Sexual Dimorphism in Sex Hormone Metabolism in Human Skeletal Muscle Cells in Response to Different Testosterone Exposure DOI Creative Commons
Paolo Sgrò, Cristina Antinozzi, Christopher W. Wasson

и другие.

Biology, Год журнала: 2024, Номер 13(10), С. 796 - 796

Опубликована: Окт. 5, 2024

Muscle tissue is an important target of sex steroids, and particularly, testosterone plays essential roles in muscle cell metabolism. Wide ranges studies have reported differences basal steroidogenesis, recently several genes been identified to be regulated by androgen response elements that show innate muscle. However, accounting for demonstrating sexual dimorphism vitro are still scarce not well characterized. Here, we demonstrated the ability 46XX 46XY human primary skeletal cells differently activate steroidogenesis vitro, likely related sex-chromosome onset, induce hormone release after increasing doses exposure. Cells were treated with at concentrations 0.5, 2, 5, 10, 32, 100 nmol/L 24 h. Variations 17β-HSD, 5α-R2, CYP-19 expression, DHT, estradiol, androstenedione release, as IL6 IL8 analyzed, respectively, RT-PCR, ELISA, luminex-assay. Following treatments, potentially any concentration level, increase expression was observed cells, accompanied elevated levels androstenedione, IL6/IL8 release. same treatment, exhibited 5α-R2 a conversion androgens estrogens, reduction In conclusion, this study may influence homeostasis, which pivotal

Язык: Английский

NMJ-related diseases beyond the congenital myasthenic syndromes DOI Creative Commons
Alejandra Navarro-Martínez, Cristina Vicente‐García, Jaime J. Carvajal

и другие.

Frontiers in Cell and Developmental Biology, Год журнала: 2023, Номер 11

Опубликована: Авг. 4, 2023

Neuromuscular junctions (NMJs) are a special type of chemical synapse that transmits electrical stimuli from motor neurons (MNs) to their innervating skeletal muscle induce response. They an ideal model for the study synapses, given manageable size and easy accessibility. Alterations in morphology or function lead neuromuscular disorders, such as congenital myasthenic syndromes, which caused by mutations proteins located NMJ. In this review, we highlight novel potential candidate genes may cause modify NMJs-related pathologies humans exploring phenotypes hundreds mouse models available literature. We also underscore fact NMJs differ between species, muscles even sexes. Hence importance choosing good organism NMJ-related diseases: only taking into account specific features mammalian NMJ, experimental results would be efficiently translated clinic.

Язык: Английский

Процитировано

2

Expression of neurotransmitters, vasculogenesis markers and myosin heavy chain isoforms in the masseter muscle of senescence‐accelerated mouse prone 8 mice DOI

Chiaki Nakamura,

Iwao Sato, Yoko Miwa

и другие.

Journal of Oral Rehabilitation, Год журнала: 2023, Номер 50(7), С. 587 - 595

Опубликована: Март 23, 2023

Learning and memory deficits pathologic changes in the hippocampus caused by toothlessness soft diet feeding are related to reduced masseter muscle (MM) function.Myosin heavy chain (MyHC) isoform expression MM also under different chewing conditions. The neurotransmitter calcitonin gene-related peptide (CGRP) vascular endothelial growth factor A (VEGF-A) involved formation. However, relationship between CGRP, VEGF-A MyHC isoforms senescence-accelerated mouse prone 8 (SAMP8) strain, a model of learning deficits, remains unclear.Changes VEGF-A, vasculogenesis marker mRNA MMs ageing SAMP8 resistant 1 (SAMR1) mice was investigated through quantitative real-time polymerase reaction (qRT-PCR) situ hybridization.qRT-PCR revealed obviously high CGRP levels (p < .001). MyHC-IId/x higher 24-week-old than SAMR1 .001) but lower slow-MyHC observed on fibres not hybridization. Principal component analysis (PCA) strong positive contributions SAMP8-MyHC-IId/x, SAMP8-CGRP, SAMR1-MyHC-emb, SAMR1-CGRP, SAMR1-VEGF-A, SAMR1-CD31, SAMP8-VEGF-A, SAMP8-CD31 at 12 24 weeks.Calcitonin is key for patterns mice.

Язык: Английский

Процитировано

1

(-)-epicatechin treatment did not modify the thermogenic pathway in the gastrocnemius muscle of male rat offspring obeses by programming DOI
María Elena Tejeda,

Sergio De los Santos,

Ramón Mauricio Coral‐Vázquez

и другие.

Journal of Developmental Origins of Health and Disease, Год журнала: 2024, Номер 15

Опубликована: Янв. 1, 2024

Abstract The aim of this study was to analyse the expression genes related regulation energy metabolism in skeletal muscle tissue by comparing male offspring two age groups [at 110 and 245 postnatal days (pnd)] from a mother with obesity induced high-fat diet (-)-epicatechin (Epi) administration. Four six different litters were randomly selected for control [C mothers maternal (MO)] or Epi intervention groups. We evaluated effect on gastrocnemius analysing mRNA protein levels Fndc5/irisin, Pgc-1α, Ucp3, Sln. significantly increased Pgc-1α MO group at pnd ( p < 0.036, vs . MO+Epi), while pnd, Fndc5/irisin MO+Epi versus = 0.006). No differences detected Ucp3 Sln (including mRNA) protein) among experimental In conclusion, treatment Pgc-α 245. Furthermore, it is suggested that flavonoid model its impact thermogenesis are regulated pathway than Fndc5/irisin.

Язык: Английский

Процитировано

0

Prazosin improves insulin-induced anabolic signaling by protecting capillary regression in the soleus muscle of hindlimb-unloaded rats DOI
Masayuki Tanaka,

Miho Kanazashi,

Toshiko Tsumori

и другие.

Journal of Diabetes & Metabolic Disorders, Год журнала: 2024, Номер 23(2), С. 1989 - 1999

Опубликована: Июнь 26, 2024

Язык: Английский

Процитировано

0

Sexual Dimorphism in Sex Hormone Metabolism in Human Skeletal Muscle Cells in Response to Different Testosterone Exposure DOI Creative Commons
Paolo Sgrò, Cristina Antinozzi, Christopher W. Wasson

и другие.

Biology, Год журнала: 2024, Номер 13(10), С. 796 - 796

Опубликована: Окт. 5, 2024

Muscle tissue is an important target of sex steroids, and particularly, testosterone plays essential roles in muscle cell metabolism. Wide ranges studies have reported differences basal steroidogenesis, recently several genes been identified to be regulated by androgen response elements that show innate muscle. However, accounting for demonstrating sexual dimorphism vitro are still scarce not well characterized. Here, we demonstrated the ability 46XX 46XY human primary skeletal cells differently activate steroidogenesis vitro, likely related sex-chromosome onset, induce hormone release after increasing doses exposure. Cells were treated with at concentrations 0.5, 2, 5, 10, 32, 100 nmol/L 24 h. Variations 17β-HSD, 5α-R2, CYP-19 expression, DHT, estradiol, androstenedione release, as IL6 IL8 analyzed, respectively, RT-PCR, ELISA, luminex-assay. Following treatments, potentially any concentration level, increase expression was observed cells, accompanied elevated levels androstenedione, IL6/IL8 release. same treatment, exhibited 5α-R2 a conversion androgens estrogens, reduction In conclusion, this study may influence homeostasis, which pivotal

Язык: Английский

Процитировано

0