Suppr超能文献

左旋肉碱和烟酰胺核糖联合治疗可改善肝脏代谢,减轻肥胖和肝脂肪变性。

Combined Treatment with L-Carnitine and Nicotinamide Riboside Improves Hepatic Metabolism and Attenuates Obesity and Liver Steatosis.

机构信息

Department of Metabolic Health Research, The Netherlands Organization for Applied Scientific Research (TNO), 2333 CK Leiden, The Netherlands.

Human and Animal Physiology, Wageningen University, 6708 WD Wageningen, The Netherlands.

出版信息

Int J Mol Sci. 2019 Sep 5;20(18):4359. doi: 10.3390/ijms20184359.

Abstract

Obesity characterized by adiposity and ectopic fat accumulation is associated with the development of non-alcoholic fatty liver disease (NAFLD). Treatments that stimulate lipid utilization may prevent the development of obesity and comorbidities. This study evaluated the potential anti-obesogenic hepatoprotective effects of combined treatment with L-carnitine and nicotinamide riboside, i.e., components that can enhance fatty acid transfer across the inner mitochondrial membrane and increase nicotinamide adenine nucleotide (NAD+) levels, which are necessary for β-oxidation and the TCA cycle, respectively. Ldlr -/-.Leiden mice were treated with high-fat diet (HFD) supplemented with L-carnitine (LC; 0.4% /), nicotinamide riboside (NR; 0.3% /) or both (COMBI) for 21 weeks. L-carnitine plasma levels were reduced by HFD and normalized by LC. NR supplementation raised its plasma metabolite levels demonstrating effective delivery. Although food intake and ambulatory activity were comparable in all groups, COMBI treatment significantly attenuated HFD-induced body weight gain, fat mass gain (-17%) and hepatic steatosis (-22%). Also, NR and COMBI reduced hepatic 4-hydroxynonenal adducts. Upstream-regulator gene analysis demonstrated that COMBI reversed detrimental effects of HFD on liver metabolism pathways and associated regulators, e.g., ACOX, SCAP, SREBF, PPARGC1B, and INSR. Combination treatment with LC and NR exerts protective effects on metabolic pathways and constitutes a new approach to attenuate HFD-induced obesity and NAFLD.

摘要

肥胖的特征是脂肪过多和异位脂肪积累,与非酒精性脂肪性肝病 (NAFLD) 的发展有关。刺激脂质利用的治疗方法可能预防肥胖和合并症的发展。本研究评估了联合使用左旋肉碱和烟酰胺核糖苷(即可以增强脂肪酸穿过线粒体内膜的转移并增加烟酰胺腺嘌呤二核苷酸 (NAD+) 水平的成分,分别是β-氧化和 TCA 循环所必需的)治疗的潜在抗肥胖肝保护作用。用高脂肪饮食 (HFD) 处理 Ldlr -/-。莱顿小鼠补充左旋肉碱 (LC;0.4% /)、烟酰胺核糖苷 (NR;0.3% /) 或两者 (COMBI) 21 周。HFD 降低了左旋肉碱的血浆水平,而 LC 使其恢复正常。NR 补充提高了其血浆代谢物水平,表明有效输送。尽管所有组的食物摄入量和活动量相似,但 COMBI 治疗显着减轻了 HFD 引起的体重增加、脂肪量增加(-17%)和肝脂肪变性(-22%)。此外,NR 和 COMBI 降低了肝 4-羟壬烯醛加合物。上游调节剂基因分析表明,COMBI 逆转了 HFD 对肝脏代谢途径和相关调节剂的有害影响,例如 ACOX、SCAP、SREBF、PPARGC1B 和 INSR。LC 和 NR 的联合治疗对代谢途径具有保护作用,是减轻 HFD 诱导的肥胖和 NAFLD 的新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e184/6770226/6d1351be4bb6/ijms-20-04359-g001.jpg

相似文献

2
Nicotinamide riboside, an NAD+ precursor, attenuates the development of liver fibrosis in a diet-induced mouse model of liver fibrosis.
Biochim Biophys Acta Mol Basis Dis. 2019 Sep 1;1865(9):2451-2463. doi: 10.1016/j.bbadis.2019.06.009. Epub 2019 Jun 11.
3
Nicotinamide riboside has minimal impact on energy metabolism in mouse models of mild obesity.
J Endocrinol. 2021 Sep 9;251(1):111-123. doi: 10.1530/JOE-21-0123.
4
Hepatic steatosis induced by nicotine plus Coca-Cola™ is prevented by nicotinamide riboside (NR).
Front Endocrinol (Lausanne). 2024 May 2;15:1282231. doi: 10.3389/fendo.2024.1282231. eCollection 2024.
7
Garcinia Cambogia attenuates diet-induced adiposity but exacerbates hepatic collagen accumulation and inflammation.
World J Gastroenterol. 2013 Aug 7;19(29):4689-701. doi: 10.3748/wjg.v19.i29.4689.
9
L-Carnitine counteracts in vitro fructose-induced hepatic steatosis through targeting oxidative stress markers.
J Endocrinol Invest. 2020 Apr;43(4):493-503. doi: 10.1007/s40618-019-01134-2. Epub 2019 Nov 8.

引用本文的文献

2
4
Metabolic dysfunction-associated steatotic liver disease is associated with effects on cerebral perfusion and white matter integrity.
Heliyon. 2024 Sep 26;10(19):e38516. doi: 10.1016/j.heliyon.2024.e38516. eCollection 2024 Oct 15.
8
l-carnitine: Nutrition, pathology, and health benefits.
Saudi J Biol Sci. 2023 Feb;30(2):103555. doi: 10.1016/j.sjbs.2022.103555. Epub 2022 Dec 30.

本文引用的文献

6
Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle.
Rev Endocr Metab Disord. 2018 Mar;19(1):93-106. doi: 10.1007/s11154-018-9448-1.
7
SCAP/SREBPs are Central Players in Lipid Metabolism and Novel Metabolic Targets in Cancer Therapy.
Curr Top Med Chem. 2018;18(6):484-493. doi: 10.2174/1568026618666180523104541.
9
Key Inflammatory Processes in Human NASH Are Reflected in Ldlr.Leiden Mice: A Translational Gene Profiling Study.
Front Physiol. 2018 Feb 23;9:132. doi: 10.3389/fphys.2018.00132. eCollection 2018.
10
Sirt2 facilitates hepatic glucose uptake by deacetylating glucokinase regulatory protein.
Nat Commun. 2018 Jan 2;9(1):30. doi: 10.1038/s41467-017-02537-6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验