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Research article summary (published 28 Jul 2008):

Influences of levodopa on adipose tissue and skeletal muscle metabolism in patients with idiopathic Parkinson's disease.

Full Abstract

OBJECTIVE: The substantial weight loss in Parkinson's patients may be related to direct influences of levodopa treatment on fat mobilization/oxidation. We assessed systemic and local metabolic responses to levodopa/benserazide in patients with idiopathic Parkinson's disease. METHODS: We studied 10 Parkinson's disease patients and examined adipose tissue and skeletal muscle metabolism directly with microdialysis. We monitored dialysate concentrations of ethanol, glucose, lactate, pyruvate, and glycerol to assess tissue blood flow and metabolism before and after levodopa/benserazide intake. We also conducted in vitro studies on adipocytes from healthy women. RESULTS: Levodopa/benserazide increased serum levodopa, 3,4-dihydroxyphenylacetic acid (DOPAC), and norepinephrine (P < 0.01). Serum adipose tissue and skeletal muscle glycerol did not change or decreased. Adipose tissue glycerol was inversely correlated with serum levodopa concentrations (P < 0.05). In isolated adipocytes, levodopa attenuated isoproterenol-induced glycerol release (P < 0.05). CONCLUSION: Levodopa/benserazide elicits pronounced metabolic changes in both adipose tissue and skeletal muscle with a switch from lipid to carbohydrate metabolism. In adipose tissue, levodopa/benserazide failed to activate lipolysis. Therefore, we suggest that levodopa/benserazide does not induce fat wasting through direct and acute influences on adipose tissue metabolism.

 

Author information

Author/s: Adams, Frauke (F); Boschmann, Michael (M); Lobsien, Elmar (E); Kupsch, Andreas (A); Lipp, Axel (A); Franke, Gabriele (G); Leisse, Marie Charlotte (MC); Janke, Juergen (J); Gottschalk, Simone (S); Spranger, Joachim (J); Jordan, Jens (J);

Affiliation: Experimental and Clinical Research Center, A Cooperation with Max Delbrueck Center for Molecular Medicine, Charité Campus Buch, and HELIOS Klinikum, Berlin, Germany. Frauke.Adams(-atsign-)charite.de

Journal and publication information

Publication Type: Journal Article

Journal: European journal of clinical pharmacology (Eur J Clin Pharmacol), published in Germany. (Language: eng)

Reference: 2008-Sep; vol 64 (issue 9) : pp 863-70

Dates: Created 2008/09/02; Completed 2008/12/09;

PMID: 18665357, status: MEDLINE (last retrieved date: 2/18/2009)

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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Associated Chemicals: Antiparkinson Agents (0) ; Levodopa (0) ; Benserazide (322-35-0) ; Glycerol (56-81-5) ; Isoproterenol (7683-59-2)

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