PRENATAL AND POSTNATAL EFFECT OF LEAD ACETATE ON THE HISTOLOGY OF FRONTAL CORTEX AND MOTOR ACTIVITY IN WISTAR RATS

Authors

  • SALEH NUHU Department of Human Anatomy, Faculty of Basic Medical Sciences, Yusuf Maitama Sule University, Kano, Nigeria.
  • HAUWA IDRIS AHMAD Department of Human Anatomy, Faculty of Basic Medical Sciences, Yusuf Maitama Sule University, Kano, Nigeria.
  • AISHA MUHAMMAD GARBA Department of Human Anatomy, Faculty of Basic Medical Sciences, Yusuf Maitama Sule University, Kano, Nigeria.
  • TASIU ABDULLAHI SULAIMAN Department of Human Anatomy, Faculty of Basic Medical Sciences, Yusuf Maitama Sule University, Kano, Nigeria.

DOI:

https://doi.org/10.22159/ijms.2021.v9i6.43098

Keywords:

Lead, Frontal cortex, Prenatal, Postnatal, Motor activity, Palmer grasp reflex

Abstract

Objectives: The objective of this study was to find the histologic and motor activity effect of lead on prenatally and postnatally exposed Wistar rats.

Methods: In this study, twelve Wistar Rats were used and grouped into four groups of two females and one male. Group I rats served as the control and allowed feed and water freely. The rats in Group II were administered 500ppm of Pb through drinking water from gestation day 8 (GD8) to parturition (GD21). While Group III rats were given 500ppm of Pb in drinking water from postnatal day 1 (PND1) to PND21. The rats in the fourth group (Group IV) were given 500ppm of Pb from GD8 to PND21. Palmer grasp reflex was conducted to assess the motor activity of the rat pups. The animals were then humanely sacrificed and the frontal cortices were isolated for routine histological processing.

Results: The histological study has shown normal neurons in the control group while degenerating cells exhibiting karyolysis, pyknosis, karyorrhexis, vacuolation were seen in the lead-treated groups. Group II and Group IV showed considerate deficit in their motor activity while Group III showed mild effect.

Conclusion: From this study, lead exposure of Wistar rats at both prenatal and postnatal period of development has effect on the histology of the frontal cortex as well as on their motor activity.

References

Naqi SZ. A Comparative study of the histological changes in cerebral cortex, hippocampus, cerebellum, pons and medulla of the albino rat due to lead toxicity. Int J Anat Res 2015;3:1173-8.

Aprioku JS, Siminialayi IM. Maternal lead exposure and pregnancy outcome in Wistar albino rats. J Toxicol Environ Health Sci 2013;5:185-93.

Adikwu E, Deo O, Geoffrey OP, Enimeya DA. Lead organ and tissue toxicity: Roles of mitigating agents (Part 1). Br J Toxicol Pharm 2013;4:232-40.

Thurtle N, Greig J, Cooney L, Amitai Y, Ariti C, Brown MJ, et al.Description of 3, 180 courses of chelation with dimercaptosuccinic acid in children ≤ 5y with severe lead poisoning in Zamfara, Northern Nigeria: A retrospective analysis of programme data. PLoS Med 2014;11:e1001739.

Iliyasu MO, Ibegbu AO, Sambo JS, Musa SA, Akpulu PS. Histopathological changes on the hippocampus of adult wistar rats exposed to lead acetate and aqueous extract of psidium guajava leaves. Afr J Cell Path 2015;31:26-31.

Bazrgar M, Goudarzi I, Abrari K, Salmani ME, Lashkarbolouki T. Effect of postnatal chronic lead exposure on spatial learning and memory in male rat. Zahedan J Res Med Sci 2015;17:e1050.

Ghareeb DA, Hussien HM, Khalil AA. Toxicological and Environmental chemistry toxic effects of lead exposure on the brain of rats: Involvement of oxidative stress, inflammation, acetylcholinesterase, and the beneficial role of flaxseed extract. Toxicol Environ Chem 2010;92:37-41.

Ahmed MB, Ahmed MI, Meki AR, Abdraboh N. Neurotoxic effect of lead on rats: Relationship to apoptosis. Int J Health Sci (Qassim) 2013;7:192-9.

McClain RM, Becker BA. Teratogenicity, fetal toxicity, and placental transfer of lead nitrate in rats. Toxicol Appl Pharmacol 1975;31:72-82.

Azza AA, Hebatalla IA, Asmaa IA. Protective effect of zinc against postnatal lead-induced alterations in the neurobehavioural development of normally-fed and protein malnourished rats. J Neurol Neurosci 2016;7:117.

Goma UE, Mahrous AA. Changes in behavior and learning ability of rats intoxicated with lead. Int Sch Sci Res Innov 7 2013;7:1096-102.

Basha MR, Murali M, Siddiqi HK, Ghosal K, Siddiqi OK, Lashuel HA, et al. Lead (Pb) exposure and its effect on APP proteolysis and Abeta aggregation. FASEB J 2005;19:2083-4.

Reddy GR, Devi BC, Chetty CS. Developmental lead neurotoxicity: Alterations in brain cholinergic system. Neurotoxicology 2007;28:402-7.

Bunn TL, Parsons PJ, Kao E, Dietert RR. Exposure to lead during critical windows of embryonic development: Differential immunotoxic outcome based on stage of exposure and gender. Toxicol Sci 2001;64:57-66.

Rao Barkur R, Bairy LK. Evaluation of passive avoidance learning and spatial memory in rats exposed to low levels of lead during specific periods of early brain development. Int J Occup Med Environ Health 2015;28:533-44.

Bancroft JD, Gamble M. Theory and Practice of Histological Techniques. 6th ed. London: Churchill Livingstone, Elsevier; 2008.

Lockman J. Advances in Child Development and Behavior. 1st ed., Vol. 61. United States: Academic Press; 2021.

Highab SM, Magaji RA, Muhammad BY. Effect of lead poisoning and antidepressant drug on the cerebral cortex of the Wistar rats. Acta Sci Pharm Sci 2018;2:16-21.

Hazell AS, Normandin L, Norenberg MD, Kennedy G, Yi JH. Alzheimer type II astrocytic changes following sub-acute exposure to manganese and its prevention by antioxidant treatment. Neurosci Lett. 2006 Apr 3;396(3):167-71.

Nuhu S. Effect of Lead on the Histology of Medulla Oblongata, Body Weight and Haematological Profile in Albino Wistar Rats, M.Sc, Bayero University, Kano, Nigeria; 2017.

Anitha KS. Effect of Water Pollution on LDH Isoenzymes in Fish from Hussain Sagar Lake, Ph.D, Osmania University, Hyderabad, India; 1998.

Jagannath BM. Effect of heavy metals on the histopathology of gills and brain of fresh water fish Catla catla. Biomed Pharm J 2013;6:99-105.

Luthman J, Oskarsson A, Olson L, Hoffer B. Postnatal lead exposure affects motor skills and exploratory behavior in rats. Environ Res 1992;58:236-52.

Grant LD, Kimmel CA, West GL, Martinez-Vargas CM, Howard JL. Chronic low-level lead toxicity in the rat. Toxicol App Pharm 1980;56:42-58.

Dietrich KN, Berger OG, Succop PA, Hammond PB, Bornschein RL. The developmental consequences of low to moderate prenatal and postnatal Pb exposure: Intellectual attainment in the Cincinnati Pb study cohort following school entry. Neurotoxicol Teratol 1993;15:37-44.

Published

01-11-2021

How to Cite

NUHU, S., AHMAD, H. I., GARBA, A. M., & TASIU ABDULLAHI SULAIMAN. (2021). PRENATAL AND POSTNATAL EFFECT OF LEAD ACETATE ON THE HISTOLOGY OF FRONTAL CORTEX AND MOTOR ACTIVITY IN WISTAR RATS. Innovare Journal of Medical Sciences, 9(6), 10–12. https://doi.org/10.22159/ijms.2021.v9i6.43098

Issue

Section

Original Article(s)