Eur J Endocrinol
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DOI: 10.1530/EJE-08-0619
European Journal of Endocrinology, Vol 160, Issue 2, 249-255
Copyright © 2009 by European Society of Endocrinology
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CLINICAL STUDY

Skeletal muscle 11β hydroxysteroid dehydrogenase type 1 activity is upregulated following elective abdominal surgery

Christina Jang1,2, Varuni R Obeyesekere1, Frank P Alford1,2 and Warrick J Inder1,2

1 Department of Endocrinology and Diabetes, St Vincent's Hospital, Melbourne2 Department of Medicine, University of Melbourne 41 Victoria Parade, Fitzroy 3065, Australia

(Correspondence should be addressed to W J Inder; Email: winder{at}medstv.unimelb.edu.au)

Objective: Cortisol has been traditionally implicated in the causation of peri-operative skeletal muscle (SkM) insulin resistance, but cortisol levels return to normal within 72 h of surgery. Tissue cortisol bioactivity may be prolonged by local upregulation of the enzyme 11βHSD1. We aimed to investigate the changes of SkM 11βHSD1 enzyme activity and mRNA expression, relative to plasma cortisol, insulin and glucose levels following elective abdominal surgery.

Patients and design: Eight non-diabetic subjects (two male, six female) underwent serial plasma hormone sampling and muscle biopsy of vastus lateralis at baseline and on day 5 following elective laparoscopic cholecystectomy.

Methods: SkM 11βHSD1 and H6PDH mRNA levels were measured by quantitative RT-PCR and enzyme activity by % conversion of 3H cortisone to cortisol. Plasma glucose, insulin, free fatty acids (FFA), tumour necrosis factor-{alpha} and cortisol by standardised assays.

Results: Compared with baseline, SkM 11βHSD1 activity was significantly increased on day 5 after surgery (14.7±2.1 vs 20.4±3.2%, P=0.005). Neither 11βHSD1 nor H6PDH mRNA levels were altered after surgery. Plasma cortisol (P=0.027), FFA (P=0.01) and glucose (P=0.004) rose rapidly following surgery and had returned to baseline values by 24 h post-surgery. There was no significant change in plasma insulin.

Conclusions: This is the first study to demonstrate an upregulation of SkM 11βHSD1 activity in response to a physiological stressor. Sustained activation of this enzyme may increase tissue cortisol bioactivity.




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