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Pathological and biochemical investigation of the effects of l-carnitine and gemfibrozil on peroxisome proliferator activated Receptors (PPARS) and lipidosis in rabbits on a high-fat diet

Year 2022, Volume: 7 Issue: 3, 346 - 360, 31.12.2022
https://doi.org/10.31797/vetbio.1136444

Abstract

Obesity and fatty liver is a widespread growing health problem in human with detrimental consequences that encouraged researchers to find ways to overcome it. In this study, gemfibrozil and L-carnitine were evaluated in prevention of obesity and hepatic lipidosis also the role of L-carnitine in avoiding side effects of gemfibrozil was investigated.
The study involved 56 New-Zealand Albino rabbits, divided into 2 main groups and then subdivided into 4 equal groups (n=7). The groups I (normal diet), II (normal diet+gemfibrozil), III (normal diet+L-carnitine) and IV (normal diet+gemfibrozil+L-carnitine) received normal diet and the groups V (fat rich diet), VI (fat rich diet+gemfibrozil), VII (fat rich diet+L-carnitine) and VIII (fat rich diet+gemfibrozil+L-carnitine) received fat rich diet for 8 weeks.
Animals were blood sampled and wieght weekly during the experiment and at the end of the experiment for determination of biochemical (HDL, High-density lipoproteins; LDL, Low-density lipoprotein; VLDL, Very low-density lipoprotein; ALT, Alanine amino transferase; AST, Aspartate aminotransferase; GGT, Gamma glutamyltransferase; GLDH, Glutamate lactate dehydrogenase; LDH, Lactate dehydrogenase) and oxidative stress (MDA, Malondialdehyde; GSH, Reduced gluthation; NO, Nitric oxide; SOD, Superoxide dismutase) parameters. All rabbits were euthanised for histopathological examination and for distrubition of Peroxisome proliferator activated receptors (PPARs) in tissues by immunohystochemistry.
Liver enzymes increased in fat rich diet group throughout the study. Addition of gemfibrozil and L-carnitin in fat rich diet resulted in statistically significant decreasein lipid profile when compared to those only received fat rich diet. Beta oxidation of fat rich diet group was significantly higher than that of groups additionally received gemfibrozil and L-carnitine. Immunohistochemistry revealed an increase in PPAR PPAR-α and β but not PPAR-γ expression in fat rich diet group. On the contrary L-carnitin administration did have any effect on tissue PPAR expression. PPAR-α expression differed between groups received gemfibrozil and fat rich diet and those did not. Fat rich diet increased MDA level while decreased GSH and catalase. Addition of gemfibrozil and L-carnitine to fat rich diet significantly decreased MDA level and increased antioxidants. The most marked macroscopy finding was abdominal fat increase in fat rich diet group (group V). On the other hand gemfibrozil administration resulted in significant abdominal fat decrease. Furthermore decreased abdominal fat was marked in gemfibrozil and L-carnitine given animals (group VIII) when compared to other groups.
In conclusion, gemfibrozil and L-carnitine administration alleviated abdominal and hepatic fattening and improved lipid profile. Gemfibrozil also caused a significant increase in PPAR-α expression in the liver. It may be of use in avoiding abdominal fat (obesity) due to high fat by use of gemfibrozil, a synthetic PPAR-a ligand, and L-carnitine.

Supporting Institution

This study was financially supported The Scientific and Technical Research Council of Turkey (Project Number 106 O 160).

Project Number

Project Number 106 O 160

Thanks

We sincerely thank The Scientific and Technical Research Council of Turkey as a study team for providing financial support.

References

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Year 2022, Volume: 7 Issue: 3, 346 - 360, 31.12.2022
https://doi.org/10.31797/vetbio.1136444

Abstract

Project Number

Project Number 106 O 160

References

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  • Akbiyik, F., Cinar, K., Demirpence, E., Ozsullu, T., Tunca, R., Haziroglu, R., Yurdaydın, C., Uzunalimoglu, O. & Bozkaya, H. (2007). Ligand-induced expression of peroxisome proliferator-activated receptor  and activation of fatty acid oxidation enzymes in fatty liver. European Journal of Clinical Investigation, 34, 429-435.
  • Ament, Z., West, J.A., Stanley, E., Ashmore, T., Roberts, L.D., Wright, J., Nicholls, A.W. & Griffin, J.L. (2016). PPAR-pan activation induces hepatic oxidative stress and lipidomic remodelling. Free Radical Biology and Medicine, 95, 357-368. doi:10.1016/j.freeradbiomed.2015.11.033
  • Arockia Rani, P.J. & Panneerselvam, C. (2001). Carnitine as a free radical scavenger in aging. Experimental Gerontology, 36, 1713-1726. doi: 10.1016/S0531-5565(01)00116-4
  • Atherton, H.J., Bailey, N.J., Zhang, W., Taylor, J., Major, H., Shockcor, J., Clarke, K. & Griffin, J.L. (2006). A combined 1H-NMR spectroscopy- and mass spectrometry-based metabolomic study of the PPAR-{alpha} null mutant mouse defines profound systemic changes in metabolism linked to the metabolic syndrome. Physiological Genomics, 27, 178-186. doi: 10.1152/physiolgenomics.00060.2006
  • Barter, P.J. & Rye, K.A. (2006). Cardioprotective properties of fibrates. Which fibrate, Which patients, What mechanism?. Circulation, 113, 1553-1555. doi: 10.1161/CIRCULATIONAHA.105.620450
  • Beutler, E., Duran, O. & Kelley, B.M. (1963). Improved method for determination of blood glutathione. Journal of Laboratory and Clinical Medicine, 61, 882-888.
  • Binienda, Z.K. & Ali, S.F. (2001). Neuroprotective role of l-carnitine in the 3-nitropropionic acid induced neurotoxicity. Toxicology Letters, 25, 67-73. DOI: 10.1016/s0378-4274(01)00415-5
  • Brown, J.D. & Plutzky, J. (2007). Peroxisome proliferator-activated receptors as transcriptional nodal points and therapeutic targets. Circulation, 115, 518-533.
  • Brown, G.C. (1999). Nitric oxide and mitochondrial respiration. Biochimica et Biophysica Acta (BBA) - Bioenergetics, 1411, 351-369. doi:10.1016/S0005-2728(99)00025-0
  • Costet, P., Legendre, J., More, J., Edgar, A., Galtier, P. & Pineau, T. (1998). Peroxisome proliferator-activated receptor alpha-isoform deficiency leads to progressive dyslipidemia with sexually dimorphic obesity and steatosis. Journal of Biological Chemistry, 273, 29577-29585. doi: 10.1074/jbc.273.45.29577
  • DeFronzo, R.A. (1999). Pharmacologic therapy for type 2 diabetes mellitus. Annals of Internal Medicine, 131, 281-303. doi: 10.7326/0003-4819-131-4-199908170-00008
  • Dokmeci, D., Akpolat, M., Aydogdu, N., Doganay, L. & Turan, F.N. (2005). L-carnitine inhibits ethanol-induced gastric mucosal injury in rats. Pharmacological Reports, 57, 481-488.
  • Dreyer, C., Krey, G., Keller, H., Givel, F., Helftenbein, G. & Wahli, W. (1992). Control of the peroxisomal -oxidation pathway by a novel family of nuclear hormone receptors. Cell, 68, 879-887. doi: 10.1016/0092-8674(92)90031-7
  • Elijah, I.E., Børsheim, E., Maybauer, D.M., Finnerty, C.C., Herndon, D.N. & Maybauer, M.O. (2012). Role of the PPAR-α agonist fenofibrate in severe pediatric burn injury. Burns, 38, 481-86. doi: 10.1016/j.burns.2011.12.004
  • Fritz, I.B. (1955). The effect of muscle extracts on the oxidation of palmitic acid by liver slices and homogenates. Acta Physiologica Scandinavica, 34, 367-385. doi: 10.1111/j.1748-1716.1955.tb01256.x
  • Frei, B, Stocker, R. & Ames, B.N. (1988). Antioxidant defences and lipid peroxidation in human blood plasma. Proceedings of the National Academy of Sciences, 85, 9748-9752. doi: 10.1073/pnas.85.24.9748
  • Guerre-Millo, M., Gervois, P., Raspé, E., Madsen, L., Poulain, P., Derudas, B., Herbert, J.M., Winegar, D.A., Willson, T.M., Fruchart, J.C., Berge, R.K. & Staels, B. (2000). Peroxisome proliferator-activated receptor α activators improve insulin sensitivity and reduce adiposity. Journal of Biological Chemistry, 275, 16638-16642. doi: 10.1074/jbc.275.22.16638
  • Hashimoto, T., Fujita, T., Usuda, N., Cook, W., Qi, C., Peters, J.M., Gonzales, F.J., Yeldandi, A.V., Rao, S.M. & Reddy JK (1999). Peroxisomal and mitochondrial fatty acid -oxidation in mice nullizygous for both PPARα and fatty acyl CoA oxidase: Genotype correlation with fatty liver phenotype. Journal of Biological Chemistry, 274, 19228-19236. doi: 10.1074/jbc.274.27.19228
  • Huang, T.H., Teoh, A.W., Lin, B.L., Lin, D.S. & Roufogalis, B. (2009). The role of herbal PPAR modulators in the treatment of cardiometabolic syndrome. Pharmacological Research, 60, 195-206. doi: 10.1016/j.phrs.2009.03.020
  • Jeffrey, M.P., Susanna, S.T.L., Wen, L., Jerrold, M.W., Oksana, G., Carrie, E., Marc, L.R., Lynn, D.H. & Frank, J.G. (2000). Growth, adipose, brain, and skin alterations resulting from targeted disruption of the mouse peroxisome proliferator-activated receptor-. Molecular and Cellular Biology, 20, 5119-5128. doi: 10.1128/mcb.20.14.5119-5128.2000
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There are 62 citations in total.

Details

Primary Language English
Subjects Veterinary Surgery
Journal Section Research Articles
Authors

Mehmet Çitil 0000-0001-9839-7533

Recai Tunca 0000-0003-0004-7485

Erdoğan Uzlu 0000-0002-3064-6633

Mahmut Karapehlivan 0000-0003-0408-534X

Yasemen Adalı 0000-0002-8004-7364

Kürşat Yapar 0000-0003-0287-4521

Hüseyin Avni Eroğlu 0000-0002-1040-3255

Ekin Emre Erkılıç 0000-0003-2461-5598

Mustafa Makav 0000-0003-1879-8180

Hidayet Metin Erdoğan 0000-0003-1261-4352

Project Number Project Number 106 O 160
Publication Date December 31, 2022
Submission Date June 28, 2022
Acceptance Date December 22, 2022
Published in Issue Year 2022 Volume: 7 Issue: 3

Cite

APA Çitil, M., Tunca, R., Uzlu, E., Karapehlivan, M., et al. (2022). Pathological and biochemical investigation of the effects of l-carnitine and gemfibrozil on peroxisome proliferator activated Receptors (PPARS) and lipidosis in rabbits on a high-fat diet. Journal of Advances in VetBio Science and Techniques, 7(3), 346-360. https://doi.org/10.31797/vetbio.1136444

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