4.7 Article

Maternal Intake of Either Fructose or the Artificial Sweetener Acesulfame-K Results in Differential and Sex-Specific Alterations in Markers of Skin Inflammation and Wound Healing Responsiveness in Mouse Offspring: A Pilot Study

Journal

NUTRIENTS
Volume 15, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/nu15112534

Keywords

developmental programming; DOHaD; animal model; maternal nutrition; fructose; artificial sweetener; inflammation; wound healing; skin; adipose tissue; pressure injury

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Growing evidence suggests that maternal consumption of artificial sweeteners may not be a beneficial alternative to sugar-sweetened beverages and may contribute to metabolic dysfunction in adult offspring. This study investigated the impact of maternal fructose or acesulfame-k consumption during pregnancy on offspring wound healing. The results showed that a maternal fructose diet had significant effects on wound severity and delayed healing, while a maternal artificial sweetener diet had a sex-specific effect on the healing process. These findings highlight the importance of understanding developmental programming and its influence on skin integrity and wound responsiveness in later life.
Growing evidence has demonstrated that maternal artificial sweetener (AS) consumption may not be a beneficial alternative when compared to sugar-sweetened beverages and potentially leads to metabolic dysfunction in adult offspring. Compromised skin integrity and wound healing associated with type 2 diabetes can lead to complications such as diabetic pressure injury (PI). In this context, the skin plays an important role in the maintenance of metabolic homeostasis, yet there is limited information on the influence of sugar- or AS-sweetened beverages during pregnancy on developmental programming and offspring skin homeostasis. This study examined the impact of maternal fructose or acesulfame-k consumption on offspring wound healing. Female C57Bl/6 mice received a chow diet ad libitum with either water (CD), fructose (FR; 34.7 mM fructose), or AS (AS; 12.5 mM Acesulfame-K) throughout pregnancy and lactation. PIs were induced in offspring at 9 weeks of age (n = 6/sex/diet). PIs and healthy skin biopsies were collected for later analysis. Maternal AS intake increased skin inflammatory markers in healthy biopsies while an FR diet increased Tgfb expression, and both diets induced subtle changes in inflammatory markers post-wound inducement in a sex-specific manner. Furthermore, a maternal FR diet had a significant effect on pressure wound severity and early wound healing delay, while AS maternal diet had a sex-specific effect on the course of the healing process. This study demonstrates the need for a better understanding of developmental programming as a mediator of later-life skin integrity and wound responsiveness.

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