Laboratory of Autonomic Neuroscience, Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808, USA.
J Neurosci. 2012 Apr 11;32(15):5237-41. doi: 10.1523/JNEUROSCI.6220-11.2012.
The early proinflammatory cytokine tumor necrosis factor (TNF) is released in significant quantities by the activated immune system in response to infection, leukemia, autoimmune disorders, and radiation sickness. Nausea, emesis, and anorexia are common features of these disorders. TNF action on vagal afferent terminals in the brainstem is a likely cause of the malaise associated with these disorders. Our previous work has shown that TNF action to excite vagal afferents occurs as a result of sensitization of ryanodine channels in afferent nerve terminals. For millennia, cannabinoids (CB) have been used to combat the visceral malaise associated with chronic disease, although the mechanism of action has not been clear. Previous work in culture systems suggests that CB1 agonists can suppress neurotransmission by downregulating ryanodine channels through a protein kinase A (PKA)-dependent mechanism. Laser confocal calcium imaging methods were used to directly examine effects of CB1 cannabinoid agonists and TNF on visceral afferent signaling in the rat hindbrain. CB1 agonists blocked the effects of TNF to amplify vagal afferent responsiveness; blockade of PKA with H89 also eliminated the TNF amplification effect. These results help to explain the effectiveness of cannabinoids in blocking the malaise generated by TNF-releasing disease processes by opposing effects on ryanodine channels.
早期炎症细胞因子肿瘤坏死因子(TNF)在感染、白血病、自身免疫性疾病和辐射病等情况下,由激活的免疫系统大量释放。恶心、呕吐和厌食是这些疾病的常见特征。TNF 作用于脑干中的迷走传入末梢,可能是与这些疾病相关的不适的原因。我们之前的工作表明,TNF 通过敏化传入神经末梢中的肌醇 1,4,5-三磷酸受体(ryanodine 受体)来兴奋迷走传入。几千年来,大麻素(CB)一直被用于对抗与慢性疾病相关的内脏不适,尽管其作用机制尚不清楚。先前的培养系统研究表明,CB1 激动剂可以通过蛋白激酶 A(PKA)依赖性机制下调肌醇 1,4,5-三磷酸受体来抑制神经传递。激光共聚焦钙成像方法用于直接研究 CB1 大麻素激动剂和 TNF 对大鼠后脑内脏传入信号的影响。CB1 激动剂阻断了 TNF 放大迷走传入反应的作用;用 H89 阻断 PKA 也消除了 TNF 放大作用。这些结果有助于解释大麻素通过对肌醇 1,4,5-三磷酸受体产生相反的作用来阻断由释放 TNF 的疾病过程产生的不适的有效性。