Abraham Premila, Sugumar Emila
Department of Biochemistry, Christian Medical College, Bagayam, Vellore, Tamil Nadu, India.
Arch Toxicol. 2008 Apr;82(4):237-8. doi: 10.1007/s00204-007-0240-3. Epub 2007 Sep 14.
Recent studies have shown that paraoxanase (PON1) has protective effect against oxidative stress and hence can act as an antioxidant. A time course study was carried out in order to find out alterations in PON1 activity in cyclophosphamide (CYP) induced renal injury. Eight to ten weeks old female rats were administered CYP at the dose of 150 mg/kg body wt. (i.p.) and sacrificed at 6, 16, or 24 h after treatment. Saline treated rats served as control. CYP exposure for 6 h caused a dramatic increase in PON1 activity (83%), which escalated to 160% at 16 h. The renal PON1 activity reached control values 24 h after treatment with CYP. The renal malondialdehyde level was unaltered 6 h after treatment with CYP and an increase by 35% was observed 16 h after treatment with CYP. The present investigation shows for the first time that an increase in renal PON1 activity is an early biochemical event in cyclophosphamide induced renal damage. It is suggested that this enzyme may have a role within the antioxidant systems of the kidney.
最近的研究表明,对氧磷酶(PON1)对氧化应激具有保护作用,因此可作为一种抗氧化剂。为了找出环磷酰胺(CYP)诱导的肾损伤中PON1活性的变化,进行了一项时间进程研究。将8至10周龄的雌性大鼠以150mg/kg体重的剂量腹腔注射CYP,并在治疗后6、16或24小时处死。用生理盐水处理的大鼠作为对照。暴露于CYP 6小时导致PON1活性急剧增加(83%),在16小时时升至160%。用CYP治疗24小时后,肾脏PON1活性恢复到对照值。用CYP治疗6小时后,肾脏丙二醛水平未改变,而用CYP治疗16小时后观察到丙二醛水平增加了35%。本研究首次表明,肾脏PON1活性增加是环磷酰胺诱导肾损伤的早期生化事件。提示该酶可能在肾脏的抗氧化系统中发挥作用。