in three different periods of time (7, 14, and 28) days, as following: Control groups (Groups 1, 2, and 3): Respectively received intraperitoneal injection with distilled water for 7, 14, and 28 days, experimental groups (Groups 4, 5, and 6): They were rats, respectively, received intraperitoneal dose (60 mg/kg) of ZnO NPs for (7, 14, and 28) days, and group (7, 8, and 9) experimental groups were rats, respectively, received intraperitoneal dose (30 mg/kg) of ZnO NPs for (7, 14, and 28) days. Data showed high significant decrease (P < 0.01) in level of T3, T4, TSH, and level of testosterone also decrease at high and low dose for 7, 14, and 28 days.

scholarly journals Alpha-Lipoic Acid Protects Co-Exposure to Lead and Zinc Oxide Nanoparticles Induced Neuro, Immuno and Male Reproductive Toxicity in Rats

2021 ◽  
Vol 12 ◽  
Author(s):  
Monika S. Deore ◽  
Keerthana S ◽  
Saba Naqvi ◽  
Anoop Kumar ◽  
S. J. S. Flora
Keyword(s):  
Zinc Oxide ◽  
Lipoic Acid ◽  
Zinc Oxide Nanoparticles ◽  
Acid Treatment ◽  
Aminolevulinic Acid ◽  
Reproductive Toxicity ◽  
Oxide Nanoparticles ◽  
Protective Agent ◽  
Protective Effects ◽  
Zno Nps

We evaluated the neuro-, immuno-, and male reproductive toxicity of zinc oxide nanoparticles (ZnO NPs) alone and in combination with lead acetate. We also studied the therapeutic role of α-lipoic acid postexposure. Lead (10 mg/kg, body weight), ZnO NPs (100 mg/kg, bwt) alone, and their combination were administered orally in Wistar rats for 28 days, followed by the administration of α-lipoic acid (15 mg/kg, bwt) for the next 15 days. Our results demonstrated protective effects of α-lipoic acid on lead and ZnO NP–induced biochemical alterations in neurological, immunological, and male reproductive organs in rats. The altered levels of blood δ-aminolevulinic acid dehydratase (ALAD), immunoglobulins (IgA, IgG, IgM, and IgE), interleukins (IL-1β, IL-4, and IL-6), caspase-3, and tumor necrosis factor (TNF-α) were attenuated by lipoic acid treatment. Lead and ZnO NP–induced oxidative stress was decreased by lipoic acid treatment, while a moderate recovery in the normal histoarchitecture of the brain section (cortex and hippocampus) and testes further confirmed the neuro- and male reproductive toxicity of lead and ZnO NPs. We also observed a significant decrease in the blood metal content in the animals treated with lipoic acid compared to the lead-administered group, indicating the moderate chelating property of lipoic acid. It may thus be concluded that lipoic acid might be a promising protective agent against lead and ZnO NP–induced alterations in the neurological, immunological, and reproductive parameters.

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