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大鼠脑中的[125I]三碘甲状腺原氨酸:源自解冻装片放射自显影的神经定位和轴突运输证据

[125I] triiodothyronine in the rat brain: evidence for neural localization and axonal transport derived from thaw-mount film autoradiography.

作者信息

Dratman M B, Crutchfield F L, Futaesaku Y, Goldberger M E, Murray M

出版信息

J Comp Neurol. 1987 Jun 15;260(3):392-408. doi: 10.1002/cne.902600306.

Abstract

Previous thaw-mount light microscopic autoradiographic studies have shown that intravenously administered [125I] triiodothyronine is saturably concentrated and retained for at least 10 hours in discrete neural systems in the rat brain. To survey the brain more completely and to gain information about the time course of labeling, serial thaw-mount film autoradiograms were prepared from rat brains obtained at intervals through 48 hours after intravenous injection of high specific activity [125I] triiodothyronine. Parallel biochemical studies of whole brain homogenate extracts revealed that, at all time intervals, the label in the brain was mainly due to triiodothyronine itself (80%), or other organic iodocompounds (15%), but probably not due to free [125I] iodide (3%), which is rapidly transported out of the brain. The highly reproducible, well-defined labeling patterns seen on film indicated a widespread but selective localization of the hormone. At early times after intravenous injection of [125I] triiodothyronine, label was nonuniformly and prominently concentrated in selected regions of gray matter; evidence for saturability of hormone processing was obtained in competition studies with unlabeled triiodothyronine. Discrete labeling of fiber tracts (usually after 10 hours) left some regions of white matter conspicuously unlabeled. At 48 hours, many originally labeled gray regions showed markedly diminished or virtually complete loss of radioactivity, whereas others became newly or more prominently labeled. At that time, certain fiber tracts were also conspicuously labeled. The observed changing profiles of regional labeling over time are best explained by movement of the hormone from original sites of saturable incorporation in specific nuclei, to terminal fields, through the mechanism of axonal transport.

摘要

以往的冻融切片光镜放射自显影研究表明,静脉注射的[125I]三碘甲状腺原氨酸在大鼠脑内离散的神经系统中以饱和方式浓聚并保留至少10小时。为了更全面地观察脑内情况并获取标记的时间进程信息,在静脉注射高比活度[125I]三碘甲状腺原氨酸后,于不同时间间隔取材大鼠脑,制备系列冻融切片放射自显影片。对全脑匀浆提取物进行的平行生化研究显示,在所有时间间隔,脑内的标记主要归因于三碘甲状腺原氨酸本身(80%)或其他有机碘化合物(15%),但可能不是由于游离的[125I]碘化物(3%),后者会迅速转运出脑外。胶片上呈现的高度可重复、界限清晰的标记模式表明该激素分布广泛但具有选择性。静脉注射[125I]三碘甲状腺原氨酸后的早期,标记物在灰质的特定区域非均匀且显著浓聚;在与未标记的三碘甲状腺原氨酸的竞争研究中获得了激素处理存在饱和性的证据。纤维束的离散标记(通常在10小时后)使得一些白质区域明显未被标记。在48小时时,许多最初标记的灰质区域放射性明显减弱或几乎完全消失,而其他区域则新出现或更显著地被标记。此时,某些纤维束也明显被标记。观察到的区域标记随时间的变化情况,最好用激素通过轴突运输机制从特定核内最初的饱和掺入位点移动到终末区域来解释。

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