Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.

BACKGROUND: Apolipoprotein M (ApoM) is a constituent of high-density lipoproteins (HDL). It plays a crucial role in HDL-mediated reverse cholesterol transport. Insulin resistance is associated with decreased ApoM levels. AIMS: To assess the effects of increased free fatty acids (FFAs) levels after s...

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Main Authors: Lu Zheng, Yuehua Feng, Yuanping Shi, Jun Zhang, Qinfeng Mu, Li Qin, Maria Berggren-Söderlund, Peter Nilsson-Ehle, Xiaoying Zhang, Guanghua Luo, Ning Xu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4140822?pdf=render
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spelling doaj-0f69d2cf5c7b49828e13b6fa056cb5672020-11-25T01:27:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0198e10568110.1371/journal.pone.0105681Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.Lu ZhengYuehua FengYuanping ShiJun ZhangQinfeng MuLi QinMaria Berggren-SöderlundPeter Nilsson-EhleXiaoying ZhangGuanghua LuoNing XuBACKGROUND: Apolipoprotein M (ApoM) is a constituent of high-density lipoproteins (HDL). It plays a crucial role in HDL-mediated reverse cholesterol transport. Insulin resistance is associated with decreased ApoM levels. AIMS: To assess the effects of increased free fatty acids (FFAs) levels after short-term Intralipid infusion on insulin sensitivity and hepatic ApoM gene expression. METHODS: Adult male Sprague-Dawley (SD) rats infused with 20% Intralipid solution for 6 h. Glucose infusion rates (GIR) were determined by hyperinsulinemic-euglycemic clamp during Intralipid infusion and plasma FFA levels were measured by colorimetry. Rats were sacrificed after Intralipid treatment and livers were sampled. Human embryonic kidney 293T cells were transfected with a lentivirus mediated human apoM overexpression system. Goto-Kakizaki (GK) rats were injected with the lentiviral vector and insulin tolerance was assessed. Gene expression was assessed by real-time RT-PCR and PCR array. RESULTS: Intralipid increased FFAs by 17.6 folds and GIR was decreased by 27.1% compared to the control group. ApoM gene expression was decreased by 40.4% after Intralipid infusion. PPARβ/δ expression was not changed by Intralipid. Whereas the mRNA levels of Acaca, Acox1, Akt1, V-raf murine sarcoma 3611 viral oncogene homolog, G6pc, Irs2, Ldlr, Map2k1, pyruvate kinase and RBC were significantly increased in rat liver after Intralipid infusion. The Mitogen-activated protein kinase 8 (MAPK8) was significantly down-regulated in 293T cells overexpressing ApoM. Overexpression of human ApoM in GK rats could enhance the glucose-lowering effect of exogenous insulin. CONCLUSION: These results suggest that Intralipid could decrease hepatic ApoM levels. ApoM overexpression may have a potential role in improving insulin resistance in vivo and modulating apoM expression might be a future therapeutic strategy against insulin resistance in type 2 diabetes.http://europepmc.org/articles/PMC4140822?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Lu Zheng
Yuehua Feng
Yuanping Shi
Jun Zhang
Qinfeng Mu
Li Qin
Maria Berggren-Söderlund
Peter Nilsson-Ehle
Xiaoying Zhang
Guanghua Luo
Ning Xu
spellingShingle Lu Zheng
Yuehua Feng
Yuanping Shi
Jun Zhang
Qinfeng Mu
Li Qin
Maria Berggren-Söderlund
Peter Nilsson-Ehle
Xiaoying Zhang
Guanghua Luo
Ning Xu
Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.
PLoS ONE
author_facet Lu Zheng
Yuehua Feng
Yuanping Shi
Jun Zhang
Qinfeng Mu
Li Qin
Maria Berggren-Söderlund
Peter Nilsson-Ehle
Xiaoying Zhang
Guanghua Luo
Ning Xu
author_sort Lu Zheng
title Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.
title_short Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.
title_full Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.
title_fullStr Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.
title_full_unstemmed Intralipid decreases apolipoprotein M levels and insulin sensitivity in rats.
title_sort intralipid decreases apolipoprotein m levels and insulin sensitivity in rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description BACKGROUND: Apolipoprotein M (ApoM) is a constituent of high-density lipoproteins (HDL). It plays a crucial role in HDL-mediated reverse cholesterol transport. Insulin resistance is associated with decreased ApoM levels. AIMS: To assess the effects of increased free fatty acids (FFAs) levels after short-term Intralipid infusion on insulin sensitivity and hepatic ApoM gene expression. METHODS: Adult male Sprague-Dawley (SD) rats infused with 20% Intralipid solution for 6 h. Glucose infusion rates (GIR) were determined by hyperinsulinemic-euglycemic clamp during Intralipid infusion and plasma FFA levels were measured by colorimetry. Rats were sacrificed after Intralipid treatment and livers were sampled. Human embryonic kidney 293T cells were transfected with a lentivirus mediated human apoM overexpression system. Goto-Kakizaki (GK) rats were injected with the lentiviral vector and insulin tolerance was assessed. Gene expression was assessed by real-time RT-PCR and PCR array. RESULTS: Intralipid increased FFAs by 17.6 folds and GIR was decreased by 27.1% compared to the control group. ApoM gene expression was decreased by 40.4% after Intralipid infusion. PPARβ/δ expression was not changed by Intralipid. Whereas the mRNA levels of Acaca, Acox1, Akt1, V-raf murine sarcoma 3611 viral oncogene homolog, G6pc, Irs2, Ldlr, Map2k1, pyruvate kinase and RBC were significantly increased in rat liver after Intralipid infusion. The Mitogen-activated protein kinase 8 (MAPK8) was significantly down-regulated in 293T cells overexpressing ApoM. Overexpression of human ApoM in GK rats could enhance the glucose-lowering effect of exogenous insulin. CONCLUSION: These results suggest that Intralipid could decrease hepatic ApoM levels. ApoM overexpression may have a potential role in improving insulin resistance in vivo and modulating apoM expression might be a future therapeutic strategy against insulin resistance in type 2 diabetes.
url http://europepmc.org/articles/PMC4140822?pdf=render
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