A novel method for the rapid detection of post-translationally modified visinin-like protein 1 in rat models of brain injury

Brain Inj. 2018;32(3):363-380. doi: 10.1080/02699052.2017.1418907. Epub 2017 Dec 28.

Abstract

Background: Although elevated serum levels of visinin-like protein 1 (VILIP-1), a neuron-specific calcium sensor protein, are associated with ischaemic stroke, only a single study has evaluated VILIP-1 as a biomarker of traumatic brain injury (TBI). The current proof-of-concept study was designed to determine whether serum VILIP-1 levels increase post-injury in a well-characterized rat unilateral cortical contusion model.

Methods: Lateral flow devices (LFDs) rapidly (< 20 min) detected trace serum levels (pg/mL) of VILIP-1 in a small input sample volume (10 µL). Temporal profiles of serum levels at baseline and post-injury were measured in male Sprague Dawley rats subjected to very mild-, mild unilateral-cortical contusion, or naïve surgery and in male Sprague Dawley rats following a diffuse TBI or sham surgery.

Results: Mean serum levels were significantly elevated by 0.5 h post-injury and remained so throughout the temporal profile compared with baseline in very mild and mild unilateral contusions but not in naïve surgeries. Serum levels were also elevated in a small cohort of animals subjected to a diffuse TBI injury.

Conclusions: Overall, the current study demonstrates that the novel LFD is a reliable and rapid point-of-care diagnostic for the detection and quantification of serum levels of UB-VILIP-1 in a clinically relevant time frame.

Keywords: Biomarker; head injury; mild brain injury; traumatic brain injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Injuries / blood*
  • Brain Injuries / diagnosis*
  • Cerebral Cortex / injuries
  • Cohort Studies
  • Disease Models, Animal
  • HEK293 Cells
  • Humans
  • Immunoprecipitation
  • Linear Models
  • Male
  • Neurocalcin / blood*
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors
  • Ubiquitin / metabolism

Substances

  • Neurocalcin
  • Ubiquitin
  • Vsnl1 protein, rat