Ito C, Onodera K, Yamatodani A, Yanai K, Sakurai E, Sato M, Watanabe T
Department of Psychiatry, Tohoku University School of Medicine, Sendai, Japan.
Tohoku J Exp Med. 1997 Dec;183(4):285-92. doi: 10.1620/tjem.183.285.
In this study, the effect of haloperidol on histamine (HA) levels, histidine decarboxylase (HDC) activities and the bindings of [3H]-(R)-alpha-methylhistamine ([3H]-(R)-alpha-MeHA) to histamine H3 receptors were investigated in the rat brain. Administration of 10 mg/kg of haloperidol decreased HA levels in the rat striatum and diencephalon, but increased HDC activities in rat striatum and diencephalon, although that of 5 mg/kg did not change them. Meanwhile, haloperidol inhibited the bindings of [3H]-(R)-alpha-MeHA to H3 receptor sites in the rat striatal membrane with a Ki value of 10.5 +/- 0.45 microM. These findings suggest that only a high dose of haloperidol increases HA synthesis and release as a histamine H3 receptor antagonist in the rat brain.
在本研究中,研究了氟哌啶醇对大鼠脑内组胺(HA)水平、组氨酸脱羧酶(HDC)活性以及[3H] -(R)-α-甲基组胺([3H] -(R)-α-MeHA)与组胺H3受体结合的影响。给予10mg/kg氟哌啶醇可降低大鼠纹状体和间脑的HA水平,但可增加大鼠纹状体和间脑的HDC活性,而5mg/kg剂量则无此作用。同时,氟哌啶醇抑制[3H] -(R)-α-MeHA与大鼠纹状体膜中H3受体位点的结合,Ki值为10.5±0.45μM。这些发现表明,只有高剂量的氟哌啶醇作为组胺H3受体拮抗剂可增加大鼠脑内HA的合成和释放。