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PMID: 10875926 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Reduced food intake and body weight in mice treated with fatty acid synthase inhibitors.

Science (New York, N.Y.) ·Vol. 288 ·No. 5475 ·2000-06-30 ·Pages 2379-81

Loftus TM, Jaworsky DE, Frehywot GL, Townsend CA, Ronnett GV, Lane MD, Kuhajda FP

Abstract

With the escalation of obesity-related disease, there is great interest in defining the mechanisms that control appetite and body weight. We have identified a link between anabolic energy metabolism and appetite control. Both systemic and intracerebroventricular treatment of mice with fatty acid synthase (FAS) inhibitors (cerulenin and a synthetic compound C75) led to inhibition of feeding and dramatic weight loss. C75 inhibited expression of the prophagic signal neuropeptide Y in the hypothalamus and acted in a leptin-independent manner that appears to be mediated by malonyl-coenzyme A. Thus, FAS may represent an important link in feeding regulation and may be a potential therapeutic target.

MeSH Terms
Acetyl-CoA Carboxylase/antagonists & inhibitors,metabolism Animals Appetite/drug effects Appetite Depressants/administration & dosage,chemical synthesis,pharmacology Cerulenin/pharmacology Dose-Response Relationship, Drug Eating/drug effects Enzyme Inhibitors/administration & dosage,chemical synthesis,pharmacology Fasting Fatty Acid Synthases/antagonists & inhibitors,metabolism Female Hypothalamus/drug effects,metabolism Injections, Intraventricular Leptin/metabolism Liver/drug effects,metabolism Male Malonyl Coenzyme A/metabolism Mice Mice, Inbred BALB C Neurons/drug effects,metabolism Neuropeptide Y/administration & dosage,genetics,metabolism,pharmacology RNA, Messenger/genetics,metabolism Weight Loss/drug effects
Chemicals
Appetite Depressants Enzyme Inhibitors Leptin Neuropeptide Y RNA, Messenger Cerulenin Malonyl Coenzyme A Fatty Acid Synthases Acetyl-CoA Carboxylase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Loftus T M
Department of Biological Chemistry, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Jaworsky D E
Frehywot G L
Townsend C A
Ronnett G V
Lane M D
Kuhajda F P
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
2000-06-30
Pages
2379-81
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIDCD NIH HHS · DC02979 · United States
NIDDK NIH HHS · DK09623 · United States
Corrections
CommentIn
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