Plewka A, Bienioszek M
Department of Histology and Embryology, Silesian School of Medicine, Katowice-Ligota, Poland.
Arch Toxicol. 1994;68(1):32-6. doi: 10.1007/BF03035707.
There is a wide range of change in both microsomal heme oxygenase activity and cytochrome P-450 level in the livers of rats of various ages. We tried to investigate the phases of heme oxygenase activity, both spontaneous and caused by typical MFO inducers in the lifetime of the rat. Wistar male rats aged 0.5, 1, 2, 4, 8, 12, 20 and 28 months received phenobarbital (50 mg/kg) twice, 3 and 2 days before being killed. beta-Naphthoflavone and dexamethasone were given three times: 3, 2 and 1 day before decapitation 20 mg/kg and 10 mg/kg, respectively). The highest heme oxygenase activity is observed in intact 2-week-old animals (1.16 +/- 0.038 nM/h per mg protein). Before maturity this activity decreases slightly up to the 2nd month of life. Then it stabilizes and remains virtually unchanged till the 8th month of life (1.02 +/- 0.03). Afterwards HO activity tends to increase until the 28th month of life (1.10 +/- 0.06), but does not reach the level observed in the 2-week-old animals. We have found that some typical MFO inducers can modify HO activity. While phenobarbital stimulates HO activity only in premature animals (1.42 +/- 0.056; 1.30 +/- 0.059 and 1.13 +/- 0.035, respectively in 0.5-, 1- and 2-month-old animals), beta-naphthoflavone enhances HO activity in all the groups studied. Dexamethasone, as a physiological inducer of the MFO system, modifies HO activity very characteristically. It induces this activity until the 2nd month of life and then its inducibility appears to remain unchanged.(ABSTRACT TRUNCATED AT 250 WORDS)
不同年龄大鼠肝脏中的微粒体血红素加氧酶活性和细胞色素P - 450水平存在广泛变化。我们试图研究大鼠一生中血红素加氧酶活性的阶段,包括自发活性以及由典型的混合功能氧化酶(MFO)诱导剂引起的活性。0.5、1、2、4、8、12、20和28月龄的雄性Wistar大鼠在处死前3天和2天各接受两次苯巴比妥(50mg/kg)。β - 萘黄酮和地塞米松分别在断头前3天、2天和1天各给药3次,剂量分别为20mg/kg和10mg/kg。在完整的2周龄动物中观察到最高的血红素加氧酶活性(每毫克蛋白质1.16±0.038nM/h)。在成熟前,这种活性在出生后2个月内略有下降。然后它稳定下来,直到8月龄几乎保持不变(1.02±0.03)。之后,血红素加氧酶活性趋于增加,直到28月龄(1.10±0.06),但未达到2周龄动物中观察到的水平。我们发现一些典型的MFO诱导剂可以改变血红素加氧酶活性。苯巴比妥仅刺激未成熟动物的血红素加氧酶活性(0.5、1和2月龄动物中分别为1.42±0.056、1.30±0.059和1.13±0.035),而β - 萘黄酮在所有研究组中均增强血红素加氧酶活性。地塞米松作为MFO系统的生理性诱导剂,对血红素加氧酶活性的改变非常具有特征性。它在出生后2个月内诱导这种活性,然后其诱导性似乎保持不变。(摘要截短于250字)