Essential oil from Citrus depressa peel exhibits antimicrobial, antioxidant and cancer chemopreventive effects

Author:

Weng Yu‐Xiang1,Wang Hsiao‐Chi2,Chu Yung‐Lin3ORCID,Wu Yun‐Zhen1,Liao Jie‐An1,Su Zheng‐Yuan1ORCID

Affiliation:

1. Department of Bioscience Technology Chung Yuan Christian University Taoyuan City Taiwan, ROC

2. Department of Oral Hygiene and Healthcare Cardinal Tien Junior College of Healthcare and Management New Taipei City Taiwan, ROC

3. Department of Food Science, College of Agriculture National Pingtung University of Science and Technology Pingtung County Taiwan, ROC

Abstract

AbstractBACKGROUNDMany diseases may be caused by pathogens and oxidative stress resulting from carcinogens. Earlier studies have highlighted the antimicrobial and antioxidant effects of plant essential oils (EO). It is crucial to effectively utilize agricultural waste to achieve a sustainable agricultural economy and protect the environment. The present study aimed to evaluate the potential benefits of EO extracted from the discarded peels of Citrus depressa Hayata (CD) and Citrus microcarpa Bunge (CM), synonyms of Citrus deliciosa Ten and Citrus japonica Thunb, respectively.RESULTSGas chromatography‐mass spectrometry analysis revealed that the main compounds in CD‐EO were (R)‐(+)‐limonene (38.97%), γ‐terpinene (24.39%) and linalool (6.22%), whereas, in CM‐EO, the main compounds were (R)‐(+)‐limonene (48.00%), β‐pinene (13.60%) and γ‐terpinene (12.07%). CD‐EO exhibited inhibitory effects on the growth of common microorganisms, including Candida albicans, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus. However, CM‐EO showed only inhibitory effects on E. coli. Furthermore, CD‐EO exhibited superior antioxidant potential, as demonstrated by its ability to eliminate 1,1‐diphenyl‐2‐picrylhydrazyl and 2,2′‐azinobis‐3‐ethylbenzthiazoline‐6‐sulfonate free radicals. Furthermore, CD‐EO at a concentration of 100 μg mL−1 significantly inhibited 12‐O‐tetradecanoylphorbol‐13‐acetate‐induced cancer transformation in mouse epidermal JB6 P+ cells (P < 0.05), possibly by up‐regulating protein expression of nuclear factor erythroid 2‐related factor 2 and its downstream antioxidant enzymes, such as NAD(P)H:quinone oxidoreductase 1, heme oxygenase‐1 and UGT1A.CONCLUSIONThese findings suggest that CD‐EO exhibits inhibitory effects on pathogenic microorganisms, possesses antioxidant properties and has cancer chemopreventive potential. © 2024 Society of Chemical Industry.

Publisher

Wiley

Subject

Nutrition and Dietetics,Agronomy and Crop Science,Food Science,Biotechnology

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