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纸质出版日期:2013
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高双荣, 梁爱华, 戴宝强, 等. 雄黄肾脏毒性的病理形态学特征[J]. 中国实验方剂学杂志, 2013,19(18):297-301.
GAO Shuang-rong, LIANG Ai-hua, DAI Bao-qiang, et al. Morphological Characteristics of Kidney Toxicity in Realgar[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(18): 297-301.
高双荣, 梁爱华, 戴宝强, 等. 雄黄肾脏毒性的病理形态学特征[J]. 中国实验方剂学杂志, 2013,19(18):297-301. DOI: 10.11653/syfj2013180297.
GAO Shuang-rong, LIANG Ai-hua, DAI Bao-qiang, et al. Morphological Characteristics of Kidney Toxicity in Realgar[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(18): 297-301. DOI: 10.11653/syfj2013180297.
目的: 研究反复灌胃给予雄黄后
大鼠肾脏毒性的病理形态学特征
为临床安全、有效地使用雄黄提供科学依据。方法: 随机将大鼠分为对照组和雄黄0.01
0.04
0.17 g·kg-1剂量组。各剂量组均每日灌胃给药1次
对照组给予高纯水
连续3个月。于给药后1
2
3个月和停药1
2个月后
计算肾脏指数
测定血清葡萄糖(GLU)、肌酐(Cr)、尿素氮(BUN)及尿蛋白等
并观察肾组织病理形态学变化。结果: 连续灌服雄黄≥0.01 g·kg-1 3个月或0.17 g·kg-1 2个月
肾组织出现不同程度的细胞肿胀
胞浆空泡变性
核固缩、溶解及血管扩张、充血等病变
近曲小管较肾小球损伤严重
病变呈现明显的量-时-毒关系
血BUN、GLU、尿蛋白也相应增高。停药1个月后
除0.17 g·kg-1剂量组有66.7%的肾小管轻度水肿、变性外
其余各组未见明显病变。结论: 大鼠连续灌服雄黄≥0.01 g·kg-1 3个月或0.17 g·kg-1 2个月对大鼠肾脏病理学产生明显影响
尤其对肾脏近曲小管的损伤作用较为明显
停药后肾脏病变逐渐恢复至正常。
Objective: To study the morphological characteristics of kidney toxicity in rats when repeated intra-gastric administration of realgar in order to provide a scientific basis for safe and effective application of realgar. Method: The rats were randomly divided into four groups:control group and realgar 0.01
0.04
0.17 g·kg-1 groups. The rats were intra-gastrically treated with realgar once a day for successively 90 days
while the control group was given ultra-filtrated water. Calculatate the kidney weight and body weight index were calculated and the glucose
ketones
blood urine nitrogen and urine protein were measured and pathological change of kidney under microscope was observed at 30
60
90
120
150 days. Result: The kidney cells showed swelling
vacuolation
nuclear condensation
breakage
vasodilation and congestion after repeated intra-gastric administration of realgar ≥0.01 g·kg-1 successively 90 days or 0.17 g·kg-1 successively 60 days. Proximal convoluted tubules were seriously damaged. The lesions showed significant dose and time and toxicity relationship
blood urine nitrogen
glucose
urine protein also increased accordingly. 66.7% of the renal tubular in 0.17 g·kg-1 group showed mild swelling and degeneration at day 30 after drug withdrawal
while the other groups had no significant lesions. Conclusion: Kidneys showed severe pathologic injuries after repeated intra-gastric administration of realgar≥0.01 g·kg-1 successively 90 days or 0.17 g·kg-1 successively 60 days. The proximal convoluted tubules may be a main target of arsenic toxicity to kidneys. The lesions can gradually restored to normal after realgar withdrawal.
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