The effects of repeated nitroglycerin administrations in rats; modeling migraine-related endpoints and chronification

Hannah M Harris; Jessica M Carpenter; Jonathan R Black; Todd A Smitherman; Kenneth J Sufka

doi:10.1016/j.jneumeth.2017.04.010

The effects of repeated nitroglycerin administrations in rats; modeling migraine-related endpoints and chronification

J Neurosci Methods. 2017 Jun 1:284:63-70. doi: 10.1016/j.jneumeth.2017.04.010. Epub 2017 Apr 23.

Authors

Hannah M Harris¹, Jessica M Carpenter², Jonathan R Black³, Todd A Smitherman⁴, Kenneth J Sufka⁵

Affiliations

¹ Department of Psychology, University of Mississippi, 207 Peabody Building, University, MS 38677, USA. Electronic address: hmharris@go.olemiss.edu.
² Research Institute of Pharmaceutical Sciences, University of Mississippi, University, MS 38677, USA. Electronic address: jmc69554@uga.edu.
³ Department of Psychology, University of Mississippi, 207 Peabody Building, University, MS 38677, USA. Electronic address: jrblack@go.olemiss.edu.
⁴ Department of Psychology, University of Mississippi, 207 Peabody Building, University, MS 38677, USA. Electronic address: tasmithe@olemiss.edu.
⁵ Department of Psychology, University of Mississippi, 207 Peabody Building, University, MS 38677, USA; Research Institute of Pharmaceutical Sciences, University of Mississippi, University, MS 38677, USA. Electronic address: pysufka@olemiss.edu.

PMID: 28442295
DOI: 10.1016/j.jneumeth.2017.04.010

Abstract

Background: Rodent models typically use a single nitroglycerin injection to induce migraine, yet migraine in clinical populations presents as recurrent episodes. Further, these models quantify behavioral endpoints that do not align with the clinical features of episodic migraine or migraine chronification and therefore may limit translational relevance.

New method: Rats received 5 nitroglycerin (10mg/kg/2ml), propylene glycol/ethanol vehicle, or saline injections every third day over 15days. Behavioral endpoints were assessed 110min post nitroglycerin administration and included time spent light/dark chambers for photophobia as well as activity, facial pain expressions, and tactile allodynia.

Results: Animals administered nitroglycerin displayed photophobia, decreased activity, and increased facial pain expression. Similar alterations in photophobia and activity were seen in the vehicle treated animals, but these tended to diminish by the 4th or 5th injection. The presentation of spontaneous tactile allodynia was observed in the nitroglycerin group by the 5th episode.

Comparison with existing methods: Most NTG migraine models entail a single NTG administration and quantification of evoked allodynia. This paradigm employs recurring NTG episodes and clinically-relevant measures of photophobia, hypoactivity and facial grimace endpoints as well as introduces a novel arena apparatus to quantify spontaneous allodynia.

Conclusions: This repeated NTG procedure and endpoint measures aligns with the frequency and clinical presentation of episodic migraine and its chronification, respectively. Further, propylene glycol ethanol vehicle contributes to migraine endpoints.

Keywords: Allodynia; Animal models; Migraine; Nitroglycerin; Translational research.

MeSH terms

Animals
Disease Models, Animal*
Drug Administration Schedule
Endpoint Determination / methods*
Hyperalgesia / chemically induced
Hyperalgesia / diagnosis
Hyperalgesia / physiopathology
Male
Migraine Disorders / chemically induced*
Migraine Disorders / physiopathology*
Nitroglycerin / administration & dosage*
Nitroglycerin / adverse effects*
Outcome Assessment, Health Care / methods*
Rats
Rats, Sprague-Dawley
Reproducibility of Results
Sensitivity and Specificity
Species Specificity
Treatment Outcome

Substances

Nitroglycerin