首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Jejunal transfer rates of 109cadmium chloride increase in rats in vitro and in vivo after oral pretreatment with cadmium or zinc chloride.
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Jejunal transfer rates of 109cadmium chloride increase in rats in vitro and in vivo after oral pretreatment with cadmium or zinc chloride.

机译:口服镉或氯化锌预处理后,大鼠体内外的109氯化镉的空肠转移速率增加。

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An increased body retention of Cd in rats orally pretreated with Cd or Zn is explained by induction of hepatic and renal metallothionein. Whether intestinal absorption of Cd increases after such treatments is not clear yet. To approach this problem we measured jejunal transfer rates of 109Cd in vitro and in vivo in pretreated rats (0.44 mmol Cd/l or 4.6 mmol Zn/l in the drinking water for 10 days) and compared them with those of untreated controls. Isolated jejunal segments were used for in vitro perfusion. In vivo perfusion was performed in anaesthetized rats with blood collected from mesenteric venules substituting corresponding losses by reinfusion of rat blood. Water and glucose transfer did not differ between controls and pretreated rats. At a luminal concentration of 5 micromol 109CdCl2/l, Cd and Zn pretreatment significantly increased the transfer rate of 109Cd in vitro and in vivo similarly. The 109Cd transfer rates in controls in the final perfusion intervals (80-120 min) were 0.06 (pmol/cm/min) in vivo and 0.05 in vitro; the corresponding rates in Cd or Zn pretreated rats were significantly higher (P<0.05) and amounted to 0.11 and 0.18 or 0.15 and 0.23, respectively. Mucosal concentrations of 109Cd measured at the end of the perfusion period tended to be lower in the pretreated animals than in the controls. This suggests that pretreatment with Cd or Zn reduces the amount of 109Cd bound to the tissue leaving more 109Cd for the transfer step. As compared to a level of mucosal metallothionein of 8 microg/g wet weight in controls, increased amounts of 67 or 52 microg/g wet weight in the Cd or Zn pretreated rats, respectively, thus did not decrease but increased transfer rates of 109Cd. Therefore, increased small intestinal transfer rates of Cd can contribute to increase the body retention of Cd seen after oral pretreatment with Cd or Zn.
机译:通过诱导肝和肾金属硫蛋白可以解释口服Cd或Zn预处理的大鼠体内Cd保留量的增加。在这种治疗后,肠道对镉的吸收是否增加尚不清楚。为了解决这个问题,我们测量了预处理大鼠在体外和体内109Cd的空肠转移速率(饮用水中0.44 mmol Cd / l或4.6 mmol Zn / l 10天),并将其与未处理的对照组进行比较。分离的空肠段用于体外灌注。在麻醉的大鼠中进行体内灌注,用从肠系膜小静脉收集的血液代替通过再灌注大鼠血液而产生的相应损失。对照和预处理大鼠之间的水和葡萄糖转移没有差异。腔内浓度为5微摩尔109CdCl2 / l时,Cd和Zn预处理在体内和体外均显着提高了109Cd的转移速率。最终灌注间隔(80-120分钟)中对照组的109 Cd转移速率在体内为0.06(pmol / cm / min),在体外为0.05;镉或锌预处理大鼠的相应比率显着更高(P <0.05),分别为0.11和0.18或0.15和0.23。在灌注期结束时测得的粘膜浓度109Cd在预处理动物中往往低于对照组。这表明用Cd或Zn预处理会减少与组织结合的109Cd的量,从而为转移步骤留下更多的109Cd。与对照组中粘膜金属硫蛋白的湿重为8微克/克湿重的水平相比,在Cd或Zn预处理的大鼠中分别增加了67或52微克/克湿重的量,因此没有降低,但增加了109Cd的转移速率。因此,在口服Cd或Zn预处理后,增加的Cd小肠转移速率有助于增加Cd的体内滞留率。

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