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对感染鼠轮状病毒的新生小鼠肠道随时间变化的电子显微镜研究。

An electron microscopic investigation of time-related changes in the intestine of neonatal mice infected with murine rotavirus.

作者信息

Osborne M P, Haddon S J, Spencer A J, Collins J, Starkey W G, Wallis T S, Clarke G J, Worton K J, Candy D C, Stephen J

机构信息

Department of Physiology, University of Birmingham, U.K.

出版信息

J Pediatr Gastroenterol Nutr. 1988 Mar-Apr;7(2):236-48. doi: 10.1097/00005176-198803000-00014.

Abstract

Seven-day-old mice were infected orally with murine rotavirus (EDIM) and regions of the gut examined at 24 h intervals up to 7 days by electron microscopy. Structural changes were correlated with data on viral antigen production, thymidine kinase activity, and clinical signs of diarrhea. No pathological changes were detected in the colon. Infection and structural damage were confined to the small intestine, with middle regions showing the most pronounced changes. Constriction of villus bases, edema of the lamina propria, and vacuolation of enterocytes occurred at 24 h postinfection (PI), i.e., before evidence of major virus replication. Transient villus atrophy occurred at 48 h PI. Recovery of villus length was evident by 72 h PI accompanied by evidence of marked enterocyte replication at villus bases. Many enterocytes were damaged with little evidence for the presence of virus particles. By 96 h PI, villi had almost recovered from infection although some enterocytes were still damaged; no virus particles were detected in these cells. A second phase of villus damage and edema of the lamina propria occurred at 120 h PI; the pathology resembled that at 24-48 h PI. By 144 to 168 h PI, recovery of the mucosa from infection was virtually complete. We suggest that many of the pathological features following rotavirus infection result from rotavirus-induced ischemia of villi and that diarrhea results from malabsorption of fluid by damaged villi and hypersecretion of ions released from increased numbers of dividing cells at villus-crypt borders.

摘要

给7日龄小鼠经口感染鼠轮状病毒(EDIM),在长达7天的时间里,每隔24小时通过电子显微镜检查肠道区域。将结构变化与病毒抗原产生、胸苷激酶活性及腹泻临床症状的数据进行关联分析。在结肠中未检测到病理变化。感染和结构损伤局限于小肠,中部区域变化最为明显。感染后24小时(PI),即主要病毒复制迹象出现之前,绒毛基部收缩、固有层水肿以及肠上皮细胞空泡化就已发生。感染后48小时出现短暂的绒毛萎缩。感染后72小时,绒毛长度明显恢复,同时伴有绒毛基部肠上皮细胞显著增殖的迹象。许多肠上皮细胞受损,但几乎没有病毒颗粒存在的证据。到感染后96小时,尽管一些肠上皮细胞仍有损伤,但绒毛已基本从感染中恢复;在这些细胞中未检测到病毒颗粒。感染后120小时,出现了绒毛损伤和固有层水肿的第二阶段;病理情况与感染后24 - 48小时相似。到感染后144至168小时,黏膜从感染中的恢复基本完成。我们认为,轮状病毒感染后的许多病理特征是由轮状病毒诱导的绒毛缺血所致,腹泻是由受损绒毛对液体的吸收不良以及绒毛 - 隐窝边界处增殖细胞数量增加释放的离子过度分泌引起的。

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