Citric acid cycle intermediates as ligands for orphan G-protein-coupled receptors

Weihai He, Frederick J.-P. Miao, Daniel C.-H. Lin, Ralf T. Schwandner, Zhulun Wang, Jinhai Gao, Jin-Long Chen, Hui Tian and Lei Ling ()
Additional contact information
Weihai He: Tularik Inc.
Frederick J.-P. Miao: Tularik Inc.
Daniel C.-H. Lin: Tularik Inc.
Ralf T. Schwandner: Tularik Inc.
Zhulun Wang: Tularik Inc.
Jinhai Gao: Tularik Inc.
Jin-Long Chen: Tularik Inc.
Hui Tian: Tularik Inc.
Lei Ling: Tularik Inc.

Nature, 2004, vol. 429, issue 6988, 188-193

Abstract: Abstract The citric acid cycle is central to the regulation of energy homeostasis and cell metabolism1. Mutations in enzymes that catalyse steps in the citric acid cycle result in human diseases with various clinical presentations2. The intermediates of the citric acid cycle are present at micromolar concentration in blood and are regulated by respiration, metabolism and renal reabsorption/extrusion. Here we show that GPR91 (ref. 3), a previously orphan G-protein-coupled receptor (GPCR), functions as a receptor for the citric acid cycle intermediate succinate. We also report that GPR99 (ref. 4), a close relative of GPR91, responds to α-ketoglutarate, another intermediate in the citric acid cycle. Thus by acting as ligands for GPCRs, succinate and α-ketoglutarate are found to have unexpected signalling functions beyond their traditional roles. Furthermore, we show that succinate increases blood pressure in animals. The succinate-induced hypertensive effect involves the renin–angiotensin system and is abolished in GPR91-deficient mice. Our results indicate a possible role for GPR91 in renovascular hypertension, a disease closely linked to atherosclerosis, diabetes and renal failure5,6.

Date: 2004
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DOI: 10.1038/nature02488

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