𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Nephrotoxicity induced by N-(3,5-dichlorophenyl)-3-hydroxysuccinamic acid in male and female Fischer 344 rats

✍ Scribed by Gary O. Rankin; Suk-kil Hong; Dianne K. Anestis


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
185 KB
Volume
28
Category
Article
ISSN
0260-437X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The agricultural fungicide N‐(3,5‐dichlorophenyl)succinimide (NDPS) is a more potent nephrotoxicant in female rats than in males. Similarly, nephrotoxicant NDPS metabolites studied to date in male and female rats have also demonstrated gender differences, being twice as potent as nephrotoxicants in females as in males. The purpose of this study was to examine the nephrotoxic potential of N‐(3,5‐dichlorophenyl)‐3‐hydroxysuccinimide (3‐NDHSA) in male and female Fisher 344 rats to determine if gender differences in nephrotoxic potential also exist for this metabolite. Rats (four per group) were administered a single intraperitoneal (i.p.) injection of 3‐NDHSA (0.1, 0.2 or 0.4  mmol kg^−1^) or vehicle, and renal function was monitored at 24 and 48 h. 3‐NDHSA 0.1 mmol kg^−1^ did not induce nephrotoxicity in male or female rats. In male rats, 3‐NDHSA 0.2 mmol kg^−1^ induced mild nephrotoxicity seen as diuresis and transient, mild proteinuria. However, 3‐NDHSA 0.4 mmol kg^−1^ induced marked nephrotoxicity. In female rats, 3‐NDHSA 0.2 mmol kg^−1^ induced mild nephrotoxicity, as evidenced by transient diuresis and proteinuria. As in males, 3‐NDHSA 0.4 mmol kg^−1^ induced marked nephrotoxicity. These results indicate that, unlike NDPS and other nephrotoxic NDPS metabolites, 3‐NDHSA does not exhibit gender differences in nephrotoxic potential. In addition, in comparison with NDPS and other nephrotoxic NDPS metabolites, 3‐NDHSA is a less potent nephrotoxicant that NDHS or 2‐NDHSA and similar to NDPS in nephrotoxic potential in male rats. Copyright © 2008 John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Effect of structural modifications on 3-
✍ Niti N. Patel; Christine M. Crincoli; Douglas M. Frederick; Ruy Tchao; Peter J. 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 381 KB

## ABSTRACT Glitazones, used for type II diabetes, have been associated with liver damage in humans. A structural feature known as a 2,4‐thiazolidinedione (TZD) ring may contribute to this toxicity. TZD rings are of interest since continued human exposure via the glitazones and various prototype dr

Protection from 1-cyano-3,4-epithiobutan
✍ Jan L. Vansteenhouse; Judith S. Prescott; David H. Swenson 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 226 KB 👁 1 views

Cyano-3,4-epithiobutane (CEB), a naturally occurring nitrile derived from cruciferous plants, causes nephrotoxicity and increased renal glutathione (GSH) concentration in male F-344 rats. This CEBinduced nephrotoxicity is dependent on GSH conjugation and bioactivation. The objectives of the present

Effect of chemical form, route of admini
✍ Herng-Hsiang Lo; Monica A. Valentovic; Gary O. Rankin; Patrick I. Brown 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 685 KB

Chloroanilines are widely used chemical intermediates for the manufacture of dyes, agricultural chemicals and industrial compounds. Nephrotoxicity occurs as one toxicity following intraperitoneal (i.p,) administration of chloroaniline hydrochlorides to rats. The purpose of this study was to examine

Urinary enzyme excretion as a parameter
✍ Monica Valentovic; Pamela Williams; John Carl Iii; Gary O. Rankin 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 452 KB

The kidney has been identified as the specific target organ for in vivo exposure to an agricultural fungicide, K(3,5-dichlorophenyl)succinimide (NDPS). The goal of this study was to determine if urinary protein and enzyme excretion were sensitive, non-invasive markers for NDPS-induced renal damage.