Chemogenetics defines a short-chain fatty acid receptor gut-brain axis

Research output: Contribution to journalJournal articleResearchpeer-review

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Chemogenetics defines a short-chain fatty acid receptor gut-brain axis. / Barki, Natasja; Bolognini, Daniele; Börjesson, Ulf; Jenkins, Laura; Riddell, John; Hughes, David I.; Ulven, Trond; Hudson, Brian D.; Ulven, Elisabeth Rexen; Dekker, Niek; Tobin, Andrew B.; Milligan, Graeme.

In: eLife, Vol. 11, e73777, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Barki, N, Bolognini, D, Börjesson, U, Jenkins, L, Riddell, J, Hughes, DI, Ulven, T, Hudson, BD, Ulven, ER, Dekker, N, Tobin, AB & Milligan, G 2022, 'Chemogenetics defines a short-chain fatty acid receptor gut-brain axis', eLife, vol. 11, e73777. https://doi.org/10.7554/eLife.73777

APA

Barki, N., Bolognini, D., Börjesson, U., Jenkins, L., Riddell, J., Hughes, D. I., Ulven, T., Hudson, B. D., Ulven, E. R., Dekker, N., Tobin, A. B., & Milligan, G. (2022). Chemogenetics defines a short-chain fatty acid receptor gut-brain axis. eLife, 11, [e73777]. https://doi.org/10.7554/eLife.73777

Vancouver

Barki N, Bolognini D, Börjesson U, Jenkins L, Riddell J, Hughes DI et al. Chemogenetics defines a short-chain fatty acid receptor gut-brain axis. eLife. 2022;11. e73777. https://doi.org/10.7554/eLife.73777

Author

Barki, Natasja ; Bolognini, Daniele ; Börjesson, Ulf ; Jenkins, Laura ; Riddell, John ; Hughes, David I. ; Ulven, Trond ; Hudson, Brian D. ; Ulven, Elisabeth Rexen ; Dekker, Niek ; Tobin, Andrew B. ; Milligan, Graeme. / Chemogenetics defines a short-chain fatty acid receptor gut-brain axis. In: eLife. 2022 ; Vol. 11.

Bibtex

@article{b2309b7d6cae4bffa3e185fb40ccd84f,
title = "Chemogenetics defines a short-chain fatty acid receptor gut-brain axis",
abstract = "Volatile small molecules, including the short-chain fatty acids (SCFAs), acetate and propionate, released by the gut microbiota from the catabolism of nondigestible starches, can act in a hormone-like fashion via specific G-protein-coupled receptors (GPCRs). The primary GPCR targets for these SCFAs are FFA2 and FFA3. Using transgenic mice in which FFA2 was replaced by an altered form called a Designer Receptor Exclusively Activated by Designer Drugs (FFA2-DREADD), but in which FFA3 is unaltered, and a newly identified FFA2-DREADD agonist 4-methoxy-3-methyl-benzoic acid (MOMBA), we demonstrate how specific functions of FFA2 and FFA3 define a SCFA-gut-brain axis. Activation of both FFA2/3 in the lumen of the gut stimulates spinal cord activity and activation of gut FFA3 directly regulates sensory afferent neuronal firing. Moreover, we demonstrate that FFA2 and FFA3 are both functionally expressed in dorsal root- and nodose ganglia where they signal through different G proteins and mechanisms to regulate cellular calcium levels. We conclude that FFA2 and FFA3, acting at distinct levels, provide an axis by which SCFAs originating from the gut microbiota can regulate central activity.",
keywords = "Designer Receptor Exclusively Activated by Designer Drugs, gut–brain axis, medicine, mouse, short-chain fatty acids",
author = "Natasja Barki and Daniele Bolognini and Ulf B{\"o}rjesson and Laura Jenkins and John Riddell and Hughes, {David I.} and Trond Ulven and Hudson, {Brian D.} and Ulven, {Elisabeth Rexen} and Niek Dekker and Tobin, {Andrew B.} and Graeme Milligan",
note = "Publisher Copyright: {\textcopyright} 2022, Barki et al.",
year = "2022",
doi = "10.7554/eLife.73777",
language = "English",
volume = "11",
journal = "eLife",
issn = "2050-084X",
publisher = "eLife Sciences Publications Ltd.",

}

RIS

TY - JOUR

T1 - Chemogenetics defines a short-chain fatty acid receptor gut-brain axis

AU - Barki, Natasja

AU - Bolognini, Daniele

AU - Börjesson, Ulf

AU - Jenkins, Laura

AU - Riddell, John

AU - Hughes, David I.

AU - Ulven, Trond

AU - Hudson, Brian D.

AU - Ulven, Elisabeth Rexen

AU - Dekker, Niek

AU - Tobin, Andrew B.

AU - Milligan, Graeme

N1 - Publisher Copyright: © 2022, Barki et al.

PY - 2022

Y1 - 2022

N2 - Volatile small molecules, including the short-chain fatty acids (SCFAs), acetate and propionate, released by the gut microbiota from the catabolism of nondigestible starches, can act in a hormone-like fashion via specific G-protein-coupled receptors (GPCRs). The primary GPCR targets for these SCFAs are FFA2 and FFA3. Using transgenic mice in which FFA2 was replaced by an altered form called a Designer Receptor Exclusively Activated by Designer Drugs (FFA2-DREADD), but in which FFA3 is unaltered, and a newly identified FFA2-DREADD agonist 4-methoxy-3-methyl-benzoic acid (MOMBA), we demonstrate how specific functions of FFA2 and FFA3 define a SCFA-gut-brain axis. Activation of both FFA2/3 in the lumen of the gut stimulates spinal cord activity and activation of gut FFA3 directly regulates sensory afferent neuronal firing. Moreover, we demonstrate that FFA2 and FFA3 are both functionally expressed in dorsal root- and nodose ganglia where they signal through different G proteins and mechanisms to regulate cellular calcium levels. We conclude that FFA2 and FFA3, acting at distinct levels, provide an axis by which SCFAs originating from the gut microbiota can regulate central activity.

AB - Volatile small molecules, including the short-chain fatty acids (SCFAs), acetate and propionate, released by the gut microbiota from the catabolism of nondigestible starches, can act in a hormone-like fashion via specific G-protein-coupled receptors (GPCRs). The primary GPCR targets for these SCFAs are FFA2 and FFA3. Using transgenic mice in which FFA2 was replaced by an altered form called a Designer Receptor Exclusively Activated by Designer Drugs (FFA2-DREADD), but in which FFA3 is unaltered, and a newly identified FFA2-DREADD agonist 4-methoxy-3-methyl-benzoic acid (MOMBA), we demonstrate how specific functions of FFA2 and FFA3 define a SCFA-gut-brain axis. Activation of both FFA2/3 in the lumen of the gut stimulates spinal cord activity and activation of gut FFA3 directly regulates sensory afferent neuronal firing. Moreover, we demonstrate that FFA2 and FFA3 are both functionally expressed in dorsal root- and nodose ganglia where they signal through different G proteins and mechanisms to regulate cellular calcium levels. We conclude that FFA2 and FFA3, acting at distinct levels, provide an axis by which SCFAs originating from the gut microbiota can regulate central activity.

KW - Designer Receptor Exclusively Activated by Designer Drugs

KW - gut–brain axis

KW - medicine

KW - mouse

KW - short-chain fatty acids

U2 - 10.7554/eLife.73777

DO - 10.7554/eLife.73777

M3 - Journal article

C2 - 35229717

AN - SCOPUS:85125559473

VL - 11

JO - eLife

JF - eLife

SN - 2050-084X

M1 - e73777

ER -

ID: 300064404