TY - JOUR
T1 - Sexual Dimorphism in Transcriptional and Functional Glucocorticoid Effects on Mouse Skeletal Muscle
AU - Li, Sheng
AU - Schönke, Milena
AU - Buurstede, Jacobus C.
AU - Moll, Tijmen J.A.
AU - Gentenaar, Max
AU - Schilperoort, Maaike
AU - Visser, Jenny A.
AU - Kaikaew, Kasiphak
AU - van de Vijver, Davy
AU - Abbassi-Daloii, Tooba
AU - Raz, Vered
AU - Aartsma-Rus, Annemieke
AU - van Putten, Maaike
AU - Meijer, Onno C.
AU - Kroon, Jan
N1 - Funding Information:
SL was supported by a Chinese Scholarship Council grant. This study was in part funded by the Leiden University Fund-Mulder Hamelers obtained by JK.
Publisher Copyright:
Copyright © 2022 Li, Schönke, Buurstede, Moll, Gentenaar, Schilperoort, Visser, Kaikaew, van de Vijver, Abbassi-Daloii, Raz, Aartsma-Rus, van Putten, Meijer and Kroon.
PY - 2022/7/11
Y1 - 2022/7/11
N2 - Muscle atrophy is common in patients with increased glucocorticoid exposure. Glucocorticoid effects are often sex-specific, and while different glucocorticoid responses between male and female subjects are reported, it is unclear why this is. In this study, we evaluated the effects of corticosterone and synthetic glucocorticoid treatment on muscle atrophy in male and female mice. We found that corticosterone treatment reduced grip strength in female mice only, whereas muscle mass was reduced in both sexes. Skeletal muscle transcriptional responses to corticosterone treatment were more pronounced and widespread in male mice. Synthetic glucocorticoid treatment reduced grip strength in both sexes, while female mice were more sensitive to muscle atrophy than male mice. To evaluate the role of androgens, chemically-castrated male mice were treated with synthetic glucocorticoids. We observed additively reduced muscle mass, but did not observe any interaction effects. Although sex differences in glucocorticoid responses in skeletal muscle are partly influenced by androgen signaling, further studies are warranted to fully delineate the underlying mechanisms.
AB - Muscle atrophy is common in patients with increased glucocorticoid exposure. Glucocorticoid effects are often sex-specific, and while different glucocorticoid responses between male and female subjects are reported, it is unclear why this is. In this study, we evaluated the effects of corticosterone and synthetic glucocorticoid treatment on muscle atrophy in male and female mice. We found that corticosterone treatment reduced grip strength in female mice only, whereas muscle mass was reduced in both sexes. Skeletal muscle transcriptional responses to corticosterone treatment were more pronounced and widespread in male mice. Synthetic glucocorticoid treatment reduced grip strength in both sexes, while female mice were more sensitive to muscle atrophy than male mice. To evaluate the role of androgens, chemically-castrated male mice were treated with synthetic glucocorticoids. We observed additively reduced muscle mass, but did not observe any interaction effects. Although sex differences in glucocorticoid responses in skeletal muscle are partly influenced by androgen signaling, further studies are warranted to fully delineate the underlying mechanisms.
UR - http://www.scopus.com/inward/record.url?scp=85134643449&partnerID=8YFLogxK
U2 - 10.3389/fendo.2022.907908
DO - 10.3389/fendo.2022.907908
M3 - Article
C2 - 35898460
AN - SCOPUS:85134643449
SN - 1664-2392
VL - 13
JO - Frontiers in Endocrinology
JF - Frontiers in Endocrinology
M1 - 907908
ER -