Abstract | PURPOSE: The aim of this work was to assess the effect(s) of de novo ceramide synthesis inhibition on lipid metabolism in skeletal muscle tissue of type 1 diabetic rats. The latter seems to be of vital importance, since previous works have shown its positive influence on lipid metabolism and glucose homeostasis in the case of its counterpart - type 2 diabetes. MATERIALS/METHODS: The animals were randomly assigned to one of the following groups: C - control, M - myriocin ( ceramide de novo synthesis inhibitor), D - diabetes (induced by streptozotocin injections); D+M - diabetes+myriocin. We have evaluated intracellular concentration of key sphingolipid species, via chromatography (GC and HPLC), and the activity of their most important enzymes, using radiometric approach. The aforementioned assessments were evaluated in respect to the three different types of muscle tissue representing different spectra of muscle metabolism (soleus - oxidative, red gastrocnemious - oxidative-glycolytic, white gastrocnemious - glycolytic). RESULTS: CONCLUSIONS: In the light of the results ensuing from this study, it seems conceivable that the reduction of intramuscular ceramide production and accumulation could bestow an insulin-sensitizing effect. If so, then SPT inhibition could find potential future applications as a therapeutic intervention aimed to mitigate the effects of insulin resistance.
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Authors | Krzysztof Kurek, Marta Garbowska, Dominika M Ziembicka, Bartłomiej Łukaszuk, Jakub Rogowski, Adrian Chabowski, Jan Górski, Małgorzata Żendzian-Piotrowska |
Journal | Advances in medical sciences
(Adv Med Sci)
Vol. 62
Issue 1
Pg. 65-73
(Mar 2017)
ISSN: 1898-4002 [Electronic] Netherlands |
PMID | 28189121
(Publication Type: Journal Article)
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Copyright | Copyright © 2016 Medical University of Bialystok. Published by Elsevier B.V. All rights reserved. |
Chemical References |
- Ceramides
- Fatty Acids, Monounsaturated
- Immunosuppressive Agents
- Serine C-Palmitoyltransferase
- thermozymocidin
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Topics |
- Animals
- Ceramides
(metabolism)
- Diabetes Mellitus, Experimental
(drug therapy, metabolism, pathology)
- Diabetes Mellitus, Type 1
(drug therapy, metabolism, pathology)
- Fatty Acids, Monounsaturated
(pharmacology)
- Immunosuppressive Agents
(pharmacology)
- Insulin Resistance
- Lipid Metabolism
(drug effects)
- Male
- Muscle, Skeletal
(drug effects, metabolism)
- Rats
- Rats, Wistar
- Serine C-Palmitoyltransferase
(antagonists & inhibitors)
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