Lucesoli F, Caligiuri M, Roberti M F, Perazzo J C, Fraga C G
School of Pharmacy and Biochemistry, University of Buenos Aires, Buenos Aires, Argentina.
Arch Biochem Biophys. 1999 Dec 1;372(1):37-43. doi: 10.1006/abbi.1999.1476.
This study describes the in vivo response of rat testes to acute iron overload. Male Wistar rats (250-300 g) were injected ip with iron dextran at doses of 250 (Fe250), 500 (Fe500), or 1000 mg/kg body wt (Fe1000) or with saline (C). Parameters of oxidative stress and iron toxicity were measured 20 h after injection. Total iron content was 3.5-, 5.3-, and 10.4-fold higher in the Fe250, Fe500, and Fe1000 groups, respectively, compared to controls (320 +/- 22 nmol/g tissue). Histological studies showed that: (a) iron accumulated in the sperm and other testes cells, and (b) spermatogenesis was markedly lower in the Fe1000 group. The concentration of alpha-tocopherol, ubiquinol-9, and ubiquinol-10 in the testes was inversely correlated with the extent of oxidation. Testes chemiluminescence was 45% higher in the Fe1000 group compared to controls (41 cps/cm(2)). Endogenous levels of lipid oxidation, evaluated as 2-thiobarbituric acid-reactive substances, were 46, 73, and 82% higher in the groups Fe250, Fe500, and Fe1000, respectively, than in controls (33.6 +/- 1.4 nmol/g tissue). Oxidative damage to DNA evaluated by the presence of 8-oxo-2'-deoxyguanosine (oxo(8)dG), was 26, 39, and 74% higher in the Fe250, Fe500, and Fe1000 groups, respectively, than in the C group (2.3 +/- 0.1 oxo(8)dG/10(5)dG). Protein oxidation was measured as protein thiols and carbonyl content in proteins and glutamine synthase activity. Protein thiols content and glutamine synthase activity were similar in all the groups, while the protein-associated carbonyls content was 96% higher in the Fe1000 group than in the C group (2.1 +/- 0.4 nmol/mg protein). No changes in the activities of superoxide dismutase, catalase, and glutathione peroxidase were observed. The results showed that in vivo iron overload induced oxidative stress and the impairment of spermatogenesis in rat testes that were dependent on the amount of iron supplemented and its accumulation in the tissue.
本研究描述了大鼠睾丸对急性铁过载的体内反应。将雄性Wistar大鼠(250 - 300 g)腹腔注射右旋糖酐铁,剂量分别为250(Fe250)、500(Fe500)或1000 mg/kg体重(Fe1000),或注射生理盐水(C)。注射后20小时测量氧化应激和铁毒性参数。与对照组(320±22 nmol/g组织)相比,Fe250、Fe500和Fe1000组的总铁含量分别高出3.5倍、5.3倍和10.4倍。组织学研究表明:(a)铁在精子和其他睾丸细胞中积累,(b)Fe1000组的精子发生明显降低。睾丸中α - 生育酚、泛醇 - 9和泛醇 - 10的浓度与氧化程度呈负相关。Fe1000组的睾丸化学发光比对照组高45%(41 cps/cm²)。以内源性脂质氧化产物2 - 硫代巴比妥酸反应性物质评估,Fe250、Fe500和Fe1000组的水平分别比对照组(33.6±1.4 nmol/g组织)高46%、73%和82%。通过8 - 氧代 - 2'-脱氧鸟苷(oxo(8)dG)的存在评估的DNA氧化损伤,Fe250、Fe500和Fe1000组分别比C组高26%、39%和74%(2.3±0.1 oxo(8)dG/10⁵dG)。蛋白质氧化通过蛋白质硫醇和蛋白质中的羰基含量以及谷氨酰胺合成酶活性来测量。所有组的蛋白质硫醇含量和谷氨酰胺合成酶活性相似,而Fe1000组与蛋白质相关的羰基含量比C组高96%(2.1±0.4 nmol/mg蛋白质)。未观察到超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶活性的变化。结果表明,体内铁过载诱导大鼠睾丸氧化应激和精子发生受损,这取决于补充铁的量及其在组织中的积累。