D'Andrea G, Cevoli S, Colavito D, Leon A
Research & Innovation (R&I), Padua, Italy.
Neurol Sci. 2015 May;36 Suppl 1:17-22. doi: 10.1007/s10072-015-2131-3.
The pathogenesis of migraine as well as cluster headache (CH) is yet a debated question. In this review, we discuss the possible role of the of tyrosine and tryptophan metabolism in the pathogenesis of these primary headaches. These include the abnormalities in the synthesis of neurotransmitters: high level of DA, low level of NE and very elevated levels of octopamine and synephrine (neuromodulators) in plasma of episodic migraine without aura and CH patients. We hypothesize that the imbalance between the levels of neurotransmitters and elusive amines synthesis is due to a metabolic shift directing tyrosine toward an increased decarboxylase and reduced hydroxylase enzyme activities. The metabolic shift of the tyrosine is favored by a state of neuronal hyperexcitability and a reduced mitochondrial activity present in migraine. In addition we present biochemical studies performed in chronic migraine and chronic tension-type headache patients to verify if the same anomalies of the tyrosine and tryptophan metabolism are present in these primary headaches and, if so, their possible role in the chronicity process of CM and CTTH. The results show that important abnormalities of tyrosine metabolism are present only in CM patients (very high plasma levels of DA, NE and tryptamine). Tryptamine plasma levels were found significantly lower in both CM and CTTH patients. In view of this, we propose that migraine and, possibly, CH attacks derive from neurotransmitter and neuromodulator metabolic abnormalities in a hyperexcitable and hypoenergetic brain that spread from the frontal lobe, downstream, resulting in abnormally activated nuclei of the pain matrix. The low tryptamine plasma levels found in CM and CTTH patients suggest that these two primary chronic headaches are characterized by a common insufficient serotoninergic control of the pain threshold.
偏头痛以及丛集性头痛(CH)的发病机制仍是一个有争议的问题。在本综述中,我们讨论了酪氨酸和色氨酸代谢在这些原发性头痛发病机制中可能发挥的作用。这些包括神经递质合成异常:无先兆发作性偏头痛和CH患者血浆中多巴胺(DA)水平高、去甲肾上腺素(NE)水平低以及章鱼胺和辛弗林(神经调质)水平极高。我们推测,神经递质水平与难以捉摸的胺类合成之间的失衡是由于代谢转变导致酪氨酸脱羧酶活性增加而羟化酶活性降低。偏头痛中存在的神经元过度兴奋状态和线粒体活性降低有利于酪氨酸的代谢转变。此外,我们展示了对慢性偏头痛和慢性紧张型头痛患者进行的生化研究,以验证这些原发性头痛中是否存在相同的酪氨酸和色氨酸代谢异常,以及如果存在,它们在慢性偏头痛(CM)和慢性紧张型头痛(CTTH)慢性化过程中的可能作用。结果表明,酪氨酸代谢的重要异常仅存在于CM患者中(血浆中DA、NE和色胺水平非常高)。在CM和CTTH患者中均发现血浆色胺水平显著降低。鉴于此,我们提出偏头痛以及可能的CH发作源于额叶下游过度兴奋和能量不足的大脑中神经递质和神经调质的代谢异常,导致疼痛矩阵的核异常激活。在CM和CTTH患者中发现的低血浆色胺水平表明,这两种原发性慢性头痛的特征是对疼痛阈值的5-羟色胺能控制普遍不足。