Mark Nixon
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Mark Nixon is a Lecturer at the University of Edinburgh, UK. His research focuses on the interactions between obesity, glucocorticoid exposure, and metabolic responses, as evidenced by his recent publications. He has conducted significant studies on sex differences in adipose tissue and the role of various proteins in modulating stress responses and metabolic diseases.
Recent Grants
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ABCC1-mediated corticosterone export protects from glucocorticoid-induced cardiometabolic toxicity
Open Date: 2022-07-01
Close Date: 2024-12-31
Grant: Close
Adipose glucocorticoid exposure is regulated by proteolytic cleavage of corticosteroid binding globulin (CBG)
Open Date: 2018-10-01
Close Date: 2024-01-06
Grant: Close
Regulation of macrophage phenotype by SIK1
Open Date: 2012-12-01
Close Date: 2013-12-01
Grant: Close
Characterisation of glucocorticoid receptor activation by 5α-reduced glucocorticoids
Open Date: 2011-02-01
Close Date: 2012-02-01
Articles (10)
Year:
2025
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2025
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2024
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2024
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2024
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2023
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2023
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2023
Year:
2022
Encoded by SerpinA6, plasma corticosteroid-binding globulin (CBG) transports glucocorticoids and regulates their access to cells. We determined how CBG influences plasma corticosterone and adrenal development in rats during the pubertal to adult transition using CRISPR/cas9 to disrupt SerpinA6 gene expression. In the absence of CBG, total plasma corticosterone levels were ∼80% lower in adult rats of both sexes, with a greater absolute reduction in females than in males. Notably, free corticosterone and adrenocorticotropic hormone were comparable between all groups. Between 30 and 90 days of age, wild-type female rats showed increases in adrenal weight and the size of the corticosterone-producing region, the zona fasciculata (zf), in tandem with increases in plasma CBG and corticosterone concentrations, whereas no such changes were observed in males. This sex difference was lost in rats without CBG, such that adrenal growth and zf expansion were similar between sexes. The sex-specific effects of CBG on adrenal morphology were accompanied by remarkable changes in gene expression: ∼40% of the adrenal transcriptome was altered in females lacking CBG, whereas almost no effect was seen in males. Over half of the adrenal genes that normally exhibit sexually dimorphic expression after puberty were similarly expressed in males and females without CBG, including those responsible for cholesterol biosynthesis and mobilization, steroidogenesis, and growth. Rat adrenal SerpinA6 transcript levels were very low or undetectable. Thus, sex differences in adrenal growth, morphology and gene expression profiles that emerge during puberty in rats are dependent on concomitant increases in plasma CBG produced by the liver.
Year:
2022
Collaborators (10)
Rebecca M Reynolds
Professor of Metabolic Medicine
University of Edinburgh
Ruth Morgan
Academic contract that is both teaching and research, Reader
Scotland's Rural College
Ewout Hoorn
Erasmus University Rotterdam
Natalie Z. M. Homer
University of Edinburgh
Michelle L. Gumz
University of Florida
Jessica Ivy
Lecturer
University of Edinburgh
Victor Viau
The University of British Columbia
Ruth Andrew
University of Edinburgh
Dawn Livingstone
University of Edinburgh
Luke Boyle
Imperial College Healthcare NHS Trust
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