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DOI 10.1002/j.1532-2149.2012.00140.x

Медицинская библиотека · European journal of pain (London, England) · 2012

The correlation between pain-related behaviour and spinal microgliosis in four distinct models of peripheral neuropathy.

Blackbeard J, Wallace V C J, O'Dea K P, Hasnie F, Segerdahl A, Pheby T, Field M J, Takata M, Rice A S C

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Peripheral nerve injury is associated with a spinal microglial response that has been correlated with the development of behaviours reflective of neuropathic pain.

METHODS

To examine whether this phenomenon is generalizable to neuropathic pain of non-traumatic aetiology, this study investigated the association between spinal microgliosis and behavioural measures of neuropathic hypersensitivity and pain-related anxiety behaviour in four distinct rat models of peripheral neuropathic pain. These were traumatic neuropathy [L5 spinal nerve transection (SNT)], HIV-related neuropathies (either treatment with the antiretroviral drug Zalcitabine (ddC) or combination of perineural exposure to the HIV-gp120 protein and ddC treatment) and varicella zoster virus (VZV) infection.

RESULTS AND

CONCLUSION

Persistent mechanical hypersensitivity developed in all 'neuropathic' rats. However, spinal microgliosis, as measured by increased CD11b/c immunohistochemical staining and increased numbers of cells expressing CD11b measured by flow cytometry, was evident in the SNT and to a lesser extent in the HIV neuropathy models but not the VZV model. These results suggest that behavioural hypersensitivity and thigmotaxis can only be linked to a microglial response in certain models of neuropathy.

Для цитирования: Blackbeard J, Wallace V C J, O'Dea K P, Hasnie F, Segerdahl A, Pheby T, Field M J, Takata M, Rice A S C. The correlation between pain-related behaviour and spinal microgliosis in four distinct models of peripheral neuropathy.. European journal of pain (London, England). 2012. DOI: 10.1002/j.1532-2149.2012.00140.x.

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