Acute Toxicity Assessment of Gallic Acid Administered Orally and Intraperitoneally in Wistar Rats
Jesús Velázquez-Antúnez1,2, Rosa I Higuera-Piedrahita3, Rolando Rojo-Rubio1
1Centro Universitario UAEM Temascaltepec, Universidad Autónoma Del Estado de México, México, Mexico.
Journal of Applied Toxicology : JAT
|November 5, 2025
Summary
Gallic acid (GA) toxicity was assessed in rats. While some biochemical changes occurred at higher doses, severe brain degeneration was observed only at medium and high intraperitoneal doses, suggesting safety at lower exposure levels.
Area of Science:
- Toxicology
- Biochemistry
- Histopathology
Background:
- Gallic acid (GA) is a phenolic compound with potential health benefits.
- Understanding its toxicological profile is crucial for safe application.
Purpose of the Study:
- To evaluate the biochemical parameters and anatomopathological changes in Wistar rats following oral and intraperitoneal administration of gallic acid.
- To determine the acute toxicity of gallic acid based on OECD guidelines.
Main Methods:
- Wistar rats were administered three single doses of gallic acid (11.46, 114.6, and 1146 mg/kg) via oral and intraperitoneal routes.
- Biochemical analyses of blood and histopathological examinations of kidney, liver, lung, heart, and brain tissues were performed.
- Acute toxicity testing followed OECD guidelines.
Main Results:
- Hypoproteinemia (low albumin and total protein) was observed in all groups, including the control, indicating it was not due to gallic acid.
- Elevated biochemical parameters at higher gallic acid doses remained within reference ranges.
- Severe diffuse neuronal and neuropil degeneration was noted in the brains of rats receiving medium and high intraperitoneal doses of gallic acid.
Conclusions:
- The observed hypoproteinemia is not attributable to gallic acid administration.
- Gallic acid may be safe at low and medium administered doses, particularly via the oral route.
- Intraperitoneal administration of medium to high doses of gallic acid may lead to neurotoxicity.


