Cited by 82Nutrition and Health in AgingClinical Nutrition and GastroenterologyCancer, Lipids, and Metabolism

Whole-body lipolysis and triglyceride-fatty acid cycling in cachectic patients with esophageal cancer.

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Klein, S, Wolfe, R R·1990·Journal of Clinical Investigation

Abstract

Whole-body lipolytic rates and the rate of triglyceride-fatty acid cycling (reesterification of fatty acids released during lipolysis) were measured with stable isotopic tracers in the basal state and during beta-adrenergic blockade with propranolol infusion in five cachectic patients with squamous cell carcinoma of the esophagus, five cachectic cancer-free, nutritionally-matched control patients, and 10 healthy volunteers. Resting energy expenditure and plasma catecholamines were normal in all three groups. The basal rate of glycerol appearance in blood in the patients with cancer (2.96 +/- 0.45 mumol.kg-1.min-1) was similar to that in the nutritionally matched controls (3.07 +/- 0.28 mumol.kg-1.min-1), but 48% greater than in the normal-weight volunteers (2.00 +/- 0.16 mumol.kg-1.min-1) (P = 0.028). The antilipolytic effect of propranolol and the rate of triglyceride-fatty acid cycling in the patients with cancer were also similar in the cachectic control group and approximately 50% greater than in the normal-weight volunteers, but the differences were not statistically significant because of the variability in the data. We conclude that the increase in lipolysis and triglyceride-fatty acid cycling in "unstressed" cachectic patients with esophageal cancer is due to alterations in their nutritional status rather than the presence of tumor itself. Increased beta-adrenergic activity may be an important contributor to the stimulation of lipolysis.

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  • Triglyceride/fatty acid cycling is involved in the thermogenesis associated with burn injuries, cancer cachexia, and after exercise.

    “This cycling is involved in the thermogenesis associated with burn injuries 26, cancer cachexia 27, and after exercise 28.”

    From Cellular bioenergetics as a target for obesity therapy (2010) · cites this paper as [27]

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Authors
Klein, S., & Wolfe, R. R.
Affiliations
  • The University of Texas Medical Branch at Galveston (US)
  • Shriners Hospitals for Children - Galveston (US)
Venue
Journal of Clinical Investigation
Published
1990-11-01
Volume
86
Issue
5
Pages
1403-1408
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2015843414
Cited by
82
References
45
Citations by year
2025: 1 · 2024: 1 · 2023: 1 · 2022: 2 · 2021: 2 · 2020: 2 · 2019: 2 · 2018: 5 · 2017: 3 · 2016: 1 · 2015: 2 · 2014: 3 · 2013: 3 · 2012: 3
FWCI
1.62
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Investigation (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • American Institute for Cancer Research
  • American Gastroenterological Association
  • National Institutes of Health (5r29ca050330-05, RR-00073)
  • National Cancer Institute (CA 50330)
  • National Institute of Diabetes and Digestive and Kidney Diseases (DK-38010, R01DK038010)
  • National Center for Research Resources (RR 00073, M01RR000073)
Topics
  • Health Sciences › Medicine › Physiology › Nutrition and Health in Aging
  • Health Sciences › Nursing › Nutrition and Dietetics › Clinical Nutrition and Gastroenterology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Lipids, and Metabolism
Keywords
fatty acid re-esterification, cancer cachexia, esophageal squamous cell carcinoma, propranolol, beta-adrenergic blockade, beta-adrenergic activity, nutritional status
MeSH terms
Adult, Aged, Cachexia, Carcinoma, Squamous Cell, Esophageal Neoplasms, Fatty Acids, Female, Glycerol, Humans, Lipolysis, Male, Middle Aged, Propranolol, Triglycerides

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