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Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats

BACKGROUND: Nitrites are mainly used in food preservation. These materials could change to nitrosamine due to the effect of heat and gastric acid. Nitrosamine is absorbed in intestine and enters the liver and hepatocytes by portal venous system, and hampers the detoxification system of liver by inte...

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Autores principales: Rezaie, Annahita, Fazlara, Ali, Haghi Karamolah, Mojtaba, Shahriari, Ali, Najaf Zadeh, Hossein, Pashmforosh, Marzieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: DocS 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941908/
https://www.ncbi.nlm.nih.gov/pubmed/24624189
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author Rezaie, Annahita
Fazlara, Ali
Haghi Karamolah, Mojtaba
Shahriari, Ali
Najaf Zadeh, Hossein
Pashmforosh, Marzieh
author_facet Rezaie, Annahita
Fazlara, Ali
Haghi Karamolah, Mojtaba
Shahriari, Ali
Najaf Zadeh, Hossein
Pashmforosh, Marzieh
author_sort Rezaie, Annahita
collection PubMed
description BACKGROUND: Nitrites are mainly used in food preservation. These materials could change to nitrosamine due to the effect of heat and gastric acid. Nitrosamine is absorbed in intestine and enters the liver and hepatocytes by portal venous system, and hampers the detoxification system of liver by interfering in cytochrome P450 enzymes, so, the liver gently proceeds to cirrhosis and cancer. OBJECTIVES: The current study aimed to investigate the hepatic and renal protective effects of aerial parts of Echinacea purpurea extract (EPE) on injury induced by diethylnitrosamine (DEN). MATERIALS AND METHODS: Twenty Wistar rats were divided into 4 groups. Groups were as follow: Control group (normal saline), DEN (200 mg/kg, IP, a single dose), EPE (100 mg/kg, orally, daily) and DEN + EPE which received as group DEN and EPE. After 30 days, Blood samples, and liver and kidney tissues were taken for further examination. Aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), BUN, Creatinine and total and direct bilirubin were estimated in serum. RESULTS: DEN induced hepatotoxicity and nephrotoxicity in all the treated animals by elevated serum ALT, AST, ALP and BUN, creatinin and total and direct bilirubin levels. AST, BUN and total and direct bilirubin significantly decreased in DEN + EPE compared to DEN group. After 30 days of DEN administration, histopathological investigation revealed proliferation of hepatic stellate cells and early fibrosis which were partly improved by EPE administration. CONCLUSIONS: The current study findings indicated that Echinacea purpurea extract played an important role in the protection against DEN toxicity in rats.
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spelling pubmed-39419082014-03-12 Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats Rezaie, Annahita Fazlara, Ali Haghi Karamolah, Mojtaba Shahriari, Ali Najaf Zadeh, Hossein Pashmforosh, Marzieh Jundishapur J Nat Pharm Prod Research Article BACKGROUND: Nitrites are mainly used in food preservation. These materials could change to nitrosamine due to the effect of heat and gastric acid. Nitrosamine is absorbed in intestine and enters the liver and hepatocytes by portal venous system, and hampers the detoxification system of liver by interfering in cytochrome P450 enzymes, so, the liver gently proceeds to cirrhosis and cancer. OBJECTIVES: The current study aimed to investigate the hepatic and renal protective effects of aerial parts of Echinacea purpurea extract (EPE) on injury induced by diethylnitrosamine (DEN). MATERIALS AND METHODS: Twenty Wistar rats were divided into 4 groups. Groups were as follow: Control group (normal saline), DEN (200 mg/kg, IP, a single dose), EPE (100 mg/kg, orally, daily) and DEN + EPE which received as group DEN and EPE. After 30 days, Blood samples, and liver and kidney tissues were taken for further examination. Aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), BUN, Creatinine and total and direct bilirubin were estimated in serum. RESULTS: DEN induced hepatotoxicity and nephrotoxicity in all the treated animals by elevated serum ALT, AST, ALP and BUN, creatinin and total and direct bilirubin levels. AST, BUN and total and direct bilirubin significantly decreased in DEN + EPE compared to DEN group. After 30 days of DEN administration, histopathological investigation revealed proliferation of hepatic stellate cells and early fibrosis which were partly improved by EPE administration. CONCLUSIONS: The current study findings indicated that Echinacea purpurea extract played an important role in the protection against DEN toxicity in rats. DocS 2013-05-04 2013 /pmc/articles/PMC3941908/ /pubmed/24624189 Text en Copyright © 2013, School of Pharmacy, Ahvaz Jundishapur University of Medical Sciences http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rezaie, Annahita
Fazlara, Ali
Haghi Karamolah, Mojtaba
Shahriari, Ali
Najaf Zadeh, Hossein
Pashmforosh, Marzieh
Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats
title Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats
title_full Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats
title_fullStr Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats
title_full_unstemmed Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats
title_short Effects of Echinacea purpurea on Hepatic and Renal Toxicity Induced by Diethylnitrosamine in Rats
title_sort effects of echinacea purpurea on hepatic and renal toxicity induced by diethylnitrosamine in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941908/
https://www.ncbi.nlm.nih.gov/pubmed/24624189
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