Alison Gurney
Professor Alison M. Gurney | |
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Born | 1957 |
Alma mater | |
Known for |
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Scientific career | |
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Institutions |
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Thesis | Effects of methonium compounds on rat submandibular ganglion cells (1982) |
Doctoral advisor | Humphrey Rang[1][2] |
Other academic advisors | Henry Lester[3]
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Website | Official website |
Alison Marion Gurney (born 1957) is professor of Pharmacology at the University of Manchester. She previously held the W.C. Bowman[4] Chair of Pharmacology at the University of Strathclyde, where she was the first female appointed to a science professorship and the first female Professor of Pharmacology in Scotland. She is known for her research into the pharmacology and physiological roles of ion channels, especially in the pulmonary circulation.
Education
Gurney was educated at Prestwick Academy before attending the University of Aberdeen, where she graduated with a BSc degree in Pharmacology in 1979, then University College London, where she obtained a PhD in Pharmacology under the supervision of Professor Humphrey Rang. Together they identified a novel mechanism by which drugs that block neurotransmission across autonomic ganglia interact with neuronal nicotinic receptors.
Career and research
In 1982, Gurney moved to California to carry out postdoctoral research with Henry Lester at the California Institute of Technology, making use of novel light-sensitive compounds to study the interactions between drugs and receptors. She returned to the UK in 1985 to take up a lectureship in pharmacology at the United Medical and Dental Schools of Guy's and St Thomas's hospitals (now part of King's College), where she established a laboratory investigating ion channels in the cardiovascular system as a target for drugs to treat cardiovascular disease. While there she identified a positive feedback effect of cytoplasmic Ca2+ on cardiac calcium channels,[5] a role for ATP-sensitive potassium channels in regulating the membrane potential of artery smooth muscle cells[6] and the main features of the ion channels that set the resting potential of pulmonary artery smooth muscle cells.[7]
After 10 years in London, Gurney moved to Glasgow to take up the W.C. Bowman Chair of Pharmacology at the University of Strathclyde. For the next 10 years she continued studying the pulmonary circulation, identifying key roles for store-operated SOC channels[8] and the two-pore-domain potassium channel TASK-1[9] in regulating pulmonary artery tone and in the development of pulmonary hypertension. Along with physicists Allister Ferguson and John Girkin, she founded the Centre for Biophotonics and acted as its Director for the next 5 years.[10] In 2005, Gurney moved to the University of Manchester, where she continues to study ion channels in pulmonary artery disease, identifying KCNQ channels[11] as a possible biological target for drugs to treat pulmonary hypertension.
Recognition
Gurney was awarded the British Pharmacological Society Sandoz prize for her research in pharmacology in 1991, the Royal Pharmaceutical Society of Great Britain Conference Science Medal in 1992 and a Royal Society Leverhulme Trust Senior Research Fellowship in 2002.
One of Gurney's papers, "The channel-blocking action of methonium compounds on rat submandibular ganglion cells"[12] was recognised in "Landmarks in Pharmacology",[13] a collection of the most significant papers published by the British Journal of Pharmacology during its first 50 years.
References
- ^ "Humphrey Rang | Royal Society". royalsociety.org.
- ^ "Rang & Dale's Pharmacology - 9780702074486 | Elsevier Health - UK". www.uk.elsevierhealth.com.
- ^ "Dr Henry A Lester | Lester Research Group". lester.caltech.edu.
- ^ "Bio" (PDF). www.rse.org.uk. Retrieved 2020-05-20.
- ^ Gurney, A. M.; Charnet, P.; Pye, J. M.; Nargeot, J. (September 1989). "Augmentation of cardiac calcium current by flash photolysis of intracellular caged-Ca 2+ molecules". Nature. 341 (6237): 65–68. Bibcode:1989Natur.341...65G. doi:10.1038/341065a0. ISSN 1476-4687. PMID 2549428. S2CID 4268164.
- ^ Clapp, L. H.; Gurney, A. M. (1992-03-01). "ATP-sensitive K+ channels regulate resting potential of pulmonary arterial smooth muscle cells". American Journal of Physiology. Heart and Circulatory Physiology. 262 (3): H916–H920. doi:10.1152/ajpheart.1992.262.3.H916. ISSN 0363-6135. PMID 1558201.
- ^ Evans, A. M.; Osipenko, O. N.; Gurney, A. M. (1996). "Properties of a novel K+ current that is active at resting potential in rabbit pulmonary artery smooth muscle cells". The Journal of Physiology. 496 ( Pt 2) (2): 407–20. doi:10.1113/jphysiol.1996.sp021694. PMC 1160886. PMID 8910225.
- ^ Ng Lih Chyuan; Gurney Alison M. (2001-11-09). "Store-Operated Channels Mediate Ca2+ Influx and Contraction in Rat Pulmonary Artery". Circulation Research. 89 (10): 923–929. doi:10.1161/hh2201.100315. PMID 11701620.
- ^ Gurney, A.M.; Osipenko, O.N.; MacMillan, D.; McFarlane, K.M.; Tate, R.J.; Kempsill, F.E.J. (2003). "Two-Pore Domain K Channel, TASK-1, in Pulmonary Artery Smooth Muscle Cells". Circulation Research. 93 (10): 957–964. doi:10.1161/01.res.0000099883.68414.61. PMID 14551239.
- ^ "Prof JM Girkin - Durham University". www.dur.ac.uk. Retrieved 2020-04-14.
- ^ Gurney, Alison M.; Joshi, Shreena; Manoury, Boris (2010). Yuan, Jason X. -J.; Ward, Jeremy P. T. (eds.). "KCNQ Potassium Channels: New Targets for Pulmonary Vasodilator Drugs?". Membrane Receptors, Channels and Transporters in Pulmonary Circulation. Advances in Experimental Medicine and Biology. 661. Totowa, NJ: Humana Press: 405–417. doi:10.1007/978-1-60761-500-2_26. ISBN 978-1-60761-500-2. PMID 20204745.
- ^ Gurney, A.M.; Rang, H.P. (1997-02-01). "The channel-blocking action of methonium compounds on rat submandibular ganglion cells". British Journal of Pharmacology. 120 (S1): 471–490. doi:10.1111/j.1476-5381.1997.tb06837.x. ISSN 0007-1188. PMC 3224332. PMID 9142425.
- ^ Birmingham, A. T; Brown, D. A (1997). Landmarks in pharmacology: a selection from papers published in the British Journal of Pharmacology since its foundation in 1946. Hampshire [UK: MacMillan Press. ISBN 978-0-333-71930-5. OCLC 36960433.