Improvement of Metabolic and Histological Changes of Adiposity in Rats by Synthetic Oleoyl Chalcones

Author:

AlKhathami Azza A. M.1,Saad Hosam A.12,Fareed Fareed A.3,El‐Shafey Eman S.4,Elsherbiny Eslam S.4,El Nahas Mamdouh R.5,Aly Mohamed R. E.13ORCID

Affiliation:

1. Department of Chemistry College of Science Taif University P. O. Box 11099 Taif 21944 Saudi Arabia

2. Chemistry Department Faculty of Science Zagazig University 44511 Zagazig Egypt

3. Chemistry Department Faculty of Science Port Said University 42522 Port Said Egypt on leave from Taif University to Port Said University

4. Biochemistry Department Faculty of Science Damietta University 34517 Damietta Egypt

5. Internal Medicine Department Faculty of Medicine Port Said University 42522 Port Said Egypt

Abstract

AbstractWe previously reported that synthetic oleoyl chalcones had a favorable effect to alleviate metabolic consequences of obesity in male SD rats. In this work, we prepared and characterized by spectroscopic tools, a set of six oleoyl chalcones (5a–c, 10 and 11a,b). The comparative effects of the previously prepared oleoyl chalcones and their new synthetic analogs on metabolic and histological changes in obese male SD rats were studied. It was found that the oleoyl chalcones IIIa and IV were the best in improving many metabolic parameters, e. g., FBG, FI, ISI, TG, and total cholesterol. They cured systemic inflammation, through inhibition of the TNF‐α and induction of adiponectin production. Moreover, chalcones IIIa and IV alleviated the oxidative stress accompanying obesity through the induction of the antioxidant enzymes GPX, SOD and CAT besides, GSH. Interestingly, chalcones IIIa and IV exerted hepatoprotective potency and ameliorated the manifestations of NAFLD via inhibition of apoptosis and induction of autophagy of hepatic cells. In conclusion, the oleoyl chalcones IIIa and IV were the most effective candidates among the series of synthetic chalcones in correcting body weight and the consequent metabolic and histological changes in adiposity.

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

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