Laurikainen E, Miller J M, Nuttall A L, Quirk W S
Kresge Hearing Research Institute, Department of Otolaryngology, University of Michigan, Ann Arbor, USA.
Eur Arch Otorhinolaryngol. 1998;255(3):119-23. doi: 10.1007/s004050050025.
The aim of this study was to investigate the mechanism and site of action of betahistine dihydrochloride in the inner ear of the guinea pig. Betahistine-evoked increases in cochlear blood flow (CBF) have been presumed to be due to the drug effect on the later wall capillary bed or larger feeding vessels in the cochlea vascular system. As such, the mechanism of action could be due to inhibition of H3 receptors. Betahistine may also have a direct effect on postsynaptic H1/H2 receptors and/or an effect modulated by other autonomic receptors. Betahistine-evoked CBF responses were assessed by laser Doppler flowmetry in the presence of an H3 agonist (alpha N-methyl-histamine dihydrochloride), an H3 antagonist (thioperamide), an H2 antagonist (cimetidine) or an alpha 2 antagonist (idazoxan). The effects of betahistine on circulation in the anterior inferior cerebellar artery (AICA) and ipsilateral stria vascularis (SV) were assessed using intravital microscopy (IVM). Findings showed that betahistine increased CBF and reduced systemic blood pressure (BP). In contrast, alpha N-methylhistamine dihydrochloride had no effect on baseline CBF or BP and did not influence betahistine-induced increases in CBF. Thioperamide reversed the effects of betahistine on CBF, but had no effect on baseline CBF or BP. Cimetidine had no marked effect on baseline CBF or betahistine-induced increases in CBF Idazoxan had no consistent effects on baseline CBF, but abolished the effect of betahistine on CBF. The mean increase of red blood cell velocity in SV capillaries was 15% and occurred without a demonstrable change in capillary diameters. In contrast, the diameter of the AICA increased by 17-20%, indicating that betahistine-evoked increases in CBF resulted primarily from vasodilatation of the AICA. We suggest that this effect may be mediated via presynaptic H3 heteroreceptors and autonomic alpha 2 receptors.
本研究的目的是探究盐酸倍他司汀在豚鼠内耳的作用机制和作用部位。据推测,倍他司汀引起的耳蜗血流量(CBF)增加是由于该药物对耳蜗血管系统的外侧壁毛细血管床或较大的供血血管产生了作用。因此,其作用机制可能是抑制H3受体。倍他司汀也可能对突触后H1/H2受体有直接作用和/或通过其他自主受体调节产生作用。在存在H3激动剂(α-N-甲基组胺二盐酸盐)、H3拮抗剂(硫代哌啶)、H2拮抗剂(西咪替丁)或α2拮抗剂(咪唑克生)的情况下,通过激光多普勒血流仪评估倍他司汀引起的CBF反应。使用活体显微镜检查(IVM)评估倍他司汀对小脑前下动脉(AICA)和同侧血管纹(SV)循环的影响。研究结果表明,倍他司汀增加了CBF并降低了全身血压(BP)。相比之下,α-N-甲基组胺二盐酸盐对基线CBF或BP没有影响,也不影响倍他司汀引起的CBF增加。硫代哌啶逆转了倍他司汀对CBF的作用,但对基线CBF或BP没有影响。西咪替丁对基线CBF或倍他司汀引起的CBF增加没有明显影响。咪唑克生对基线CBF没有一致的影响,但消除了倍他司汀对CBF的作用。SV毛细血管中红细胞速度平均增加了15%,且毛细血管直径没有明显变化。相比之下,AICA的直径增加了17 - 20%,表明倍他司汀引起的CBF增加主要是由AICA的血管舒张所致。我们认为这种作用可能是通过突触前H3异受体和自主α2受体介导产生的。