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A Silver Nanoparticle Method for Ameliorating Biliary Atresia Syndrome in Mice
Published on: October 13, 2018
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Ultrastructural hepatocytic alterations induced by silver nanoparticle toxicity
Mansour Almansour1, Laszlo Sajti2, Walid Melhim3
1a Department of Zoology , College of Science, King Saud University , Saudi Arabia.
Ultrastructural Pathology
|March 3, 2016
Summary
Silver nanoparticles (SNPs) can cause significant ultrastructural damage to liver cells in rats. These findings highlight potential health risks associated with nanosilver exposure from consumer products and nanomedicine.
Area of Science:
- Nanotoxicology
- Hepatopathology
- Cellular Biology
Background:
- Silver nanoparticles (SNPs) are increasingly used in medicine and consumer goods.
- Potential human health risks from SNPs are a growing concern.
- Limited data exists on the ultrastructural pathological effects of nanosilver.
Purpose of the Study:
- To investigate the ultrastructural alterations in rat hepatocytes induced by silver nanoparticle (SNP) exposure.
- To assess the potential cellular damage and functional impact on the liver.
Main Methods:
- Male rats received daily doses of SNPs (15-35 nm diameter) at 2 mg/kg for 21 days.
- Liver biopsies were collected and examined using transmission electron microscopy.
- Ultrastructural changes in hepatocytes were systematically documented.
Main Results:
- Observed alterations include mitochondrial swelling/crystolysis, endoplasmic reticulum disruption, cytoplasmic vacuolization, and lipid accumulation.
- Other findings include glycogen depletion, karyopyknosis, apoptosis, sinusoidal dilatation, Kupffer cell activation, and myelin figures.
- These changes indicate significant organelle damage and cellular stress within hepatocytes.
Conclusions:
- SNP exposure can induce significant hepatocyte organelle alterations, leading to cellular damage.
- These ultrastructural changes may impair liver function, posing potential health risks.
- Further research is needed to understand nanosilver toxicity in vital organs.

