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Derangement of Serotonin System in Migrainous Patients With Analgesic Abuse Headache: Clues From Platelets

Authors

  • Anan Srikiatkhachorn MD,

    Corresponding author
    1. From the Department of Physiology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand (Dr. Srikiatkhachorn) and
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  • Supang Maneesri MS,

    1. Department of Pathology (Ms. Maneesri and Dr. Kasantikul), Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand and the
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  • Piyarat Govitrapong PhD,

    1. Department of Neuro- and Behavioral Biology (Dr. Govitrapong), Institute of Science and Technology for Research and Development, Mahidol University, Nakorn Pathom, Thailand.
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  • Vira Kasantikul MD

    1. Department of Pathology (Ms. Maneesri and Dr. Kasantikul), Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand and the
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Address all correspondence to Dr. Anan Srikiatkhachorn, Department of Physiology, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.

Abstract

Accumulating evidence indicates that serotonin (5-HT) may be involved in the process of analgesic-induced headache transformation. In order to clarify this hypothesis, we investigated the 5-HT system in migraine patients with analgesic abuse headache by using platelets as a neuronal model. Our results revealed a significant decrease in platelet 5-HT content in these patients compared to migraine patients and nonheadache controls (179.24 ± 10.18, 451.22 ± 14.35, and 480.22 ± 13.98 ng/109 platelets, respectively; P<0.001). This biochemical result was well correlated with a significant decrease (P<O.OOl) in platelet dense body number observed in these patients (5.9 ± 0.4 and 9.2 ± 0.6 granules/10 platelets, for migraine patients with and without analgesic abuse headache, respectively). Beside the 5-HT depletion, the presence of numerous large intracytoplasmic vacuoles formed from the surface-connecting canaliculi system was found in this condition. Such a finding has not been previously described. The total area occupied by these vacuoles was significantly greater (P<0.01) in migraine patients with analgesic overuse than in migraine patients and nonheadache controls (249.2 ± 19.5, 164.1 ± 19.5, and 183.1 ± 20.3 nm2/cells, respectively). As this canaliculi system plays a significant role in the platelet secretory response, such dilatation may imply an excessive release of substances from this system. Based on this platelet model, we suggest that excessive use of analgesics alters the central 5-HT system by depleting 5-HT from its storage sites and results in the hyposerotonergic state. This analgesic-induced 5-HT alteration may be a possible mechanism of headache transformation observed in this condition.

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