Koçtürk Semra, Oktay Gülgün, Güner Gül, Pekçetin Cetin, Güre Ataman
Biochemistry Department, Faculty of Medicine, Dokuz Eylul University, Turkey.
Cell Biochem Funct. 2006 Mar-Apr;24(2):167-72. doi: 10.1002/cbf.1209.
This study was designed to clarify the effects of D-penicillamine (DPA), a drug used for treatment of various pathological events, on lung elastin formation and maturation of the newborn in the perinatal period. The investigation was conducted on 20 newborn rats bred from 40 female and six male rats. DPA doses 400 mg kg(-1) day(-1) and physiological saline were given intraperitoneally (i.p) to experimental and control groups. To assess newborn maturation, their body and lung weights were determined. Serum Cu levels were measured by atomic absorption spectroscopy and ceruloplasmin (Cp) activities were measured spectrophotometrically. Newborn lung tissue elastin, desmosine (DES) and isodesmosine (IDES) levels were measured by HPLC. The results showed that DPA treatment caused loss of skin elasticity and reduction in body and lung weight in newborns of the experimental group. The serum Cu levels and Cp activity were found to be significantly lower in both maternal and newborn of the experimental groups compared with the control group. The lung DES, IDES and elastin values of newborns in the experimental group were decreased compared with the control group. In conclusion, our results indicate that 400 mg kg(-1) day(-1) DPA, a dose that is used in the treatment of Wilson's disease, rheumatoid arthritis and cystinuria, caused the retardation of newborn maturation, a decrease in DES-IDES cross-links and levels of lung elastin of offspring in the perinatal period. Another conclusion to be drawn from this study is that even low levels of Cu depletion due to DPA administration induces a change in cross-linking in lung elastin during the perinatal period.
本研究旨在阐明用于治疗各种病理情况的药物 D-青霉胺(DPA)对围产期新生鼠肺弹性蛋白形成和成熟的影响。对由 40 只雌鼠和 6 只雄鼠繁育的 20 只新生大鼠进行了研究。分别向实验组和对照组腹腔注射 400 mg kg(-1) day(-1) 的 DPA 剂量和生理盐水。为评估新生鼠的成熟情况,测定了它们的体重和肺重。采用原子吸收光谱法测定血清铜水平,用分光光度法测定铜蓝蛋白(Cp)活性。通过高效液相色谱法测定新生鼠肺组织弹性蛋白、锁链素(DES)和异锁链素(IDES)水平。结果显示,DPA 处理导致实验组新生鼠皮肤弹性丧失,体重和肺重减轻。与对照组相比,实验组母鼠和新生鼠的血清铜水平和 Cp 活性均显著降低。实验组新生鼠的肺 DES、IDES 和弹性蛋白值与对照组相比有所下降。总之,我们的结果表明,用于治疗威尔逊病、类风湿性关节炎和胱氨酸尿症的 400 mg kg(-1) day(-1) DPA 剂量,导致围产期新生鼠成熟迟缓,后代肺弹性蛋白的 DES-IDES 交联和水平降低。本研究得出的另一个结论是,即使由于给予 DPA 导致的低水平铜缺乏,也会在围产期引起肺弹性蛋白交联的变化。