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腹腔内给予短链脂肪酸以性别特异性方式改善长爪沙鼠的脂代谢。

Intraperitoneal Administration of Short-Chain Fatty Acids Improves Lipid Metabolism of Long-Evans Rats in a Sex-Specific Manner.

机构信息

Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL A1B 3X9, Canada.

School of Science and the Environment/Boreal Ecosystem Research Initiative, Grenfell Campus, Memorial University of Newfoundland, Corner Brook, NL A2H 5G4, Canada.

出版信息

Nutrients. 2021 Mar 10;13(3):892. doi: 10.3390/nu13030892.


DOI:10.3390/nu13030892
PMID:33801984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8000072/
Abstract

Short-chain fatty acids (SCFAs) are microbial metabolites, mainly generated by the action of gut microbiota on dietary fibers. Acetate, propionate, and butyrate are the three main SCFAs produced typically in a 60:20:20 molar ratio in the colon. Acetate, propionate, and butyrate, when given individually as supplements, have shown a protective role in obesity and hyperglycemia; however, the sex-specific effects of a mixture of SCFAs, when given in 60:20:20 ratio, on the regulation of lipid metabolism and lipid profile are not known. Male and female Long-Evans rats were given a mixture of SCFAs (acetate, propionate, and butyrate; molar ratio 60:20:20) each day for seven days intraperitoneally; plasma and hepatic lipids, gene expression, and lipidomics profile were analyzed. SCFAs significantly decreased plasma and hepatic triglycerides and cholesterol in males, whereas the fatty acyl composition of cholesteryl esters, triglycerides, and phospholipids was modulated in females. SCFAs decreased the mRNA expression of hepatic acetyl-CoA carboxylase-1 in both males and females. Our findings demonstrate for the first time that SCFAs (60:20:20) improved plasma and hepatic lipid levels and fatty acyl composition in a manner that may provide cardio-protective and anti-inflammatory effects in both sexes, via independent mechanisms.

摘要

短链脂肪酸(SCFAs)是微生物代谢物,主要由肠道微生物对膳食纤维的作用产生。乙酸盐、丙酸盐和丁酸盐是结肠中通常以 60:20:20 摩尔比产生的三种主要 SCFA。当作为补充剂单独给予时,乙酸盐、丙酸盐和丁酸盐在肥胖和高血糖症中显示出保护作用;然而,当以 60:20:20 的比例给予 SCFA 混合物时,其对脂质代谢和脂质谱的调节的性别特异性影响尚不清楚。雄性和雌性长耳大仓鼠每天通过腹膜内给予 SCFA(乙酸盐、丙酸盐和丁酸盐;摩尔比 60:20:20)混合物 7 天;分析血浆和肝脂质、基因表达和脂质组学谱。SCFA 显著降低了雄性血浆和肝甘油三酯和胆固醇,而雌性的胆固醇酯、甘油三酯和磷脂的脂肪酸酰基组成被调节。SCFA 降低了雄性和雌性肝乙酰辅酶 A 羧化酶-1 的 mRNA 表达。我们的研究结果首次表明,SCFA(60:20:20)以可能通过独立机制在两性中提供心脏保护和抗炎作用的方式改善了血浆和肝脂质水平和脂肪酸酰基组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/c9fbc7aae83f/nutrients-13-00892-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/e5ca2ca9c14b/nutrients-13-00892-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/7372fa24b424/nutrients-13-00892-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/e3a7de8e0495/nutrients-13-00892-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/8e22267c011e/nutrients-13-00892-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/6901b2eeae37/nutrients-13-00892-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/c9fbc7aae83f/nutrients-13-00892-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/e5ca2ca9c14b/nutrients-13-00892-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/7372fa24b424/nutrients-13-00892-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/e3a7de8e0495/nutrients-13-00892-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/8e22267c011e/nutrients-13-00892-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/6901b2eeae37/nutrients-13-00892-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4658/8000072/c9fbc7aae83f/nutrients-13-00892-g006.jpg

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[3]
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[4]
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Mol Cell Biochem. 2025-5

[5]
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Int J Mol Sci. 2024-9-27

[6]
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Nutrients. 2024-7-19

[7]
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Nutr Metab (Lond). 2024-7-18

[8]
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Int J Mol Sci. 2024-4-13

[9]
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[10]
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本文引用的文献

[1]
The influence of biological sex and sex hormones on bile acid synthesis and cholesterol homeostasis.

Biol Sex Differ. 2019-11-27

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Sci Rep. 2019-3-25

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Front Endocrinol (Lausanne). 2018-1-11

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Structure-Specific Effects of Short-Chain Fatty Acids on Plasma Cholesterol Concentration in Male Syrian Hamsters.

J Agric Food Chem. 2017-12-20

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Arachidonic acid-containing phosphatidylcholine characterized by consolidated plasma and liver lipidomics as an early onset marker for tamoxifen-induced hepatic phospholipidosis.

J Appl Toxicol. 2017-8

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