Short-chain fatty acid delivery: assessing exogenous administration of the microbiome metabolite acetate in mice

被引:27
作者
Shubitowski, Tyler B. [1 ]
Poll, Brian G. [1 ]
Natarajan, Niranjana [2 ]
Pluznick, Jennifer L. [1 ]
机构
[1] Johns Hopkins Sch Med, Dept Physiol, 725 N Wolfe St WBSB 205, Baltimore, MD 21205 USA
[2] Harvard Univ, Harvard Stem Cell Inst, Dept Stem Cell & Regenerat Biol, Cambridge, MA USA
来源
PHYSIOLOGICAL REPORTS | 2019年 / 7卷 / 04期
基金
美国国家卫生研究院;
关键词
Drinking water; i; p; injection; oral gavage; plasma acetate; PROTEIN-COUPLED RECEPTOR; GUT MICROBIOTA; INFLAMMATORY RESPONSES; BLOOD-PRESSURE; ACTIVATION; LIPOLYSIS; BUTYRATE; DIET;
D O I
10.14814/phy2.14005
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Short-chain fatty acids (SCFAs) are fermentation by-products of gut microbes which have been linked to positive effects on host physiology; the most abundant SCFA is acetate. Exogenous administration of acetate alters host metabolism, immune function, and blood pressure, making it a biologic of interest. The effects of acetate have been attributed to activation of G-protein-coupled receptors and other proteins (i.e., HDACs), often occurring at locations distant from the gut such as the pancreas or the kidney. However, due to technical difficulties and costs, studies have often delivered exogenous acetate without determining if systemic plasma acetate levels are altered. Thus, it is unclear to what extent each method of acetate delivery may alter systemic plasma acetate levels. In this study, we aimed to determine if acetate is elevated after exogenous administration by drinking water (DW), oral gavage (OG), or intraperitoneal (IP) injection, and if so, over what timecourse, to best inform future studies. Using a commercially available kit, we demonstrated that sodium acetate delivered over 21 days in DW does not elicit a measurable change in systemic acetate over baseline. However, when acetate is delivered by OG or IP injection, there are rapid, reproducible, and dose-dependent changes in plasma acetate. These studies report, for the first time, the timecourse of changes in plasma acetate following acetate administration by three common methods, and thus inform the best practices for exogenous acetate delivery.
引用
收藏
页数:11
相关论文
共 43 条
  • [11] Butyrate stimulates adipose lipolysis and mitochondrial oxidative phosphorylation through histone hyperacetylation- associated β3-adrenergic receptor activation in high-fat diet-induced obese mice
    Jia, Yimin
    Hong, Jian
    Li, Huifang
    Hu, Yun
    Jia, Longfei
    Cai, Demin
    Zhao, Ruqian
    [J]. EXPERIMENTAL PHYSIOLOGY, 2017, 102 (02) : 273 - 281
  • [12] Short-Chain Fatty Acids Activate GPR41 and GPR43 on Intestinal Epithelial Cells to Promote Inflammatory Responses in Mice
    Kim, Myung H.
    Kang, Seung G.
    Park, Jeong H.
    Yanagisawa, Masashi
    Kim, Chang H.
    [J]. GASTROENTEROLOGY, 2013, 145 (02) : 396 - +
  • [13] Short-chain fatty acids and ketones directly regulate sympathetic nervous system via G protein-coupled receptor 41 (GPR41)
    Kimura, Ikuo
    Inoue, Daisuke
    Maeda, Takeshi
    Hara, Takafumi
    Ichimura, Atsuhiko
    Miyauchi, Satoshi
    Kobayashi, Makio
    Hirasawa, Akira
    Tsujimoto, Gozoh
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (19) : 8030 - 8035
  • [14] Korecka A, 2012, J ORAL MICROBIOL, V4
  • [15] HIGH PROPIONIC-ACID FERMENTATIONS AND MINERAL ACCUMULATION IN THE CECUM OF RATS ADAPTED TO DIFFERENT LEVELS OF INULIN
    LEVRAT, MA
    REMESY, C
    DEMIGNE, C
    [J]. JOURNAL OF NUTRITION, 1991, 121 (11) : 1730 - 1737
  • [16] Butyrate reduces appetite and activates brown adipose tissue via the gut-brain neural circuit
    Li, Zhuang
    Yi, Chun-Xia
    Katiraei, Saeed
    Kooijman, Sander
    Zhou, Enchen
    Chung, Chih Kit
    Gao, Yuanqing
    van den Heuvel, Jose K.
    Meijer, Onno C.
    Berbee, Jimmy F. P.
    Heijink, Marieke
    Giera, Martin
    van Dijk, Ko Willems
    Groen, Albert K.
    Rensen, Patrick C. N.
    Wang, Yanan
    [J]. GUT, 2018, 67 (07) : 1269 - 1279
  • [17] Butyrate and Propionate Protect against Diet-Induced Obesity and Regulate Gut Hormones via Free Fatty Acid Receptor 3-Independent Mechanisms
    Lin, Hua V.
    Frassetto, Andrea
    Kowalik, Edward J., Jr.
    Nawrocki, Andrea R.
    Lu, Mofei M.
    Kosinski, Jennifer R.
    Hubert, James A.
    Szeto, Daphne
    Yao, Xiaorui
    Forrest, Gail
    Marsh, Donald J.
    [J]. PLOS ONE, 2012, 7 (04):
  • [18] Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss
    Lucas, Sebastien
    Omata, Yasunori
    Hofmann, Joerg
    Boettcher, Martin
    Iljazovic, Aida
    Sarter, Kerstin
    Albrecht, Olivia
    Schulz, Oscar
    Krishnacoumar, Brenda
    Kroenke, Gerhard
    Herrmann, Martin
    Mougiakakos, Dimitrios
    Strowig, Till
    Schett, Georg
    Zaiss, Mario M.
    [J]. NATURE COMMUNICATIONS, 2018, 9
  • [19] Regulation of inflammatory responses by gut microbiota and chemoattractant receptor GPR43
    Maslowski, Kendle M.
    Vieira, Angelica T.
    Ng, Aylwin
    Kranich, Jan
    Sierro, Frederic
    Yu, Di
    Schilter, Heidi C.
    Rolph, Michael S.
    Mackay, Fabienne
    Artis, David
    Xavier, Ramnik J.
    Teixeira, Mauro M.
    Mackay, Charles R.
    [J]. NATURE, 2009, 461 (7268) : 1282 - U119
  • [20] Gut microbiome-derived metabolites modulate intestinal epithelial cell damage and mitigate graft-versus-host disease
    Mathewson, Nathan D.
    Jenq, Robert
    Mathew, Anna V.
    Koenigsknecht, Mark
    Hanash, Alan
    Toubai, Tomomi
    Oravecz-Wilson, Katherine
    Wu, Shin-Rong
    Sun, Yaping
    Rossi, Corinne
    Fujiwara, Hideaki
    Byun, Jaeman
    Shono, Yusuke
    Lindemans, Caroline
    Calafiore, Marco
    Schmidt, Thomas C.
    Honda, Kenya
    Young, Vincent B.
    Pennathur, Subramaniam
    van den Brink, Marcel
    Reddy, Pavan
    [J]. NATURE IMMUNOLOGY, 2016, 17 (05) : 505 - +