大鼠亚慢性暴露于铅或锌对离体输精管α -肾上腺素受体介导的收缩反应的影响。

V Mutafova-Yambolieva, D Staneva-Stoytcheva, L Lasova, R Radomirov
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摘要

研究了亚慢性(30 d)饮水暴露大鼠单独或联合暴露于ZnSO4或Pb(CH3COO)2对离体输精管肾上腺素能介导的收缩反应的影响。锌暴露后,α 1、α 2-肾上腺素受体激动剂去甲肾上腺素(NA)和α 1-肾上腺素受体激动剂1-苯肾上腺素(1- phe)的收缩作用减弱,而铅暴露或铅加锌暴露后则无变化。与对照组相比,在所有金属处理的制备中,电场电刺激(FES, 0.1 Hz, 1 msec, 80 V)的收缩反应幅度减小。在铅处理和锌处理的制剂中,育亨宾诱导的可定抑制收缩的恢复在FES反应中都有所降低,育亨宾的EC50在对照制剂中为0.018 +/- 0.001微米,在铅处理的制剂中为0.073 +/- 0.019微米,在锌处理的制剂中为0.056 +/- 0.021微米。钙通道阻滞剂维拉帕米在低浓度时可抑制大鼠锌暴露制剂中fes诱导的收缩反应,在高浓度时可增加fes诱导的收缩反应。累积应用尼群地平对fes诱导的收缩的抑制作用在铅和锌处理的大鼠平滑肌中都有所增加,但在铅加锌处理的大鼠制剂中没有改变。因此,亚慢性暴露于亚毒性剂量的铅或锌导致离体输精管肾上腺素能介导的收缩力的不同变化。铅加锌暴露后,未观察到锌暴露引起的变化。所有这些发现可能具有药理、毒理学或临床意义。
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Effects of subchronic exposure of rats to lead or zinc on alpha-adrenoceptor-mediated contractile responses in isolated vas deferens.

The effects of subchronic (30 days) drinking water exposure of rats to ZnSO4 or Pb(CH3COO)2 alone or in combination on the adrenergically-mediated contractile responses of isolated vas deferens were studied. The contractile effects of the alpha 1, alpha 2-adrenoceptor agonist noradrenaline (NA) and to the alpha 1-adrenoceptor agonist 1-phenylephrine (1-PhE) were decreased after zinc exposure, whereas after lead exposure or lead plus zinc exposure they were not changed. The contractile responses to field electrical stimulation (FES, 0.1 Hz, 1 msec, 80 V) were diminished in amplitude in all metal-treated preparations as compared to controls. The yohimbine-induced restoration of the clonidine inhibited contractions in response to FES was decreased in both lead- and zinc-treated preparations, the EC50 for yohimbine being 0.018 +/- 0.001 microM in control preparations, 0.073 +/- 0.019 microM in lead-treated preparations and 0.056 +/- 0.021 microM in zinc-treated preparations. The calcium-channel blocker verapamil was found to inhibit at low concentrations and to increase at higher concentrations the FES-induced contractile responses in preparations from zinc-exposed rats. The inhibitory effect of cumulatively applied nitrendipine on the FES-induced contractions was increased in both lead- and zinc-treated smooth muscles, but was not altered in the preparations from lead plus zinc-treated rats. Therefore, subchronic exposure to subtoxic doses of lead of zinc led to different changes in the adrenergically-mediated contractility of isolated vas deferens. The changes induced by zinc exposure were not observed after lead plus zinc exposure. All these findings might be of pharmacological, toxicological or clinical importance.

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