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玻璃体内注射药物后脊椎动物眼球运动的分析。III. 自发性眼球震颤受GABAa受体调节。

Analysis of vertebrate eye movements following intravitreal drug injections. III. Spontaneous nystagmus is modulated by the GABAa receptor.

作者信息

Ariel M

机构信息

Department of Behavioral Neuroscience, University of Pittsburgh, PA 15260.

出版信息

J Neurophysiol. 1989 Aug;62(2):469-80. doi: 10.1152/jn.1989.62.2.469.

Abstract
  1. Turtle eye movements were recorded in response to horizontal motion of patterned stimuli and intravitreal injections of selective GABAergic drugs by using a contact lens search-coil technique. Similar to results from rabbit and cat, injection of picrotoxin into the turtle's eye results in a spontaneous horizontal nystagmus, with its slow-phase movement in a temporal-to-nasal direction with respect to the injected eye. In contrast, there were no prominent vertical eye movements in response to either horizontal optokinetic stimuli or drug injections. 2. Injections of bicuculline or bicuculline methyl iodide (BMI), which selectively block the GABAa receptor, had effects similar to those of picrotoxin. The GABAa agonist muscimol, on the other hand, blocked optokinetic nystagmus (OKN). Furthermore, combinations of these drugs demonstrated competitive interactions between the agonists and antagonists. 3. The threshold dose for the eye-movement effects of each drug was ascertained with the use of a radioactive calibration procedure. Tritiated inulin was injected into the vitreous. After 1 h, ocular components were assayed for radioactivity. Then, by the use of an estimate of vitreal/retinal dilution, the retinal concentrations of these threshold doses were calculated. The computed threshold retinal concentrations of the GABAa drugs were found to be in the low micromolar range. 4. These results are discussed in terms of the directionally sensitive (DS) processing which occurs in the retina, and the output of retinal DS cells to pathways involved in oculomotor control of retinal image stabilization. It is known that intravitreal application of picrotoxin makes DS retinal ganglion cells lose their selectivity for any one direction. Based on the effect of picrotoxin on OKN, it is argued that DS retinal cells provide a major input to oculomotor subsystems involved in the stabilization of gaze. Furthermore, these intravitreal drug effects on OKN are selective for GABAa drugs, suggesting that GABAa receptors play a major role in DS processing in the retina.
摘要
  1. 通过使用隐形眼镜搜索线圈技术,记录乌龟对图案刺激的水平运动以及玻璃体内注射选择性GABA能药物的眼动反应。与兔子和猫的结果相似,向乌龟眼睛注射印防己毒素会导致自发性水平眼球震颤,其慢相运动相对于注射眼是从颞侧到鼻侧方向。相比之下,无论是对水平视动刺激还是药物注射,都没有明显的垂直眼动。2. 注射选择性阻断GABAA受体的荷包牡丹碱或甲基碘化荷包牡丹碱(BMI),其效果与印防己毒素相似。另一方面,GABAA激动剂蝇蕈醇可阻断视动性眼球震颤(OKN)。此外,这些药物的组合显示出激动剂和拮抗剂之间的竞争性相互作用。3. 使用放射性校准程序确定每种药物眼动效应的阈值剂量。将氚标记的菊粉注入玻璃体。1小时后,检测眼部成分的放射性。然后,通过估计玻璃体/视网膜稀释度,计算这些阈值剂量的视网膜浓度。发现GABAA药物的计算阈值视网膜浓度处于低微摩尔范围内。4. 根据视网膜中发生的方向敏感(DS)处理以及视网膜DS细胞向参与视网膜图像稳定眼动控制的通路的输出,对这些结果进行了讨论。已知玻璃体内应用印防己毒素会使DS视网膜神经节细胞失去对任何一个方向的选择性。基于印防己毒素对OKN的影响,有人认为DS视网膜细胞为参与注视稳定的眼动子系统提供主要输入。此外,这些玻璃体内药物对OKN的作用对GABAA药物具有选择性,表明GABAA受体在视网膜的DS处理中起主要作用。

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