Caloric restriction suppresses apoptotic cell death in the mammalian cochlea and leads to prevention of presbycusis.

Abstract

Presbycusis is characterized by an age-related progressive decline of auditory function, and arises mainly from the degeneration of hair cells or spiral ganglion (SG) cells in the cochlea. Here we show that caloric restriction suppresses apoptotic cell death in the mouse cochlea and prevents late onset of presbycusis. Calorie restricted (CR) mice, which maintained body weight at the same level as that of young control (YC) mice, retained normal hearing and showed no cochlear degeneration. CR mice also showed a significant reduction in the number of TUNEL-positive cells and cleaved caspase-3-positive cells relative to middle-age control (MC) mice. Microarray analysis revealed that CR down-regulated the expression of 24 apoptotic genes, including Bak and Bim. Taken together, our findings suggest that loss of critical cells through apoptosis is an important mechanism of presbycusis in mammals, and that CR can retard this process by suppressing apoptosis in the inner ear tissue.

• Authors: Shinichi Someya, Tatsuya Yamasoba, Richard Weindruch, Tomas A Prolla, Masaru Tanokura
• Journal: Neurobiology of aging (Neurobiol Aging) Vol. 28 Issue 10 Pg. 1613-22 (Oct 2007) ISSN: 1558-1497 [Electronic] United States
• PMID: 16890326 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Casp3 protein, mouse
• Caspase 3

Topics

• Aging (metabolism, pathology)
• Animals
• Apoptosis (physiology)
• Body Weight (physiology)
• Caloric Restriction (methods)
• Caspase 3 (metabolism)
• Cochlea (metabolism, physiopathology)
• Eating (physiology)
• Food Deprivation (physiology)
• In Situ Nick-End Labeling
• Male
• Mice
• Mice, Inbred C57BL
• Presbycusis (metabolism, physiopathology, prevention & control)