Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats
Context: Stachys pilifera Benth (Lamiaceae) has long been used to treat infectious diseases, respiratory and rheumatoid disorders in Iranian folk medicine. Antitumor and antioxidant activity of the plant have been reported. Objective: The study was designed to assess the hepatoprotective activity of...
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doaj-777c153182c848c7ad68a9d1dd9f89222020-11-25T03:33:52ZengTaylor & Francis GroupPharmaceutical Biology1388-02091744-51162017-01-015511389139310.1080/13880209.2017.13024841302484Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in ratsEsmaeel Panahi Kokhdan0Kyomarth Ahmadi1Heibatollah Sadeghi2Hossein Sadeghi3Fahemeh Dadgary4Nazanin Danaei5Mahmoud Reza Aghamaali6University of GuilanAJA University of Medical Sciences, Yasuj University of Medical Sciences, Yasuj University of Medical SciencesSchool of Nursing, AJA University of Medical Sciences, Yasuj University of Medical SciencesUniversity of GuilanContext: Stachys pilifera Benth (Lamiaceae) has long been used to treat infectious diseases, respiratory and rheumatoid disorders in Iranian folk medicine. Antitumor and antioxidant activity of the plant have been reported. Objective: The study was designed to assess the hepatoprotective activity of ethanol extract of Stachys pilifera in carbon tetrachloride (CCl4)-induced hepatotoxicity in rats. Materials and methods: The rats were randomly divided into six equal groups (n = 7). Group I was treated with normal saline; Group II received CCl4 (1 mL/kg. i.p., twice a week) for 60 consecutive days; Groups III, IV and V were given CCl4 plus Stachys pilifera (100, 200 and 400 mg/kg/d,p.o.); Group VI received the extract (400 mg/kg/d, p.o.). Histopathological analysis and measurement of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), malondialdehyde (MDA), total protein (TP) and albumin (ALB) were performed. Results: CCl4 caused a significant increase in the serum levels of AST, ALT, ALP and MDA as well as decreased ALB, and TP serum levels (p < 0.001). The extract (200 and 400 mg/kg/d) significantly normalized the CCl4-elevated levels of ALT, AST, ALP and MDA (p < 0.001). The extract (200 and 400 mg/kg/d) also increased the serum levels of TP compared to CCl4 group (p< 0.01). The extract (200 and 400 mg/kg/d) also decreased the histological injuries (inflammation and fatty degeneration) by CCl4. Discussion: The results revealed that the Stachys pilifera extract could provide considerable protection against CCl4 hepatotoxicity in rats that may be related to its antioxidant properties.http://dx.doi.org/10.1080/13880209.2017.1302484astalphepatotoxicitymda |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Esmaeel Panahi Kokhdan Kyomarth Ahmadi Heibatollah Sadeghi Hossein Sadeghi Fahemeh Dadgary Nazanin Danaei Mahmoud Reza Aghamaali |
spellingShingle |
Esmaeel Panahi Kokhdan Kyomarth Ahmadi Heibatollah Sadeghi Hossein Sadeghi Fahemeh Dadgary Nazanin Danaei Mahmoud Reza Aghamaali Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats Pharmaceutical Biology ast alp hepatotoxicity mda |
author_facet |
Esmaeel Panahi Kokhdan Kyomarth Ahmadi Heibatollah Sadeghi Hossein Sadeghi Fahemeh Dadgary Nazanin Danaei Mahmoud Reza Aghamaali |
author_sort |
Esmaeel Panahi Kokhdan |
title |
Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats |
title_short |
Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats |
title_full |
Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats |
title_fullStr |
Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats |
title_full_unstemmed |
Hepatoprotective effect of Stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats |
title_sort |
hepatoprotective effect of stachys pilifera ethanol extract in carbon tetrachloride-induce hepatotoxicity in rats |
publisher |
Taylor & Francis Group |
series |
Pharmaceutical Biology |
issn |
1388-0209 1744-5116 |
publishDate |
2017-01-01 |
description |
Context: Stachys pilifera Benth (Lamiaceae) has long been used to treat infectious diseases, respiratory and rheumatoid disorders in Iranian folk medicine. Antitumor and antioxidant activity of the plant have been reported. Objective: The study was designed to assess the hepatoprotective activity of ethanol extract of Stachys pilifera in carbon tetrachloride (CCl4)-induced hepatotoxicity in rats. Materials and methods: The rats were randomly divided into six equal groups (n = 7). Group I was treated with normal saline; Group II received CCl4 (1 mL/kg. i.p., twice a week) for 60 consecutive days; Groups III, IV and V were given CCl4 plus Stachys pilifera (100, 200 and 400 mg/kg/d,p.o.); Group VI received the extract (400 mg/kg/d, p.o.). Histopathological analysis and measurement of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), malondialdehyde (MDA), total protein (TP) and albumin (ALB) were performed. Results: CCl4 caused a significant increase in the serum levels of AST, ALT, ALP and MDA as well as decreased ALB, and TP serum levels (p < 0.001). The extract (200 and 400 mg/kg/d) significantly normalized the CCl4-elevated levels of ALT, AST, ALP and MDA (p < 0.001). The extract (200 and 400 mg/kg/d) also increased the serum levels of TP compared to CCl4 group (p< 0.01). The extract (200 and 400 mg/kg/d) also decreased the histological injuries (inflammation and fatty degeneration) by CCl4. Discussion: The results revealed that the Stachys pilifera extract could provide considerable protection against CCl4 hepatotoxicity in rats that may be related to its antioxidant properties. |
topic |
ast alp hepatotoxicity mda |
url |
http://dx.doi.org/10.1080/13880209.2017.1302484 |
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