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氯化汞对发育中大鼠肾脏的毒性。II. 剂量增加对乳鼠肾功能的影响。

Toxicity of mercuric chloride to the developing rat kidney. II. Effect of increased dosages on renal function in suckling pups.

作者信息

Daston G P, Gray J A, Carver B, Kavlock R J

出版信息

Toxicol Appl Pharmacol. 1984 Jun 15;74(1):35-45. doi: 10.1016/0041-008x(84)90267-9.

Abstract

It has been demonstrated that the sensitivity to HgCl2 nephrotoxicity increases with maturity in the rat, and that neonates are largely unaffected by a dose of 5 mg/kg. In the present study, immature rat pups were exposed to higher doses of HgCl2 to determine whether this effect was attributable to a quantitative or qualitative difference in the renal sensitivity to HgCl2. Sprague-Dawley rats were injected with a single dose of 5, 7.5, 10, 12.5, 20, or 30 mg/kg on Postnatal Day 1; 5, 7.5, 10, 12.5, 15, or 20 mg/kg on Day 8; or 6.25, 7.5, 10, or 12.5 mg/kg on Day 15. Renal function was evaluated at 24, 48, and 120 hr after treatment by measuring urine volume, osmolality, urinary pH, and chloride content, the ability to concentrate urine during water deprivation, and the presence of protein, glucose, or hemoglobin in urine. Animals were then killed and their kidneys weighed. A dose of 20 mg/kg was needed to induce mortality in pups treated at 1 day of age, and 15 mg/kg was needed in pups treated at 8 days of age. In contrast, the 6.25-mg/kg dose given to 15-day-old pups produced some mortality, and all rats given higher doses at 15 days of age died within 2 days. There was marked oliguria or anuria in the rats that died. Kidney weight was increased in a dose-related fashion at all ages. In those animals not rendered oliguric by the treatment, urine volume increased and the ability to secrete a more concentrated urine during water deprivation decreased. Urinary pH was decreased in a dose-related manner. Urinary chloride excretion was temporarily decreased after HgCl2 treatment on Day 1 , but was increased thereafter. Proteinuria, glucosuria, and hematuria were detected in the treated rats, again increasing in frequency and severity with age and dose.

摘要

已证实,大鼠对氯化汞肾毒性的敏感性随成熟度增加,且新生大鼠对5mg/kg的剂量基本无影响。在本研究中,对未成熟的幼鼠给予更高剂量的氯化汞,以确定这种效应是否归因于肾脏对氯化汞敏感性的数量或质量差异。在出生后第1天,给斯普拉格-道利大鼠单次注射5、7.5、10、12.5、20或30mg/kg;在第8天注射5、7.5、10、12.5、15或20mg/kg;在第15天注射6.25、7.5、10或12.5mg/kg。在治疗后24、48和120小时,通过测量尿量、渗透压、尿pH值和氯化物含量、禁水期间浓缩尿液的能力以及尿中蛋白质、葡萄糖或血红蛋白的存在情况来评估肾功能。然后处死动物并称重其肾脏。1日龄幼鼠需要20mg/kg的剂量才能诱导死亡,8日龄幼鼠需要15mg/kg的剂量。相比之下,给15日龄幼鼠注射6.25mg/kg的剂量会导致一些死亡,所有15日龄给予更高剂量的大鼠在2天内死亡。死亡的大鼠出现明显的少尿或无尿。所有年龄段的大鼠肾脏重量均呈剂量相关增加。在未因治疗而少尿的动物中,尿量增加,禁水期间分泌更浓缩尿液的能力下降。尿pH值呈剂量相关下降。第1天氯化汞治疗后尿氯化物排泄暂时减少,但此后增加。在接受治疗的大鼠中检测到蛋白尿、糖尿和血尿,其频率和严重程度也随年龄和剂量增加。

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