Pian K L, Westenberg H G, van Megen H J, den Boer J A
Department of Psychiatry, University Hospital Utrecht, The Netherlands.
Psychopharmacology (Berl). 1998 Dec;140(3):365-70. doi: 10.1007/s002130050777.
The non-selective serotonin (5-HT) receptor agonist meta-chlorophenylpiperazine (mCPP) has been reported to elicit symptoms in patients with obsessive compulsive disorder (OCD). MK-212, another non-selective 5-HT receptor agonist, does not seem to induce obsessive compulsive symptoms in OCD patients. The major pharmacological difference between mCPP and MK-212 is their affinity for the 5-HT(ID) receptor. The aim of this study was to explore the role of the 5-HT(ID) receptor in the pathophysiology of OCD, by using a challenge paradigm with the selective 5-HT(ID) receptor agonist sumatriptan (Imigran). A randomized, double-blind, placebo-controlled crossover challenge with sumatriptan (100 mg PO) was performed in 15 OCD patients. Neither the obsessive compulsive symptoms nor mood or anxiety symptoms changed significantly following sumatriptan administration as compared to placebo. Sumatriptan did induce a significant increase in plasma growth hormone (GH) levels. In the present study, no indication were found for the role of the 5-HT(ID) receptor in the pathophysiology of OCD. It should be noted, however, that sumatriptan does not readily pass the blood-brain barrier. Selective 5-HT(ID) receptors with better brain penetrating properties may shed more light on the role of this 5-HT receptor subtype in OCD.
据报道,非选择性5-羟色胺(5-HT)受体激动剂间氯苯哌嗪(mCPP)可在强迫症(OCD)患者中引发症状。另一种非选择性5-HT受体激动剂MK-212似乎不会在OCD患者中诱发强迫症状。mCPP与MK-212之间的主要药理学差异在于它们对5-HT(ID)受体的亲和力。本研究的目的是通过使用选择性5-HT(ID)受体激动剂舒马曲坦(英明格)的激发范式,探讨5-HT(ID)受体在OCD病理生理学中的作用。对15名OCD患者进行了舒马曲坦(100mg口服)的随机、双盲、安慰剂对照交叉激发试验。与安慰剂相比,服用舒马曲坦后强迫症状、情绪或焦虑症状均无显著变化。舒马曲坦确实导致血浆生长激素(GH)水平显著升高。在本研究中,未发现5-HT(ID)受体在OCD病理生理学中起作用的迹象。然而,应该注意的是,舒马曲坦不易通过血脑屏障。具有更好脑穿透特性的选择性5-HT(ID)受体可能会更清楚地揭示这种5-HT受体亚型在OCD中的作用。