Ilan Z, Yaron Z
J Endocrinol. 1980 Nov;87(2):185-93. doi: 10.1677/joe.0.0870185.
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.
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。