» Articles » PMID: 27311610

Protective Effects of Ascorbic Acid and Garlic Extract Against Lead-induced Apoptosis in Developing Rat Hippocampus

Overview
Journal Metab Brain Dis
Publisher Springer
Specialties Endocrinology
Neurology
Date 2016 Jun 18
PMID 27311610
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Lead exposure has negative effects on developing nervous system and induces apoptosis in newly generated neurons. Natural antioxidants (i.e. Ascorbic acid and Garlic) might protect against lead-induced neuronal cell damage. The aim of the present study was to investigate the protective effects of Ascorbic acid and Garlic administration during pregnancy and lactation on lead-induced apoptosis in rat developing hippocampus. Timed pregnant Wistar rats were administrated with Lead (1500 ppm) via drinking water (Pb group) or lead plus Ascorbic acid (Pb + AA Group, 500 mg/kg, IP), or lead plus Garlic Extract (Pb + G Group, 1 ml garlic juice/100 g BW, via Gavage) from early gestation (GD 0) until postnatal day 50 (PN 50). At the end of experiments, the pups' brains were carefully dissected. To identify neuronal death, the brain sections were stained with TUNEL assay. Mean of blood and brain lead levels increased significantly in Pb group comparing to other studied groups (P < 0.01). There was significant reduction in blood and brain lead level in Pb + AA and Pb + G groups when compared to those of Pb group (P < 0.01). The mean number of TUNEL positive cells in the CA1, CA3, and DG was significantly lower in the groups treated by either Ascorbic acid or Garlic (P < 0.05). Administration of Ascorbic acid and Garlic during pregnancy and lactation protect against lead-induced neuronal cell apoptosis in the hippocampus of rat pups partially via the reduction of Pb concentration in the blood and in the brain.

Citing Articles

Garlic bioactive substances and their therapeutic applications for improving human health: a comprehensive review.

El-Saadony M, Saad A, Korma S, Salem H, Abd El-Mageed T, Sami Alkafaas S Front Immunol. 2024; 15:1277074.

PMID: 38915405 PMC: 11194342. DOI: 10.3389/fimmu.2024.1277074.


The interplay between vitamin C and thyroid.

Far B, Behnoush A, Ghondaghsaz E, Habibi M, Khalaji A Endocrinol Diabetes Metab. 2023; 6(4):e432.

PMID: 37246589 PMC: 10335618. DOI: 10.1002/edm2.432.


Potential diagnostic biomarkers for lead-induced hepatotoxicity and the role of synthetic chelators and bioactive compounds.

Lakka N, Pai B, Mani M, Dsouza H Toxicol Res (Camb). 2023; 12(2):178-188.

PMID: 37125327 PMC: 10141777. DOI: 10.1093/toxres/tfad014.


Nanomedicine of Plant Origin for the Treatment of Metabolic Disorders.

Hu F, Sun D, Wang K, Shang D Front Bioeng Biotechnol. 2022; 9:811917.

PMID: 35223819 PMC: 8873594. DOI: 10.3389/fbioe.2021.811917.


Herbal Medicines-Are They Effective and Safe during Pregnancy?.

Sarecka-Hujar B, Szulc-Musiol B Pharmaceutics. 2022; 14(1).

PMID: 35057067 PMC: 8802657. DOI: 10.3390/pharmaceutics14010171.


References
1.
Alfano D, Petit T . Behavioral effects of postnatal lead exposure: possible relationship to hippocampal dysfunction. Behav Neural Biol. 1981; 32(3):319-33. DOI: 10.1016/s0163-1047(81)92372-4. View

2.
Munoz-Pinedo C . Signaling pathways that regulate life and cell death: evolution of apoptosis in the context of self-defense. Adv Exp Med Biol. 2012; 738:124-43. DOI: 10.1007/978-1-4614-1680-7_8. View

3.
Senapati S, Dey S, Dwivedi S, Swarup D . Effect of garlic (Allium sativum L.) extract on tissue lead level in rats. J Ethnopharmacol. 2001; 76(3):229-32. DOI: 10.1016/s0378-8741(01)00237-9. View

4.
Winneke G, Kramer U . Neurobehavioral aspects of lead neurotoxicity in children. Cent Eur J Public Health. 1997; 5(2):65-9. View

5.
Needleman H . Low level lead exposure and the development of children. Southeast Asian J Trop Med Public Health. 2005; 35(2):252-4. View