Protective Effect of Electroacupuncture on Chemotherapy-Induced Salivary Gland Hypofunction in a Mouse Model

Author:

Nguyen Thanh-Hien Vu12ORCID,Chiu Kuo-Chou3,Shih Yin-Hwa4ORCID,Liu Chung-Ji5ORCID,Bao Quach Tran Van2,Hsia Shih-Min67ORCID,Chen Yi-Hung189ORCID,Shieh Tzong-Ming2ORCID

Affiliation:

1. Graduate Institute of Acupuncture Science, China Medical University, Taichung 40402, Taiwan

2. School of Dentistry, China Medical University, Taichung 40402, Taiwan

3. Division of Oral Diagnosis and Family Dentistry, Tri-Service General Hospital, National Defense Medical Center, Taipei 11490, Taiwan

4. Department of Healthcare Administration, Asia University, Taichung 41354, Taiwan

5. Department of Oral and Maxillofacial Surgery, MacKay Memorial Hospital, Taipei 10449, Taiwan

6. School of Nutrition and Health Sciences, Taipei Medical University, Taipei 110301, Taiwan

7. Nutrition Research Center, Taipei Medical University Hospital, Taipei 110301, Taiwan

8. Chinese Medicine Research Center, China Medical University, Taichung 40402, Taiwan

9. Department of Photonics and Communication Engineering, Asia University, Taichung 41354, Taiwan

Abstract

Radiotherapy and chemotherapy can impair salivary gland (SG) function, which causes xerostomia and exacerbate other side effects of chemotherapy and oral infection, reducing patients’ quality of life. This animal study aimed to assess the efficacy of electroacupuncture (EA) as a means of preventing xerostomia induced by 5−fluorouracil (5−FU). A xerostomia mouse model was induced via four tail vein injections of 5−FU (80 mg/kg/dose). EA was performed at LI4 and LI11 for 7 days. The pilocarpine-stimulated salivary flow rate (SFR) and salivary glands weight (SGW) were recorded. Salivary immunoglobulin A (SIgA) and lysozyme were determined via enzyme-linked immunosorbent assay (ELISA). SG was collected for hematoxylin and eosin staining to measure acini number and acinar cell size. Tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), and aquaporin 5 (AQP5) mRNA expressions in SG were quantified via RT-qPCR. 5−FU caused significant decreases in SFR, SGW, SIgA, lysozyme, AQP5 expression, and acini number, while TNF-α and IL-1β expressions and acinar cell size were significantly increased. EA treatment can prevent 5−FU damage to the salivary gland, while pilocarpine treatment can only elevate SFR and AQP5 expression. These findings provide significant evidence to support the use of EA as an alternative treatment for chemotherapy-induced salivary gland hypofunction and xerostomia.

Funder

Ministry of Science and Technology

China Medical University

Chinese Medicine Research Center of China Medical University

the Ministry of Education, Taiwan

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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