Carbohydrate-restricted diet promotes skin senescence in senescence-accelerated prone mice

Biogerontology. 2019 Feb;20(1):71-82. doi: 10.1007/s10522-018-9777-1. Epub 2018 Oct 3.

Abstract

This study used senescence-accelerated prone mice (SAMP8) to examine the effects of a carbohydrate-restricted diet on aging and skin senescence, to determine how long-term carbohydrate restriction affects the aging process. Three-week-old male SAMP8 mice were divided into three groups after 1 week of preliminary feeding: one was given a controlled diet, the other was given a high-fat diet, and the third was given a carbohydrate-restricted diet. Ad libitum feeding was administered until the mice reached 50 weeks of age. Before the end of the test period, a grading test was used to evaluate visible aging in the mice. After the test period, serum and skin samples in mice were obtained and submitted for analysis. As a result, the grading test demonstrated that there was significant progression of visible aging in the carbohydrate-restricted group, as well as a decreased survival rate. Histological examination of the skin revealed that the epidermis and dermis in the carbohydrate-restricted group had become thinner. Analysis of the mechanisms involved demonstrated an increase in serum interleukin-6, aggravated skin senescence, inhibition of skin autophagy and activation of skin mTOR. Therefore, this study proved that a carbohydrate-restricted diet promoted skin senescence in senescence-accelerated mice.

Keywords: Aging; Autophagy; Carbohydrate-restricted diet; IL-6; Senescence-accelerated mice; mTOR.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Aging, Premature* / metabolism
  • Aging, Premature* / pathology
  • Animals
  • Autophagy / physiology
  • Cellular Senescence / physiology
  • Diet, Carbohydrate-Restricted* / adverse effects
  • Diet, Carbohydrate-Restricted* / methods
  • Diet, High-Fat / methods
  • Interleukin-6 / metabolism
  • Mice
  • Models, Animal
  • Skin / metabolism
  • Skin / pathology
  • Skin Aging / physiology*
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Interleukin-6
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases