Oral administration of an herbal medicine to prevent progressive hearing loss in a mouse model of diabetes

Tsumura Suzuki Obese Diabetes (TSOD) mice exhibit early age-associated hearing loss. Histopathological analysis of these mice shows narrowing of capillaries in the stria vascularis and chronic reduction of blood flow in the cochlea. In this study, we investigated the effect of oral administration of...

Full description

Saved in:
Bibliographic Details
Published inAuris, nasus, larynx Vol. 46; no. 5; pp. 703 - 708
Main Authors Hori, Takeshi, Sugahara, Kazuma, Tsuda, Junko, Hirose, Yoshinobu, Hashimoto, Makoto, Takemoto, Yousuke, Tarumoto, Shunsuke, Yamashita, Hiroshi
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.10.2019
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Tsumura Suzuki Obese Diabetes (TSOD) mice exhibit early age-associated hearing loss. Histopathological analysis of these mice shows narrowing of capillaries in the stria vascularis and chronic reduction of blood flow in the cochlea. In this study, we investigated the effect of oral administration of a herbal medicine or calorie restriction on hearing in TSOD mice. TSOD mice were divided into 4 groups: CR (calorie restriction), BF and DS (treated with the herbal medicines, Bofutsushosan and Daisaikoto, respectively), and the control group. Body weight, blood glucose levels, and auditory brainstem responses (ABRs) were measured. The cochleae were excised and evaluated histopathologically. Blood glucose levels were suppressed in the CR, BF, and DS groups. In addition, the elevation of ABR thresholds was inhibited in the CR, BF, and DS groups. Cochlear blood vessels remained wide in the three treatment groups compared with the control group. These results suggested that the administration of these herbal medicines improved glucose tolerance and yielded results similar to those on calorie restriction. Oral administration of 2 herbal medicines can prevent hearing function disorder in a model mouse of diabetes. The results may clarify the possibility of clinical application.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0385-8146
1879-1476
DOI:10.1016/j.anl.2019.01.011