Geetha A, Sankar R, Marar T, Devi C S
Department of Biochemistry, A.C. College of Technology, Guindy Campus, Madras.
Indian J Physiol Pharmacol. 1990 Apr;34(2):94-100.
The beneficial effect of alpha-tocopherol on doxorubicin-induced toxicity was studied in rats. alpha-Tocopherol (400 mg/kg/day) was administered orally, daily for a period of 2 months along with/without doxorubicin (2.5 mg/kg, i v weekly once for 8 weeks). Histology showed liver necrosis, heart myocyte degeneration, glomerular and tubular degeneration, cellular infiltration and desquammation of intestinal mucosa in doxorubicin treated animals. There was a significant increase in lipid peroxide levels measured in terms of "TBA reactants" in all these organs. These changes were associated with elevated levels of serum enzymes such as transaminases, creatine kinase and lactate dehydrogenase. The pathological observations, were minimal in animals receiving both doxorubicin and alpha-tocopherol. The lipid peroxide levels were low with concomitant normal levels of serum and intestinal enzymes in those animals.
在大鼠中研究了α-生育酚对阿霉素诱导毒性的有益作用。α-生育酚(400毫克/千克/天)口服给药,每天一次,持续2个月,同时给予/不给予阿霉素(2.5毫克/千克,静脉注射,每周一次,共8周)。组织学检查显示,接受阿霉素治疗的动物出现肝坏死、心肌细胞变性、肾小球和肾小管变性、细胞浸润以及肠黏膜脱屑。所有这些器官中以“TBA反应物”衡量的脂质过氧化物水平显著升高。这些变化与血清酶如转氨酶、肌酸激酶和乳酸脱氢酶水平升高有关。在同时接受阿霉素和α-生育酚的动物中,病理观察结果轻微。这些动物的脂质过氧化物水平较低,同时血清和肠道酶水平正常。