Details

Autor(en) / Beteiligte

• Dillon, E.L
• Volpi, Elena
• Wolfe, Robert R
• Sinha, Sandeep
• Sanford, Arthur P
• Arrastia, Concepcion D
• Urban, Randall J
• Casperson, Shanon L
• Paddon-Jones, Douglas
• Sheffield-Moore, Melinda

Titel

Amino acid metabolism and inflammatory burden in ovarian cancer patients undergoing intense oncological therapy

Ist Teil von

• Clinical nutrition (Edinburgh, Scotland), 2007-12, Vol.26 (6), p.736-743

Ort / Verlag

Kidlington: Elsevier Ltd

Erscheinungsjahr

2007

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Summary Background & aims Cancer and oncological therapy are associated with a progressive physical deterioration, malnutrition, and enhanced inflammatory burden. Our considerable data showing the strong anabolic potential of amino acids (AA) led us to test whether AA can acutely stimulate muscle protein synthesis in cancer patients (CA) undergoing intense chemotherapy. Methods Mixed muscle fractional synthesis rate (FSR), rates of phenylalanine appearance and disappearance (Ra and Rd), and net phenylalanine balance (NB) were measured during a primed constant infusion of l -[ring-2 H5 ]phenylalanine. Blood and muscle tissue samples were collected in the basal state and following ingestion of 40 g of AA given in 30 mL boluses every 10 min for 3 h. Serum and tissue cytokines and NF-κB expression in skeletal muscle were measured and compared to normative, healthy older controls (OC). Results Skeletal muscle TNF-α, IL-6, and NF-κB were elevated in CA. FSR and model-derived protein synthesis (Rd) increased significantly from basal to AA (FSR: 0.052±0.009 vs. 0.120±0.008% h−1 , P <0.001; Rd: 23.1±4.1 vs. 36.4±5.0 nmol min−1 100 mL leg−1 , P ⩽0.05). Model-derived protein breakdown (Ra) remained unchanged from basal to AA. Phenylalanine NB improved from a negative basal value (−16±2) to zero (0.8±6 nmol min−1 100 ml leg−1 , P ⩽0.05) following AA. Conclusion Despite advanced cancer, ongoing therapy, and an enhanced inflammatory burden, AA were capable of acutely stimulating muscle protein synthesis in these patients.