Projects per year
Abstract / Description of output
Androgens are essential for male development and reproductive function. They are transported to their site of action as blood-borne endocrine hormones, but can also be produced within tissues to act in intracrine and paracrine fashions. Because of this, circulating concentrations may not accurately reflect the androgenic influence within specific tissue microenvironments. Mass spectrometry imaging permits regional analysis of small molecular species directly from tissue surfaces. However, due to poor ionization and localized ion suppression, steroid hormones are difficult to detect. Here derivatization with Girard T reagent was used to charge-tag testosterone and 5α-dihydrotestosterone allowing direct detection of these steroids in mouse testes, in both basal and maximally-stimulated states and in rat prostate. Limits of detection were ~0.1 pg for testosterone. Exemplary detection of endogenous steroids was achieved by matrix-assisted laser desorption ionization and either Fourier transform ion cyclotron resonance detection (at 150 μm spatial resolution) or quadrupole-time of flight detection (at 50 μm spatial resolution). Structural confirmation was achieved by collision induced fragmentation following liquid extraction surface desorption and electrospray ionization. This application broadens the scope for derivatization strategies on tissue surfaces to elucidate local endocrine signaling in health and disease
Original language | English |
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Journal | Analytical Chemistry |
Volume | 88 |
Issue number | 21 |
Early online date | 27 Sept 2016 |
DOIs | |
Publication status | E-pub ahead of print - 27 Sept 2016 |
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Dive into the research topics of 'Spatial Localization and Quantitation of Androgens in Mouse Testis by Mass Spectrometry Imaging'. Together they form a unique fingerprint.Projects
- 2 Finished
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Research Excellence Award - Cardiovascular Surgery / Zebrafish Support
Mullin, N., Azzoni, E., Fox, K., Mullins, J., Newby, D., Seckl, J., Walker, B., Webb, D. & Wilmut, I.
1/04/08 → 30/09/17
Project: Research
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Tissue specific disruption of glucocorticoid signalling: new mechanisms and therapies for cardiovascular risk. Renewal
Walker, B.
1/04/06 → 31/03/11
Project: Research