Chirulli Vera, Longo Vincenzo, Marini Sandra, Mazzaccaro Arturo, Fiorio Roberto, Gervasi Pier Giovanni
Istituto di Fisiologia Clinica, Area della Ricerca CNR, Via Moruzzi, 1, 56127, Pisa, Italy.
Life Sci. 2005 Apr 15;76(22):2535-46. doi: 10.1016/j.lfs.2004.09.042.
Several CYP enzymes are expressed in the lung of mammals but studies on their regulation have been rather neglected. In this study, the CAR and PXR expression and the inducibility of CYP 2B and CYP 3A isoforms in the lung rats and rabbits were investigated. Rats were treated with phenobarbital, clotrimazole or a mixture of dexametasone plus pregnenolone 16alpha-carbonitrile, whereas rabbits were treated with phenobarbital or rifampicin. A low constitutive expression of CAR mRNA was demonstrated by RT-PCR analysis in the lung of rat but not in rabbit. Phenobarbital treatment did not change the CAR expression profiles and did not induce in either rats and rabbits the pulmonary CYP 2B isoforms, as judged by western blot analysis and the marker pentoxyresorufin O-dealkylase and 7-ethoxy-4-trifluoroethylcoumarin O-deethylase activities. On the contrary, these marker activities were strongly induced by phenobarbital in the liver of both species. A low constitutive level of PXR mRNA was also detected by RT-PCR in the lung of rabbit but not in rat. However, also in this case, their expressions were not altered by the administration of strong CYP 3A inducers such as clotrimazole or a mixture of dexametasone plus pregnenolone 16alpha-carbonitrile for the rat and rifampicin or phenobarbital for the rabbit. For the first time, it was demonstrated by RT-PCR that rat lung expresses CYP 3A2, 3A9, 3A18 and 3A23 whereas the rabbit lung expresses the CYP 3A6, the only CYP 3A isoform identified in the rabbit so far. However, notwithstanding the differences observed in the constitutive presence of PXR and CYP 3A transcripts in both species, the above mentioned treatments did not affect in their lungs, unlike their livers, neither the anti-rat 3A immunoreactive proteins nor the CYP 3A marker 7-benzyloxyquinoline O-debenzylase and the 6beta-testosterone hydroxylase activities. The results obtained indicate that the role of CAR and PXR in the lung of rat and rabbit is different from that observed in the liver or other extrahepatic tissues where the induction of the CYP 2B and CYP 3A isoforms is regulated by these receptors.
几种细胞色素P450(CYP)酶在哺乳动物肺中表达,但对其调控的研究却相当被忽视。在本研究中,对大鼠和兔肺中组成型雄烷受体(CAR)和孕烷X受体(PXR)的表达以及CYP 2B和CYP 3A亚型的诱导性进行了研究。大鼠用苯巴比妥、克霉唑或地塞米松加孕烯醇酮16α-腈混合物处理,而兔用苯巴比妥或利福平处理。通过逆转录聚合酶链反应(RT-PCR)分析表明,大鼠肺中有低水平的CAR mRNA组成型表达,而兔肺中没有。通过蛋白质免疫印迹分析以及标记物戊氧异吩唑酮O-脱烷基酶和7-乙氧基-4-三氟乙基香豆素O-脱乙基酶活性判断,苯巴比妥处理并未改变CAR的表达谱,也未在大鼠和兔中诱导肺CYP 2B亚型。相反,在两个物种的肝脏中,这些标记物活性均被苯巴比妥强烈诱导。通过RT-PCR还检测到兔肺中有低水平的PXR mRNA组成型表达,而大鼠肺中没有。然而,同样在这种情况下,给予大鼠强CYP 3A诱导剂如克霉唑或地塞米松加孕烯醇酮16α-腈混合物,以及给予兔利福平或苯巴比妥,并未改变它们的表达。通过RT-PCR首次证明大鼠肺表达CYP 3A2、3A9、3A18和3A23,而兔肺表达CYP 3A6,这是迄今为止在兔中鉴定出的唯一CYP 3A亚型。然而,尽管在两个物种中观察到PXR和CYP 3A转录本组成型存在的差异,但上述处理对它们的肺没有影响,与肝脏不同,既不影响抗大鼠3A免疫反应性蛋白,也不影响CYP 3A标记物7-苄氧基喹啉O-脱苄基酶和6β-睾酮羟化酶活性。所得结果表明,CAR和PXR在大鼠和兔肺中的作用与在肝脏或其他肝外组织中观察到的不同,在这些组织中CYP 2B和CYP 3A亚型的诱导受这些受体调控。