2. Academic Validation
  3. GTP cyclohydrolase and tetrahydrobiopterin regulate pain sensitivity and persistence

GTP cyclohydrolase and tetrahydrobiopterin regulate pain sensitivity and persistence

  • Nat Med. 2006 Nov;12(11):1269-77. doi: 10.1038/nm1490.
Irmgard Tegeder 1,  Michael Costigan,  Robert S Griffin,  Andrea Abele,  Inna Belfer,  Helmut Schmidt,  Corina Ehnert,  Jemiel Nejim,  Claudiu Marian,  Joachim Scholz,  Tianxia Wu,  Andrew Allchorne,  Luda Diatchenko,  Alexander M Binshtok,  David Goldman,  Jan Adolph,  Swetha Sama,  Steven J Atlas,  William A Carlezon,  Aram Parsegian,  Jörn Lötsch,  Roger B Fillingim,  William Maixner,  Gerd Geisslinger,  Mitchell B Max,  Clifford J Woolf
Affiliations

Affiliation

  • 1 Neural Plasticity Research Group, Department of Anesthesia and Critical Care, Massachusetts General Hospital & Harvard Medical School, 149 13th Street, Room 4309, Charlestown, Massachusetts 02129, USA.
PMID: 17057711 DOI: 10.1038/nm1490
Abstract

We report that GTP cyclohydrolase (GCH1), the rate-limiting Enzyme for tetrahydrobiopterin (BH4) synthesis, is a key modulator of peripheral neuropathic and inflammatory pain. BH4 is an essential cofactor for Catecholamine, serotonin and nitric oxide production. After axonal injury, concentrations of BH4 rose in primary sensory neurons, owing to upregulation of GCH1. After peripheral inflammation, BH4 also increased in dorsal root ganglia (DRGs), owing to enhanced GCH1 Enzyme activity. Inhibiting this de novo BH4 synthesis in rats attenuated neuropathic and inflammatory pain and prevented nerve injury-evoked excess nitric oxide production in the DRG, whereas administering BH4 intrathecally exacerbated pain. In humans, a haplotype of the GCH1 gene (population frequency 15.4%) was significantly associated with less pain following diskectomy for persistent radicular low back pain. Healthy individuals homozygous for this haplotype exhibited reduced experimental pain sensitivity, and forskolin-stimulated immortalized leukocytes from haplotype carriers upregulated GCH1 less than did controls. BH4 is therefore an intrinsic regulator of pain sensitivity and chronicity, and the GTP cyclohydrolase haplotype is a marker for these traits.

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