首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Beneficial cardio-renovascular effects of a low-molecular-weight heparin-derivative on adriamycin-induced glycosaminoglycanuria and tissue lipid abnormalities.
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Beneficial cardio-renovascular effects of a low-molecular-weight heparin-derivative on adriamycin-induced glycosaminoglycanuria and tissue lipid abnormalities.

机译:低分子量肝素衍生物对阿霉素诱导的糖胺基尿症和组织脂质异常的有益的心血管作用。

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摘要

The present work includes a study on the glycosaminoglycanuric condition induced by adriamycin (ADR, a chemotherapeutic agent) and the accompanying secondary hyperlipidemia, wherein the treatment with a low-molecular-weight heparin-derivative (LMWH), certoparin, is evaluated for its protective role (if any) on these parameters. Two groups of male albino rats of the Wistar strain (140+/-10g) received a single intravenous injection of adriamycin (7.5mg/kg), and one of these groups was treated with a low-molecular-weight heparin-derivative (Certoparin Sodium, Troparin((R)); 300mug/day/rat s.c.), commencing on day 8, for a week. Urinary total glycosaminoglycans excretion of the untreated ADR-induced group was found to increase on the 8th and the 15th days of observation, when compared with the controls. The LMWH treatment commencing on day 8 resulted in minimising the glycosaminoglycans (GAGs) excretion by day 15 (p<0.001). Plasma, cardiac, hepatic and renal lipids (cholesterol, triglycerides and phospholipids) showed a sharp increase in the pathologic group, along with a rise in plasma LDL and VLDL cholesterol and drop in HDL cholesterol levels, paralleled by abnormal activities of the enzymes involved in lipid metabolism. LMWH treated group showed a normalised lipid profile and the activities of the lipid-metabolising enzymes was close to that of controls. It is concluded herein that adriamycin administration resulted in severe nephropathy manifested by increased glycosaminoglycanuria and abnormal lipid metabolism, and that LMWH treatment afforded substantial protection by restoring glomerular structure and function, and normalised the plasma and tissue lipid levels, lipoprotein profile and the activities of lipid-metabolising enzymes.
机译:目前的工作包括对由阿霉素(ADR,化学治疗剂)和伴随的继发性高脂血症引起的糖胺基尿酸状况的研究,其中评估了低分子肝素衍生物(LMWH)certoparin的保护作用。在这些参数上的作用(如果有)。两组Wistar品系(140 +/- 10g)的雄性白化病大鼠接受单次静脉注射阿霉素(7.5mg / kg),其中一组接受低分子量肝素衍生物(Certoparin)的治疗。钠,Troparin(R); 300杯/天/大鼠sc),从第8天开始,持续一周。与对照组相比,未观察到的ADR诱导组的尿总糖胺聚糖排泄在观察的第8天和第15天增加。从第8天开始的LMWH治疗导致第15天的糖胺聚糖(GAGs)排泄最小化(p <0.001)。血浆,心脏,肝脏和肾脏脂质(胆固醇,甘油三酸酯和磷脂)在病理组中急剧增加,同时血浆LDL和VLDL胆固醇升高,HDL胆固醇水平下降,同时所涉及的酶的异常活动脂质代谢。 LMWH治疗组显示归一化的脂质分布,并且脂质代谢酶的活性接近于对照。在此得出结论,阿霉素的给药导致严重的肾病,表现为糖胺基糖尿过多和脂质代谢异常,LMWH治疗通过恢复肾小球结构和功能提供了实质性保护,并使血浆和组织脂质水平,脂蛋白谱和脂质活性正常化代谢酶。

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