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富含可可的饮食可增强三叉神经节神经元中磷酸酶的表达,并降低炎症分子的表达。

Cocoa-enriched diets enhance expression of phosphatases and decrease expression of inflammatory molecules in trigeminal ganglion neurons.

机构信息

Center for Biomedical and Life Sciences, Missouri State University, Springfield, MO 65806, USA.

出版信息

Brain Res. 2010 Apr 6;1323:18-32. doi: 10.1016/j.brainres.2010.01.081. Epub 2010 Feb 6.

Abstract

Activation of trigeminal nerves and release of neuropeptides that promote inflammation are implicated in the underlying pathology of migraine and temporomandibular joint (TMJ) disorders. The overall response of trigeminal nerves to peripheral inflammatory stimuli involves a balance between enzymes that promote inflammation, kinases, and those that restore homeostasis, phosphatases. The goal of this study was to determine the effects of a cocoa-enriched diet on the expression of key inflammatory proteins in trigeminal ganglion neurons under basal and inflammatory conditions. Rats were fed a control diet or an isocaloric diet enriched in cocoa for 14days prior to an injection of noxious stimuli to cause acute or chronic excitation of trigeminal neurons. In animals fed a cocoa-enriched diet, basal levels of the mitogen-activated kinase (MAP) phosphatases MKP-1 and MKP-3 were elevated in neurons. Importantly, the stimulatory effects of acute or chronic peripheral inflammation on neuronal expression of the MAPK p38 and extracellular signal-regulated kinases (ERK) were significantly repressed in response to cocoa. Similarly, dietary cocoa significantly suppressed basal neuronal expression of calcitonin gene-related peptide (CGRP) as well as stimulated levels of the inducible form of nitric oxide synthase (iNOS), proteins implicated in the underlying pathology of migraine and TMJ disorders. To our knowledge, this is the first evidence that a dietary supplement can cause upregulation of MKP, and that cocoa can prevent inflammatory responses in trigeminal ganglion neurons. Furthermore, our data provide evidence that cocoa contains biologically active compounds that would be beneficial in the treatment of migraine and TMJ disorders.

摘要

三叉神经的激活和神经肽的释放促进炎症,这与偏头痛和颞下颌关节(TMJ)紊乱的潜在病理有关。三叉神经对周围炎症刺激的总体反应涉及促进炎症的酶、激酶和恢复体内平衡的酶(磷酸酶)之间的平衡。本研究的目的是确定富含可可的饮食对基础和炎症条件下三叉神经节神经元中关键炎症蛋白表达的影响。在对三叉神经神经元进行有害刺激注射以引起急性或慢性兴奋之前,大鼠喂食对照饮食或富含可可的等热量饮食 14 天。在喂食富含可可的饮食的动物中,神经元中丝裂原激活蛋白激酶(MAP)磷酸酶 MKP-1 和 MKP-3 的基础水平升高。重要的是,急性或慢性外周炎症对 MAPK p38 和细胞外信号调节激酶(ERK)的神经元表达的刺激作用在可可的作用下明显受到抑制。同样,饮食可可显著抑制了降钙素基因相关肽(CGRP)的基础神经元表达,并刺激了诱导型一氧化氮合酶(iNOS)的水平,这些蛋白与偏头痛和 TMJ 紊乱的潜在病理有关。据我们所知,这是第一个证明膳食补充剂可以上调 MKP 的证据,并且可可可以防止三叉神经节神经元的炎症反应。此外,我们的数据提供了证据表明可可含有生物活性化合物,这将有益于偏头痛和 TMJ 紊乱的治疗。

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