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心脏作为2,3,7,8-四氯二苯并对二恶英毒性作用的靶器官:β-肾上腺素能反应性降低及细胞内钙增加的证据

Heart as a target organ in 2,3,7,8-tetrachlorodibenzo-p-dioxin toxicity: decreased beta-adrenergic responsiveness and evidence of increased intracellular calcium.

作者信息

Canga L, Levi R, Rifkind A B

机构信息

Department of Pharmacology, Cornell University Medical College, New York, NY 10021.

出版信息

Proc Natl Acad Sci U S A. 1988 Feb;85(3):905-9. doi: 10.1073/pnas.85.3.905.

Abstract

The heart has not been regarded as a major target organ of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) toxicity notwithstanding that lethal cardiac dysfunction can occur in the absence of histopathological changes. To assess possible TCDD cardiotoxicity, we studied the effect of TCDD five days after treatment (10 micrograms/kg of body weight; single dose given i.p. in corn oil) on the contractility of guinea pig right ventricular papillary muscle. Controls were treated with corn oil. TCDD treatment significantly decreased beta-adrenergic responsiveness. In papillary muscles from TCDD-treated guinea pigs, the positive inotropic effect of isoproterenol (0.03-0.3 microM) was decreased by a mean of 65% (P less than 0.001), and the enhancement in the velocity of relaxation was 60% less than in the controls (P less than 0.05). On the other hand, TCDD treatment did not alter the positive inotropic effect of lower concentrations of isoproterenol (0.1-10 nM). After TCDD, responsiveness to low-frequency stimulation (0.1 and 0.25 Hz) was enhanced, responsiveness to increases in extracellular Ca2+ concentration was attenuated, and isoproterenol-elicited aftercontractions in K+-depolarized preparations were increased in magnitude. Collectively, the latter findings suggest that in addition to decreasing beta-adrenergic responsiveness, TCDD increases the intracellular Ca2+ concentration in papillary muscle. Finally, slow Ca2+ channels were not blocked after TCDD treatment, inasmuch as isoproterenol restored contractility equally effectively in K+-depolarized TCDD-treated and control papillary muscles. Our findings indicate that TCDD causes a specific pattern of cardiac dysfunction in a mammalian species, selectively augmenting or decreasing different cardiac responses. The cardiac changes are consistent with reported membrane effects of TCDD; further, they suggest that the heart may be a major target organ for TCDD toxicity.

摘要

尽管在没有组织病理学变化的情况下可能会发生致命的心脏功能障碍,但心脏尚未被视为2,3,7,8-四氯二苯并对二恶英(TCDD)毒性的主要靶器官。为了评估TCDD可能的心脏毒性,我们研究了处理后五天(10微克/千克体重;腹腔注射单剂量于玉米油中)TCDD对豚鼠右心室乳头肌收缩性的影响。对照组用玉米油处理。TCDD处理显著降低了β-肾上腺素能反应性。在TCDD处理的豚鼠的乳头肌中,异丙肾上腺素(0.03 - 0.3微摩尔)的正性肌力作用平均降低了65%(P < 0.001),舒张速度的增强比对照组少60%(P < 0.05)。另一方面,TCDD处理并未改变较低浓度异丙肾上腺素(0.1 - 10纳摩尔)的正性肌力作用。TCDD处理后,对低频刺激(0.1和0.25赫兹)的反应性增强,对细胞外Ca2+浓度增加的反应性减弱,并且在K+去极化制剂中异丙肾上腺素引发的后收缩幅度增加。总的来说,后一组发现表明,除了降低β-肾上腺素能反应性外,TCDD还增加了乳头肌中的细胞内Ca2+浓度。最后,TCDD处理后慢Ca2+通道未被阻断,因为异丙肾上腺素在K+去极化的TCDD处理的和对照乳头肌中同样有效地恢复了收缩性。我们的发现表明,TCDD在哺乳动物物种中引起特定模式的心脏功能障碍,选择性地增强或降低不同的心脏反应。心脏变化与报道的TCDD的膜效应一致;此外,它们表明心脏可能是TCDD毒性的主要靶器官。

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