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6-巯基嘌呤对胎鼠中枢神经系统的组织学影响:一项光学显微镜研究

Histological effects of 6-mercaptopurine on the fetal rat central nervous system: a light-microscopic study.

作者信息

Adhami H, Noack W

出版信息

Teratology. 1975 Jun;11(3):297-311. doi: 10.1002/tera.1420110309.

DOI:10.1002/tera.1420110309
PMID:1154292
Abstract

Wistar rats were administered single doses of 16 or 50 mg/kg 6-mercaptopurine (6-MP) on day 12 of pregnancy. Necrosis in the fetal forebrain and spinal cord was studied by light microscope 6, 12, 14, 48, 72, and 81 h and 8 days afterward. The extent of necrosis was dose dependent. The first necroses were seen after 24 h, regardless of location (brain, spinal cord) or dose; but the extent was greatest after 48 h. All necrotic cells had a typical appearance; they were ballooned and often fragmented, their nuclei were darkly colored and frequently pyknotic, and they were often karyorhexic. Necroses appeared almost exclusively at sites of beginning cellular differentiation, i.e., in the intermediate zone. In the spinal cord the ventricular zone was also necrotic and the alar plate (dorsal horn) always affected. Phagocytizing cells (macrophages) appeared in the spinal cord after 48 h and in the brain after 72 h. After 81 h all the necrotic material had been phagocytized, at which time there was a massive congestion of the extra- and intracerebral vessels. Hemorrhages appeared in defined localizations. Eight days after exposure to 16 mg/kg 6-MP fetuses no longer showed any visible deviations. Fetuses exposed to 50 mg/kg showed deviations in the cytoarchitecture of the neopallium: an extremely broadened ventricular zone, few cells in the intermediate zone, and extensive rarefaction cells in the cortical plate with no clear layer structure. In the spinal cord, cleft formations were especially noticeable in the dorsal-horn region. All fetuses showed a hydrocephalus externus after 50 mg/kg. The mechanism leading to necrosis is discussed.

摘要

在妊娠第12天给Wistar大鼠单次注射16或50mg/kg的6-巯基嘌呤(6-MP)。在给药后6、12、14、48、72和81小时以及8天后,通过光学显微镜研究胎儿前脑和脊髓的坏死情况。坏死程度呈剂量依赖性。无论位置(脑、脊髓)或剂量如何,首次坏死在24小时后出现;但坏死程度在48小时后最大。所有坏死细胞都有典型的外观;它们呈气球样且常破碎,细胞核染色深且常固缩,并且常核溶解。坏死几乎仅出现在细胞开始分化的部位,即中间带。在脊髓中,室管膜带也坏死,翼板(背角)总是受到影响。吞噬细胞(巨噬细胞)在48小时后出现在脊髓中,72小时后出现在脑中。81小时后所有坏死物质都已被吞噬,此时脑内外血管出现大量充血。出血出现在特定部位。暴露于16mg/kg 6-MP的胎儿在8天后不再显示任何可见的异常。暴露于50mg/kg的胎儿在新皮质的细胞结构上出现异常:室管膜带极度增宽,中间带细胞很少,皮质板中有广泛的细胞稀疏且无清晰的层结构。在脊髓中,背角区域的裂隙形成尤为明显。所有暴露于50mg/kg的胎儿都出现了外部脑积水。本文讨论了导致坏死的机制。

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