PAIN
Volume 148, Issue 3 , Pages 407-413, March 2010

NGF induces non-inflammatory localized and lasting mechanical and thermal hypersensitivity in human skin

  • Roman Rukwied

      Affiliations

    • Corresponding Author InformationCorresponding author. Address: Department of Anaesthesiology and Intensive Care Medicine, Medical Faculty Mannheim, University of Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany. Tel.: +49 621 383 3170; fax: +49 621 383 1463.
  • ,
  • Alexandra Mayer

      Affiliations

    • These authors contributed equally to the manuscript.
  • ,
  • Olga Kluschina

      Affiliations

    • These authors contributed equally to the manuscript.
  • ,
  • Otilia Obreja
  • ,
  • Marcus Schley
  • ,
  • Martin Schmelz

Department of Anaesthesiology and Intensive Care Medicine Mannheim, Heidelberg University, Germany

Received 23 July 2009; received in revised form 3 November 2009; accepted 25 November 2009. published online 21 December 2009.

Abstract 

Nerve growth factor (NGF) modulates sensitivity and sprouting of nociceptors. We explored the spatial and temporal sensitization induced by NGF injection (1μg) in human skin. Hyperalgesia was investigated in 16 volunteers (36±9years) at day 1, 3, 7, 21, and 49. Areas of mechanical (brush, pin-prick) and heat (43°C) sensitization were mapped and thermal (heat and cold) pain thresholds, mechanical (impact stimulation) and electrically evoked pain, and axon reflex flare were assessed. No spontaneous pain or local inflammation was recorded upon NGF injection and during 49days. Sensitization to heat was maximum at day 3 and lasted 21days. Hyperalgesia to cold was recorded at day 7 and 21. Hypersensitivity to mechanical impact stimuli developed delayed, reached maximum at day 21, and persisted throughout 49days. Fifty percent of all volunteers reported a static allodynia to tonic pressure until day 21. Electrical stimulation at 7.5mA was more painful at the NGF site at day 21, which correlated significantly to maximum impact pain. Axon reflex flare was unaffected by NGF. Sensitization was limited to the NGF injection site, no touch- or pin-prick evoked secondary hyperalgesia was observed. Spatially restricted hyperalgesia indicates a peripheral rather than central mechanism. The temporal profile of lasting nociceptor sensitization suggests an altered peripheral axonal expression of sensory proteins specifically leading to mechanical and thermal sensitization. Intradermal NGF administration provokes a pattern of sensitization that can be used as experimental model for neuropathic pain.

Keywords: Hyperalgesia, Static allodynia, Axonal protein biosynthesis

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PII: S0304-3959(09)00688-5

doi:10.1016/j.pain.2009.11.022

PAIN
Volume 148, Issue 3 , Pages 407-413, March 2010