Friedman L, Gaines D W, Alleva F R, Seidler F J, Flynn T J, Slotkin T A, Balazs T
Toxicol Ind Health. 1986 Sep;2(2):57-68. doi: 10.1177/074823378600200207.
Sprague-Dawley male and female rats were treated with 6-mercaptopurine (6-MP) (2 mg/kg sc) daily from 2 to 22 days of age and killed at 7, 15, 27 and 64 days of age. At 7 and 27 days of age rats were injected with 3H thymidine for measurement of DNA synthesis. Fore- and hindlimb muscles were removed and analyzed for ornithine decarboxylase (ODC) activity (all ages), DNA radioactivity (7 and 27 days), DNA level (27 and 64 days) and RNA level (64 days). As expected, ODC activity and DNA synthesis were higher in muscles of 7-day-old rats than in muscles of the older rats studied. A consistently lower ODC activity was seen in 6-MP-treated vs. control rats for 5-25 days after start of treatment, but the effect was essentially the same for the hindlimb and forelimb muscles. During the 7-27-day time course ODC activity was higher in hindlimb than forelimb muscles. By 27 days of age DNA synthesis was also higher in the hindlimb muscles. DNA synthesis was decreased after 5 days of treatment relative to that of control rats, to an approximately equal extent in forelimb and hindlimb muscles. Five days after the last treatment a trend was seen for slower recovery from inhibition of DNA synthesis in hindlimb muscles, particularly in male rats. DNA levels were reduced in treated rats relative to those in control rats 5 days after the last treatment to approximately the same degree in forelimb and hindlimb muscles. Forty-two days after the last treatment a trend toward increased activity of ODC and increased DNA and RNA levels was seen in muscles of treated rats, probably reflective of recovery processes. These early biochemical effects of 6-MP, which were seen to about the same extent in the forelimb and hindlimb muscles cannot explain by themselves the delayed hindlimb fat atrophy resulting from 6-MP treatment of neonatal rats.
将2至22日龄的Sprague-Dawley雄性和雌性大鼠每天皮下注射6-巯基嘌呤(6-MP)(2mg/kg),并在7、15、27和64日龄时处死。在7和27日龄时,给大鼠注射3H胸腺嘧啶核苷以测量DNA合成。切除前肢和后肢肌肉并分析鸟氨酸脱羧酶(ODC)活性(所有年龄段)、DNA放射性(7和27日龄)、DNA水平(27和64日龄)以及RNA水平(64日龄)。如预期的那样,7日龄大鼠肌肉中的ODC活性和DNA合成高于所研究的老年大鼠肌肉。在开始治疗后5至25天,6-MP处理的大鼠与对照大鼠相比,ODC活性持续较低,但后肢和前肢肌肉的效果基本相同。在7至27日龄期间,后肢肌肉中的ODC活性高于前肢肌肉。到27日龄时,后肢肌肉中的DNA合成也更高。与对照大鼠相比,治疗5天后DNA合成减少,前肢和后肢肌肉减少程度大致相同。最后一次治疗5天后,后肢肌肉中DNA合成抑制后的恢复趋势较慢,尤其是雄性大鼠。最后一次治疗5天后,与对照大鼠相比,处理大鼠的DNA水平降低,前肢和后肢肌肉降低程度大致相同。最后一次治疗42天后,处理大鼠的肌肉中ODC活性增加以及DNA和RNA水平增加的趋势,这可能反映了恢复过程。6-MP的这些早期生化效应在前肢和后肢肌肉中出现的程度大致相同,但其本身无法解释新生大鼠6-MP治疗导致的后肢脂肪萎缩延迟现象。