The potential therapeutic effect of loaded ginger nanoparticles against Ehrlich ascites carcinoma (EAC) bearing mice-induced renal toxicity

Document Type : Research and Reference

Authors

1 Histology, Zoology Department, faculty of science, Tanta University

2 Zoology Department, faculty of science, Tanta University

3 Institute of Nanoscience and Nanotechnology, Kafrelsheikh University, 33516, Kafr ElSheikh, Egypt.

4 Zoology department, faculty of science, Tanta university, Tanta, Egypt

Abstract

Ehrlich ascites carcinoma (EAC) are undifferentiated, natural mouse mammary adenocarcinomas that are primarily used for research. The current study aims to assess whether loaded ginger nanoparticles have a protective effect against renal toxicity induced by EAC in mice. This study employed forty-nine mice, which were separated into seven groups as follows: Group1(GR1) was utilized as the negative control. EACs were implanted in GR2 mice. The GR3 was treated with Cis (40 μg/mouse) on the first day post-inoculation. The fourth, fifth, and sixth treatment groups received Gin, AGNPS, and Gin/AGNPS (0.4 mg/mouse for 6 days). The seventh treated group was injected with Cis (40 μg/mice) and then administered with Gin/AGNPS for 6 days. All mice were slaughtered to examine the biochemical, histological and immunohistochemical alterations in the kidney. The findings demonstrated a substantial increase in the EAC group's overall body weight. However, in contrast to (GR2), groups that received Cis, AGNPS, Gin, Gin/AGNPS, and Cis/Gin/AGNPS displayed a small percentage increase in body weight. Furthermore, EAC produced renal impairment, as demonstrated by increase in serum urea and creatinine levels. While the treatment group with Gin/AGNPS and Cis/Gin/AGNPS improved and reduced these differences in renal function stress. Histological and immunohistochemical staining verified these results. Present results imply that loaded ginger nanoparticles may possess anti-oxidant, anti-cancer, and renal protective qualities in addition to inhibiting the damage that EAC causes to the kidney dysfunction.

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