Labelled ketone bodies were produced readily from [U−14C]palmitate, [2−14C]palmitate and [1−14C]glycerol by sheep rumen-epithelial and liver tissues in vitro. On a tissue-nitrogen basis, both tissues had similar capacities for ketogenesis. Palmitate was a ketogenic substrate in both rumen-epithelial tissue and liver, and more of its 14C appeared in ketone bodies than in the 14CO2 liberated. Glycerol was actively metabolized to ketone bodies, but more readily underwent complete oxidation to carbon dioxide; this complete oxidation was most pronounced in rumen-epithelial tissue from ketotic ewes. These experiments with labelled compounds confirm earlier observations that rumen-epithelial tissue, like liver, actively forms ketone bodies from long-chain fatty acids and show further that normal rumen-epithelial tissue can convert palmitate into ketone bodies as readily as into carbon dioxide. Free glycerol, which is metabolized only by liver tissue in non-ruminants, is also metabolized by rumen epithelium. The rumen epithelium thus has unique metabolic capacity among extrahepatic tissues.
Skip Nav Destination
Follow us on Twitter @Biochem_Journal
Article navigation
January 1968
-
Cover Image
Cover Image
- PDF Icon PDF LinkTable of Contents
- PDF Icon PDF LinkEditorial Board
Research Article|
January 01 1968
Formation of ketone bodies from [14C]palmitate and [14C]glycerol by tissues from ketotic sheep
J. A. Taylor;
J. A. Taylor
1Departments of Biochemistry and of Veterinary Physiology and Pharmacology, Purdue University, Lafayette, Ind. 47907, U.S.A.
Search for other works by this author on:
H. D. Jackson
H. D. Jackson
1Departments of Biochemistry and of Veterinary Physiology and Pharmacology, Purdue University, Lafayette, Ind. 47907, U.S.A.
Search for other works by this author on:
Publisher: Portland Press Ltd
© 1968 The Biochemical Society
1968
Biochem J (1968) 106 (1): 289–292.
Citation
J. A. Taylor, H. D. Jackson; Formation of ketone bodies from [14C]palmitate and [14C]glycerol by tissues from ketotic sheep. Biochem J 1 January 1968; 106 (1): 289–292. doi: https://doi.org/10.1042/bj1060289
Download citation file:
Sign in
Don't already have an account? Register
Sign in to your personal account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Biochemical Society Member Sign in
Sign InSign in via your Institution
Sign in via your InstitutionGet Access To This Article
Cited By
Follow us on Twitter @Biochem_Journal
Open Access for all
We offer compliant routes for all authors from 2025. With library support, there will be no author nor reader charges in 5 journals. Check here |
![]() View past webinars > |