Department of Neurobiology and Anatomy, University of Texas Medical School at Houston, Houston, Texas, USA.
Invest Ophthalmol Vis Sci. 2011 May 10;52(6):3083-8. doi: 10.1167/iovs.10-6160.
Previously, retinopetal axons containing histamine and dopaminergic neurons expressing histamine H(1)-receptor had been localized in mouse retinas using anatomic techniques. The goal of these experiments was to demonstrate that these receptors are functional.
Dopaminergic cells were acutely isolated from retinas of transgenic mice expressing red fluorescent protein under control of the tyrosine hydroxylase promoter and loaded with the calcium indicator Fura-2.
Under control conditions, there were spontaneous oscillations in the levels of free intracellular calcium in dopaminergic cells. These oscillations were abolished in nominally calcium-free extracellular medium and in 1 μM tetrodotoxin, findings suggesting that the oscillations were mediated by calcium entry across the plasma membrane in response to sodium-dependent action potentials. Histamine increased the mean free intracellular calcium in the dopaminergic cells by increasing the frequency and/or amplitude of the calcium oscillations. The effects of histamine were dose-dependent and reached maximum at 5 μM. With this dose, there was a 65% increase in the mean free intracellular calcium concentration. The histamine H(1)-receptor antagonist, pyrilamine, blocked the effects of 5 μM histamine when applied at 50 μM. The selective histamine H(1)-receptor agonists, 2-(3-trifluoromethylphenyl) histamine and methylhistaprodifen significantly increased mean free intracellular calcium when applied at 5 μM.
Histamine released from retinopetal axons in the mouse retina can elevate intracellular calcium levels in the perikarya of dopaminergic cells via the activation of histamine H(1)-receptors.
先前,通过解剖技术已经在小鼠视网膜中定位了含有组胺的视网膜神经纤维和表达组氨酸 H(1)-受体的多巴胺能神经元。这些实验的目的是证明这些受体是功能性的。
从表达酪氨酸羟化酶启动子控制下的红色荧光蛋白的转基因小鼠的视网膜中急性分离多巴胺能细胞,并加载钙指示剂 Fura-2。
在对照条件下,多巴胺能细胞内游离钙的水平存在自发的振荡。这些振荡在无钙的细胞外介质中和 1 μM 河豚毒素中被消除,这表明振荡是由钠依赖性动作电位引起的质膜钙内流介导的。组胺通过增加钙振荡的频率和/或幅度来增加多巴胺能细胞内的平均游离钙。组胺的作用呈剂量依赖性,在 5 μM 时达到最大值。在此剂量下,平均游离钙浓度增加了 65%。组胺 H(1)-受体拮抗剂,哌嗪,在 50 μM 时可阻断 5 μM 组胺的作用。选择性组胺 H(1)-受体激动剂,2-(3-三氟甲基苯基)组胺和甲基组氨酸 prodifen 在 5 μM 时显著增加了平均游离细胞内钙。
从鼠标视网膜中的视网膜神经纤维释放的组胺可以通过激活组胺 H(1)-受体来升高多巴胺能细胞体的细胞内钙水平。