1.Effects on Salivation, Xerostomia and Halitosis in Elders after Oral Function Improvement Exercises.
Young Jin KIM ; Kyung Min PARK
Journal of Korean Academy of Nursing 2012;42(6):898-906
PURPOSE: The purpose of this study was to investigate effects of Oral Function Improvement Exercises on salivation, xerostomia and halitosis in elderly people. METHODS: The participants in the study were 48 female community-dwelling elders in D city. The Oral Function Improvement Exercises were given 3 times a week, for a total of 24 times from August to October 2011. Spitting method, Visual Analogue Scale, and halimeter (mBA-21) were used to evaluate the effects of Oral Function Improvement Exercises on salivation, xerostomia, and halitosis. The data were analyzed using chi2-test and t-test with the SPSS program. RESULTS: The experimental group had significantly better salivation, and less xerostomia and halitosis than the control group. CONCLUSION: The results indicate that Oral Function Improvement Exercises were effective for salivation, xerostomia and halitosis in the elders. Therefore, it was suggested that Oral Function Improvement Exercise are applicable in a community nursing intervention program to improve the quality of life for elders.
Aged
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*Exercise
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Female
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Halitosis/*physiopathology
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Humans
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Program Evaluation
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Quality of Life
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Questionnaires
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Salivation/*physiology
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Xerostomia/*physiopathology
2.Human salivary gland stem cells ameliorate hyposalivation of radiation-damaged rat salivary glands.
Jaemin JEONG ; Hyunjung BAEK ; Yoon Ju KIM ; Youngwook CHOI ; Heekyung LEE ; Eunju LEE ; Eun Sook KIM ; Jeong Hun HAH ; Tack Kyun KWON ; Ik Joon CHOI ; Heechung KWON
Experimental & Molecular Medicine 2013;45(11):e58-
Salivary function in mammals may be defective for various reasons, such as aging, Sjogren's syndrome or radiation therapy in head and neck cancer patients. Recently, tissue-specific stem cell therapy has attracted public attention as a next-generation therapeutic reagent. In the present study, we isolated tissue-specific stem cells from the human submandibular salivary gland (hSGSCs). To efficiently isolate and amplify hSGSCs in large amounts, we developed a culture system (lasting 4-5 weeks) without any selection. After five passages, we obtained adherent cells that expressed mesenchymal stem cell surface antigen markers, such as CD44, CD49f, CD90 and CD105, but not the hematopoietic stem cell markers, CD34 and CD45, and that were able to undergo adipogenic, osteogenic and chondrogenic differentiation. In addition, hSGSCs were differentiated into amylase-expressing cells by using a two-step differentiation method. Transplantation of hSGSCs to radiation-damaged rat salivary glands rescued hyposalivation and body weight loss, restored acinar and duct cell structure, and decreased the amount of apoptotic cells. These data suggest that the isolated hSGSCs, which may have characteristics of mesenchymal-like stem cells, could be used as a cell therapy agent for the damaged salivary gland.
Amylases/genetics/metabolism
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Animals
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Antigens, CD/genetics/metabolism
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Apoptosis
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Cell Differentiation
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Humans
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Male
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Mesenchymal Stromal Cells/*cytology/metabolism
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Radiation Injuries, Experimental
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Rats
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Rats, Wistar
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*Regeneration
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Salivary Glands/cytology/injuries/physiology/*surgery
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*Salivation
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*Stem Cell Transplantation