Sarchielli P, Alberti A, Russo S, Codini M, Panico R, Floridi A, Gallai V
Interuniversity Center for the Study of Headache and Neurotransmitter Disorders of the Central Nervous System, Perugia, Rome, Italy.
Cephalalgia. 1999 Nov;19(9):810-6. doi: 10.1046/j.1468-2982.1999.1909810.x.
An alteration in serotonin concentration has been found in patients with chronic headache caused by abuse of analgesic substances as well as an up-regulation of 5HT2 platelet receptors, which has been correlated with chronicization of the headache. In a previous study we demonstrated an increase in L-arginine/nitric oxide (NO) pathway activity in platelets from patients affected by migraine with or without aura, particularly during attacks. In the present research we assessed the variations in platelet L-arginine/NO pathway and cyclic guanosine monophosphate (cGMP) levels in 32 patients affected by chronic daily headache (CDH) (8 M, 24 F, age range 34-50 years) both during and between attacks. In these same patients, the platelet aggregation to different collagen concentrations (0.3, 1, 3 micrograms/ml) was determined as well as the intracellular platelet calcium concentration using fluorescence polarization spectrometry. These parameters were compared with those of an age- and sex-matched control group (n = 25; n = 10, n = 15, age range 35-51 years). A reduction found in platelet aggregation response to each collagen concentration used (p < 0.001) was coupled with an increased NO and cGMP production (NO: p < 0.0001; cGMP: p < 0.001). This was accompanied by a significant increase in intracytosolic Ca2+ (p < 0.0001) concentration and a reduced platelet serotonin content compared to those in control individuals (p < 0.0002). Changes in the above platelet parameters were accentuated more in patients with analgesic abuse than in CDH patients with no drug abuse. These findings suggest the occurrence of an activation of cGMP-Ca2+ mediated events in CDH patients with analgesic abuse. This physiologic compensatory mechanism, which intervenes in overcoming the increase in cytosolic Ca2+ levels, is not as efficient at limiting serotonin depletion by platelet dense bodies. A similar depletion in the central serotoninergic pathway can be assumed in the same patients.
在因滥用止痛药物导致慢性头痛的患者中,已发现血清素浓度改变以及5HT2血小板受体上调,这与头痛的慢性化相关。在先前的一项研究中,我们证明了患有或不患有先兆偏头痛的患者血小板中L-精氨酸/一氧化氮(NO)途径活性增加,尤其是在发作期间。在本研究中,我们评估了32例慢性每日头痛(CDH)患者(8例男性,24例女性,年龄范围34 - 50岁)在发作期间和发作间隔期血小板L-精氨酸/NO途径及环磷酸鸟苷(cGMP)水平的变化。在这些相同的患者中,还测定了血小板对不同胶原蛋白浓度(0.3、1、3微克/毫升)的聚集情况以及使用荧光偏振光谱法测定细胞内血小板钙浓度。将这些参数与年龄和性别匹配的对照组(n = 25;n = 10,n = 15,年龄范围35 - 51岁)的参数进行比较。发现对所使用的每种胶原蛋白浓度的血小板聚集反应均降低(p < 0.001),同时NO和cGMP生成增加(NO:p < 0.0001;cGMP:p < 0.001)。这伴随着细胞内Ca²⁺浓度显著增加(p < 0.0001)以及与对照组个体相比血小板血清素含量降低(p < 0.0002)。与无药物滥用的CDH患者相比,上述血小板参数的变化在滥用止痛药物的患者中更为明显。这些发现表明在滥用止痛药物的CDH患者中发生了cGMP - Ca²⁺介导事件的激活。这种生理补偿机制在克服细胞内Ca²⁺水平升高方面发挥作用,但在限制血小板致密体导致的血清素耗竭方面效率不高。可以假定在这些相同的患者中,中枢血清素能途径也存在类似的耗竭。