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庆大霉素肾毒性。II. 对大鼠长期给药的生理、生化及形态学影响。

Gentamicin nephrotoxicity. II. Physiological, biochemical and morphological effects of prolonged administration to rats.

作者信息

Cuppage F E, Setter K, Sullivan P, Reitzes E J, Melnykovych A O

出版信息

Virchows Arch B Cell Pathol. 1977 Jun 24;24(2):121-38.

PMID:407707
Abstract

The purpose of this investigation was to determine the morphological, physiological and biochemical effects of gentamicin upon the rat kidney following prolonged administration of the antibiotic. Sprague-Dawley and Fischer 344 strain rats were given 3, 10, 20 or 40 mg gentamicin per kg body weight per day for 28 days. Morphologic alterations were evaluated by light and electron microscopy. Functional parameters included glomerular filtration rate, PAH secretion, renal plasma flow, sodium reabsorption, potassium excretion, urine volume and protein, and serum urea nitrogen. Oxidative metabolism of mitochondrial fractions from renal cortical homogenates was evaluated by oxygen uptake and P:O ratios. The results indicate focal proximal tubular injury, decreased tubular maximum secretion of PAH, and altered oxidative metabolism at the higher dose levels of gentamicin. Neither elevations of serum urea nitrogen nor alterations in glomerular filtration rate, renal plasma flow, or sodium or potassium excretion were observed. Thus, it appears that high dose levels (40 mg per kg per day) alter the structure and function of some proximal tubular segments when administered over prolonged periods. The alterations appear reversible. Although nephro-toxicity is identified under these conditions in rats, extrapolation to human patients usually receiving much lower doses must be guarded.

摘要

本研究的目的是确定长期给予庆大霉素后,其对大鼠肾脏的形态学、生理学和生物化学影响。将Sprague-Dawley和Fischer 344品系的大鼠每天按每千克体重给予3、10、20或40毫克庆大霉素,持续28天。通过光学显微镜和电子显微镜评估形态学改变。功能参数包括肾小球滤过率、对氨基马尿酸(PAH)分泌、肾血浆流量、钠重吸收、钾排泄、尿量和蛋白质以及血清尿素氮。通过摄氧量和磷氧比评估肾皮质匀浆线粒体部分的氧化代谢。结果表明,在较高剂量水平的庆大霉素作用下,出现局灶性近端肾小管损伤、PAH肾小管最大分泌量降低以及氧化代谢改变。未观察到血清尿素氮升高,也未观察到肾小球滤过率、肾血浆流量或钠或钾排泄的改变。因此,似乎长期给予高剂量水平(每天每千克40毫克)会改变一些近端肾小管节段的结构和功能。这些改变似乎是可逆的。尽管在这些条件下大鼠出现了肾毒性,但对于通常接受低得多剂量的人类患者进行推断时必须谨慎。

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