4.5 Review

Responses to Many Anti-Aging Interventions Are Sexually Dimorphic

Journal

WORLD JOURNAL OF MENS HEALTH
Volume -, Issue -, Pages -

Publisher

KOREAN SOC SEXUAL MEDICINE & ANDROLOGY
DOI: 10.5534/wjmh.230015

Keywords

Aging; Caloric restriction; Estradiol-17 alpha; IGF-1; Rapamycin; Sex

Ask authors/readers for more resources

There is growing recognition that sex differences extend beyond reproductive organs and traits related to reproduction, and that sex is a significant biological variable in most characteristics of living organisms. This article focuses on sex differences in responses to anti-aging interventions, which have been shown to vary substantially between females and males. While calorie restriction and certain genetic alterations can extend longevity in both sexes, specific metabolic changes and health benefits differ between women and men. It is clear that understanding the unique mechanisms of aging in females and males is crucial for developing effective and tailored anti-aging interventions.
There is increasing appreciation that sex differences are not limited to reproductive organs or traits related to reproduction and that sex is an important biological variable in most characteristics of a living organism. The biological process of aging and aging-related traits are no exception and exhibit numerous, often major, sex differences. This article explores one aspect of these differences, namely sex differences in the responses to anti-aging interventions. Aging can be slowed down and/or postponed by a variety of environmental (lifestyle), genetic or pharmacological interventions. Although many, particularly older studies utilized only one sex of experimental animals, there is considerable evidence that responses to these interven-tions can be very different in females and males. Calorie restriction (CR), that is reducing food intake without malnutrition can extend longevity in both sexes, but specific metabolic alterations and health benefits induced by CR are not the same in women and men. In laboratory mice, several of the genetic alterations that reduce insulin-like growth factor I (IGF-1) signal -ing extend longevity more effectively in females or in females only. Beneficial effects of rapamycin, an inhibitor of mTOR sig-naling, on mouse longevity are greater in females. In contrast, several anti-aging compounds, including a weak estrogen, 17 alpha estradiol, extend longevity of male, but not female, mice. Apparently, fundamental mechanisms of aging are not identi-cal in females and males and it is essential to use both sexes in studies aimed at identifying novel anti-aging interventions. Recommendations for lifestyle modifications, drugs, and dietary supplements to maintain good health and functionality into advanced age and to live longer will likely need to be tailored to the sex of the user.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available