Literature DB >> 10807352

Effects of dietary restriction and antioxidants on presbyacusis.

M D Seidman1.   

Abstract

OBJECTIVES/HYPOTHESIS: The premise of this study is that the membrane hypothesis of aging, also known as the mitochondrial clock theory of aging, is the basis for presbyacusis. Furthermore, it is proposed that treatment with antioxidants or dietary restriction can attenuate age-related hearing loss. Many studies have demonstrated a reduction in blood flow to specific tissues, including the cochlea, with aging. Hypoperfusion leads to the formation of reactive oxygen metabolites (ROM). ROM are highly toxic molecules that directly affect tissues including inner ear structures. In addition, ROM can damage mitochondrial DNA (mtDNA), resulting in the production of specific mtDNA deletions (mtDNA del4977 [human] or mtDNA del4834 [rat]; also known as the common aging deletion]. Previous corroborating data suggest that the common aging deletion mtDNA4834 may be associated not only with aging but also with presbyacusis, thus further strengthening the basis of the current studies. In this study, experiments provide compelling evidence that long-term treatment with compounds that block or scavenge reactive oxygen metabolites attenuate age-related hearing loss and reduce the impact of associated deleterious changes at the molecular level. STUDY
DESIGN: Prospective randomized study.
METHODS: One hundred thirty rats were randomly assigned to one of six groups with appropriate controls. Animals were divided into the following treatment arms: group 1, 30% caloric restriction; group 2, vitamin E oversupplementation; group 3, vitamin C over-supplementation; group 4, melatonin treatment; group 5, lazaroid treatment; and group 6, placebo. In addition, 10 animals were used to determine the appropriate caloric restriction. All subjects underwent baseline and every-3-month testing until their health failed (range, 18-28 mo; average, 25 mo). This testing included auditory sensitivity studies using auditory brainstem response (ABR) testing, as well as tissue analysis for mtDNA deletions using molecular biological techniques. At the conclusion of the study, animals underwent a final ABR test and were tested for mtDNA deletions in brain and inner ear tissues, and the opposite ear was used for histological analysis.
RESULTS: Results indicated that the 30%-caloric-restricted group maintained the most acute auditory sensitivities, the lowest quantity of mtDNA deletions, and the least amount of outer hair cell loss. The antioxidant-treated subjects had improved auditory sensitivities, and a trend for fewer mtDNA deletions was observed compared with the placebo subjects. The placebo subjects had the poorest auditory sensitivity, the most mtDNA deletions, and the greatest degree of outer hair cell loss.
CONCLUSIONS: Intervention designed to reduce reactive oxygen metabolite damage appears to protect against age-related hearing loss specifically and aging in general. This is reflected by an overall reduction in mtDNA deletions. These data also suggest that the common aging deletion appears to be associated with presbyacusis, as demonstrated by an increased frequency of the mtDNA del4834 in the cochleae with the most significant hearing loss. Nutritional and pharmacological strategies may very well provide rational treatment options that would limit the age-associated increase in ROM generation, reduce mtDNA damage, and reduce the degree of hearing loss as the organism advances in age.

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Year:  2000        PMID: 10807352     DOI: 10.1097/00005537-200005000-00003

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  68 in total

1.  Why do hair cells and spiral ganglion neurons in the cochlea die during aging?

Authors:  Philip Perez; Jianxin Bao
Journal:  Aging Dis       Date:  2011-04-28       Impact factor: 6.745

Review 2.  Mitochondrial oxidative damage and apoptosis in age-related hearing loss.

Authors:  Shinichi Someya; Tomas A Prolla
Journal:  Mech Ageing Dev       Date:  2010-04-29       Impact factor: 5.432

Review 3.  Effects of caloric restriction on age-related hearing loss in rodents and rhesus monkeys.

Authors:  Shinichi Someya; Masaru Tanokura; Richard Weindruch; Tomas A Prolla; Tatsuya Yamasoba
Journal:  Curr Aging Sci       Date:  2010-02

Review 4.  Mechanisms of noise-induced hearing loss indicate multiple methods of prevention.

Authors:  Colleen G Le Prell; Daisuke Yamashita; Shujiro B Minami; Tatsuya Yamasoba; Josef M Miller
Journal:  Hear Res       Date:  2006-12-04       Impact factor: 3.208

5.  Oxidative imbalance in the aging inner ear.

Authors:  Hongyan Jiang; Andra E Talaska; Jochen Schacht; Su-Hua Sha
Journal:  Neurobiol Aging       Date:  2006-08-22       Impact factor: 4.673

Review 6.  Recognition and control of the progression of age-related hearing loss.

Authors:  Hong Miao Ren; Jihao Ren; Wei Liu
Journal:  Rejuvenation Res       Date:  2013-12       Impact factor: 4.663

7.  Age-related hearing loss in C57BL/6J mice is mediated by Bak-dependent mitochondrial apoptosis.

Authors:  Shinichi Someya; Jinze Xu; Kenji Kondo; Dalian Ding; Richard J Salvi; Tatsuya Yamasoba; Peter S Rabinovitch; Richard Weindruch; Christiaan Leeuwenburgh; Masaru Tanokura; Tomas A Prolla
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-09       Impact factor: 11.205

8.  Hypertension, Diuretic Use, and Risk of Hearing Loss.

Authors:  Brian M Lin; Sharon G Curhan; Molin Wang; Roland Eavey; Konstantina M Stankovic; Gary C Curhan
Journal:  Am J Med       Date:  2015-11-30       Impact factor: 4.965

9.  Adenosine and the auditory system.

Authors:  Srdjan M Vlajkovic; Gary D Housley; Peter R Thorne
Journal:  Curr Neuropharmacol       Date:  2009-09       Impact factor: 7.363

Review 10.  Noise and quality of life.

Authors:  Michael D Seidman; Robert T Standring
Journal:  Int J Environ Res Public Health       Date:  2010-10-19       Impact factor: 3.390

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