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金黄色罗非鱼(硬骨鱼纲)肾间组织对促肾上腺皮质激素反应的有机氯抑制作用

Suppression by organochlorines of the response to adrenocorticotrophin of the interrenal tissue in Sarotherodon aureus (Teleostei).

作者信息

Ilan Z, Yaron Z

出版信息

J Endocrinol. 1980 Nov;87(2):185-93. doi: 10.1677/joe.0.0870185.

Abstract

Superfused interrenal tissue of Sarotherodon aureus responded to ACTH with increased release of cortisol. The response to ACTH of interrenal tissue taken from fish treated with the organochlorine insecticide 1,1-dichloro-2-(o-chlorophenyl)-2-(p-chlorophenyl) ethane (o,p-DDD; 50 mg/kg) in vivo was almost totally abolished. Lower doses were less effective. The response was also suppressed by exposure in vitro of the interrenal tissue to the organochlorine; there seemed to be a dose-response to o,p-DDD over the range of 0.023 to 1 mg/l. Also 1,1-dichloro-2,2-bis (p-chlorophenyl) ethylene (p,p'-DDE) was effective in suppressing the response to ACTH at concentrations of 50--150 mg/l; 1,1,1-trichloro-2,2-bis (p-chlorophenyl) ethane (p,p'-DDT) or the polychlorinated biphenyl, Aroclor 1254, were ineffective at 50 mg/l. No suppressive effect of o,p-DDD on output of cortisol could be detected in superfusion when N6,O2'-dibutyryl cyclic AMP (20 mmol/L) was substituted for ACTH. This may indicate that the interference of o,p-DDD with the interrenal response to ACTH results from an interruption in the generation of cyclic AMP.

摘要

金黄色罗非鱼的肾上腺组织在受到促肾上腺皮质激素(ACTH)刺激时,皮质醇释放量会增加。从经体内注射有机氯杀虫剂1,1-二氯-2-(邻氯苯基)-2-(对氯苯基)乙烷(o,p-DDD;50毫克/千克)处理的鱼身上获取的肾上腺组织,对ACTH的反应几乎完全消失。较低剂量的效果较差。肾上腺组织在体外暴露于该有机氯时,其反应也受到抑制;在0.023至1毫克/升的范围内,似乎存在对o,p-DDD的剂量反应。此外,1,1-二氯-2,2-双(对氯苯基)乙烯(p,p'-DDE)在浓度为50 - 150毫克/升时可有效抑制对ACTH的反应;1,1,1-三氯-2,2-双(对氯苯基)乙烷(p,p'-DDT)或多氯联苯Aroclor 1254在50毫克/升时无效。当用N6,O2'-二丁酰环磷酸腺苷(20毫摩尔/升)替代ACTH进行灌流时,未检测到o,p-DDD对皮质醇输出有抑制作用。这可能表明o,p-DDD对肾上腺对ACTH反应的干扰是由于环磷酸腺苷生成的中断所致。

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