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Institut für Physiologie und Experimentelle Pathophysiologie, and Institut für Klinische und Molekulare Virologie, Friedrich-Alexander-Universität Erlangen-Nürnberg, D-91054 Erlangen, Germany
1Correspondence: Institut für Physiologie und Experimentelle Pathophysiologie, Universitätsstr. 17, D-91054 Erlangen, Germany. E-mail: kress{at}physiologie1.uni-erlangen.de
Varicella-zoster virus (VZV) is a widespread human herpes virus causing
chicken pox on primary infection and persisting in sensory
neurons. Reactivation causes shingles, which are characterized by
severe pain and often lead to postherpetic neuralgia. To elucidate the
mechanisms of VZV-associated hyperalgesia, we elaborated an in
vitro model for the VZV infection of sensory neurons from rat
dorsal root ganglia. Between 35 and 50% of the neurons showed strong
expression of the immediate-early virus antigens IE62 and IE63 and the
late glycoprotein gE. When the intracellular calcium concentration was
monitored microfluorometrically for individual cells after infection,
the sensitivity to GABA or capsaicin was similar in controls and in
VZV-infected neurons. However, the baseline calcium concentration was
increased. Neurons became de novo sensitive to
adrenergic stimulation after VZV infection. Norepinephrine-responsive
neurons were more frequent and calcium responses to norepinephrine were
significantly higher after infection with wild-type isolates than with
the attenuated vaccine strain OKA. The adrenergic agonists
phenylephrine and isoproterenol had similar efficacy. We suggest that
the infection with wild-type VZV isolates confers norepinephrine
sensitivity to sensory neurons by using
1- and/or
ß1-adrenergic receptors providing a model for the
pathophysiology of the severe pain associated with the acute
reactivation of VZV.Kress, M., Fickenscher, H. Infection by human
varicella-zoster virus confers norepinephrine sensitivity to sensory
neurons from rat dorsal root ganglia.
Key Words: DRG cells norepinephrine postherpetic neuralgia sensory neurons
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