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. 2022 Feb 2;12:837509. doi: 10.3389/fphar.2021.837509

TABLE 1.

Summary of the studies about the effects of butyrate on atherosclerosis.

Reference Type of study Butyrate dose Model Result
Aguilar et al. (2018) In vivo 1%wt/wt butyrate in diet for 10 weeks HFD fed ApoE knockout mice decreased atherosclerosis lesions of aorta
decreased CCL2, VCAM1
increased MMP2 and9
decreased migration of macrophage
increased collagen depositions and plaque stability
In vitro 0.5 mM butyrate for 2 h Macrophage decreased ox-LDL uptake, CD36, VCAM1, CCL2, TNFα, IL1β and IL6
endothelial cells increased IL10 levels
inhibited NF-kB activity
Kasahara et al. (2018) In vivo 6% wt/wt tributyrin in diet for 14 weeks ApoE knockout mice inhibited the development of atherosclerosis, lipid deposition and macrophage accumulation in the plaque
reduced gut permeability
Du et al. (2020) In vivo SB 200 and 400 mg/kg/day for 16 weeks HFD fed ApoE knockout mice improved the gut microbial diversity
increased the abundance of Firmicutes
decreased cholesterol deposition
decreased atherosclerotic lesions of aortae
decreased TC
increased the ABCA1 level in liver
In vitro 2 and 5 mM butyrate for 24 h Murine RAW 264.7 macrophages increased ABCA1 protein level
ABCA1p-Luc HepG2 cells increased the cholesterol efflux in RAW 264.7 macrophages in a dose-dependent manner
Primary peritoneal macrophages
Wang et al. (2020) In vitro 100 and 200 μM butyrate for 24 h TNF-α induced HUVECs cells decreased VCAM-1 and E-selectin
reduced oxidative stress by reducing the levels of ROS and 4-HNE
decreased MCP-1 and IL-8
improved protective factor KLF2,via the ERK5 pathway

Abbreviations: HFD, high fat diet; APO E, apolipoprotein E; CCL2, C–C motif chemokine ligand 2; VCAM1, vascular adhesion molecule-1; MMP, matrix metalloproteinases; ox-LDL, oxidized-low density lipoprotein; TNFα, Tumor necrosis factorα; IL, interleukin, NF-kB, Nuclear factor kappa B; SB, sodium butyrate; Hep G2, hepatocye G2; TC, total cholesterol; ABCA1, ATP Binding Cassette Subfamily A Member 1; HUVECs, human umbilical vein endothelial cells; ROS, reactive oxygen species; 4-HNE, 4-Hydroxynonenal; MCP1, monocyte chemoattractant protein-1; KLF2, Kruppel Like Factor 2; ERK5, Extracellular-signal-regulated kinase 5.