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Microglial reactions after subcutaneous formalin injection into the rat hind paw
K Y Fu1, A R Light, G K Matsushima
1Dental Research Center, School of Dentistry, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA.
Abstract:
Microglia in primary afferent projection territories are activated and proliferate after peripheral nerve injury. However, it is not known whether stimulation of peripheral nerves by noxious stimuli applied to their receptive fields activates microglial cells in the spinal cord. This study was designed to investigate the response of microglia in the lumbar spinal cord and in the brainstem to a tonic noxious stimulus. Thirty-two male Sprague-Dawley rats received subcutaneous injections of 5% formalin (50 microliter) into the plantar surface of the right hind paw, and 24 rats were injected with 50 microliter saline as a control. The lumbar spinal cord and brainstem were evaluated for immunoreactivity (IR) to complement receptor C3bi (monoclonal antibody OX-42) and major histocompatibility complex class II (monoclonal antibody OX-6) on postinjection hours 0, 2, 4 and 8 and days 1, 3, 7, 14 and 28. A qualitative and quantitative increase of OX-42-IR microglial cells were observed in the medial portion of the dorsal horn and in the gracile nucleus of the brainstem on the side ipsilateral to the formalin injection, starting on days 1-3 and peaking on day 7 postinjection. OX-6-positive cells were scattered both in gray and white matter, but no difference was detected between the two sides of the spinal cord or between formalin-injected and control animals. This is the first study that reports that subcutaneous injection of formalin into the rat's hind paw induces microglial activation in the spinal cord as well as in the brainstem. Although we have not determined whether these responses result from nociceptor activity, peripheral inflammation, or degeneration of primary afferents and/or central neurons, this method provides a simple, effective and stable animal model that will permit the future study of the mechanisms that contribute to microglial activation and its pathophysiological consequences.
Insights
Noxious stimuli, like formalin injections in rats, activate microglia in the spinal cord and brainstem. This study establishes a model for investigating microglial activation mechanisms and consequences.
Area of Science:
- Neuroscience
- Immunology
- Pain Research
Background:
- Microglia activation and proliferation occur after peripheral nerve injury.
- The effect of noxious stimuli on microglia in the spinal cord remains unclear.
Purpose of the Study:
- To investigate microglial activation in the rat lumbar spinal cord and brainstem in response to a tonic noxious stimulus.
- To establish an animal model for studying microglial activation mechanisms.
Main Methods:
- Thirty-two rats received formalin injections into the hind paw; 24 received saline as a control.
- Lumbar spinal cord and brainstem were analyzed for microglial markers (OX-42, OX-6) at various time points.
- Immunoreactivity was assessed qualitatively and quantitatively.
Main Results:
- Increased OX-42 immunoreactivity in microglia was observed in the spinal cord dorsal horn and brainstem gracile nucleus ipsilateral to formalin injection.
- Microglial activation began 1-3 days post-injection, peaking at day 7.
- No significant changes in OX-6 positive cells were detected between groups or sides.
Conclusions:
- Subcutaneous formalin injection in rats induces microglial activation in the spinal cord and brainstem.
- This study provides a model for future research into the mechanisms and consequences of microglial activation in response to noxious stimuli.