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PMID: 6021210 Published · ppublish English Journal Article

Studies on lipolysis in human adipose cells.

The Journal of clinical investigation ·Vol. 46 ·No. 4 ·1967-04-00 ·Pages 621-9

Galton DJ, Bray GA

Abstract

Epinephrine stimulated lipolysis and the uptake of oxygen by subcutaneous adipose cells of man. When glucose-(14)C was present in the medium, its utilization was not increased by epinephrine, although lipolysis was accelerated. Insulin did not reduce the production of fatty acids that had been stimulated by epinephrine. The combination of human growth hormone and cortisol stimulated the production of fatty acids by isolated human adipose cells to a lesser extent than epinephrine. When human growth hormone or cortisol was used singly, or when bovine growth hormone was added in combination with cortisol, no effect on fatty acid production was observed. Furthermore, an acetone-dried preparation of human pituitary glands, which was shown to stimulate lipolysis in rat adipose cells, had no effect on fatty acid formation in human adipose cells. This suggested that the human pituitary gland contained no more potent lipolytic agents than growth hormone and was supported by the lack of response of human adipose cells to purified corticotropin.

MeSH Terms
Adipose Tissue/metabolism Adolescent Adult Aged Animals Carbon Isotopes Cattle Epinephrine/pharmacology Fatty Acids/analysis,biosynthesis Glucose/metabolism Growth Hormone/pharmacology Humans Hydrocortisone/pharmacology Insulin/pharmacology Lipids/biosynthesis Middle Aged Oxygen Consumption/drug effects Pituitary Gland/physiology Rats Swine
Chemicals
Carbon Isotopes Fatty Acids Insulin Lipids Growth Hormone Glucose Hydrocortisone Epinephrine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Galton D J
Bray G A
References (12)
12 references, click to expand
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1967-04-00
Pages
621-9
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC442046
Subset
IM
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