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. 2023 Sep 21;28(18):6732.
doi: 10.3390/molecules28186732.

Antioxidant and Hypolipidemic Activities of Cinnamic Acid Derivatives

Affiliations

Antioxidant and Hypolipidemic Activities of Cinnamic Acid Derivatives

Christina Nouni et al. Molecules. .

Abstract

Oxidative stress and hyperlipidemia are important factors for the initiation and progression of various cell degenerative pathological conditions, including cardiovascular and neurological diseases. A series of cinnamic acid-derived acids, such as ferulic acid, sinapic acid, 3,4-dimethoxycinnamic acid, p-coumaric acid, and (E)-3-(3,5-di-tert-butyl-4-hydroxyphenyl)acrylic acid, were esterified or amidated with various moieties, bearing different biological activities, and evaluated. The antioxidant and radical scavenging abilities of the compounds via inhibition of rat hepatic microsomal membrane lipid peroxidation, as well as their interaction with the stable radical 2,2-diphenyl-1-picrylhydrazyl (DPPH), were assessed. Further, their hypolipidemic activity in vivo was tested. The majority of the obtained compounds demonstrated considerable radical scavenging and antioxidant action, with a parallel decrease in Triton-induced hyperlipidemia in rats. The (E)-3-(3,5-di-tert-butyl-4-hydroxyphenyl)acrylic acid derivative with morpholine and 4-methylpiperidine (compounds 4 and 13, respectively) significantly decreased triglycerides and total cholesterol in the plasma of hyperlipidemic rats, with an antioxidant capacity similar to that of the antioxidant Trolox. The compounds were designed to exhibit antioxidant and hypolipidemic pharmacological actions, and this succeeded for the majority of them. Thus, such agents may be of interest in conditions and diseases implicating oxidative stress and dyslipidemia.

Keywords: 3-phenylacrylic acid; antioxidants; cinnamic acid derivatives; hyperlipidemia; hypolipidemic agents; morpholine.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Structures of the synthesized compounds.
Figure 2
Figure 2
Synthesis of the examined compounds 113. The corresponding acids (IV) were activated with DCC and with the corresponding alcohol or amine. In the presence of DMAP, the esterification or amidation reaction was carried out, providing the corresponding 113 compounds.

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References

    1. Sánchez A., Calpena A.C., Clares B. Evaluating the oxidative stress in inflammation: Role of melatonin. Int. J. Mol. Sci. 2015;16:16981–17004. doi: 10.3390/ijms160816981. - DOI - PMC - PubMed
    1. Li H., Horke S., Förstermann U. Oxidative stress in vascular disease and its pharmacological prevention. Trends Pharmacol. Sci. 2013;34:313–319. doi: 10.1016/j.tips.2013.03.007. - DOI - PubMed
    1. Apryatin S.A., Sidorova Y.S., Shipelin V.A., Balakina A., Trusov N.V., Mazo V.K. Neuromotor activity, anxiety and cognitive function in the in vivo model of alimentary hyperlipidemia and obesity. Bull. Exp. Biol. Med. 2017;163:37–44. doi: 10.1007/s10517-017-3732-z. - DOI - PubMed
    1. Gancheva S., Galunska B., Zhelyazkova-Savova M. Diets rich in saturated fat and fructose induce anxiety and depression-like behaviours in the rat: Is there a role for lipid peroxidation? Int. J. Exp. Pathol. 2017;98:296–306. doi: 10.1111/iep.12254. - DOI - PMC - PubMed
    1. Liao J.C., Deng J.S., Chiu C.S., Hou W.C., Huang S.S., Shie P.H., Huang G.J. Anti-inflammatory activities of cinnamomum cassia constituents in vitro and in vivo. Evid. Based Complement. Alternat. Med. 2012;2012:429320. doi: 10.1155/2012/429320. - DOI - PMC - PubMed

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