open access

Vol 79, No 4 (2020)
Original article
Submitted: 2019-09-09
Accepted: 2019-11-17
Published online: 2019-11-26
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Protective effect of propolis on manganese chloride neurotoxicity of olfactory bulb in adult male albino rat

O. M. Mahmoud1, N. A. Salem1, M. H. Al Badawi2
·
Pubmed: 31777945
·
Folia Morphol 2020;79(4):672-680.
Affiliations
  1. Department of Human Anatomy and Embryology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt
  2. Department of Human Anatomy and Embryology, Faculty of Medicine, Helwan University, Cairo, Egypt

open access

Vol 79, No 4 (2020)
ORIGINAL ARTICLES
Submitted: 2019-09-09
Accepted: 2019-11-17
Published online: 2019-11-26

Abstract

Background: Manganese (Mn) is widely used for industrial purposes and exposure to high levels of Mn may cause an irreversible brain disease. Propolis is a natural plant product; it acts as a powerful reactive oxygen species scavenger and improves the neurodegeneration process. Materials and methods: In this study 40 adult male albino rats were divided randomly into four groups 10 rats each: group I (control group), group II manganese chloride (MnCl2) received 10 mg/kg/day/orally for 4 weeks by intra-gastric tube, group III (propolis group) received 50 mg/kg/day/orally for 4 weeks by intra-gastric tube, and group IV (MnCl2 + propolis group) received the same doses with the same duration and route as in groups II and III. Rats were sacrificed after 24 h of last dose. The olfactory bulbs removed, the right bulb cut to be processed for haematoxylin and eosin, immunohistochemical staining and the left cut for electron microscopic studies. Results: Results revealed that rat olfactory bulb from MnCl2 group showed darkly stained mitral cells with dark pyknotic nuclei, some show pericellular spaces and vacuolation, dark apoptotic cells in granular cells, neuropil vacuolation and pyknotic astrocyte. Electron microscopic examination showed abnormal granular cell with irregular damaged nuclear membrane, rupture of myelin fibre. Mitral nerve cell with destructed nucleus, many cytoplasmic vacuoles, swollen rough endoplasmic reticulum, vacuolated mitochondria and neuropil were observed. Manganese chloride + propolis group showed improvement compared to MnCl2 group. Conclusions: It was concluded that propolis can ameliorate the toxic changes of manganese chloride on rat olfactory bulb.

Abstract

Background: Manganese (Mn) is widely used for industrial purposes and exposure to high levels of Mn may cause an irreversible brain disease. Propolis is a natural plant product; it acts as a powerful reactive oxygen species scavenger and improves the neurodegeneration process. Materials and methods: In this study 40 adult male albino rats were divided randomly into four groups 10 rats each: group I (control group), group II manganese chloride (MnCl2) received 10 mg/kg/day/orally for 4 weeks by intra-gastric tube, group III (propolis group) received 50 mg/kg/day/orally for 4 weeks by intra-gastric tube, and group IV (MnCl2 + propolis group) received the same doses with the same duration and route as in groups II and III. Rats were sacrificed after 24 h of last dose. The olfactory bulbs removed, the right bulb cut to be processed for haematoxylin and eosin, immunohistochemical staining and the left cut for electron microscopic studies. Results: Results revealed that rat olfactory bulb from MnCl2 group showed darkly stained mitral cells with dark pyknotic nuclei, some show pericellular spaces and vacuolation, dark apoptotic cells in granular cells, neuropil vacuolation and pyknotic astrocyte. Electron microscopic examination showed abnormal granular cell with irregular damaged nuclear membrane, rupture of myelin fibre. Mitral nerve cell with destructed nucleus, many cytoplasmic vacuoles, swollen rough endoplasmic reticulum, vacuolated mitochondria and neuropil were observed. Manganese chloride + propolis group showed improvement compared to MnCl2 group. Conclusions: It was concluded that propolis can ameliorate the toxic changes of manganese chloride on rat olfactory bulb.

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Keywords

olfactory bulb, manganese chloride, propolis, rat

About this article
Title

Protective effect of propolis on manganese chloride neurotoxicity of olfactory bulb in adult male albino rat

Journal

Folia Morphologica

Issue

Vol 79, No 4 (2020)

Article type

Original article

Pages

672-680

Published online

2019-11-26

Page views

1061

Article views/downloads

1142

DOI

10.5603/FM.a2019.0127

Pubmed

31777945

Bibliographic record

Folia Morphol 2020;79(4):672-680.

Keywords

olfactory bulb
manganese chloride
propolis
rat

Authors

O. M. Mahmoud
N. A. Salem
M. H. Al Badawi

References (46)
  1. Al Badawi MH, Mahmoud O, Salem N. Therapeutic potential of omega-3 against sodium fluoride toxicity on the cerebellar cortex of adult male albino rats. Egyptian J Histol. 2016; 39(2): 170–178.
  2. Arai MA, Koryudzu K, Koyano T, et al. Naturally occurring Ngn2 promoter activators from Butea superba. Mol Biosyst. 2013; 9(10): 2489–2497.
  3. Aschner M, Erikson KM, Herrero Hernández E, et al. Manganese and its role in Parkinson's disease: from transport to neuropathology. Neuromolecular Med. 2009; 11(4): 252–266.
  4. Aschner M, Guilarte TR, Schneider JS, et al. Manganese: recent advances in understanding its transport and neurotoxicity. Toxicol Appl Pharmacol. 2007; 221(2): 131–147.
  5. Aschner M, Vrana KE, Zheng W. Manganese uptake and distribution in the central nervous system (CNS). Neurotoxicology. 1999; 20(2-3): 173–180.
  6. Bankova V, de Castro SL, Marcucci MC. Propolis: recent advances in chemistry and plant origin. Apidologie. 2000; 31(1): 3–15.
  7. Bowler RM, Nakagawa S, Drezgic M, et al. Sequelae of fume exposure in confined space welding: a neurological and neuropsychological case series. Neurotoxicology. 2007; 28(2): 298–311.
  8. Cersosimo MG, Koller WC. The diagnosis of manganese-induced parkinsonism. Neurotoxicology. 2006; 27(3): 340–346.
  9. Chen CJ, Liao SL. Oxidative stress involves in astrocytic alterations induced by manganese. Exp Neurol. 2002; 175(1): 216–225.
  10. Chen P, Bornhorst J, Aschner M. Manganese metabolism in humans. Front Biosci (Landmark Ed). 2018; 23: 1655–1679.
  11. Crossgrove J, Zheng W. Manganese toxicity upon overexposure. NMR Biomed. 2004; 17(8): 544–553.
  12. Devanand DP, Michaels-Marston KS, Liu X, et al. Olfactory deficits in patients with mild cognitive impairment predict Alzheimer's disease at follow-up. Am J Psychiatry. 2000; 157(9): 1399–1405.
  13. Dorman DC, Brenneman KA, McElveen AM, et al. Olfactory transport: a direct route of delivery of inhaled manganese phosphate to the rat brain. J Toxicol Environ Health A. 2002; 65(20): 1493–1511.
  14. Dringen R. Metabolism and functions of glutathione in brain. Prog Neurobiol. 2000; 62(6): 649–671.
  15. El-Masry TA, Emara AM, El-Shitany NA. Possible protective effect of propolis against lead-induced neurotoxicity in animal model. J Evol Biol Res. 2011; 3: 4–11.
  16. Ennis M, Hamilton KA, Hayar A. Neurochemistry of the main olfactory system. Handbook of Neurochemistry and Molecular Neurobiology. 2007: 137–204.
  17. Farooqui T, Farooqui AA. Beneficial effects of propolis on human health and neurological diseases. Front Biosci (Elite Ed). 2012; 4: 779–793.
  18. Fishman JB, Rubin JB, Handrahan JV, et al. Receptor-mediated transcytosis of transferrin across the blood-brain barrier. J Neurosci Res. 1987; 18(2): 299–304.
  19. Flora S. Nutritional components modify metal absorption, toxic response and chelation therapy. J Nutr Environ Med. 2009; 12(1): 53–67.
  20. Flynn MR, Susi P. Neurological risks associated with manganese exposure from welding operations--a literature review. Int J Hyg Environ Health. 2009; 212(5): 459–469.
  21. Fordahl SC. Effects of manganese exposure and antioxidant therapy on oxidative stress and stereotypic behaviors in rats. The University of North Carolina at Greensboro. 2009.
  22. Ilhan A, Koltuksuz U, Ozen S, et al. The effects of caffeic acid phenethyl ester (CAPE) on spinal cord ischemia/reperfusion injury in rabbits. Eur J Cardiothorac Surg. 1999; 16(4): 458–463.
  23. Iregren A. Manganese neurotoxicity in industrial exposures: proof of effects, critical exposure level, and sensitive tests. Neurotoxicology. 1999; 20(2-3): 315–323.
  24. Jaishankar M, Tseten T, Anbalagan N, et al. Toxicity, mechanism and health effects of some heavy metals. Interdiscip Toxicol. 2014; 7(2): 60–72.
  25. Jin X, Liu Q, Jia L, et al. Pinocembrin attenuates 6-OHDA-induced neuronal cell death through Nrf2/ARE pathway in SH-SY5Y cells. Cell Mol Neurobiol. 2015; 35(3): 323–333.
  26. Leavens TL, Rao D, Andersen ME, et al. Evaluating transport of manganese from olfactory mucosa to striatum by pharmacokinetic modeling. Toxicol Sci. 2007; 97(2): 265–278.
  27. Lehmkuhl AM, Dirr ER, Fleming SM. Olfactory assays for mouse models of neurodegenerative disease. J Vis Exp. 2014(90): e51804.
  28. Liu R, Wu CX, Zhou D, et al. Pinocembrin protects against β-amyloid-induced toxicity in neurons through inhibiting receptor for advanced glycation end products (RAGE)-independent signaling pathways and regulating mitochondrion-mediated apoptosis. BMC Med. 2012; 10: 105.
  29. Liu Y, Wu Z, Zhang X, et al. Leptomeningeal cells transduce peripheral macrophages inflammatory signal to microglia in reponse to Porphyromonas gingivalis LPS. Mediators Inflamm. 2013; 2013: 407562.
  30. Maier CM, Chan PH. Role of superoxide dismutases in oxidative damage and neurodegenerative disorders. Neuroscientist. 2002; 8(4): 323–334.
  31. Ni J, Wu Z, Meng J, et al. The neuroprotective effects of brazilian green propolis on neurodegenerative damage in human neuronal SH-SY5Y cells. Oxid Med Cell Longev. 2017; 2017: 7984327.
  32. Ramadan A, Soliman G, Mahmoud S, et al. Evaluation of the safety and antioxidant activities of Crocus sativus and Propolis ethanolic extracts. J Saudi Chem Soc. 2012; 16(1): 13–21.
  33. Ramos-Vara JA, Kiupel M, Baszler T, et al. Suggested guidelines for immunohistochemical techniques in veterinary diagnostic laboratories. J Vet Diagn Invest. 2008; 20(4): 393–413.
  34. Salem NA, Al Ba, Hussein HH. Protective role of propolis on diazinon induced nephrotoxicity in adult male albino rats. Eur J Anat. 2015; 19: 331–342.
  35. Santos AP, Lucas RL, Andrade V, et al. Protective effects of ebselen (Ebs) and para-aminosalicylic acid (PAS) against manganese (Mn)-induced neurotoxicity. Toxicol Appl Pharmacol. 2012; 258(3): 394–402.
  36. Schneider CA, Rasband WS, Eliceiri KW. NIH Image to ImageJ: 25 years of image analysis. Nat Methods. 2012; 9(7): 671–675.
  37. Seven I, Aksu T, Seven P. The Effects of Propolis on Biochemical Parameters and Activity of Antioxidant Enzymes in Broilers Exposed to Lead-Induced Oxidative Stress. Asian-Australasian J Animal Scien. 2010; 23(11): 1482–1489.
  38. Sforcin JM. Propolis and the immune system: a review. J Ethnopharmacol. 2007; 113(1): 1–14.
  39. Stallings WC, Metzger AL, Pattridge KA, et al. Structure-function relationships in iron and manganese superoxide dismutases. Free Radic Res Commun. 1991; 12-13 Pt 1: 259–268.
  40. Swamy M, Suhaili D, Sirajudeen KNS, et al. Propolis ameliorates tumor nerosis factor-α, nitric oxide levels, caspase-3 and nitric oxide synthase activities in kainic acid mediated excitotoxicity in rat brain. Afr J Tradit Complement Altern Med. 2014; 11(5): 48–53.
  41. Takeda A. Manganese action in brain function. Brain Res Brain Res Rev. 2003; 41(1): 79–87.
  42. Thompson KJ, Molina RM, Donaghey T, et al. Manganese uptake and distribution in the brain after methyl bromide-induced lesions in the olfactory epithelia. Toxicol Sci. 2011; 120(1): 163–172.
  43. Yang Mu, Crawley JN. Simple behavioral assessment of mouse olfaction. Curr Protoc Neurosci. 2009; Chapter 8: Unit 8.24.
  44. Young IS, Woodside JV. Antioxidants in health and disease. J Clin Pathol. 2001; 54(3): 176–186.
  45. Zaiyang L, Yue-Ming J, Xiang-Rong Li, et al. Vulnerability of welders to manganese exposure – A neuroimaging study. NeuroToxicology. 2014; 45: 285–292.
  46. Zhang S, Fu J, Zhou Z. In vitro effect of manganese chloride exposure on reactive oxygen species generation and respiratory chain complexes activities of mitochondria isolated from rat brain. Toxicol In Vitro. 2004; 18(1): 71–77.

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