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Effects of nicotinic acid on gene expression: potential mechanisms and implications for wanted and unwanted effects of the lipid-lowering drug.烟酸对基因表达的影响:潜在机制及对降脂药期望和非期望作用的影响。
J Clin Endocrinol Metab. 2011 Oct;96(10):3048-55. doi: 10.1210/jc.2011-1104. Epub 2011 Aug 3.
2
Continuous 24-h nicotinic acid infusion in rats causes FFA rebound and insulin resistance by altering gene expression and basal lipolysis in adipose tissue.在大鼠中持续 24 小时给予烟酸输注会通过改变脂肪组织中的基因表达和基础脂肪分解来引起 FFA 反弹和胰岛素抵抗。
Am J Physiol Endocrinol Metab. 2011 Jun;300(6):E1012-21. doi: 10.1152/ajpendo.00650.2010. Epub 2011 Mar 8.
3
Widespread effects of nicotinic acid on gene expression in insulin-sensitive tissues: implications for unwanted effects of nicotinic acid treatment.烟酸对胰岛素敏感组织中基因表达的广泛影响:对烟酸治疗不良作用的启示。
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Nicotinic acid supplementation in diet favored intramuscular fat deposition and lipid metabolism in finishing steers.日粮中添加烟酸有利于育肥牛的肌内脂肪沉积和脂质代谢。
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Insulin Signaling in Liver and Adipose Tissues in Periparturient Dairy Cows Supplemented with Dietary Nicotinic Acid.围产期补充膳食烟酸的奶牛肝脏和脂肪组织中的胰岛素信号传导
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Effect of Extended-Release Niacin/Laropiprant Combination on Plasma Adiponectin and Insulin Resistance in Chinese Patients with Dyslipidaemia.缓释烟酸/拉罗匹仑组合对中国血脂异常患者血浆脂联素和胰岛素抵抗的影响。
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Effects of phenotypic and genotypic factors on the lipid responses to niacin in Chinese patients with dyslipidemia.表型和基因型因素对中国血脂异常患者烟酸脂质反应的影响。
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Evidence for fatty acids mediating CL 316,243-induced reductions in blood glucose in mice.脂肪酸介导 CL 316,243 降低小鼠血糖的证据。
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本文引用的文献

1
Continuous 24-h nicotinic acid infusion in rats causes FFA rebound and insulin resistance by altering gene expression and basal lipolysis in adipose tissue.在大鼠中持续 24 小时给予烟酸输注会通过改变脂肪组织中的基因表达和基础脂肪分解来引起 FFA 反弹和胰岛素抵抗。
Am J Physiol Endocrinol Metab. 2011 Jun;300(6):E1012-21. doi: 10.1152/ajpendo.00650.2010. Epub 2011 Mar 8.
2
Niacin results in reduced monocyte adhesion in patients with type 2 diabetes mellitus.烟酸可降低 2 型糖尿病患者的单核细胞黏附。
Atherosclerosis. 2011 Mar;215(1):176-9. doi: 10.1016/j.atherosclerosis.2010.12.020. Epub 2010 Dec 25.
3
Regulation of hepatic ApoC3 expression by PGC-1β mediates hypolipidemic effect of nicotinic acid.PGC-1β 调控肝 ApoC3 表达介导烟酸的降脂作用。
Cell Metab. 2010 Oct 6;12(4):411-419. doi: 10.1016/j.cmet.2010.09.001.
4
Modulation of HDL metabolism by the niacin receptor GPR109A in mouse hepatocytes.载脂蛋白代谢的调节在小鼠肝细胞中的烟酸受体 GPR109A。
Biochem Pharmacol. 2010 Nov 1;80(9):1450-7. doi: 10.1016/j.bcp.2010.07.023. Epub 2010 Jul 22.
5
Nicotinic acid decreases apolipoprotein B100-containing lipoprotein levels by reducing hepatic very low density lipoprotein secretion through a possible diacylglycerol acyltransferase 2 inhibition in obese dogs.烟酸通过可能抑制二酰基甘油酰基转移酶 2 减少肥胖犬肝脏极低密度脂蛋白分泌,从而降低载脂蛋白 B100 脂蛋白水平。
J Pharmacol Exp Ther. 2010 Aug;334(2):583-9. doi: 10.1124/jpet.110.167478. Epub 2010 May 4.
6
Widespread effects of nicotinic acid on gene expression in insulin-sensitive tissues: implications for unwanted effects of nicotinic acid treatment.烟酸对胰岛素敏感组织中基因表达的广泛影响:对烟酸治疗不良作用的启示。
Metabolism. 2011 Jan;60(1):134-44. doi: 10.1016/j.metabol.2010.02.013. Epub 2010 Mar 29.
7
Epac: defining a new mechanism for cAMP action.Epac:定义 cAMP 作用的新机制。
Annu Rev Pharmacol Toxicol. 2010;50:355-75. doi: 10.1146/annurev.pharmtox.010909.105714.
8
Niacin promotes cholesterol efflux through stimulation of the PPARgamma-LXRalpha-ABCA1 pathway in 3T3-L1 adipocytes.烟酸通过刺激 3T3-L1 脂肪细胞中的 PPARγ-LXRα-ABCA1 通路促进胆固醇外流。
Pharmacology. 2009;84(5):282-7. doi: 10.1159/000242999. Epub 2009 Oct 1.
9
Anti-inflammatory effects of nicotinic acid in adipocytes demonstrated by suppression of fractalkine, RANTES, and MCP-1 and upregulation of adiponectin.烟酰胺在脂肪细胞中发挥抗炎作用,表现为抑制 fractalkine、RANTES 和 MCP-1,以及上调脂联素。
Atherosclerosis. 2010 Mar;209(1):89-95. doi: 10.1016/j.atherosclerosis.2009.08.045. Epub 2009 Aug 31.
10
Statins, fibrates, nicotinic acid, cholesterol absorption inhibitors, anion-exchange resins, omega-3 fatty acids: which drugs for which patients?他汀类药物、贝特类药物、烟酸、胆固醇吸收抑制剂、阴离子交换树脂、ω-3 脂肪酸:哪些药物适合哪些患者?
Fundam Clin Pharmacol. 2009 Dec;23(6):687-92. doi: 10.1111/j.1472-8206.2009.00745.x. Epub 2009 Aug 14.

烟酸对基因表达的影响:潜在机制及对降脂药期望和非期望作用的影响。

Effects of nicotinic acid on gene expression: potential mechanisms and implications for wanted and unwanted effects of the lipid-lowering drug.

机构信息

Department of Biochemistry and Molecular Biology, Kyung Hee University School of Medicine, Seoul 1130-701, Korea.

出版信息

J Clin Endocrinol Metab. 2011 Oct;96(10):3048-55. doi: 10.1210/jc.2011-1104. Epub 2011 Aug 3.

DOI:10.1210/jc.2011-1104
PMID:21816780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3200242/
Abstract

CONTEXT

Nicotinic acid (NA), or niacin, lowers circulating levels of lipids, including triglycerides, very low-density lipoprotein-cholesterol, and low-density lipoprotein-cholesterol. The lipid-lowering effects have been attributed to its effect to inhibit lipolysis in adipocytes and thus lower plasma free fatty acid (FFA) level. However, evidence accumulates that the FFA-lowering effect may account for only a fraction of NA effects on plasma lipids, and other mechanisms may be involved. Recent studies have reported NA effects on gene expression in various tissues in vivo and in cultured cells in vitro.

EVIDENCE ACQUISITION

We reviewed articles reporting NA effects on gene expression, identified by searching PubMed, focusing on potential underlying mechanisms and implications for unexplained NA effects.

CONCLUSION

The effects of NA on gene expression may be mediated directly via the NA receptor in the affected cells, indirectly via changes in circulating FFA or hormone levels induced by NA, or by activating the transcription factor FOXO1 in insulin-sensitive tissues. NA effects on gene expression provide new insights into previously unexplained NA effects, such as FFA-independent lipid-lowering effects, FFA rebound, and insulin resistance observed in clinics during NA treatment.

摘要

背景

烟酸(NA),又称尼克酸,可降低包括甘油三酯、极低密度脂蛋白胆固醇和低密度脂蛋白胆固醇在内的循环脂质水平。降脂作用归因于其抑制脂肪细胞脂肪分解的作用,从而降低血浆游离脂肪酸(FFA)水平。然而,越来越多的证据表明,FFA 降低作用可能仅占 NA 对血浆脂质影响的一部分,可能涉及其他机制。最近的研究报告了 NA 在体内各种组织和体外培养细胞中对基因表达的影响。

证据获取

我们通过搜索 PubMed 综述了报告 NA 对基因表达影响的文章,重点关注潜在的潜在机制及其对 NA 未解释作用的影响。

结论

NA 对基因表达的影响可能通过受影响细胞中的 NA 受体直接介导,通过 NA 诱导的循环 FFA 或激素水平的变化间接介导,或通过激活胰岛素敏感组织中的转录因子 FOXO1 介导。NA 对基因表达的影响为以前未解释的 NA 作用提供了新的见解,例如临床 NA 治疗期间观察到的 FFA 独立降脂作用、FFA 反弹和胰岛素抵抗。