Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.

INTRODUCTION: Development of novel metallodrugs with enhanced anti-proliferative potential and reduced toxicity has become the prime focus of the evolving medicinal chemistry. In this regards, gold (III) complexes with various ligands are being extensively investigated. In the current study renal an...

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Main Authors: Ayesha Ahmed, Dalal M Al Tamimi, Anvarhusein A Isab, Abdulaziz M Mansour Alkhawajah, Mohamed A Shawarby
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3531431?pdf=render
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spelling doaj-5fbad44c17a44a76ae7552282afddc762020-11-25T00:12:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5188910.1371/journal.pone.0051889Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.Ayesha AhmedDalal M Al TamimiAnvarhusein A IsabAbdulaziz M Mansour AlkhawajahMohamed A ShawarbyINTRODUCTION: Development of novel metallodrugs with enhanced anti-proliferative potential and reduced toxicity has become the prime focus of the evolving medicinal chemistry. In this regards, gold (III) complexes with various ligands are being extensively investigated. In the current study renal and hepatic toxicity of a newly developed gold (III) compound [Au(en)Cl(2)]Cl was assessed by histopathological evaluation of liver and kidney specimens of rats exposed to the compound. METHODS: Male rats (n = 42) weighing 200-250 gram were injected single, varying doses of gold (III) compound [(dichlorido(ethylenediamine)aurate((III)]chloride [Au(en)Cl(2)]Cl in the acute toxicity component of the study. In the sub-acute toxicity part, a dose of 32.2 mg/kg (equivalent to 1/10 of LD50) was administered intraperitoneally for 14 consecutive days before sacrificing the animals. After autopsy, the renal and hepatic tissues were preserved in buffered formalin. Processing of the samples was followed by histopathological evaluation. The results were compared with the normal controls (n = 11). RESULTS: A dose of 32.2 mg/kg (1/10 of LD(50)) revealed no renal tubular necrosis. The predominant histopathological finding was mild pyelitis, a prominence of eosinophils and mild congestion. The hepatic lesions comprised varying extents of ballooning degeneration with accompanying congestion and focal portal inflammation. CONCLUSION: Gold (III) compound [Au(en)Cl(2)]Cl causes minimal histological changes in kidney and liver of rats, reflecting its relative safety as compared to other clinically established antineoplastic drugs.http://europepmc.org/articles/PMC3531431?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ayesha Ahmed
Dalal M Al Tamimi
Anvarhusein A Isab
Abdulaziz M Mansour Alkhawajah
Mohamed A Shawarby
spellingShingle Ayesha Ahmed
Dalal M Al Tamimi
Anvarhusein A Isab
Abdulaziz M Mansour Alkhawajah
Mohamed A Shawarby
Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.
PLoS ONE
author_facet Ayesha Ahmed
Dalal M Al Tamimi
Anvarhusein A Isab
Abdulaziz M Mansour Alkhawajah
Mohamed A Shawarby
author_sort Ayesha Ahmed
title Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.
title_short Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.
title_full Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.
title_fullStr Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.
title_full_unstemmed Histological changes in kidney and liver of rats due to gold (III) compound [Au(en)Cl(2)]Cl.
title_sort histological changes in kidney and liver of rats due to gold (iii) compound [au(en)cl(2)]cl.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description INTRODUCTION: Development of novel metallodrugs with enhanced anti-proliferative potential and reduced toxicity has become the prime focus of the evolving medicinal chemistry. In this regards, gold (III) complexes with various ligands are being extensively investigated. In the current study renal and hepatic toxicity of a newly developed gold (III) compound [Au(en)Cl(2)]Cl was assessed by histopathological evaluation of liver and kidney specimens of rats exposed to the compound. METHODS: Male rats (n = 42) weighing 200-250 gram were injected single, varying doses of gold (III) compound [(dichlorido(ethylenediamine)aurate((III)]chloride [Au(en)Cl(2)]Cl in the acute toxicity component of the study. In the sub-acute toxicity part, a dose of 32.2 mg/kg (equivalent to 1/10 of LD50) was administered intraperitoneally for 14 consecutive days before sacrificing the animals. After autopsy, the renal and hepatic tissues were preserved in buffered formalin. Processing of the samples was followed by histopathological evaluation. The results were compared with the normal controls (n = 11). RESULTS: A dose of 32.2 mg/kg (1/10 of LD(50)) revealed no renal tubular necrosis. The predominant histopathological finding was mild pyelitis, a prominence of eosinophils and mild congestion. The hepatic lesions comprised varying extents of ballooning degeneration with accompanying congestion and focal portal inflammation. CONCLUSION: Gold (III) compound [Au(en)Cl(2)]Cl causes minimal histological changes in kidney and liver of rats, reflecting its relative safety as compared to other clinically established antineoplastic drugs.
url http://europepmc.org/articles/PMC3531431?pdf=render
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