Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin

Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disorder worldwide with no curative therapy.+eaim of this study was to investigate the hepatoprotective effects of a novel Trihoney against biochemical and histological manifestations of NAFLD in hypercholesterolemic rabb...

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Main Authors: Hamad Alfarisi, Hamad Abdulsalam, Ibrahim, Muhammad, Hamad Mohamed, Zenab, Azahari, Nuraniza, Hamdan, Asmah Hanim, Che Mohamad, Che Anuar
Format: Article
Language:English
Published: Hindawi 2020
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Online Access:http://irep.iium.edu.my/83661/1/hindawi.pdf
http://irep.iium.edu.my/83661/
https://www.hindawi.com/journals/tswj/2020/4503253/
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spelling my.iium.irep.836612023-11-21T02:04:24Z http://irep.iium.edu.my/83661/ Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin Hamad Alfarisi, Hamad Abdulsalam Ibrahim, Muhammad Hamad Mohamed, Zenab Azahari, Nuraniza Hamdan, Asmah Hanim Che Mohamad, Che Anuar Q Science (General) Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disorder worldwide with no curative therapy.+eaim of this study was to investigate the hepatoprotective effects of a novel Trihoney against biochemical and histological manifestations of NAFLD in hypercholesterolemic rabbits. Methodology. Forty-eight male New Zealand white (NZW) rabbits were grouped into normal diet (C), normal diet with 0.6 g/kg/day of Trihoney (C + H), 1% cholesterol diet (HCD), 1% cholesterol diet with 0.3 g/kg/ day of Trihoney (HCD +H1), 1% cholesterol diet with 0.6 g/kg/day of Trihoney (HCD +H2), and 1% cholesterol diet with 2 mg/kg/ day of atorvastatin (HCD + At.). Animals were sacrificed after 12 weeks of treatment. Serum lipids and liver function test (LFT) were measured prior to and at the endpoint of the experiment for total cholesterol (TC), low-density lipoprotein (LDL-c), alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), gamma-glutamyl transferase (GGT), and total bilirubin (T. Bil.). Liver was processed for histopathology study. Liver homogenate was analysed for oxidative stress parameters: superoxide dismutase (SOD), glutathione peroxidase (GPx), and malondialdehyde (MDA). Results. Lipid analysis approved the induction of hypercholesterolemia. A significant elevation (p < 0.01) of serum AST and ALT levels showed by the HCD group was compared to C and C+H groups. Trihoney exhibited a significant reduction (p < 0.001) of AST and ALT compared to the HCD group. Likewise, AST and ALT reduced significantly in the HCD+ At. group (p < 0.001). Trihoney supplementation induced significant (p < 0.05) enhancement of SOD and GPx activities. Atorvastatin treatment was associated with significant (p < 0.05) reduction of SOD and GPx activities in the liver. Trihoney and atorvastatin showed marked (p < 0.001) reduction of hepatic lipid peroxidation. Trihoney showed histological protection against progression of NAFLD to nonalcoholic steatohepatitis (NASH). Atorvastatin exhibited no beneficial impact on hepatic architecture. Conclusion. Trihoney was able to maintain normal liver function and showed hepatoprotection against progression of NAFLD to NASH probably through hypocholesterolaemic and antioxidant functions. Hindawi 2020-10-09 Article NonPeerReviewed application/pdf en http://irep.iium.edu.my/83661/1/hindawi.pdf Hamad Alfarisi, Hamad Abdulsalam and Ibrahim, Muhammad and Hamad Mohamed, Zenab and Azahari, Nuraniza and Hamdan, Asmah Hanim and Che Mohamad, Che Anuar (2020) Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin. The Scientifiec World Journal, 2020. pp. 1-14. ISSN 2356-6140 E-ISSN 1537-744X https://www.hindawi.com/journals/tswj/2020/4503253/ 4503253
institution Universiti Islam Antarabangsa Malaysia
building IIUM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider International Islamic University Malaysia
content_source IIUM Repository (IREP)
url_provider http://irep.iium.edu.my/
language English
topic Q Science (General)
spellingShingle Q Science (General)
Hamad Alfarisi, Hamad Abdulsalam
Ibrahim, Muhammad
Hamad Mohamed, Zenab
Azahari, Nuraniza
Hamdan, Asmah Hanim
Che Mohamad, Che Anuar
Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin
description Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic liver disorder worldwide with no curative therapy.+eaim of this study was to investigate the hepatoprotective effects of a novel Trihoney against biochemical and histological manifestations of NAFLD in hypercholesterolemic rabbits. Methodology. Forty-eight male New Zealand white (NZW) rabbits were grouped into normal diet (C), normal diet with 0.6 g/kg/day of Trihoney (C + H), 1% cholesterol diet (HCD), 1% cholesterol diet with 0.3 g/kg/ day of Trihoney (HCD +H1), 1% cholesterol diet with 0.6 g/kg/day of Trihoney (HCD +H2), and 1% cholesterol diet with 2 mg/kg/ day of atorvastatin (HCD + At.). Animals were sacrificed after 12 weeks of treatment. Serum lipids and liver function test (LFT) were measured prior to and at the endpoint of the experiment for total cholesterol (TC), low-density lipoprotein (LDL-c), alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), gamma-glutamyl transferase (GGT), and total bilirubin (T. Bil.). Liver was processed for histopathology study. Liver homogenate was analysed for oxidative stress parameters: superoxide dismutase (SOD), glutathione peroxidase (GPx), and malondialdehyde (MDA). Results. Lipid analysis approved the induction of hypercholesterolemia. A significant elevation (p < 0.01) of serum AST and ALT levels showed by the HCD group was compared to C and C+H groups. Trihoney exhibited a significant reduction (p < 0.001) of AST and ALT compared to the HCD group. Likewise, AST and ALT reduced significantly in the HCD+ At. group (p < 0.001). Trihoney supplementation induced significant (p < 0.05) enhancement of SOD and GPx activities. Atorvastatin treatment was associated with significant (p < 0.05) reduction of SOD and GPx activities in the liver. Trihoney and atorvastatin showed marked (p < 0.001) reduction of hepatic lipid peroxidation. Trihoney showed histological protection against progression of NAFLD to nonalcoholic steatohepatitis (NASH). Atorvastatin exhibited no beneficial impact on hepatic architecture. Conclusion. Trihoney was able to maintain normal liver function and showed hepatoprotection against progression of NAFLD to NASH probably through hypocholesterolaemic and antioxidant functions.
format Article
author Hamad Alfarisi, Hamad Abdulsalam
Ibrahim, Muhammad
Hamad Mohamed, Zenab
Azahari, Nuraniza
Hamdan, Asmah Hanim
Che Mohamad, Che Anuar
author_facet Hamad Alfarisi, Hamad Abdulsalam
Ibrahim, Muhammad
Hamad Mohamed, Zenab
Azahari, Nuraniza
Hamdan, Asmah Hanim
Che Mohamad, Che Anuar
author_sort Hamad Alfarisi, Hamad Abdulsalam
title Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin
title_short Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin
title_full Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin
title_fullStr Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin
title_full_unstemmed Hepatoprotective effects of a novel Trihoney against Nonalcoholic Fatty Liver Disease: A comparative study with Atorvastatin
title_sort hepatoprotective effects of a novel trihoney against nonalcoholic fatty liver disease: a comparative study with atorvastatin
publisher Hindawi
publishDate 2020
url http://irep.iium.edu.my/83661/1/hindawi.pdf
http://irep.iium.edu.my/83661/
https://www.hindawi.com/journals/tswj/2020/4503253/
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