Adrenal Steroid

Adrenal Steroid Laboratory

Group Head: Professor Mark Cooper

About the Laboratory:

 

The adrenal glands make steroid hormones that are critical to survival and play essential roles in the way the body responds to stress. Adrenal hormones regulate blood pressure and have effects on almost all tissues in the body. Prominent features that develop when too much of these adrenal steroids are produced include bone and muscle loss, skin thinning, obesity, high blood pressure and suppression of the immune system. These features are very common in the population even when the level of adrenal steroids is normal in the circulation. However, we have found that some of these people have an excessive level of these steroids within their tissues due to local production.

In the Adrenal Steroid Lab we examine the role of adrenal steroids in these common conditions.

Research Areas:
People:
people_mcooper

Prof Mark S Cooper (BMBCh, PhD, FRCP(London), FRACP)
Professor of Medicine
ANZAC Research Institute
Concord Repatriation General Hospital

  

Mark Cooper studied Physiology and Medicine at the University of Oxford, UK. Specialist training in Endocrinology and General Medicine was at the University of Birmingham, UK where he also completed a PhD in Medical Sciences. At the beginning of 2013 he moved to Sydney to take up the position of the Professor of Medicine at Concord Repatriation General Hospital. In 2011 he was awarded the Bertram Abrahams Lectureship in Physiology at the Royal College of Physicians of London. He collaborates extensively with other research groups within the ANZAC Research Institute and also with the endocrinology, respiratory and rheumatology research groups at the University of Birmingham where he is an Honorary Senior Research Fellow.

people_jtu

Dr Jinwen Tu (PhD)
Research Fellow
ANZAC Research Institute
Concord Repatriation General Hospital

Dr Jinwen Tu obtained her PhD (Biomedicine) in 2014 from the University of Sydney. Prior to this she completed her Master’s project investigating osteoinductivity of mesenchymal stem cells on a novel scaffold using mouse and rabbit’s models. Her PhD thesis work investigated the effects that the body’s own glucocorticoids have on chondrocytes, the cells that line the surface of our joints. She has explored the effects of glucocorticoids on normal cartilage and bone development, as well as in conditions such as fracture healing and arthritis. This work indicates that chondrocytes have important functions that were not predicted previously but could be targeted therapeutically. Dr Jinwen Tu joined the Adrenal Steroid Lab in October 2013. Since then, she has examined the role and regulation of local steroid production in the development and persistence of rheumatoid arthritis, including its possible role in bone and cartilage damage during joint inflammation.

Research:

1. The role of local steroid production in post-menopausal osteoporosis

Although it has been known for many decades that high levels of cortisol (anti-inflammatory steroids) can cause bone loss, Prof Cooper was first to demonstrate that high local production of cortisol within bone tissue could account for age-related bone loss. These studies have led to a phase II clinical trial studying the effectiveness of a chemical inhibitor of the steroid producing enzyme in post-menopausal women with low bone density.

  • Dr Jinwen Tu
  • Prof Mark Cooper

References:
 Tiganescu A, Tahrani AA, Morgan SA, Otranto M, Desmoulière A, Abrahams L, Hassan-Smith Z, Walker EA, Rabbitt EH, Cooper MS, Amrein K, Lavery GG, Stewart PM. 11-Hydroxysteroid dehydrogenase blockade prevents age-induced skin structure and function defects. J Clin Invest. 2013 Jul 1;123(7):3051-60.
 Hardy R, Cooper MS. Glucocorticoid-induced osteoporosis – a disorder of mesenchymal stromal cells? Frontiers in Endocrinology 2011 2:24
 Cooper MS, Walker EA, Bland R, Fraser WD, Hewison M, Stewart PM. Expression and functional consequences of 11-hydroxysteroid dehydrogenase activity in human bone. Bone 2000; 27:375-81

2. The role of local steroid production in the development and persistence of rheumatoid arthritis

Anti-inflammatory steroids have been used since the 1950s as treatments for rheumatoid arthritis (RA). Defects in the body’s own production of steroids have also been implicated in the development or persistence of RA but the exact nature of these abnormalities has been difficult to define. In association with rheumatology colleagues at the University of Birmingham we have shown that active steroids are generated in large amounts within the inflamed joint. Although this local production can reduce the amount of inflammation within the joint it is unclear if this is a help or a hindrance in the resolution of inflammatory arthritis. This is an important question to answer since it might allow us to develop ways of switching off arthritis before it becomes persistent.

  • Dr Jinwen Tu
  • Prof Mark Cooper

References:
 Nanus DE, Filer AD, Hughes B, Fisher BA, Taylor PC, Stewart PM, Buckley CD, McInnes I, Cooper MS, Raza K. TNFα regulates cortisol metabolism in vivo in patients with inflammatory arthritis. Ann Rheum Dis. 2014 Jan 2. [Epub ahead of print]
 Kaur K, Hardy R, Ahasan MM, Eijken M, van Leeuwen JP, Filer A, Thomas AM, Raza K, Buckley CD, Stewart PM, Rabbitt EH, Hewison M, Cooper MS. Synergistic induction of local glucocorticoid generation by inflammatory cytokines and glucocorticoids: implications for inflammation associated bone loss. Annals of the Rheumatic Diseases. 2010 69:1185-90
 Hardy RS, Rabbitt EH, Filer A, Emery P, Hewison M, Stewart PM, Gittoes N, Buckley CD, Raza K, Cooper MS. Local and systemic glucocorticoid metabolism in inflammatory arthritis. Annals of the Rheumatic Diseases. 2008 67:1204-10

3. The role of local steroid production in bone and cartilage damage during joint inflammation

Bone loss is very common in people with joint disease and contributes significantly to long-term disability. We have shown that osteoblasts make anti-inflammatory steroids during inflammation and that this production is likely to be a major factor in inflammation-associated bone loss. Cartilage is the joint lining tissue and is made by a specialised type of cell called the chondrocyte. These cells are very sensitive to the effects of glucocorticoids. We have previously shown that cells that are closely related to chondrocytes and chondrocytes themselves have the capacity to generate glucocorticoids. In association with Hong Zhou and Markus Seibel at the ANZAC Research Institute we are exploring whether this regulation is important in normal cartilage function and the response of cartilage to joint inflammation.

  • Dr Jinwen Tu
  • Prof Mark Cooper

References:
 Hardy R, Juarez M, Naylor A, Tu J, Rabbitt EH, Filer A, Stewart PM, Buckley CD, Raza K, Cooper MS. Synovial DKK1 expression is regulated by local glucocorticoid metabolism in inflammatory arthritis. Arthritis Research and Therapy 2012 Oct 18; 14:R226
 de Pablo P, Cooper MS, Buckley CD. Association between bone mineral density and C-reactive protein in a large population-based sample. Arthritis and Rheumatism 2012 64(8):2624-31
 Kaur K, Hardy R, Ahasan MM, Eijken M, van Leeuwen JP, Filer A, Thomas AM, Raza K, Buckley CD, Stewart PM, Rabbitt EH, Hewison M, Cooper MS. Synergistic induction of local glucocorticoid generation by inflammatory cytokines and glucocorticoids: implications for inflammation associated bone loss. Annals of the Rheumatic Diseases 2010 69:1185-90

4. The endocrinology of critical illness

During severe illness there are many changes in the level of adrenal steroids and other hormones. These changes appear to be important in the body’s ability to survive the severe stress of major illness. In collaboration with the University of Birmingham we are currently examining aspects of the body’s response to critical illness and the implications that this has in severe sepsis and acute lung injury.

  • Prof Mark Cooper

References:
 Cooper MS, Thickett DR, Stewart PM. Reduced cortisol metabolism during critical illness. N Engl J Med. 2013 Aug 1;369(5):480.
 Parek D, Dancer RC, Lax S, Cooper MS, Martineau AR, Fraser WD, Tucker O, Alderson D, Perkins GD, Gao-Smith F, Thickett DR. Vitamin D to prevent acute lung injury following oesophagectomy (VINDALOO): study protocol for a randomised placebo controlled trial. Trials 2013 14:100
 Cooper MS, Stewart PM. Corticosteroid insufficiency in acutely ill patients. New England Journal of Medicine 2003; 348:727-34

5. The role of glucocorticoid metabolism in osteosarcoma

Osteosarcoma is the commonest primary bone cancer in children and adolescents. We have demonstrated that these tumour cells can break down anti-inflammatory adrenal steroids and thus become resistant to their effects. We are currently determining the clinical importance of this effect and whether preventing this break down of steroids might lead to better outcomes in osteosarcoma.

  • Dr Jinwen Tu
  • Prof Mark Cooper

References:
 Patel P, Hardy R, Sumathi V, Bartle G, Kindblom LG, Grimer R, Bujalska I, Stewart PM, Rabbitt E, Gittoes N, Cooper MS. Expression of 11-Hydroxysteroid dehydrogenase enzymes in human osteosarcoma: Potential role in pathogenesis and as targets for treatments. Endocrine-Related Cancer 2012 19:589-98
 Rabbitt EH, Lavery GG, Walker EA, Cooper MS, Stewart PM, Hewison M. Pre-receptor regulation of glucocorticoid action by 11-hydroxysteroid dehydrogenase: a novel determinant of cell proliferation. FASEB Journal 2002; 16:36-44

Selected Publications:
  • Cooper MC, Seibel MJ, Zhou H Glucocorticoids, bone and energy metabolism Bone 2015 [Epub ahead of print]. 2015 26051468
  • Dancer RC, Parekh D, Lax S, D’Souza V, Zheng S, Bassford CR, Park D, Bartis DG, Mahida R, Turner AM, Sapey E, Wei W, Naidu B, Stewart PM, Fraser WD, Christopher KB, Cooper M.S, Gao F,Sansom DM, Martineau AR, Perkins GD, Thickett DR. Vitamin D deficiency contributes directly to the acute respiratory distress syndrome (ARDS). Thorax (2015) 70 617 – 624 2015 25903964
  • Nanus DE, Filer AD, Hughes B, Fisher BA, Taylor PC, Stewart PM, Buckley CD, McInnes I, Cooper MS and Raza K TNFalpha regulates cortisol metabolism in vivo in patients with inflammatory arthritis. Ann Rheum Dis 74 (2): 464-469, 2015. 2015 24385202
  • Nanus DE, Filer AD, Yeo L, Scheel-Toellner D, Hardy R, Lavery GG, Stewart PM, Buckley CD, Tomlinson JW, Cooper MS and Raza K Differential glucocorticoid metabolism in patients with persistent versus resolving inflammatory arthritis. Arthritis Res Ther 17 (1): 121, 2015. 2015 25971255
  • Venkatesh B, Cohen J, Cooper M. Ten false beliefs about cortisol in critically ill patients Intensive Care Medicine (2015) 41(10):1817-9. doi: 10.1007/s00134-014-3635-7 2015 25605468