Skip to main content

Advertisement

Log in

Increased neopterin production and tryptophan degradation in advanced Parkinson's disease

  • Published:
Journal of Neural Transmission Aims and scope Submit manuscript

Summary.

Large amounts of neopterin are produced by interferon-(IFN)-γ-stimulated human monocytes/macrophages, and increased neopterin concentrations indicate cellular immune activation. In parallel, IFN-γ induces indoleamine 2,3-dioxygenase which degrades l_-tryptophan to kynurenine. Increased tryptophan degradation rates are indicated by an increased kynurenine/tryptophan ratio (kyn/trp-ratio), reflecting immune system activation, too. In 22 patients with Parkinson's disease (PD) and in 11 age-matched controls, serum and cerebrospinal fluid (CSF) neopterin concentrations were measured by ELISA. Tryptophan and kynurenine concentrations were determined by HPLC. Neopterin concentrations and kyn/trp-ratios were increased both in serum and CSF of patients as compared to controls. Serum tryptophan was lower in patients. Patients with the highest disease activity presented with highest degree of immune activation. Significant correlations existed between neopterin concentrations and kyn/trp-ratios in serum and CSF. Increased formation of neopterin and enhanced degradation of tryptophan suggest activated cell-mediated immune response in a subgroup of patients with advanced Parkinson's disease.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received March 12, 2001; accepted October 9, 2001

Rights and permissions

Reprints and permissions

About this article

Cite this article

Widner, B., Leblhuber, F. & Fuchs, D. Increased neopterin production and tryptophan degradation in advanced Parkinson's disease. J Neural Transm 109, 181–189 (2002). https://doi.org/10.1007/s007020200014

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s007020200014

Navigation