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Muscle carnitine availability plays a central role in regulating fuel metabolism in the rodent

Porter, Craig; Constantin-Teodosiu, Dumitru; Constantin, Despina; Leighton, Brendan; Poucher, Simon M.; Greenhaff, Paul L.

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Authors

Craig Porter

Dumitru Constantin-Teodosiu

Despina Constantin

Brendan Leighton

Simon M. Poucher

PAUL GREENHAFF PAUL.GREENHAFF@NOTTINGHAM.AC.UK
Professor of Muscle Metabolism



Abstract

The body carnitine pool is primarily confined to skeletal muscle, where it regulates carbohydrate (CHO) and fat usage. Mildronate (3-(2,2,2-trimethylhydrazinium)-propionate) inhibits carnitine synthesis and tissue uptake, but the impact of carnitine depletion on whole-body fuel selection, muscle fuel metabolism and its molecular regulation is under-investigated. Male lean Zucker rats received water (control, n=8) or mildronate-supplemented water (mildronate, n=8) for 10 days (1.6 g.kg-1 body mass (bm).day-1 day 1-2, 0.8 g.kg-1 bm.day-1 thereafter). From day 7-10, animals were housed in indirect calorimetry chambers after which soleus muscle and liver were harvested. Food and fluid intake, weight gain and physical activity levels were similar between groups from day 7-10. Compared to control, mildronate depleted muscle total carnitine (P<0.001) and all carnitine esters. Furthermore, whole-body fat oxidation was less (P<0.001) and CHO oxidation was greater (P<0.05) compared to control, whilst soleus and liver glycogen content were less (P<0.01 and P<0.01, respectively).

In a second study, male Wistar rats received water (n=8) or mildronate-supplemented water (n=8) as above, and kidney, heart, and EDL and soleus muscles were collected. Compared to control, mildronate depleted total carnitine content (all P<0.001), reduced carnitine transporter protein and glycogen content, and increased PDK4 mRNA abundance in heart, EDL, and soleus. 189 mRNAs regulating fuel selection were differentially expressed in soleus in mildronate vs control, and a number of cellular functions and pathways strongly associated with carnitine depletion were identified. Collectively, these data firmly support the premise that muscle carnitine availability is a primary regulator of fuel selection in vivo.

Citation

Porter, C., Constantin-Teodosiu, D., Constantin, D., Leighton, B., Poucher, S. M., & Greenhaff, P. L. (2017). Muscle carnitine availability plays a central role in regulating fuel metabolism in the rodent. Journal of Physiology, 595(17), 5765-5780. https://doi.org/10.1113/jp274415

Journal Article Type Article
Acceptance Date May 31, 2017
Online Publication Date Aug 30, 2017
Publication Date Sep 1, 2017
Deposit Date Jul 3, 2017
Publicly Available Date Aug 31, 2018
Journal Journal of Physiology
Print ISSN 0022-3751
Electronic ISSN 1469-7793
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 595
Issue 17
Pages 5765-5780
DOI https://doi.org/10.1113/jp274415
Keywords Physiology
Public URL https://nottingham-repository.worktribe.com/output/863867
Publisher URL https://physoc.onlinelibrary.wiley.com/doi/full/10.1113/JP274415
Additional Information This is the peer reviewed version of the article, which has been published in final form at https://physoc.onlinelibrary.wiley.com/doi/full/10.1113/JP274415. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Contract Date Jul 3, 2017