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氯丙嗪与负载黑色素的培养视网膜色素上皮细胞的结合。

Binding of chlorpromazine to cultured retinal pigment epithelial cells loaded with melanin.

作者信息

Basu P K, Menon I A, Persad S D, Wiltshire J D

机构信息

Department of Ophthalmology, University of Toronto, Canada.

出版信息

Lens Eye Toxic Res. 1989;6(1-2):229-40.

PMID:2488019
Abstract

The accumulation of chlorpromazine (CPZ) in cultured bovine amelanotic retinal pigment epithelial (RPE) cells artificially loaded with melanin was investigated. The melanin was isolated from human eye bank eyes. Suspensions of the melanin were added to the RPE cells and incubated for 3 hrs. The cells ingested the melanin which was dispersed in the cytoplasm of the cells. They were not adhering to the cell membrane. The melanin-loaded cells grew in culture, although their rate of growth was slower than that of the control RPE cells not loaded with melanin. When the melanin-loaded cells were treated with CPZ, these cells accumulated a greater amount of CPZ than the control cells. A greater amount of CPZ was released from the melanin-loaded cells than from the control cells. The results suggest that some drugs or chemicals such as CPZ could accumulate in vivo in larger quantities and for longer periods in melanotic cells than in nonmelanotic cells. These compounds may subsequently be released into the extracellular fluid, thus affecting the neighbouring cells. This phenomenon may play an important role in the activities of these drugs in the melanotic cells and in the cells adjacent to the melanotic cells. These results suggested that cultured cells loaded with melanin could be used as a suitable model for studying the mechanisms of binding of drugs to intracellular melanin, and of their subsequent release outside the cells.

摘要

研究了氯丙嗪(CPZ)在人工加载黑色素的培养牛无黑色素视网膜色素上皮(RPE)细胞中的蓄积情况。黑色素从人眼库的眼中分离得到。将黑色素悬浮液添加到RPE细胞中并孵育3小时。细胞摄取了分散在细胞质中的黑色素。它们不附着于细胞膜。加载黑色素的细胞在培养中生长,尽管其生长速度比未加载黑色素的对照RPE细胞慢。当用CPZ处理加载黑色素的细胞时,这些细胞比对照细胞积累了更多的CPZ。加载黑色素的细胞比对照细胞释放出更多的CPZ。结果表明,某些药物或化学物质,如CPZ,在体内黑色素细胞中比在无黑色素细胞中蓄积的量更大、时间更长。这些化合物随后可能释放到细胞外液中,从而影响邻近细胞。这种现象可能在这些药物在黑色素细胞和与黑色素细胞相邻的细胞中的活性中起重要作用。这些结果表明,加载黑色素的培养细胞可作为研究药物与细胞内黑色素结合机制及其随后在细胞外释放机制的合适模型。

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