James E. Bowe
King's College London
40 Papers
229 Citations
James E. Bowe is an academic researcher from King's College London. The author has contributed to research in topics: Internal medicine & Insulin. The author has an hindex of 18, co-authored 35 publications.
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Papers
Metabolic phenotyping guidelines: assessing glucose homeostasis in rodent models.
James E. Bowe,Zara J. Franklin,Astrid C Hauge-Evans,Aileen King,Shanta J. Persaud,Peter M. Jones +5 more
TL;DR: This review outlines the most commonly used techniques for assessing glucose tolerance in rodents and details the factors that should be taken into account in their use.
Animal models for diabetes: Understanding the pathogenesis and finding new treatments
Aileen King,James E. Bowe +1 more
TL;DR: Information is gathered on the currently used experimental animal models of both Type 1 and Type 2 diabetes and their advantages and disadvantages for research purposes and details the factors that should be taken into account in their use.
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The hop phytoestrogen, 8-prenylnaringenin, reverses the ovariectomy-induced rise in skin temperature in an animal model of menopausal hot flushes.
James E. Bowe,Xiao Feng Li,J. S. Kinsey-Jones,Arne Heyerick,Susan D. Brain,Stuart Milligan,Kevin T. O'Byrne +6 more
TL;DR: Observations suggest that the regulation of the vasomotor response by oestrogens and phytoestrogens is mediated, at least in part, by peripheral mechanisms involving both ERalpha and ERbeta.
Kisspeptin stimulation of insulin secretion: mechanisms of action in mouse islets and rats
James E. Bowe,Aileen King,J. S. Kinsey-Jones,Victoria L. Foot,Xiao Feng Li,Kevin T. O'Byrne,Shanta J. Persaud,Peter M. Jones +7 more
TL;DR: The observations suggest that neither typical protein kinase C isoforms nor p38 MAPK are involved in the potentiation of glucose-induced insulin release by kisspeptin, but intracellular signalling pathways involving phospholipase C, p42/44 MAPK and increased [Ca2+]i are required for the stimulatory effects on insulin secretion.
Expression and function of cannabinoid receptors in mouse islets
TL;DR: Investigation of cannabinoid receptor expression by mouse islet β-and α-cells and the effects of selective receptor agonists on cyclic AMP and calcium levels, and on dynamic insulin secretory responses found that mouse islets expressed both CB1 and CB2 receptors, and they were localised to β-cells.
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