کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6018612 1186523 2012 12 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Macrophage migration inhibitory factor (MIF) is essential for inflammatory and neuropathic pain and enhances pain in response to stress
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی عصب شناسی
پیش نمایش صفحه اول مقاله
Macrophage migration inhibitory factor (MIF) is essential for inflammatory and neuropathic pain and enhances pain in response to stress
چکیده انگلیسی

Stress and glucocorticoids exacerbate pain via undefined mechanisms. Macrophage migration inhibitory factor (MIF) is a constitutively expressed protein that is secreted to maintain immune function when glucocorticoids are elevated by trauma or stress. Here we show that MIF is essential for the development of neuropathic and inflammatory pain, and for stress-induced enhancement of neuropathic pain. Mif null mutant mice fail to develop pain-like behaviors in response to inflammatory stimuli or nerve injury. Pharmacological inhibition of MIF attenuates pain-like behaviors caused by nerve injury and prevents sensitization of these behaviors by stress. Conversely, injection of recombinant MIF into naïve mice produces dose-dependent mechanical sensitivity that is exacerbated by stress. MIF elicits pro-inflammatory signaling in microglia and activates sensory neurons, mechanisms that underlie pain. These data implicate MIF as a key regulator of pain and provide a mechanism whereby stressors exacerbate pain. MIF inhibitors warrant clinical investigation for the treatment of chronic pain.

► Mif null mice do not develop pain hypersensitivity after nerve injury or CFA. ► rMIF causes dose-dependent pain hypersensitivity. ► rMIF increases electrical discharge in small diameter nociceptive neurons. ► rMIF increases axon sprouting and induces pro-inflammatory cytokines. ► MIF inhibitor prevents stress-induced exacerbation of pain hypersensitivity.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Experimental Neurology - Volume 236, Issue 2, August 2012, Pages 351-362
نویسندگان
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