Migraine inhibitor olcegepant reduces weight loss and IL-6 release in SARS-CoV-2-infected older mice with neurological signs

J Virol. 2024 Jul 23;98(7):e0006624. doi: 10.1128/jvi.00066-24. Epub 2024 May 30.

Abstract

COVID-19 can cause neurological symptoms such as fever, dizziness, and nausea. However, such neurological symptoms of SARS-CoV-2 infection have been hardly assessed in mouse models. In this study, we infected two commonly used wild-type mouse lines (C57BL/6J and 129/SvEv) and a 129S calcitonin gene-related peptide (αCGRP) null-line with mouse-adapted SARS-CoV-2 and demonstrated neurological signs including fever, dizziness, and nausea. We then evaluated whether a CGRP receptor antagonist, olcegepant, a "gepant" antagonist used in migraine treatment, could mitigate acute neuroinflammatory and neurological signs of SARS-COV-2 infection. First, we determined whether CGRP receptor antagonism provided protection from permanent weight loss in older (>18 m) C57BL/6J and 129/SvEv mice. We also observed acute fever, dizziness, and nausea in all older mice, regardless of treatment. In both wild-type mouse lines, CGRP antagonism reduced acute interleukin 6 (IL-6) levels with virtually no IL-6 release in mice lacking αCGRP. These findings suggest that migraine inhibitors such as those blocking CGRP receptor signaling protect against acute IL-6 release and subsequent inflammatory events after SARS-CoV-2 infection, which may have repercussions for related pandemic or endemic coronavirus outbreaks.IMPORTANCECoronavirus disease (COVID-19) can cause neurological symptoms such as fever, headache, dizziness, and nausea. However, such neurological symptoms of severe acute respiratory syndrome CoV-2 (SARS-CoV-2) infection have been hardly assessed in mouse models. In this study, we first infected two commonly used wild-type mouse lines (C57BL/6J and 129S) with mouse-adapted SARS-CoV-2 and demonstrated neurological symptoms including fever and nausea. Furthermore, we showed that the migraine treatment drug olcegepant could reduce long-term weight loss and IL-6 release associated with SARS-CoV-2 infection. These findings suggest that a migraine blocker can be protective for at least some acute SARS-CoV-2 infection signs and raise the possibility that it may also impact long-term outcomes.

Keywords: COVID; SARS-CoV-2; inhibitor; migraine; viral infection; virus.

MeSH terms

  • Animals
  • COVID-19 Drug Treatment
  • COVID-19* / virology
  • Calcitonin Gene-Related Peptide / metabolism
  • Calcitonin Gene-Related Peptide Receptor Antagonists* / pharmacology
  • Calcitonin Gene-Related Peptide Receptor Antagonists* / therapeutic use
  • Disease Models, Animal*
  • Female
  • Humans
  • Interleukin-6* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Migraine Disorders* / drug therapy
  • Migraine Disorders* / virology
  • Piperazines
  • Quinazolines / pharmacology
  • Quinazolines / therapeutic use
  • SARS-CoV-2* / drug effects
  • Weight Loss* / drug effects

Substances

  • Interleukin-6
  • olcegepant
  • Calcitonin Gene-Related Peptide Receptor Antagonists
  • Quinazolines
  • Calcitonin Gene-Related Peptide
  • interleukin-6, mouse
  • Piperazines