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F344大鼠实验性镇痛剂肾病中髓质间质的不可逆损伤。

Irreversible damage to the medullary interstitium in experimental analgesic nephropathy in F344 rats.

作者信息

Burrell J H, Yong J L, MacDonald G J

机构信息

School of Physiology and Pharmacology, University of NSW, Australia.

出版信息

J Pathol. 1991 Aug;164(4):329-38. doi: 10.1002/path.1711640409.

Abstract

Renal papillary necrosis (RPN) and a decreased urinary concentrating ability developed during continuous long-term treatment with aspirin and paracetamol in female Fischer 344 rats. Renal structure and concentrating ability were examined after a recovery period of up to 18 weeks, when no analgesics were given, to investigate whether the analgesic-induced changes were reversible. There was no evidence of repair to the damaged medullary interstitial matrix, or proliferation of remaining undamaged type 1 medullary interstitial cells after the recovery period following analgesic treatment. The recovery of urinary concentrating ability was related to the length of analgesic treatment and the extent of the resulting inner medullary structural damage. During the early stages of analgesic treatment, the changes in urinary concentrating ability were reversible, but after prolonged analgesic treatment, maximum urinary concentrating ability failed to recover. This study shows that prolonged analgesic treatment in Fischer 344 rats causes progressive and irreversible damage to the interstitial matrix and type 1 interstitial cells leading to RPN. The associated urinary concentrating defect is reversible only during the early stages of structural damage to the inner medulla.

摘要

在雌性Fischer 344大鼠中,连续长期使用阿司匹林和对乙酰氨基酚治疗期间出现了肾乳头坏死(RPN)和尿浓缩能力下降。在长达18周的恢复期(不给任何镇痛药)后,检查肾脏结构和浓缩能力,以研究镇痛药引起的变化是否可逆。在镇痛药治疗后的恢复期,没有证据表明受损的髓质间质基质得到修复,或剩余未受损的1型髓质间质细胞增殖。尿浓缩能力的恢复与镇痛药治疗的时长以及由此导致的内髓结构损伤程度有关。在镇痛药治疗的早期阶段,尿浓缩能力的变化是可逆的,但在长期镇痛药治疗后,最大尿浓缩能力未能恢复。本研究表明,Fischer 344大鼠长期接受镇痛药治疗会对间质基质和1型间质细胞造成渐进性和不可逆的损伤,导致RPN。相关的尿浓缩缺陷仅在内髓结构损伤的早期阶段是可逆的。

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