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2018 | 77 | 1 |

Tytuł artykułu

Protective effect of garlic extract against maternal and foetal cerebellar damage induced by lead administration during pregnancy in rats

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Background: In spite of its industrial usefulness and varied daily uses, lead (Pb) pollution is a widespread ecological problem that faces the humans in the 21th century. Pb was found to produces a wide range of toxic effects including neurotoxicity especially to the developing and young offspring. Recently, the utilisation of herbal plants has received a significant attention where there has been rising awareness in their therapeutic use; among these is the garlic. In light of the above, the current study is designed experimentally in female pregnant rats in order to investigate the beneficial role of garlic extract in the protection from the maternal and foetal cerebellar damage produced by administration of different doses of Pb during pregnancy. Materials and methods: Positively pregnant female rats were divided into five groups; one control group, two Pb-treated groups (exposed to 160 and 320 mg/kg b.w. of Pb, respectively) and two groups treated with both Pb and garlic (exposed to Pb as previous groups together with 250 mg/kg b.w./day of garlic extract). Treatments started from day 1 to day 20 of pregnancy, where the mother rats of different experimental groups were sacrificed to obtain the foetuses. Pb level in the maternal and foetal blood and cerebellum was estimated by spectrophotometry. Specimens of the cerebellum of different mother and foetal groups were processed to histological and immunohistochemical staining for microscopic examination. Results: The results showed that administration of Pb to pregnant rats resulted in a dose-dependent toxicity for both mothers and foetuses in the form of decrease in maternal weight gain, placental and foetal weights, brain weight and diminished foetal growth parameters, which were prominent in rat’s group treated with larger dose of Pb. In Pb-treated rats, Pb level in blood and cerebellum was high when compared with the control group. The histopathological examination of the cerebellum of treated dams and foetuses showed marked alterations mainly in the form of Purkinje cell degeneration and lack of development of foetal cerebellum. Co-treatment of garlic extract along with Pb resulted in a significant decrease in Pb levels as compared with those treated with Pb alone with improvement of the histopathological changes. Conclusions: This study was useful in evaluating the hazardous effects of uncontrolled use of Pb in general and in assessing the developmental and neurotoxicity of foetuses due to exposure during pregnancy in particular. Co-administration of garlic has beneficial effects in amelioration of Pb-induced neurotoxicity and reversing the histopathological changes of the cerebellum of mother rats and foetuses. (Folia Morphol 2018; 77, 1: 1–15)

Słowa kluczowe

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Czasopismo

Rocznik

Tom

77

Numer

1

Opis fizyczny

p.1-15,fig.,ref.

Twórcy

autor
  • Anatomy Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
  • Anatomy Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
autor
  • Anatomy Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
autor
  • Anatomy Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia
autor
  • Marine Biology Department, Faculty of Marine Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
  • Anatomy Department, Faculty of Medicine, Arabian Gulf University, Bahrain
autor
  • Biological Sciences Department, Faculty of Sciences, King Abdulaziz University, Jeddah, Saudi Arabia

Bibliografia

  • 1. Abd El-Monem DD. The modulating effect of melatonin against the genotoxicity of lead acetate. JOBAZ. 2012; 65(4): 223–231, doi: 10.1016/j.jobaz.2012.07.001.
  • 2. Abdel Moneim AE. Flaxseed oil as a neuroprotective agent on lead acetate-induced monoamineric alterations and neurotoxicity in rats. Biol Trace Elem Res. 2012; 148(3): 363–370, doi: 10.1007/s12011-012-9370-4, indexed in Pubmed: 22395955.
  • 3. Adu EK, Yeboah S. The efficacy of the vaginal plug formation after mating for pregnancy diagnosis, and embyonic resorption in utero in the greater cane rat (Thryonomys swinderianus, Temminck). Trop Anim Health Prod. 2000; 32(1): 1–10, indexed in Pubmed: 10717938.
  • 4. Afifi O, Embaby A. Histological Study on the Protective Role of Ascorbic Acid on Cadmium Induced Cerebral Cortical Neurotoxicity in Adult Male Albino Rats. J Microsc Ultrastruct. 2016; 4(1): 36–45, doi: 10.1016/j.jmau.2015.10.001.
  • 5. Allam A, El-Ghareeb AA, Abdul-Hamid M, et al. Prenatal and perinatal acrylamide disrupts the development of cerebellum in rat: Biochemical and morphological studies. Toxicol Ind Health. 2011; 27(4): 291–306, doi: 10.1177/0748233710386412, indexed in Pubmed: 21310778.
  • 6. Attia M, Ibrahim FA, Nabil GM, et al. Antioxidant effects of ginger (Zingiber officinale Roscoe) against lead acetateinduced hepatotoxicity in rats. Afr J Pharm Pharmacol. 2013; 7(20): 1213–1219, doi: 10.5897/ajpp2013.3465.
  • 7. Baranowska-Bosiacka I, Gutowska I, Marchetti C, et al. Altered energy status of primary cerebellar granule neuronal cultures from rats exposed to lead in the pre- and neonatal period. Toxicology. 2011; 280(1-2): 24–32, doi: 10.1016/j.tox.2010.11.004, indexed in Pubmed: 21108985.
  • 8. Barkur RR, Bairy LK. Histological study on hippocampus, amygdala and cerebellum following low lead exposure during prenatal and postnatal brain development in rats. Toxicol Ind Health. 2016; 32(6): 1052–1063, doi: 10.1177/0748233714545624, indexed in Pubmed: 25147304.
  • 9. Bellé LP, De Bona KS, Abdalla FH, et al. Comparative evaluation of adenosine deaminase activity in cerebral cortex and hippocampus of young and adult rats: effect of garlic extract (Allium sativum L.) on their susceptibility to heavy metal exposure. Basic Clin Pharmacol Toxicol. 2009; 104(5): 408–413, doi: 10.1111/j.1742-7843.2009.00390.x, indexed in Pubmed: 19413661.
  • 10. Bongiorno P, Fratellone P, LoGiudice P. Potential Health Benefits of Garlic (Allium Sativum): A Narrative Review. J Complement Integr Med. 2008; 5(1), doi: 10.2202/1553-3840.1084.
  • 11. Butler Walker J, Houseman J, Seddon L, et al. Maternal and umbilical cord blood levels of mercury, lead, cadmium, and essential trace elements in Arctic Canada. Environ Res. 2006; 100(3): 295–318, doi: 10.1016/j.envres.2005.05.006, indexed in Pubmed: 16081062.
  • 12. Celiktas O, Kocabas E, Bedir E, et al. Antimicrobial activities of methanol extracts and essential oils of Rosmarinus officinalis, depending on location and seasonal variations. Food Chem. 2007; 100(2): 553–559, doi: 10.1016/j.foodchem.2005.10.011.
  • 13. Chetty CS, Reddy GR, Murthy KS, et al. Perinatal lead exposure alters the expression of neuronal nitric oxide synthase in rat brain. Int J Toxicol. 2001; 20(3): 113–120, doi: 10.1080/109158101317097692, indexed in Pubmed: 11488553.
  • 14. Cory-Slechta DA, Virgolini MB, Rossi-George A, et al. Lifetime consequences of combined maternal lead and stress. Basic Clin Pharmacol Toxicol. 2008; 102(2): 218–227, doi: 10.1111/j.1742-7843.2007.00189.x, indexed in Pubmed: 18226077.
  • 15. Dribben WH, Creeley CE, Farber N. Low-level lead exposure triggers neuronal apoptosis in the developing mouse brain. Neurotoxicol Teratol. 2011; 33(4): 473–480, doi: 10.1016/j.ntt.2011.05.006, indexed in Pubmed: 21640820.
  • 16. Gargouri M, Ghorbel-Koubaa F, Bonenfant-Magné M, et al. Spirulina or dandelion-enriched diet of mothers alleviates lead-induced damages in brain and cerebellum of newborn rats. Food Chem Toxicol. 2012; 50(7): 2303–2310, doi: 10.1016/j.fct.2012.04.003, indexed in Pubmed: 22504531.
  • 17. González A, Pariente JA, Salido GM. Ethanol stimulates ROS generation by mitochondria through Ca2+ mobilization and increases GFAP content in rat hippocampal astrocytes. Brain Res. 2007; 1178: 28–37, doi: 10.1016/j.brainres.2007.08.040, indexed in Pubmed: 17888892.
  • 18. Grandjean P, Bellinger D, Bergman A, et al. The faroes statement: human health effects of developmental exposure to chemicals in our environment. Basic Clin Pharmacol Toxicol. 2008; 102(2): 73–75, doi: 10.1111/j.1742-7843.2007.00114.x, indexed in Pubmed: 18226057.
  • 19. Han JM, Chang BJ, Li TZ, et al. Protective effects of ascorbic acid against lead-induced apoptotic neurodegeneration in the developing rat hippocampus in vivo. Brain Res. 2007; 1185: 68–74, doi: 10.1016/j.brainres.2007.09.044, indexed in Pubmed: 17959157.
  • 20. Hussain AI, Anwar F, Hussain Sherazi ST, et al. Chemical composition, antioxidant and antimicrobial activities of basil (Ocimum basilicum) essential oils depends on seasonal variations. Food Chem. 2008; 108(3): 986–995, doi: 10.1016/j.foodchem.2007.12.010, indexed in Pubmed: 26065762.
  • 21. Hussein AM, Saleh HA, H N M. Effect of sodium selenite and vitamin E on the renal cortex in rats: an ultrastructure study. Tissue Cell. 2014; 46(3): 170–177, doi: 10.1016/j.tice.2014.03.002, indexed in Pubmed: 24799186.
  • 22. Iciek M, Kwiecień I, Włodek L. Biological properties of garlic and garlic-derived organosulfur compounds. Environ Mol Mutagen. 2009; 50(3): 247–265, doi: 10.1002/em.20474, indexed in Pubmed: 19253339.
  • 23. Kern JK, Jones AM. Evidence of toxicity, oxidative stress, and neuronal insult in autism. J Toxicol Environ Health B Crit Rev. 2006; 9(6): 485–499, doi: 10.1080/10937400600882079, indexed in Pubmed: 17090484.
  • 24. Khan M, Mostofa M, Jahan MS, et al. Effect of garlic and vitamin B-complex in lead acetate induced toxicities in mice. Bangl J Vet Med. 2009; 6(2), doi: 10.3329/bjvm.v6i2.2337.
  • 25. Kilikdar D, Mukherjee D, Mitra E, et al. Protective effect of aqueous garlic extract against lead-induced hepatic injury in rats. Indian J Exp Biol. 2011; 49(7): 498–510, indexed in Pubmed: 21800501.
  • 26. Liu J, Han D, Li Y, et al. Lead affects apoptosis and related gene XIAP and Smac expression in the hippocampus of developing rats. Neurochem Res. 2010; 35(3): 473–479, doi: 10.1007/s11064-009-0083-9, indexed in Pubmed: 19911273.
  • 27. Lu X, Jin C, Yang J, et al. Prenatal and lactational lead exposure enhanced oxidative stress and altered apoptosis status in offspring rats’ hippocampus. Biol Trace Elem Res. 2013; 151(1): 75–84, doi: 10.1007/s12011-012-9531-5, indexed in Pubmed: 23086308.
  • 28. Mabrouk A, Ben Cheikh H. Thymoquinone supplementation ameliorates lead-induced testis function impairment in adult rats. Toxicol Ind Health. 2016; 32(6): 1114–1121, doi: 10.1177/0748233714548474, indexed in Pubmed: 25216800.
  • 29. Massadeh AM, Al-Safi SA, Momani IF, et al. Garlic (Allium sativum L.) as a potential antidote for cadmium and lead intoxication: cadmium and lead distribution and analysis in different mice organs. Biol Trace Elem Res. 2007; 120(1-3): 227–234, doi: 10.1007/s12011-007-8017-3, indexed in Pubmed: 17916975.
  • 30. Meyer PA, Brown MJ, Falk H. Global approach to reducing lead exposure and poisoning. Mutat Res. 2008; 659(1-2): 166–175, doi: 10.1016/j.mrrev.2008.03.003, indexed in Pubmed: 18436472.
  • 31. Miodovnik A. Environmental neurotoxicants and developing brain. Mt Sinai J Med. 2011; 78(1): 58–77, doi: 10.1002/msj.20237, indexed in Pubmed: 21259263.
  • 32. Mustafa HN, Hegazy GA, Awdan SA, et al. Protective role of CoQ10 or L-carnitine on the integrity of the myocardium in doxorubicin induced toxicity. Tissue Cell. 2017; 49(3): 410–426, doi: 10.1016/j.tice.2017.03.007, indexed in Pubmed: 28410798.
  • 33. Mustafa HN, Hussein AM. Does allicin combined with vitamin B-complex have superior potentials than alpha-tocopherol alone in ameliorating lead acetate-induced Purkinje cell alterations in rats? An immunohistochemical and ultrastructural study. Folia Morphol. 2016; 75(1): 76–86, doi: 10.5603/FM.a2015.0076, indexed in Pubmed: 26365852.
  • 34. Mustafa HN. The role of curcumin in streptozotocininduced hepatic damage and the trans-differentiation of hepatic stellate cells. Tissue Cell. 2016; 48(2): 81–88, doi: 10.1016/j.tice.2016.02.003, indexed in Pubmed: 26905192.
  • 35. Patrick L. Lead toxicity part II: the role of free radical damage and the use of antioxidants in the pathology and treatment of lead toxicity. Altern Med Rev. 2006; 11(2): 114–127, indexed in Pubmed: 16813461.
  • 36. Pizzol M, Thomsen M, Andersen MS. Long-term human exposure to lead from different media and intake pathways. Sci Total Environ. 2010; 408(22): 5478–5488, doi: 10.1016/j.scitotenv.2010.07.077, indexed in Pubmed: 20797773.
  • 37. Pourjafar M, Aghbolaghi PA, Shakhse-Niaie M. Effect of garlic along with lead acetate administration on lead burden of some tissues in mice. Pak J Biol Sci. 2007; 10(16): 2772–2774, indexed in Pubmed: 19070102.
  • 38. Ronchetti R, van den Hazel P, Schoeters G, et al. Lead neurotoxicity in children: is prenatal exposure more important than postnatal exposure? Acta Paediatr Suppl. 2006; 95(453): 45–49, doi: 10.1080/08035320600886224, indexed in Pubmed: 17000569.
  • 39. Sanders T, Liu Y, Buchner V, et al. Neurotoxic effects and biomarkers of lead exposure: a review. Rev Environ Health. 2009; 24(1): 15–45, indexed in Pubmed: 19476290.
  • 40. Shahsavani D, Baghshani H, Alishahi E. Efficacy of allicin in decreasing lead (Pb) accumulation in selected tissues of lead-exposed common carp (Cyprinus carpio). Biol Trace Elem Res. 2011; 142(3): 572–580, doi: 10.1007/s12011-010-8801-3, indexed in Pubmed: 20711682.
  • 41. Sharma S, Shrivastava S, Shukla S. Reversal of lead-induced toxicity due to the effect of antioxidants. J Environ Pathol Toxicol Oncol. 2013; 32(2): 177–187, indexed in Pubmed: 24099431.
  • 42. Sharma V, Sharma A, Kansal L. The effect of oral administration of Allium sativum extracts on lead nitrate induced toxicity in male mice. Food Chem Toxicol. 2010; 48(3): 928–936, doi: 10.1016/j.fct.2010.01.002, indexed in Pubmed: 20060875.
  • 43. Valko M, Rhodes CJ, Moncol J, et al. Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chem Biol Interact. 2006; 160(1): 1–40, doi: 10.1016/j.cbi.2005.12.009, indexed in Pubmed: 16430879.
  • 44. Verina T, Rohde CA, Guilarte TR. Environmental lead exposure during early life alters granule cell neurogenesis and morphology in the hippocampus of young adult rats. Neuroscience. 2007; 145(3): 1037–1047, doi: 10.1016/j.neuroscience.2006.12.040, indexed in Pubmed: 17276012.
  • 45. Villeda-Hernández J, Méndez Armenta M, Barroso-Moguel R, et al. Morphometric analysis of brain lesions in rat fetuses prenatally exposed to low-level lead acetate: correlation with lipid peroxidation. Histol Histopathol. 2006; 21(6): 609–617, doi: 10.14670/HH-21.609, indexed in Pubmed: 16528671.
  • 46. Zhang YM, Liu XZ, Lu H, et al. Lipid peroxidation and ultrastructural modifications in brain after perinatal exposure to lead and/or cadmium in rat pups. Biomed Environ Sci. 2009; 22(5): 423–429, doi: 10.1016/S0895-3988(10)60021-9, indexed in Pubmed: 20163068.

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Bibliografia

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