Navarro C E, Otoya R, Donoso A O
Laboratorio de Investigaciones Cerebrales (LINCE-CONICET), Facultad de Ciencias Medicas, Universidad Nacional de Cuyo, Mendoza, Argentina.
Neuroendocrinology. 1993 Apr;57(4):654-7. doi: 10.1159/000126421.
Histamine (HA) stimulates prolactin secretion via H1 and H2 receptors. In the present study, we examined the role of a third subtype of receptor recently described in brain, the H3-HA receptor, on prolactin secretion in male rats. R(-)alpha-methyl-HA (alpha-MHA), a selective H3 receptor agonist, was injected into the lateral ventricle of the brain in freely moving rats. alpha-MHA produced a dose-dependent (1-5 micrograms) and long-lasting increase in plasma prolactin levels. This increase was observed from 15 to 60 min after injection of alpha-MHA. Its stimulatory action was prevented by thioperamide (20 micrograms i.v.t), a selective H3 antagonist. This compound, injected intraventricularly, lacked effect by itself on basal plasma prolactin levels. Neither pyrilamine (H1 antagonist; 60 micrograms i.v.t.) nor ranitidine (H2 antagonist; 60 micrograms i.v.t.) affected alpha-MHA-induced prolactin release. The stimulatory effect was still present when brain HA was depleted by alpha-fluoromethylhistidine (30 mg/kg i.p.). Our findings suggest that alpha-MHA evokes prolactin release by activation of postsynaptic H3 receptors.
组胺(HA)通过H1和H2受体刺激催乳素分泌。在本研究中,我们检测了最近在脑中发现的第三种受体亚型——H3-HA受体对雄性大鼠催乳素分泌的作用。将选择性H3受体激动剂R(-)α-甲基-HA(α-MHA)注射到自由活动大鼠的脑侧脑室中。α-MHA可使血浆催乳素水平呈剂量依赖性(1-5微克)且持久升高。在注射α-MHA后15至60分钟可观察到这种升高。其刺激作用可被选择性H3拮抗剂硫代哌啶(静脉推注20微克)阻断。该化合物经脑室内注射后,自身对基础血浆催乳素水平无影响。组胺H1拮抗剂吡苄明(静脉推注60微克)和组胺H2拮抗剂雷尼替丁(静脉推注60微克)均不影响α-MHA诱导的催乳素释放。当用α-氟甲基组氨酸(腹腔注射30毫克/千克)耗尽脑内HA时,刺激作用仍然存在。我们的研究结果表明,α-MHA通过激活突触后H3受体引起催乳素释放。