Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654.
In fed rat livers perfused with [1-14C]oleic acid, Ro 22-0654 (4-amino-5-ethyl-3-thiophenecarboxylic acid methyl ester hydrochloride), an inhibitor of fatty acid synthesis, activated ketogenesis and decreased the secretion of triglyceride in very low density lipoproteins (VLDL). Ro 22-0654 was witho...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
1985-10-01
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| Series: | Journal of Lipid Research |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S002222752034267X |
| _version_ | 1818672247208935424 |
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| author | M Yamamoto N Fukuda J Triscari A C Sullivan J A Ontko |
| author_facet | M Yamamoto N Fukuda J Triscari A C Sullivan J A Ontko |
| author_sort | M Yamamoto |
| collection | DOAJ |
| description | In fed rat livers perfused with [1-14C]oleic acid, Ro 22-0654 (4-amino-5-ethyl-3-thiophenecarboxylic acid methyl ester hydrochloride), an inhibitor of fatty acid synthesis, activated ketogenesis and decreased the secretion of triglyceride in very low density lipoproteins (VLDL). Ro 22-0654 was without effect on total oleic acid uptake and utilization by the liver. The liver triglyceride content, urea synthesis, and bile production were also unaffected. Ro 22-0654 increased the conversion of both exogenous and endogenous fatty acid substrates to ketone bodies, while decreasing the secretion of triglyceride synthesized from both of these sources. Depressed fatty acid synthesis accounted for a relatively small portion of the decrease in secretory triglyceride derived from endogenous sources. 14CO2 from [1-14C]oleic acid was unchanged by Ro 22-0654. This drug decreased the malonyl-CoA content of rat liver freeze-clamped in vivo, providing an explicable mechanism for its activation of fatty acid oxidation. Hepatic citrate was also diminished. The present studies indicate the following sequence of events in the liver of fed rats following the administration of Ro 22-0654: decreased formation of citrate and malonyl-CoA, decreased fatty acid synthesis via decreased carbon supply and increased fatty acid oxidation via stimulation of acylcarnitine formation, decreased synthesis of triglyceride from both endogenous and exogenous fatty acids, resulting in the decreased formation and secretion of VLDL. |
| first_indexed | 2024-12-17T07:36:52Z |
| format | Article |
| id | doaj.art-44afc60e43fa4d1bb178b3d295c5563d |
| institution | Directory Open Access Journal |
| issn | 0022-2275 |
| language | English |
| last_indexed | 2024-12-17T07:36:52Z |
| publishDate | 1985-10-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Journal of Lipid Research |
| spelling | doaj.art-44afc60e43fa4d1bb178b3d295c5563d2022-12-21T21:58:18ZengElsevierJournal of Lipid Research0022-22751985-10-01261011961204Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654.M YamamotoN FukudaJ TriscariA C SullivanJ A OntkoIn fed rat livers perfused with [1-14C]oleic acid, Ro 22-0654 (4-amino-5-ethyl-3-thiophenecarboxylic acid methyl ester hydrochloride), an inhibitor of fatty acid synthesis, activated ketogenesis and decreased the secretion of triglyceride in very low density lipoproteins (VLDL). Ro 22-0654 was without effect on total oleic acid uptake and utilization by the liver. The liver triglyceride content, urea synthesis, and bile production were also unaffected. Ro 22-0654 increased the conversion of both exogenous and endogenous fatty acid substrates to ketone bodies, while decreasing the secretion of triglyceride synthesized from both of these sources. Depressed fatty acid synthesis accounted for a relatively small portion of the decrease in secretory triglyceride derived from endogenous sources. 14CO2 from [1-14C]oleic acid was unchanged by Ro 22-0654. This drug decreased the malonyl-CoA content of rat liver freeze-clamped in vivo, providing an explicable mechanism for its activation of fatty acid oxidation. Hepatic citrate was also diminished. The present studies indicate the following sequence of events in the liver of fed rats following the administration of Ro 22-0654: decreased formation of citrate and malonyl-CoA, decreased fatty acid synthesis via decreased carbon supply and increased fatty acid oxidation via stimulation of acylcarnitine formation, decreased synthesis of triglyceride from both endogenous and exogenous fatty acids, resulting in the decreased formation and secretion of VLDL.http://www.sciencedirect.com/science/article/pii/S002222752034267X |
| spellingShingle | M Yamamoto N Fukuda J Triscari A C Sullivan J A Ontko Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654. Journal of Lipid Research |
| title | Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654. |
| title_full | Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654. |
| title_fullStr | Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654. |
| title_full_unstemmed | Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654. |
| title_short | Decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by Ro 22-0654. |
| title_sort | decreased hepatic production of very low density lipoproteins following activation of fatty acid oxidation by ro 22 0654 |
| url | http://www.sciencedirect.com/science/article/pii/S002222752034267X |
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