The salubrious effects of ascorbic acid on cyclophosphamide instigated lipid abnormalities in fibrosarcoma bearing rats.

Cancer biochemistry biophysics Pub Date : 1998-06-01
H Vasavi, M Thangaraju, J R Babu, P Sachdanandam
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Abstract

The combined effect of cyclophosphamide and ascorbic acid on plasma lipids and lipoprotein profiles are important since, ascorbic acid encumbered the lipid abnormalities initiated by cyclophosphamide during cancer chemotherapy. Hence, the study was launched to appraise the salutary role of ascorbic acid in cyclophosphamide administered fibrosarcoma bearing rats. Fibrosarcoma cell line induced rats were treated with cyclophosphamide (10 mg/kg body weight) and ascorbic acid (200 mg/kg body weight) individually and in combination for 28 days. The concentration of plasma lipids and lipoprotein profiles were determined in control and experimental animals. The untreated, as well as cyclophosphamide administered fibrosarcoma bearing rats, divulged significantly increased levels of plasma total cholesterol, triglycerides, phospholipids, VLDL- and LDL-cholesterol, as compared with their respective control animals. In contrast, ester and HDL-cholesterol levels exhibited a marked decrease in these animals. Similar observations were also noticed in liver lipid values, as well. However, these lipid abnormalities were corrected by the co-administration of ascorbic acid. These results suggested, that some clinical entanglement of cyclophosphamide was refrained by co-administration of ascorbic acid in tumor stress condition.

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抗坏血酸对环磷酰胺诱导的纤维肉瘤大鼠脂质异常的有益作用。
环磷酰胺和抗坏血酸对血浆脂质和脂蛋白谱的联合作用是重要的,因为抗坏血酸阻碍了癌症化疗期间环磷酰胺引起的脂质异常。因此,本研究旨在评估抗坏血酸对环磷酰胺给药的纤维肉瘤大鼠的有益作用。用环磷酰胺(10 mg/kg体重)和抗坏血酸(200 mg/kg体重)单独或联合治疗纤维肉瘤细胞系诱导大鼠28 d。测定对照动物和实验动物血浆脂质浓度和脂蛋白谱。与对照动物相比,未经治疗和注射环磷酰胺的纤维肉瘤大鼠的血浆总胆固醇、甘油三酯、磷脂、VLDL-和ldl -胆固醇水平显著升高。相比之下,这些动物的酯和高密度脂蛋白胆固醇水平明显下降。肝脏脂质值也有类似的观察结果。然而,这些脂质异常可以通过联合服用抗坏血酸来纠正。这些结果表明,在肿瘤应激条件下,抗坏血酸可抑制环磷酰胺的一些临床缠结。
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Lactoferrin expression in human breast cancer. Modulation of the impaired drug metabolism in sarcoma-180-bearing mice by echitamine chloride. Magnetic field induced inhibition of human osteosarcoma cells treated with adriamycin. Modulating effect of new potential antimelanomic agents, spin-labeled triazenes and nitrosoureas on the DOPA-oxidase activity of tyrosinase. Molecular basis of specific inhibition of urokinase plasminogen activator by amiloride.
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