Literature DB >> 19851097

Increasing intravenous glucose load in the presence of normoglycemia: effect on outcome and metabolism in critically ill rabbits.

Sarah Derde1, Ilse Vanhorebeek, Eric-Jan Ververs, Ine Vanhees, Veerle M Darras, Erik Van Herck, Lars Larsson, Greet Van den Berghe.   

Abstract

OBJECTIVES: Endocrine disturbances and a feeding-resistant wasting syndrome, characterized by a negative protein balance, promote delayed recovery and poor outcome of critical illness. Parenteral nutrition alone cannot counteract the hypercatabolic state, possibly in part as a result of aggravation of the hyperglycemic response to illness. In critically ill rabbits, we investigated the impact of varying amounts of intravenous glucose while maintaining normoglycemia on mortality, organ damage, and markers of catabolism/anabolism.
DESIGN: Prospective, randomized laboratory investigation.
SETTING: University animal and molecular laboratory.
SUBJECTS: Three-month-old male rabbits.
INTERVENTIONS: Critically ill rabbits were randomized into a fasting group, a standard parenteral nutrition group, and two groups receiving either intermediate or high additional physiological amounts of intravenous glucose while maintained normoglycemic with insulin. These groups were compared with a hyperglycemic group and healthy rabbits. Protein and lipid load was equal for all fed groups.
MEASUREMENTS AND MAIN RESULTS: Varying intravenous glucose load did not affect mortality or organ damage provided hyperglycemia was prevented. Fasted critically ill rabbits lost weight, which was attenuated by increasing intravenous glucose load. As compared with healthy rabbits, mRNA expression and/or activity of several ubiquitin-proteasome pathway components, cathepsin-L and calpain-1, was elevated in skeletal muscle of fasted critically ill rabbits. Intravenous feeding was able to counteract this response. Excessive glucose load and/or hyperglycemia, however, reduced the protective effect of feeding. Genes investigated in the diaphragm and myocardium revealed roughly a similar response. Except in the normoglycemic group with intermediate glucose load, circulating thyroid hormone and insulin-like growth factor-1 levels decreased, most pronounced in hyperglycemic rabbits.
CONCLUSIONS: Increasing intravenous glucose infusion within the physiological range, while maintaining normoglycemia, was safe for organ function and survival of critically ill rabbits. Concomitantly, it reduced the catabolic responses as compared with fasting. Whether this has a beneficial effect on muscle function and mass remains to be investigated.

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Year:  2010        PMID: 19851097     DOI: 10.1097/CCM.0b013e3181c03f65

Source DB:  PubMed          Journal:  Crit Care Med        ISSN: 0090-3493            Impact factor:   7.598


  9 in total

1.  Blood glucose control in the ICU: don't throw out the baby with the bathwater!

Authors:  Jan Gunst; Greet Van den Berghe
Journal:  Intensive Care Med       Date:  2016-05-09       Impact factor: 17.440

Review 2.  The Sick and the Weak: Neuropathies/Myopathies in the Critically Ill.

Authors:  O Friedrich; M B Reid; G Van den Berghe; I Vanhorebeek; G Hermans; M M Rich; L Larsson
Journal:  Physiol Rev       Date:  2015-07       Impact factor: 37.312

3.  Short acting insulin analogues in intensive care unit patients.

Authors:  Federico Bilotta; Carolina Guerra; Rafael Badenes; Simona Lolli; Giovanni Rosa
Journal:  World J Diabetes       Date:  2014-06-15

4.  Impact of early parenteral nutrition on metabolism and kidney injury.

Authors:  Jan Gunst; Ilse Vanhorebeek; Michaël P Casaer; Greet Hermans; Pieter J Wouters; Jasperina Dubois; Kathleen Claes; Miet Schetz; Greet Van den Berghe
Journal:  J Am Soc Nephrol       Date:  2013-03-28       Impact factor: 10.121

Review 5.  Critical Care Management of Stress-Induced Hyperglycemia.

Authors:  Ilse Vanhorebeek; Jan Gunst; Greet Van den Berghe
Journal:  Curr Diab Rep       Date:  2018-02-26       Impact factor: 4.810

6.  Impact of early parenteral nutrition completing enteral nutrition in adult critically ill patients (EPaNIC trial): a study protocol and statistical analysis plan for a randomized controlled trial.

Authors:  Michaël P Casaer; Greet Hermans; Alexander Wilmer; Greet Van den Berghe
Journal:  Trials       Date:  2011-01-24       Impact factor: 2.279

7.  Premorbid obesity, but not nutrition, prevents critical illness-induced muscle wasting and weakness.

Authors:  Chloë Goossens; Mirna Bastos Marques; Sarah Derde; Sarah Vander Perre; Thomas Dufour; Steven E Thiessen; Fabian Güiza; Thomas Janssens; Greet Hermans; Ilse Vanhorebeek; Katrien De Bock; Greet Van den Berghe; Lies Langouche
Journal:  J Cachexia Sarcopenia Muscle       Date:  2016-07-20       Impact factor: 12.910

8.  The Effect of Nutritional Status in the Pathogenesis of Critical Illness Myopathy (CIM).

Authors:  Hannah Ogilvie; Lars Larsson
Journal:  Biology (Basel)       Date:  2014-05-30

9.  Hyperglycemia-induced diaphragm weakness is mediated by oxidative stress.

Authors:  Leigh A Callahan; Gerald S Supinski
Journal:  Crit Care       Date:  2014-05-03       Impact factor: 9.097

  9 in total

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