Purple Sweet Potato Powder Containing Anthocyanin Mitigates High-Fat-Diet-Induced Dry Eye Disease

Author:

Chiang Ming-Cheng12ORCID,Liu Ying-Chung23,Chen Bo-Yi4,Wu Dai-Lin1ORCID,Wu Chia-Lian4,Cheng Chun-Wen3,Chang Wen-Lung35,Lee Huei-Jane67ORCID

Affiliation:

1. School of Medicine, Chung Shan Medical University, Taichung 40221, Taiwan

2. Department of Ophthalmology, Cathay General Hospital, Taipei 10687, Taiwan

3. Institute of Medicine, Chung Shan Medical University, Taichung 40221, Taiwan

4. Department of Optometry, Chung Shan Medical University, Taichung 40221, Taiwan

5. Yi-Yeh Biotechnology Co., Taichung 40221, Taiwan

6. Department of Biochemistry, School of Medicine, Chung Shan Medical University, Taichung 40221, Taiwan

7. Department of Clinical Laboratory, Chung Shan Medical University Hospital, Taichung 40201, Taiwan

Abstract

Purple sweet potato (PSP) powder with anthocyanins possesses the ability to reduce oxidative stress and inflammation. Studies have presumed a positive correlation between body fat and dry eye disease (DED) in adults. The regulation of oxidative stress and inflammation has been proposed as the mechanism underlying DED. This study developed an animal model of high fat diet (HFD)-induced DED. We added 5% PSP powder to the HFD to evaluate the effects and underlying mechanisms in mitigating HFD-induced DED. A statin drug, atorvastatin, was also added to the diet separately to assess its effect. The HFD altered the structure of lacrimal gland (LG) tissue, reduced LG secretory function, and eliminated the expression of proteins related to DED development, including α-smooth muscle actin and aquaporin-5. Although PSP treatment could not significantly reduce body weight or body fat, it ameliorated the effects of DED by preserving LG secretory function, preventing ocular surface erosion, and preserving LG structure. PSP treatment increased superoxide dismutase levels but reduced hypoxia-inducible factor 1-α levels, indicating that PSP treatment reduced oxidative stress. PSP treatment increased ATP-binding cassette transporter 1 and acetyl-CoA carboxylase 1 levels in LG tissue, signifying that PSP treatment regulated lipid homeostasis maintenance to reduce the effects of DED. In conclusion, PSP treatment ameliorated the effects of HFD-induced DED through the regulation of oxidative stress and lipid homeostasis in the LG.

Funder

National Science and Technology Council

Chung Shan Medical University

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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