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首页> 外文期刊>Archives of Toxicology >Biochemical changes in Achilles tendon from juvenile dogs after treatment with ciprofloxacin or feeding a magnesium-deficient diet.
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Biochemical changes in Achilles tendon from juvenile dogs after treatment with ciprofloxacin or feeding a magnesium-deficient diet.

机译:环丙沙星治疗或缺镁饮食后幼犬的跟腱生物化学变化。

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Quinolones are antibacterial agents that have the potential to induce Achilles tendon disorders - such as tendinitis or even ruptures - in patients treated with these drugs. We studied the effects of ciprofloxacin on several proteins of Achilles tendons from immature dogs, 10- to 11-weeks-old. The dogs were treated orally for 5 days with 30 or 200 mg ciprofloxacin/kg body weight or with the vehicle alone. Since quinolone-like alterations in joint cartilage were observed in magnesium-deficient animals, another group was fed a magnesium-deficient diet for 6 weeks. At necropsy, tendons (n=3 from each group) were frozen and stored until analysis when they were homogenized in a lysis buffer to release a soluble fraction of the tendon proteins. Densitometric analysis of the immunoblots with anticollagen type I, anti-elastin, anti-fibronectin, and antiintegrin antibodies showed a significant reduction of all proteins. For example, collagen type I concentrations (mean +/-SD, arbitrary densitometric units) were 3190+/-217 (controls), 1890+/-468 (30mg/kg), 1695+/-135 (200mg/kg) and 2053+/-491 in the magnesium-deficient dogs. The differences between concentrations in controls and all treated groups were statistically significant (P<0.01, t-test). Similarly, compared with control samples, relative concentrations of other proteins in tendons from ciprofloxacin-treated dogs (30 mg/kg) decreased by 73% (elastin), 88% (fibronectin), and 96% (beta1 integrin) (data from low-dose group only). A very similar pattern of protein alterations was detected in samples from magnesium-deficient dogs. In conclusion, rather low doses of a fluoroquinolone or a diet-induced magnesium deficiency caused similar biochemical alterations in the soluble fraction of proteins from canine tendons. These findings support our hypothesis that quinolone-induced toxic effects on connective tissue structures are due to the magnesium-antagonistic effects of these antibacterial agents. They also indicate that patients with a latent magnesium deficiency could be at an increased risk of quinolone-induced tendon disorders.
机译:喹诺酮类药物是可能在用这些药物治疗的患者中诱发跟腱疾病(如肌腱炎甚至破裂)的抗菌剂。我们研究了环丙沙星对10至11周大的未成熟狗的跟腱蛋白的影响。用30或200mg环丙沙星/ kg体重或单独用赋形剂对狗进行口服治疗5天。由于在缺镁动物中观察到关节软骨样喹诺酮样变化,因此另一组饲喂缺镁饮食6周。尸检时,将肌腱(每组n = 3)冷冻并保存,直到分析时将它们在裂解缓冲液中匀浆以释放肌腱蛋白的可溶部分。用I型抗胶原蛋白,抗弹性蛋白,抗纤连蛋白和抗整联蛋白抗体进行的免疫印迹光密度分析表明,所有蛋白质均显着减少。例如,I型胶原蛋白浓度(平均值+/- SD,任意光密度单位)为3190 +/- 217(对照),1890 +/- 468(30mg / kg),1695 +/- 135(200mg / kg)和缺镁狗中的2053 +/- 491。对照组和所有治疗组之间的浓度差异具有统计学意义(P <0.01,t检验)。同样,与对照样品相比,环丙沙星治疗的狗(30 mg / kg)的肌腱中其他蛋白质的相对浓度分别降低了73%(弹性蛋白),88%(纤连蛋白)和96%(β1整合素)(数据来自-剂量组)。在缺镁狗的样本中检测到非常相似的蛋白质变化模式。总之,相当低剂量的氟喹诺酮或饮食引起的镁缺乏会导致犬肌腱蛋白质的可溶性部分发生类似的生化变化。这些发现支持了我们的假设,即喹诺酮对结缔组织结构的毒性作用是由于这些抗菌剂的镁拮抗作用所致。他们还表明,潜在的镁缺乏症患者可能会增加喹诺酮引起的肌腱疾病的风险。

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