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Stress, Sex, and Sugar: Glucocorticoids and Sex-Steroid Crosstalk in the Sex-Specific Misprogramming of Metabolism

期刊

JOURNAL OF THE ENDOCRINE SOCIETY
卷 4, 期 8, 页码 -

出版社

ENDOCRINE SOC
DOI: 10.1210/jendso/bvaa087

关键词

glucocorticoid; estrogen; androgen; progestogen; crosstalk; sex-specific; metabolism; diabetes; developmental programming; endocrine-disrupting chemicals

资金

  1. National Institutes of Health [R21 ES021354, R01 ES028879, T32 HD007009, P30 ES027792]

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Early-life exposures to environmental insults can misprogram development and increase metabolic disease risk in a sex-dependent manner by mechanisms that remain poorly characterized. Modifiable factors of increasing public health relevance, such as diet, psychological stress, and endocrine-disrupting chemicals, can affect glucocorticoid receptor signaling during gestation and lead to sex-specific postnatal metabolic derangements. Evidence from humans and animal studies indicate that glucocorticoids crosstalk with sex steroids by several mechanisms in multiple tissues and can affect sex-steroid-dependent developmental processes. Nonetheless, glucocorticoid sex-steroid crosstalk has not been considered in the glucocorticoid-induced misprogramming of metabolism. Herein we review what is known about the mechanisms by which glucocorticoids crosstalk with estrogen, androgen, and progestogen action. We propose that glucocorticoid sex-steroid crosstalk is an understudied mechanism of action that requires consideration when examining the developmental misprogramming of metabolism, especially when assessing sex-specific outcomes. (C) Endocrine Society 2020.

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