Effects of serine palmitoyltransferase inhibition by myriocin in ad libitum-fed and nutrient-restricted ewes.


Journal

Journal of animal science
ISSN: 1525-3163
Titre abrégé: J Anim Sci
Pays: United States
ID NLM: 8003002

Informations de publication

Date de publication:
01 Aug 2021
Historique:
received: 08 04 2021
accepted: 27 07 2021
pubmed: 30 7 2021
medline: 7 9 2021
entrez: 29 7 2021
Statut: ppublish

Résumé

The fungal isolate myriocin inhibits serine palmitoyltransferase and de novo ceramide synthesis in rodents; however, the effects of myriocin on ceramide concentrations and metabolism have not been previously investigated in ruminants. In our study, 12 non-lactating crossbred ewes received an intravenous bolus of myriocin (0, 0.1, 0.3, or 1.0 mg/kg/body weight [BW]; CON, LOW, MOD, or HIGH) every 48 h for 17 d. Ewes consumed a high-energy diet from day 1 to 14 and were nutrient-restricted (straw only) from day 15 to 17. Blood was collected preprandial and at 1, 6, and 12 h relative to bolus and nutrient restriction. Tissues were collected following euthanasia on day 17. Plasma was analyzed for free fatty acids (FFAs), glucose, and insulin. Plasma and tissue ceramides were quantified using mass spectrometry. HIGH selectively decreased metabolizable energy intake, BW, and plasma insulin, and increased plasma FFA (Dose, P < 0.05). Myriocin linearly decreased plasma very-long-chain (VLC) ceramide and dihydroceramide (DHCer) by day 13 (Linear, P < 0.05). During nutrient restriction, fold-change in FFA was lower with increasing dose (P < 0.05). Nutrient restriction increased plasma C16:0-Cer, an effect suppressed by MOD and HIGH (Dose × Time, P < 0.05). Myriocin linearly decreased most ceramide and DHCer species in the liver and omental and mesenteric adipose, VLC ceramide and DHCer in the pancreas, and C18:0-Cer in skeletal muscle and subcutaneous adipose tissue (Linear, P ≤ 0.05). We conclude that the intravenous delivery of 0.3 mg of myriocin/kg of BW/48 h decreases circulating and tissue ceramide without modifying energy intake in ruminants.

Identifiants

pubmed: 34324668
pii: 6330562
doi: 10.1093/jas/skab221
pmc: PMC8378221
pii:
doi:

Substances chimiques

Ceramides 0
Fatty Acids, Monounsaturated 0
Insulin 0
Serine C-Palmitoyltransferase EC 2.3.1.50
thermozymocidin YRM4E8R9ST

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : U.S. Department of Agriculture
ID : USDA-2016-67015-24582
Organisme : National Science Foundation
ID : DGE-1650441

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Amanda N Davis (AN)

Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.
Biological Sciences Department, State University of New York College at Cortland, Cortland, NY 13045, USA.

William A Myers (WA)

Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.

Jorge Eduardo Rico (J)

Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.

Lin Feng Wang (L)

Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.
College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zengzhou 450002, China.

Crystal Chang (C)

Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.

Andrew T Richards (AT)

Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.

Mohammed Moniruzzaman (M)

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

Norman J Haughey (NJ)

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

Joseph W McFadden (JW)

Department of Animal Science, Cornell University, Ithaca, NY 14853, USA.

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Classifications MeSH