Vascular and metabolic effects of the haem oxygenase-1 inducer haem arginate in subjects with the metabolic syndrome: A translational cross-over study

Publication date

2016-01-01

Authors

Dekker, DouweISNI 0000000396416926
Dorresteijn, Mirrin J.
Peters, Wilbert H M
Bilos, Albert
Pennings, Sebastiaan W C
Wagener, Frank Adtg
Smits, Paul

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Abstract

This translational randomized and vehicle-controlled cross-over study was performed to assess the impact of haem arginate treatment on haem oxygenase-1 induction, endothelial function and insulin sensitivity in subjects with the metabolic syndrome (n = 14). Both treatment periods consisted of 5 days. Haem arginate or vehicle (l-arginine) was administered intravenously on Days 1 and 3. Forearm blood flow in response to acetylcholine and nitroglycerine was measured by venous occlusion plethysmography (Day 3), insulin sensitivity by a hyperinsulinaemic clamp procedure (Day 5). Haem arginate did not improve endothelial function or insulin sensitivity but significantly reduced the vasodilator response to nitroglycerine (p < 0.01). These negative findings are in contrast to the preclinical data, which may be due to short duration of therapy and limited haem oxygenase-1 induction as well as interference by markedly elevated plasma haem levels observed after haem arginate treatment (p < 0.01). Future studies should pay attention to the delicate balance between sufficient dosing and timely normalization of plasma haem levels.

Keywords

endothelial function, haem arginate, haem oxygenase, insulin resistance, metabolic syndrome, Translational medical research, Endocrinology, Diabetes and Metabolism, Internal Medicine, Cardiology and Cardiovascular Medicine, Journal Article, Research Support, Non-U.S. Gov't

Citation

Dekker, D, Dorresteijn, M J, Peters, W H M, Bilos, A, Pennings, S W C, Wagener, F A & Smits, P 2016, 'Vascular and metabolic effects of the haem oxygenase-1 inducer haem arginate in subjects with the metabolic syndrome : A translational cross-over study', Diabetes and Vascular Disease Research, vol. 13, no. 1, pp. 41-48. https://doi.org/10.1177/1479164115605047