The role of antioxidant activity of nano-chitosan-hydroalcoholic extract of Bee pollen in combating aluminum chloride-induced toxicity in rat brain tissue
Subject Areas : biochemistry
1 - Assistant Prof , Department of Biology, CT.C., Islamic Azad University, Tehran, Iran
Keywords: Bee pollen, aluminum chloride, brain tissue, oxidative stress indices, rat.,
Abstract :
Introduction: Aluminum is a metal with known toxicity to humans and animals that plays a role in the pathogenesis of various diseases. Plants contain a wide range of antioxidants that can neutralize free radicals and thus prevent the progression of many chronic diseases associated with oxidative stress. The aim of this study was to investigate the effects of nanochitosan carrying a hydroalcoholic extract of flower pollen on the antioxidant level of brain tissue in male rats exposed to aluminum chloride.
Materials and Methods: In this experimental study, 28 adult male Wistar rats were divided into 4 groups of 7: control, receiving aluminum chloride (100 mg/kg), nanochitosan (1 ml), aluminum chloride + nanochitosan carrying a hydroalcoholic extract of Bee pollen (200 mg/kg). Contamination induction and nanochitosan intake were performed by gavage. After the end of the treatment period and dissection of the animals, brain tissue was extracted to measure some oxidative stress indices in different groups. Data analysis in different groups was performed with SPSS software and one-way variance statistical test, and P<0.05 was considered significant.
Results: The results obtained from this study showed that in the group receiving aluminum chloride, an increase in malondialdehyde and a decrease in superoxide dismutase and glutathione peroxidase were significantly shown compared to the control group (P<0.001), while in the group treated with nanochitosan carrying the hydroalcoholic extract of Bee pollen grains, a decrease in malondialdehyde and an increase in superoxide dismutase and glutathione peroxidase were shown compared to the infected group (P<0.05).
Conclusion: According to the findings of this study, nanochitosan carrying the hydroalcoholic extract of Bee pollen grains can probably be used as a pharmaceutical product for the prevention or treatment of damage caused by pollutants such as aluminum chloride.
1. Zghari O, Azirar S, Lamtai M, El Hessni A, Ouichou A, Mesfioui A. Intrahippocampal dose-dependent effects of aluminum injection on affective and cognitive response in male Wistar rat: potential role of oxidative stress. Egypt J Basic Appl Sci. 2023;10(1):460–75. doi: 10.1080/2314808X.2023.2229623.
2. Geravand S, Karami M, Sahraei H, Rahimi F. Protective effects of L-arginine on Alzheimer's disease: Modulating hippocampal nitric oxide levels and memory deficits in aluminum chloride-induced rat model. Eur J Pharmacol. 2023;958:176030. doi: 10.1016/j.ejphar.2023.176030.
3. Shahabuddin F, Naseem S, Alam T, Khan AA, Khan F. Chronic aluminium chloride exposure induces redox imbalance, metabolic distress, DNA damage, and histopathologic alterations in Wistar rat liver. Toxicol Ind Health. 2024;40(11):581–95. doi: 10.1177/07482337241269784.
4. Kaya S, Yalçın T, Boydak M, Dönmez HH. Protective effect of N-acetylcysteine against aluminum-induced kidney tissue damage in rats. Biol Trace Elem Res. 2023;201(4):1806–15.
5. Elganzoury SS, Abdelfattah MS, Habotta OA, et al. Neuro-amelioration of Ficus lyrata extract conjugated with selenium nanoparticles against aluminium toxicity in rat brain: relevance to neurotransmitters, oxidative, inflammatory, and apoptotic events. Environ Sci Pollut Res. 2023;30(24):65822–34. doi: 10.1007/s11356-023-27057-3.
6. Mert H, Kerem Ö, Mıs L, Yıldırım S, Mert N. Effects of protocatechuic acid against cisplatin-induced neurotoxicity in rat brains: an experimental study. Int J Neurosci. 2024;134(7):725–34. doi: 10.1080/00207454.2022.2147430.
7. Kadhim A, Ben Slima A, Alneamah G, Makni M. Assessment of histopathological alterations and oxidative stress in the liver and kidney of male rats following exposure to aluminum chloride. J Toxicol. 2024;2024:3997463. doi: 10.1155/2024/3997463.
8. Ebhodaghe CI, Enogieru AB. Aluminium chloride-induced cerebral toxicity in Wistar rats: anticholinesterase and antioxidant effects of ascorbic acid. JOPAT. 2024;23(2):1548–56. doi: 10.4314/jopat.v23i2.12.
9. Ben Bacha A, Norah AO, Al-Osaimi M, et al. The therapeutic and protective effects of bee pollen against prenatal methylmercury induced neurotoxicity in rat pups. Metab Brain Dis. 2020;35:215–24. doi: 10.1007/s11011-019-00496-z.
10. Hu Y, Chen S, Yan W, et al. Rape bee pollen alleviates renal tissue damage in diabetic rats via anti‐inflammation, anti‐oxidation, and modulating gut microbiota. eFood. 2023;4(4):e101. doi: 10.1002/efd2.101.
11. Boshra AE, Hassan NM, Ibrahim S, Elsayed S. A comparative study of Egyptian bee pollen and propolis extracts: impacts on metabolic profile, liver, and kidney functions in diabetic rats induced by streptozotocin. VMJG. 2024;70(1):106–30. doi: 10.21608/VMJG.2024.319718.1039.
12. Farid A, Mohamed A, Ahmed A, Mehanny F, Safwat G. Preparation of bee venom-loaded chitosan nanoparticles for treatment of streptozotocin-induced diabetes in male Sprague Dawley rats. BJBAS. 2024;13:97. doi: 10.1186/s43088-024-00557-y.
13. Alshehri KM, Abdella EM. Development of ternary nanoformulation comprising bee pollen-thymol oil extracts and chitosan nanoparticles for anti-inflammatory and anticancer applications. Int J Biol Macromol. 2023;242:124584. doi: 10.1016/j.ijbiomac.2023.124584.
14. Samak DH, Abd-Ellatieff HA, Khalil RH, Saleh NA, Saleh HM. Mitigation of cadmium toxicity in African catfish using biological nano chitosan: insights into biochemical, genotoxic, and histopathological effects. BMC Vet Res. 2025;21:278. doi: 10.1186/s12917-025-04673-4.
15. Kira AY, Elmorsy EA, Hamad RS, et al. Nicardipine-chitosan nanoparticles alleviate thioacetamide-induced acute liver injury by targeting NFκB/NLRP3/IL-1β signaling in rats: Unraveling new roles beyond calcium channel blocking. Int Immunopharmacol. 2024;141:113000. doi: 10.1016/j.intimp.2024.113000.
16. Hindawy RF, Manawy SM, Nafea OE, Abdelhameed AA, Hendawi FF. Moringa oleifera leaves ethanolic extract counteracts cortical neurodegeneration induced by aluminum chloride in rats. Toxicol Res. 2024;13(2):tfae028. doi: 10.1093/toxres/tfae028.
17. El-Amawy AA, Zaahkouk SA, AbdelRasheed HG, Elarabi BE. The protective efficacy of propolis against multi heavy metals-induced oxidative stress and hepato-renal damage in males of albino rats. Egypt J Chem. 2023;66(3):289–300. doi: 10.21608/EJCHEM.2022.132369.5843.
18. Ghudhaib KK, Khaleel FM. Evaluation of SOD and MDA levels with the cytotoxicity of some plant extracts toward human rhabdomyosarcoma cell lines. Baghdad Sci J. 2025;22(3). doi: 10.21123/bsj.2024.10992.
19. Fouda K, Mohamed RS. Alginate beads with encapsulated date palm pollen extract: development, characterization and their potential role in hepato-protection and fertility-stimulating hormones improvement in bisphenol A-treated rats. Polymers. 2025;17(7):912. doi: 10.3390/polym17070912.
20. Okasha H, Dahroug H, Gouda AE, Shemis MA. A novel antibacterial approach of Cecropin-B peptide loaded on chitosan nanoparticles against MDR Klebsiella pneumoniae isolates. Amino Acids. 2023;55:1965–80. doi: 10.1007/s00726-023-03356-4.
21. Benamer Oudih S, Tahtat D, Nacer Khodja A, Mahlous M, Hammache Y, Guittoum AE, Kebbouche Gana S. Chitosan nanoparticles with controlled size and zeta potential. Polym Eng Sci. 2023;63(3):1011–21. doi: 10.1002/pen.26261.
22. Adel Mohamed Mahmoud N, Salah E, Abd Elrhman E, Elkomy A. Propolis alleviated cisplatin-induced hepatorenal oxidative stress and apoptosis. BVMJ. 2024;46(1):12–9. doi: 10.21608/BVMJ.2024.250114.1755.
23. Mirkov I, Stojković D, Aleksandrov AP, et al. Plant extracts and isolated compounds reduce parameters of oxidative stress induced by heavy metals: an up-to-date review on animal studies. Curr Pharm Des. 2020;26(16):1799–815. doi: 10.2174/1381612826666200407163408.
24. Ceramella J, De Maio AC, Basile G, et al. Phytochemicals involved in mitigating silent toxicity induced by heavy metals. Foods. 2024;13(7):978. doi: 10.3390/foods13070978.
25. Pathak A, Singh S, Sharma S. Unveiling the hepatoprotective and lipid-boosting power of Cichorium intybus extract in countering lead and nickel-induced toxicity. JVPT. 2023;22(1):77–83. doi: 10.1016/j.fct.2024.114595.
26. Renu K, Mukherjee AG, Gopalakrishnan AV, et al. Protective effects of macromolecular polyphenols, metals (zinc, selenium, and copper)-polyphenol complexes, and different organs with an emphasis on arsenic poisoning: a review. Int J Biol Macromol. 2023;253:126715. doi: 10.1016/j.ijbiomac.2023.126715.
27. Mohammadbaghban E, Taravati A, Najafzadehvarzi H, Khaleghzadeh‐Ahangar H, Tohidi F. Oral administration of encapsulated catechin in chitosan‐alginate nanoparticles improves cognitive function and neurodegeneration in an aluminum chloride‐induced rat model of Alzheimer's disease. Physiol Rep. 2024;12(13):e16095. doi: 10.14814/phy2.16095.
28. El-Demerdash FM, Ahmed MM, Kang W, Mohamed TM, Radwan AM. Hepatoprotective effect of silymarin-chitosan nanocomposite against aluminum-induced oxidative stress, inflammation, and apoptosis. Tissue Cell. 2024;91:102591. doi: 10.1016/j.tice.2024.102591.
29. Othman MS, Fareid MA, Abdel Hameed RS, Abdel Moneim AE. The protective effects of melatonin on aluminum‐induced hepatotoxicity and nephrotoxicity in rats. Oxid Med Cell Longev. 2020;2020:7375136. doi: 10.1155/2020/7375136.
30. Zbiabani Z, Keshtmand Z. The effect of nanochitosan carrying bee pollen extract on the level of antioxidants and lipid peroxidation in the liver tissue of mice infected with Staphylococcus aureus. Dev Biol. 2025;17(1):1–13.
31. Sistani Karampour N, Bagheri MJ, Khorsandi LS, Dehghan Mohammadi Z, Salehcheh M, Honarmand H. Investigating the safety of bee pollen on performance, oxidative stress, and histopathological changes in the liver, kidney, and pancreas of rats. CMJA. 2022;11(4):330–45.
32. Eraslan G, Kanbur M, Silici S, Liman BC, Altinordulu S, Sarica ZS. Evaluation of protective effect of bee pollen against propoxur toxicity in rat. Ecotoxicol Environ Saf. 2009;72(3):931–7. doi: 10.1016/j.ecoenv.2008.06.008.
33. Eraslan G, Kanbur M, Silici S. Effect of carbaryl on some biochemical changes in rats: the ameliorative effect of bee pollen. Food Chem Toxicol. 2009;47(1):86–91. doi: 10.1016/j.fct.2008.10.013.
34. Sarić A, Balog T, Sobocanec S, et al. Antioxidant effects of flavonoid from Croatian Cystus incanus L. rich bee pollen. Food Chem Toxicol. 2009;47(3):547–54. doi: 10.1016/j.fct.2008.12.007.
35. Kacemi R, Campos MG. Translational proofs on bee pollen as a source of biopharmaceuticals for neurodegeneration and cancer research: a scoping review and prospective reflections. Molecules. 2024;29:5893. doi: 10.3390/molecules29245893.
36. Abedi H, Shahpiri A. Functional characterization of a manganese superoxide dismutase from Avicennia marina: insights into its role in salt, hydrogen peroxide, and heavy metal tolerance. Sci Rep. 2024;14:406. doi: 10.1038/s41598-023-50851-5.
37. Sani A, Darma AI, Abdullahi IL, Musa BU, Imam FA. Heavy metals mixture affects the blood and antioxidant defense system of mice. J Hazard Mater Adv. 2023;11:100340. doi: 10.1016/j.hazadv.2023.100340.
38. Anjum SI, Ullah A, Gohar F, et al. Bee pollen as a food and feed supplement and a therapeutic remedy: recent trends in nanotechnology. Front Nutr. 2024;11:1371672. doi: 10.3389/fnut.2024.1371672.
39. Rupanar SV, Satpute R, Gadhave P, Kakade N. Bee pollen beyond nutrition: an integrated review of its chemical, pharmacological, and biological properties. JDRAS. 2024;9(4):211–21. doi: 10.1177/22785315241257338.