Shah G M, Bhattacharya R K
Cancer Lett. 1987 May;35(2):191-8. doi: 10.1016/0304-3835(87)90044-9.
Single intraperitoneal administration of benzo[a]pyrene (B[a]P) at 20 mg/kg body weight to male Wistar rats caused an early (2 h) inhibition in liver of gross transcription as measured by incorporation of [14C] orotic acid into nuclear RNA. This inhibition was reversed gradually into a partial stimulation at 2-4 days after administration of B[a]P, followed by another period of inhibition at 7 days which persisted up to 14 days. The early reversible inhibition at 2 h was probed further by studies on in vitro transcription using isolated nuclei from treated rats. It was observed that total expression of RNA polymerase activity was only marginally inhibited because, while expression of RNA polymerases II and III showed remarkable inhibition, RNA polymerase I showed stimulation in activity.
以20毫克/千克体重的剂量对雄性Wistar大鼠进行苯并[a]芘(B[a]P)腹腔内单次给药,通过将[14C]乳清酸掺入核RNA来测量,结果显示肝脏的总体转录在早期(2小时)受到抑制。这种抑制在B[a]P给药后2至4天逐渐逆转,转变为部分刺激,随后在7天出现另一段抑制期,并持续至14天。通过使用来自处理过的大鼠的分离细胞核进行体外转录研究,进一步探究了2小时时的早期可逆抑制。结果观察到,RNA聚合酶活性的总体表达仅受到轻微抑制,因为虽然RNA聚合酶II和III的表达显示出显著抑制,但RNA聚合酶I的活性却表现出刺激作用。