Nada Hussien Arafa, Mohamed Refaat Shehata, A. S. Mohamed
{"title":"Ovothiol-A Mitigates High-Fat Diet-Induced Non-alcoholic Fatty Liver\nDisease in Rats","authors":"Nada Hussien Arafa, Mohamed Refaat Shehata, A. S. Mohamed","doi":"10.2174/0115734072272429231106090645","DOIUrl":null,"url":null,"abstract":"\n\nObesity is frequently linked to multiple comorbid and chronic illnesses,\nincluding non-alcoholic fatty liver disease, type 2 diabetes, cancer, and heart disease. Ovothiol-A\nis one of the most powerful natural antioxidants found in marine invertebrates like sea urchins.\n\n\n\nThe current study aimed to investigate ovothiol-A's hypolipidemic and hypoglycemic\npotential in obese rats.\n\n\n\nAll groups get a high-fat diet (HFD) for four weeks except for the control group. The\ncontrol and HFD groups received distilled water, while the Ovothiol-A groups received two doses\nof Ovothiol-A (200 and 400 mg/kg orally) concurrent with HFD.\n\n\n\nWeight gain, glucose, insulin, alanine aminotransferase, aspartate aminotransferase,\ngamma-glutamyl transferase, alkaline phosphatase, total cholesterol, triglycerides, low-density\nlipoprotein, malondialdehyde, and nitric oxide were all decreased after oral administration of Ovo\nat either the 200 or 400 mg/kg dose, while levels of high-density lipoprotein (HDL), glutathionereduced, catalase and glutathione-S-transferase increased. Histopathological alterations were less\nnoticeable in the liver tissue of Ovothiol-A groups, with only a few vacuolated or pyknotic nuclei\namongst a few dispersed hepatocytes.\n\n\n\nThe current findings indicate that ovothiol-A protects against high-fat diet-induced\nfatty liver in rats. The anti-obesity mechanism of Ovothiol-A is associated with its hypolipidemic,\nhypoglycemic, and antioxidant properties.\n","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":"13 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Bioactive Compounds","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0115734072272429231106090645","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
Obesity is frequently linked to multiple comorbid and chronic illnesses,
including non-alcoholic fatty liver disease, type 2 diabetes, cancer, and heart disease. Ovothiol-A
is one of the most powerful natural antioxidants found in marine invertebrates like sea urchins.
The current study aimed to investigate ovothiol-A's hypolipidemic and hypoglycemic
potential in obese rats.
All groups get a high-fat diet (HFD) for four weeks except for the control group. The
control and HFD groups received distilled water, while the Ovothiol-A groups received two doses
of Ovothiol-A (200 and 400 mg/kg orally) concurrent with HFD.
Weight gain, glucose, insulin, alanine aminotransferase, aspartate aminotransferase,
gamma-glutamyl transferase, alkaline phosphatase, total cholesterol, triglycerides, low-density
lipoprotein, malondialdehyde, and nitric oxide were all decreased after oral administration of Ovo
at either the 200 or 400 mg/kg dose, while levels of high-density lipoprotein (HDL), glutathionereduced, catalase and glutathione-S-transferase increased. Histopathological alterations were less
noticeable in the liver tissue of Ovothiol-A groups, with only a few vacuolated or pyknotic nuclei
amongst a few dispersed hepatocytes.
The current findings indicate that ovothiol-A protects against high-fat diet-induced
fatty liver in rats. The anti-obesity mechanism of Ovothiol-A is associated with its hypolipidemic,
hypoglycemic, and antioxidant properties.
Current Bioactive CompoundsPharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.90
自引率
0.00%
发文量
112
期刊介绍:
The journal aims to provide comprehensive review articles on new bioactive compounds with proven activities in various biological screenings and pharmacological models with a special emphasis on stereoeselective synthesis. The aim is to provide a valuable information source of bioactive compounds synthesized or isolated, which can be used for further development of pharmaceuticals by industry and academia. The journal should prove to be essential reading for pharmacologists, natural product chemists and medicinal chemists who wish to be kept informed and up-to-date with the most important developments on new bioactive compounds of natural or synthetic origin, including their stereoeselective synthesis.