Nicotinamide and ascorbic acid nanoparticles against the hepatic insult induced in rats by high fat high fructose diet: A comparative study

Non-alcoholic fatty liver disease (NAFLD) caused by consumption of high levels of fat and sugars (HFHS) in diet is considered one of the most dangerous medical complications among children and adolescents. Nicotinamide is among the promising candidates in ameliorating HFHS diet-induced NAFLD, but it...

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Veröffentlicht in:Life sciences (1973) 2020-12, Vol.263, p.118540, Article 118540
Hauptverfasser: Abd-Allah, Hend, Nasr, Maha, Ahmed-Farid, Omar A.H., Ibrahim, Bassant M.M., Bakeer, Rofanda M., Ahmed, Rania F.
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container_issue
container_start_page 118540
container_title Life sciences (1973)
container_volume 263
creator Abd-Allah, Hend
Nasr, Maha
Ahmed-Farid, Omar A.H.
Ibrahim, Bassant M.M.
Bakeer, Rofanda M.
Ahmed, Rania F.
description Non-alcoholic fatty liver disease (NAFLD) caused by consumption of high levels of fat and sugars (HFHS) in diet is considered one of the most dangerous medical complications among children and adolescents. Nicotinamide is among the promising candidates in ameliorating HFHS diet-induced NAFLD, but its use is limited by the possibility of prompting hepatotoxicity in high doses. Ascorbic acid is another promising candidate, however its use as a hepatoprotective agent is limited by its chemical instability. Therefore, the aim of the study was to overcome their delivery limitations and enhance their hepatoprotective activity by loading into nanoparticles. In the present study, upon incorporating nicotinamide or ascorbic acid in chitosan nanoparticles, they ameliorated the insulin-resistant status induced in rats by a high-fat-high-fructose (HFHF) diet. Both formulae decreased serum level of ALT and AST, as well as liver tissue total cholesterol, triglycerides and 8-hydroxy-2-deoxyguanosine (8-OHdG) levels. They also decreased oxidative and nitrosative stresses along with a significant increase in the hepatocellular energy. The biochemical findings were further confirmed by histopathological examination. Finally from the obtained data it could be concluded that chitosan nicotinamide nanoparticles at a dose level (10 mg/kg, p.o.) demonstrated beneficial pharmacological effect with safer toxicity profile than chitosan ascorbic acid nanoparticles. Nicotinamide chitosan nanoparticles could be recommended as daily supplement in the recovery from NAFLD.
doi_str_mv 10.1016/j.lfs.2020.118540
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Nicotinamide is among the promising candidates in ameliorating HFHS diet-induced NAFLD, but its use is limited by the possibility of prompting hepatotoxicity in high doses. Ascorbic acid is another promising candidate, however its use as a hepatoprotective agent is limited by its chemical instability. Therefore, the aim of the study was to overcome their delivery limitations and enhance their hepatoprotective activity by loading into nanoparticles. In the present study, upon incorporating nicotinamide or ascorbic acid in chitosan nanoparticles, they ameliorated the insulin-resistant status induced in rats by a high-fat-high-fructose (HFHF) diet. Both formulae decreased serum level of ALT and AST, as well as liver tissue total cholesterol, triglycerides and 8-hydroxy-2-deoxyguanosine (8-OHdG) levels. They also decreased oxidative and nitrosative stresses along with a significant increase in the hepatocellular energy. The biochemical findings were further confirmed by histopathological examination. Finally from the obtained data it could be concluded that chitosan nicotinamide nanoparticles at a dose level (10 mg/kg, p.o.) demonstrated beneficial pharmacological effect with safer toxicity profile than chitosan ascorbic acid nanoparticles. 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The biochemical findings were further confirmed by histopathological examination. Finally from the obtained data it could be concluded that chitosan nicotinamide nanoparticles at a dose level (10 mg/kg, p.o.) demonstrated beneficial pharmacological effect with safer toxicity profile than chitosan ascorbic acid nanoparticles. 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dosage</subject><subject>Nanoparticles - chemistry</subject><subject>Niacinamide - pharmacology</subject><subject>Nicotinamide</subject><subject>Non-alcoholic fatty liver disease</subject><subject>Non-alcoholic Fatty Liver Disease - drug therapy</subject><subject>Non-alcoholic Fatty Liver Disease - etiology</subject><subject>Non-alcoholic Fatty Liver Disease - metabolism</subject><subject>Non-alcoholic Fatty Liver Disease - pathology</subject><subject>Protective Agents - pharmacology</subject><subject>Rats</subject><subject>Sugar</subject><subject>Sweetening Agents - toxicity</subject><subject>Toxicity</subject><subject>Triglycerides</subject><subject>Vitamin B Complex - pharmacology</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFuGyEQhlHUKHGdPEAvFVLO68KwrNfNKbKatJKVXtozYofZGMteXGAt-Rn60iWyk2NPP4z--RAfY5-kmEkhmy-b2bZPMxBQ7rLVtbhgE9nOF5VolPzAJkJAXSkQ-pp9TGkjhNB6rq7YtVJCad22E_b32WPIfrA774jbwXGbMMTOI7foHR_sEPY2Zo9bSty-WD-kzPOa-Jr2tox5GYzbXMKNSK4kjzYn3h352r-seW_z-RBHzCERd57yV_7AMewKuTAOxFMe3fGGXfZ2m-j2nFP2-_Hbr-X3avXz6cfyYVWhamWunKIFAi2gIdm5BhrpdK8bAqWtnUtZK6s7ACccQqO063CBGgHrktArVFN2d-LuY_gzUspmE8Y4lCcNaIAaVK3r0pKnFsaQUqTe7KPf2Xg0UphX_WZjin7zqt-c9Jedz2fy2O3IvW-8-S6F-1OByv8OnqJJ6Gko4nwkzMYF_x_8P6ssl2I</recordid><startdate>20201215</startdate><enddate>20201215</enddate><creator>Abd-Allah, Hend</creator><creator>Nasr, Maha</creator><creator>Ahmed-Farid, Omar A.H.</creator><creator>Ibrahim, Bassant M.M.</creator><creator>Bakeer, Rofanda M.</creator><creator>Ahmed, Rania F.</creator><general>Elsevier Inc</general><general>Elsevier BV</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20201215</creationdate><title>Nicotinamide and ascorbic acid nanoparticles against the hepatic insult induced in rats by high fat high fructose diet: A comparative study</title><author>Abd-Allah, Hend ; 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The biochemical findings were further confirmed by histopathological examination. Finally from the obtained data it could be concluded that chitosan nicotinamide nanoparticles at a dose level (10 mg/kg, p.o.) demonstrated beneficial pharmacological effect with safer toxicity profile than chitosan ascorbic acid nanoparticles. Nicotinamide chitosan nanoparticles could be recommended as daily supplement in the recovery from NAFLD.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>33035588</pmid><doi>10.1016/j.lfs.2020.118540</doi></addata></record>
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subjects 8-Hydroxydeoxyguanosine
Acids
Animals
Antioxidants - pharmacology
Ascorbic acid
Ascorbic Acid - pharmacology
Biomarkers - analysis
Children
Chitosan
Cholesterol
Comparative studies
Deoxyguanosine
Diet
Diet, High-Fat - adverse effects
Dietary Supplements
Dosage
Fatty liver
Fructose
Fructose - toxicity
Hepatotoxicity
High fat diet
Insulin
Liver
Liver diseases
Male
Nanoparticles
Nanoparticles - administration & dosage
Nanoparticles - chemistry
Niacinamide - pharmacology
Nicotinamide
Non-alcoholic fatty liver disease
Non-alcoholic Fatty Liver Disease - drug therapy
Non-alcoholic Fatty Liver Disease - etiology
Non-alcoholic Fatty Liver Disease - metabolism
Non-alcoholic Fatty Liver Disease - pathology
Protective Agents - pharmacology
Rats
Sugar
Sweetening Agents - toxicity
Toxicity
Triglycerides
Vitamin B Complex - pharmacology
title Nicotinamide and ascorbic acid nanoparticles against the hepatic insult induced in rats by high fat high fructose diet: A comparative study
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