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Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes

Our previous studies showed that kisspeptin-10 (Kp-10) injected in vivo can markedly increase lipid anabolism in liver of quails. In order to investigate the direct effect of Kp-10 on lipid metabolism of hepatocytes in birds, cells were separated from embryos livers and cultured in vitro with 0, 100...

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Autores principales: Wu, J., Fu, W., Huang, Y., Ni, Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4092939/
https://www.ncbi.nlm.nih.gov/pubmed/25049685
http://dx.doi.org/10.5713/ajas.2012.12189
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author Wu, J.
Fu, W.
Huang, Y.
Ni, Y.
author_facet Wu, J.
Fu, W.
Huang, Y.
Ni, Y.
author_sort Wu, J.
collection PubMed
description Our previous studies showed that kisspeptin-10 (Kp-10) injected in vivo can markedly increase lipid anabolism in liver of quails. In order to investigate the direct effect of Kp-10 on lipid metabolism of hepatocytes in birds, cells were separated from embryos livers and cultured in vitro with 0, 100 and 1,000 nM Kp-10, respectively. The results showed that after 24 h treatment, cells viability was not affected by 100 nM Kp-10, but showed a mild decrease with 1,000 nM Kp-10 compared to the control cells. Based on the results of the cell viability, 100 nM dosage of Kp-10 was selected for the further study and analysis. Compared with control cells, total cholesterol (Tch) contents in 100 nM treated cells were increased by 51.23%, but did not reach statistical significance, while the level of triglyceride (TG), high density of lipoprotein-cholesterol (HDL-C) and low density of lipoprotein-cholesterol (LDL-C) were significantly increased. Real-time PCR results showed that ApoVLDL-II mRNA expression had a tendency to increase, genes including sterol regulatory element-binding protein-1 (SREBP-1), acetyl coenzyme A carboxylase α (ACCα), carnitine palmitoyltransferase 1 (CPT1), 3-hydroxyl-3-methylglutaryl-coenzyme A reductases (HMGCR) and stearyl coenzyme A dehydrogenase-1 (SCD1) mRNA in hepatocytes were significantly down-regulated by 100 nM Kp-10. However, contrary to its gene expression, SREBP-1 protein expression was significantly up-regulated by 100 nM Kp-10. Some of the significant correlations in mRNA expression were found between genes encoding hepatic factors or enzymes involved in lipid metabolism in liver of birds. These results indicate that Kp-10 stimulates lipid synthesis directly in primary cultured hepatocytes of chickens.
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spelling pubmed-40929392014-07-21 Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes Wu, J. Fu, W. Huang, Y. Ni, Y. Asian-Australas J Anim Sci Article Our previous studies showed that kisspeptin-10 (Kp-10) injected in vivo can markedly increase lipid anabolism in liver of quails. In order to investigate the direct effect of Kp-10 on lipid metabolism of hepatocytes in birds, cells were separated from embryos livers and cultured in vitro with 0, 100 and 1,000 nM Kp-10, respectively. The results showed that after 24 h treatment, cells viability was not affected by 100 nM Kp-10, but showed a mild decrease with 1,000 nM Kp-10 compared to the control cells. Based on the results of the cell viability, 100 nM dosage of Kp-10 was selected for the further study and analysis. Compared with control cells, total cholesterol (Tch) contents in 100 nM treated cells were increased by 51.23%, but did not reach statistical significance, while the level of triglyceride (TG), high density of lipoprotein-cholesterol (HDL-C) and low density of lipoprotein-cholesterol (LDL-C) were significantly increased. Real-time PCR results showed that ApoVLDL-II mRNA expression had a tendency to increase, genes including sterol regulatory element-binding protein-1 (SREBP-1), acetyl coenzyme A carboxylase α (ACCα), carnitine palmitoyltransferase 1 (CPT1), 3-hydroxyl-3-methylglutaryl-coenzyme A reductases (HMGCR) and stearyl coenzyme A dehydrogenase-1 (SCD1) mRNA in hepatocytes were significantly down-regulated by 100 nM Kp-10. However, contrary to its gene expression, SREBP-1 protein expression was significantly up-regulated by 100 nM Kp-10. Some of the significant correlations in mRNA expression were found between genes encoding hepatic factors or enzymes involved in lipid metabolism in liver of birds. These results indicate that Kp-10 stimulates lipid synthesis directly in primary cultured hepatocytes of chickens. Asian-Australasian Association of Animal Production Societies (AAAP) and Korean Society of Animal Science and Technology (KSAST) 2012-09 /pmc/articles/PMC4092939/ /pubmed/25049685 http://dx.doi.org/10.5713/ajas.2012.12189 Text en Copyright © 2012 by Asian-Australasian Journal of Animal Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/ which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Wu, J.
Fu, W.
Huang, Y.
Ni, Y.
Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes
title Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes
title_full Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes
title_fullStr Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes
title_full_unstemmed Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes
title_short Effects of Kisspeptin-10 on Lipid Metabolism in Cultured Chicken Hepatocytes
title_sort effects of kisspeptin-10 on lipid metabolism in cultured chicken hepatocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4092939/
https://www.ncbi.nlm.nih.gov/pubmed/25049685
http://dx.doi.org/10.5713/ajas.2012.12189
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