TRPV1, CGRP and SP in scalp arteries of patients suffering from chronic migraine

J Neurol Neurosurg Psychiatry. 2015 Apr;86(4):393-7. doi: 10.1136/jnnp-2014-308813. Epub 2014 Oct 6.

Abstract

Objective: The transient receptor potential vanilloid type-1 receptor (TRPV1) and the neuropeptides calcitonin gene-related peptide (CGRP) and substance P (SP) appear to be differently involved in migraine pain. A role of neurovascular scalp structures is also suggested by several data. We performed a quantitative study of TRPV1-like immunoreactive (LI), CGRP-LI and SP-LI innervation of scalp arterial samples from patients affected with chronic migraine (CM).

Methods: Short segments of scalp arteries were collected from 17 participants undergoing vascular surgery for treatment-resistant CM and from 6 controls who underwent neurosurgery for various indications. The immunoreactivity of the arterial innervation to TRPV1, CGRP, SP and to the pan-neuronal marker protein gene product 9.5 (PGP9.5) was examined. Immunoreactive nerve fibres in vessel cross-sections were quantified by computerised image analysis.

Results: A significant increase of TRPV1-LI nerve fibres was found in the arterial wall from CM compared with control patients (p<0.05), while no significant difference was found for CGRP and SP.

Conclusions: This study yields the first evidence for the existence of a TRPV1-LI innervation in human scalp arteries and provides the first quantitative assessment of the TRPV1-LI, CGRP-LI and SP-LI innervation of those vessels. The increase of TRPV1-LI periarterial nociceptive fibres of scalp arteries may represent, at least in some participants, a structural condition favouring CM (and possibly migraine), for example, by causing a higher sensitivity to algogenic agents.

Keywords: HEADACHE; MIGRAINE.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Arteries / metabolism*
  • Calcitonin Gene-Related Peptide / genetics*
  • Calcitonin Gene-Related Peptide / metabolism*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Migraine Disorders / genetics*
  • Migraine Disorders / metabolism*
  • Nerve Fibers / metabolism
  • Regional Blood Flow
  • Scalp / blood supply*
  • Substance P / genetics*
  • Substance P / metabolism*
  • TRPV Cation Channels / genetics*
  • TRPV Cation Channels / metabolism*
  • Young Adult

Substances

  • TRPV Cation Channels
  • TRPV1 protein, human
  • Substance P
  • Calcitonin Gene-Related Peptide