Whole-Body and Forearm Muscle Protein Metabolism in Patients With Acromegaly Before and After Treatment

Author:

Arlien-Søborg Mai C12ORCID,Dal Jakob134ORCID,Madsen Michael Alle1,Høgild Morten Lyng12ORCID,Pedersen Steen B5ORCID,Jessen Niels567ORCID,Jørgensen Jens O L12ORCID,Møller Niels12ORCID

Affiliation:

1. Department of Endocrinology and Internal Medicine, Aarhus University Hospital , Aarhus 8200 , Denmark

2. Medical Research Laboratory, Department of Clinical Medicine, Aarhus University Hospital , Aarhus 8200 , Denmark

3. Department of Endocrinology, Aalborg University Hospital , Aalborg 9000 , Denmark

4. Steno Diabetes Centre North, Aalborg University Hospital , Aalborg 9000 , Denmark

5. Steno Diabetes Centre, Department of endocrinology and Internal Medicine , Aarhus 8200 , Denmark

6. Department of Clinical Pharmacology, University of Aarhus , Aarhus 8200 , Denmark

7. Department of Biomedicine, Aarhus University , Aarhus 8200 , Denmark

Abstract

Abstract Background Active acromegaly is characterized by increased lean body mass, but the mechanisms underlying the protein anabolic effect are unclear. Aim To study if active acromegaly induces reversible changes in whole-body and skeletal muscle protein kinetics. Patients and Methods Eighteen patients with acromegaly were investigated before and 47 ± 10 weeks after disease control by surgery (n = 8) and/or medical treatment (n = 10). Labeled phenylalanine and tyrosine tracers were employed to assess whole-body and regional forearm muscle protein kinetics. Intramyocellular protein signaling was assessed in skeletal muscle biopsies, and whole-body dual-energy X-ray absorptiometry scan and indirect calorimetry assessed lean body mass (LBM) and resting energy expenditure, respectively. Results Disease control induced a 7% decrease in lean body mass (P < .000) and a 14% decrease in LBM-adjusted energy expenditure. Whole-body phenylalanine breakdown decreased after disease control (P = .005) accompanied by a decrease in the degradation of phenylalanine to tyrosine (P = .005) and a decrease in whole-body phenylalanine synthesis (P = .030). Skeletal muscle protein synthesis tended to decrease after disease control (P = .122), whereas the muscle protein breakdown (P = .437) and muscle protein loss were unaltered (P = .371). Unc-51 like autophagy activating kinase 1 phosphorylation, an activator of protein breakdown, increased after disease control (P = .042). Conclusions Active acromegaly represents a reversible high flux state in which both whole-body protein breakdown and synthesis are increased, whereas forearm muscle protein kinetics are unaltered. Future studies are needed to decipher the link between protein kinetics and the structure and function of the associated growth hormone-induced increase in lean body mass.

Funder

Independent Research Fund

Growth Innovation

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference55 articles.

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