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气管内滴注博来霉素对仓鼠肺组织切片磷脂合成的影响。

Effects of intratracheal instillation of bleomycin on phospholipid synthesis in hamster lung tissue slices.

作者信息

Giri S N

机构信息

Department of Veterinary Pharmacology and Toxicology, School of Veterinary Medicine, University of California, Davis 95616.

出版信息

Proc Soc Exp Biol Med. 1987 Dec;186(3):327-32. doi: 10.3181/00379727-186-42621.

Abstract

Bleomycin, an antineoplastic drug, is known to produce interstitial pulmonary fibrosis (IPF). As a result, it is commonly employed in various species to produce animal models of fibrosis. We have examined the uptake of [14C]acetate by lung slices and its incorporation into lipids in the slices at various times following intratracheal administration of a fibrogenic dose (10 units/kg) of bleomycin in hamsters. As compared to saline controls, bleomycin had no effect on [14C]acetate uptake at 4 and 7 days but it increased the uptake at 2 and 14 days after treatment. The incorporation of [14C]acetate into total lipid was significantly reduced to 44, 62, 62, and 75% of the control at 2, 4, 7, and 14 days after bleomycin treatment, respectively. The incorporation into lipid as a percentage of the uptake was 12.2 in control animals whereas in bleomycin-treated animals, it was 4.7, 8.0, 7.3, and 6.9 at the corresponding times. Separation of lipids into various fractions revealed that bleomycin treatment specifically inhibited the synthesis of phosphatidylcholine and neutral lipid at all times of the study. The synthesis of all other phospholipids except phosphatidylethanolamine was depressed at 2 days. The latter was, however, depressed at 7 and 14 days after bleomycin treatment. It was concluded from the present study that bleomycin treatment inhibits the synthesis of phospholipid and neutral lipid and this may eventually lead to decreased surfactant production.

摘要

博来霉素是一种抗肿瘤药物,已知会导致间质性肺纤维化(IPF)。因此,它常用于各种物种以建立纤维化动物模型。我们研究了在仓鼠气管内给予致纤维化剂量(10单位/千克)的博来霉素后,肺切片对[14C]乙酸盐的摄取及其在不同时间掺入切片脂质中的情况。与生理盐水对照组相比,博来霉素在治疗后第4天和第7天对[14C]乙酸盐摄取没有影响,但在第2天和第14天增加了摄取。博来霉素治疗后第2、4、7和14天,[14C]乙酸盐掺入总脂质中的量分别显著降至对照组的44%、62%、62%和75%。在对照组动物中,脂质掺入量占摄取量的百分比为12.2,而在博来霉素治疗组动物中,在相应时间分别为4.7、8.0、7.3和6.9。将脂质分离成不同组分显示,在研究的所有时间里,博来霉素治疗均特异性抑制磷脂酰胆碱和中性脂质的合成。除磷脂酰乙醇胺外,所有其他磷脂的合成在第2天受到抑制。然而,磷脂酰乙醇胺在博来霉素治疗后第7天和第14天受到抑制。本研究得出结论,博来霉素治疗会抑制磷脂和中性脂质的合成,这最终可能导致表面活性剂产生减少。

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